Registrant Actions - 2011
[Federal Register Volume 76, Number 168 (Tuesday, August 30, 2011)]
[Notices]
[Pages 53942-53961]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-22093]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. 09-33]
Richard A. Herbert, M.D.; Decision and Order
On June 15, 2010, Administrative Law Judge (ALJ) Mary Ellen Bittner
issued the attached recommended decision. Thereafter, Respondent filed
Exceptions to the ALJ's decision.
Having reviewed the entire record including Respondent's
Exceptions, I have decided to adopt the ALJ's rulings, findings of
fact, conclusions of law, and recommended Order except as expressly set
forth below.\1\
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\1\ Pursuant to 5 U.S.C. 552(a)(2), the ALJ's recommended
decision has been edited to eliminate the names of various persons
who were either witnesses or were referred to in the proceeding. All
citations to the ALJ's decision are to the slip opinion attached to
this Decision and Order.
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In his Exceptions, Respondent raises several issues. First,
Respondent argues that he "was irreparably harmed" because he was
forced to represent himself "pro se" after the ALJ granted his
previous attorney's motion to withdraw but did not grant his motion for
a continuance of the hearing to allow him to obtain new counsel.\2\
Exc. at 6-7. Respondent argues that his previous attorney had requested
that he "be given leave of 21 days to obtain new counsel," and that
"[t]he ALJ mistakenly assumed that the attorney and Respondent were
not asking for a delay of the hearing" and did not grant a continuance
in her October 13, 2009 order. Id. at 7. Respondent further asserts
that the ALJ "unfairly denied a continuance" and that he "must be
given a fair hearing with representation for a proper outcome in this
matter." Id. at 10.
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\2\ Respondent does not, however, contend that the ALJ erred in
granting the motion to withdraw. See Resp. Exc. at 6-10.
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The record establishes that on October 9, 2009, Respondent's prior
counsel filed a motion for leave to withdraw; in his motion,
Respondent's prior counsel "further requested that Respondent be given
leave of twenty-one (21) days to secure new counsel." ALJ Ex. 5. On
October 13, 2009, the ALJ granted the motion to withdraw. Id. However,
the ALJ found "it unnecessary to provide leave of twenty-one (21) days
for Respondent to secure new counsel * * * as Respondent is free to
retain counsel at any time." Id. The ALJ further ordered that "the
hearing in this matter, scheduled to begin on November 3, 2009, shall
proceed as scheduled." Id. A copy of this ruling was served on
Respondent by Federal Express. Id. In addition, the following day, the
ALJ's law clerk wrote Respondent noting that it appeared that he was no
longer represented by counsel and calling his attention to his "right
to be represented by an attorney"; the letter also included verbatim
the language of 21 CFR 1316.50, which addresses a party's right to
representation. ALJ Ex. 6. The letter further advised Respondent that
he could contact the ALJ's law clerk if he had any questions. Id.
At the hearing, Respondent argued that his prior counsel had sought
a continuance of twenty-one days. Tr. 11. However, the ALJ noted that
Respondent's prior attorney "did not ask for a postponement of the
hearing" and that he had simply requested that Respondent "be given
leave of 21 days to secure new counsel." Id. at 12-13. Respondent
replied that his prior lawyer's intent was "to get [him] time"
because "we have blocked out four days" for the hearing, and no
"major league attorney is going to have four days [open] on his
calendar," having been notified approximately three weeks before the
hearing date. Id. at 13. The ALJ responded that she did not
[[Page 53943]]
know what Respondent's prior lawyer had "intended," but only "what
he asked for." Id. Respondent then stated that he understood, and that
ALJ "ha[d] made [her] ruling." Id. The ALJ then proceeded to conduct
the hearing.
I conclude that the ALJ did not abuse her discretion in proceeding
to conduct the hearing. Whatever the intent of Respondent's counsel was
in asking for "leave * * * to secure new counsel," Respondent had at
least three weeks between his prior attorney's moving to withdraw and
the commencement of the hearing to find new counsel. While it may be
the case that most capable attorneys would not have four days clear on
their calendar on three weeks' notice, it is not as if Respondent had
secured new counsel who, because his calendar was not clear, sought a
continuance, which was denied. Indeed, it is notable that at the
hearing, Respondent made no claim that he had actually contacted any
attorney, let alone that an attorney had declined to represent him
because the attorney had a scheduling conflict. I therefore reject
Respondent's exception and conclude that he is not entitled to a new
hearing.
Respondent takes further exception to the ALJ's conclusion that the
OxyContin prescriptions he issued to E.M. lacked "a legitimate medical
purpose" and that he "was at least reckless or negligent in ignoring
the warning signs of diversion." Exc. at 10-16. Respondent raises a
number of contentions regarding the weight the ALJ gave to the
testimony of various witnesses and exhibits; Respondent also notes that
after the Agency's hearing, the Illinois Department of Financial and
Professional Regulation (IDFPR) held a hearing on the same allegations
and "found that the State did not prove that any diversion occurred."
Id. at 15.
Having reviewed each of these contentions, I concluded that a
preponderance of the evidence supports the ALJ's conclusions that the
OxyContin prescriptions which Respondent issued in the name of E.M.
were issued outside of the "usual course of * * * professional
practice" and lacked "a legitimate medical purpose" and therefore
violated the CSA. 21 CFR 1306.04(a). The evidence shows that beginning
in September 2003, Respondent prescribed 60 tablets of Oxycontin 80 mg.
(BID, twice a day), to E.M., who was then 93 years old, on a monthly
basis through May 2009, one month before her death. RX 16. Yet on
various occasions throughout this period, E.M. was an in-patient in
either a hospital or nursing home. See GX 42. Moreover, E.M. was under
hospice care from June 9 through October 11, 2006; December 8, 2006
through June 1, 2007; and from July 11, 2007 through the date of her
death.
According to the testimony of a hospice nurse who treated E.M. for
between eight months to a year, under the hospice agreement, E.M.'s
family was required to disclose whether any other physicians were
treating her. Tr. 35, 38. In addition, the testimony established that
the hospice was required to know what medications E.M. was taking. Id.
at 35. As the hospice nurse explained, a doctor would need to
communicate with hospice what drugs he was prescribing so that
contraindicated drugs were not prescribed by another doctor. Id. at 65.
Yet E.M.'s family, including her son I.S., who was a long-standing
friend of Respondent and who also received the same monthly
prescriptions for 60 tablets of OxyContin 80 mg (see id. at 686) and
filled his mother's prescriptions (id. at 690), did not disclose to the
hospice either that E.M. was being treated by Respondent or that she
was taking OxyContin 80 mg. Id. at 66. According to the hospice nurse,
the only controlled substance she was aware of being prescribed to E.M.
was Valium. Id. at 35. Moreover, on those occasions when the hospice
nurse determined that E.M. needed some medicine for her arm or knee
pain, I.S. told the hospice nurse that Tylenol (acetaminophen, a non-
controlled drug) worked for his mother and that his mother could not
handle stronger medicine. Id. at 65.
The Government also called as a witness Dr. S.D., a specialist in
internal medicine who was E.M.'s primary care physician for the last
four years of her life, including when she was in hospice. Id. at 72,
76. According to Dr. S.D., E.M. had lower back pain, shoulder and knee
pain, for which he prescribed Tylenol or Darvocet. Id. at 89-90.
However, she did not require constant medication, and he never
prescribed OxyContin 80 mg, which he considered to be "too strong for
her." Id. at 91-92. While Dr. S.D. once prescribed Vicodin to E.M.
upon her discharge from the hospital, GX 21, at 31; he did not
prescribe Vicodin to her on a monthly basis. Tr. 143.
While Dr. S.D. talked with I.S.'s live-in girlfriend regarding
E.M.'s condition, he further testified that he was never told that
Respondent was prescribing OxyContin to her. Id. at 92, 95, 109, 141-
42. Moreover, the hospice nurse never told him that E.M. was seeing
another doctor and never listed OxyContin as one of her medications.
Id. at 96, 102. Dr. S.D. further testified that if E.M. had, in fact,
been taking two OxyContin 80 mg each day and had stopped (as when she
was in the hospital), she would have undergone "severe withdrawal,"
including such symptoms as abdominal pain, diarrhea, and vomiting. Id.
at 105-06. Dr. S.D. also testified that when a patient is hospitalized,
a family member is not allowed to give the patient medication. Id. at
107. There was, however, no evidence that E.M. underwent withdrawal
during any of the various occasions when she was hospitalized. Id. at
106, 143-44.
Dr. S.D. further testified that because he was E.M.'s primary care
physician, Respondent had "the legal responsibility to send [him] a
consult that [Respondent was] treating her for pain and prescribing"
OxyContin 80 mg to her. Id. at 140. Dr. S.D. testified that if doctors
do not coordinate their prescribing to a patient, the patient could
overdose. Id. at 144. Dr. S.D. then testified that it is outside of the
normal course of medical practice for a physician, who is aware that a
patient is being treated by another physician, to prescribe drugs and
fail to consult with the other physician.\3\ Id.
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\3\ Respondent acknowledged that he was aware that E.M. was
being treated by other doctors, and the chart he maintained on her
shows that he was aware at various points that she was a patient in
a rehab facility and a nursing home. RX 16, at 5-6. Yet he never
notified either her physicians or these facilities that he was
prescribing OxyContin to her. While Respondent maintained he did not
notify E.M.'s physicians and the facilities regarding the OxyContin
prescriptions because E.M's family did not want him to, Respondent
offered no credible explanation for why he continued to prescribe to
E.M. when he knew she was under the care of other physicians.
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As noted above, during the period in which Respondent issued the
OxyContin prescriptions in E.M.'s name, E.M. was admitted as an in-
patient to a hospital on approximately twenty occasions.\4\ See GX 42.
Yet there is no evidence that she ever underwent withdrawal. Moreover,
in the voluminous medical records entered into evidence, Respondent
points to only a single instance (involving a January 18, 2006
emergency room visit for a potential stroke (CVA)), in which the
medical records listed her medications as including OxyContin. GX 21,
at 29. If E.M. was actually taking the OxyContin, this begs the
question of why her family was so reluctant to disclose this
information (as well as Respondent's) name to the hospitals where she
was treated.
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\4\ She was also taken to the Emergency Room approximately ten
times.
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There is further evidence establishing that Respondent's
prescriptions were unlawful. The evidence shows that on November 10,
2004, E.M. was discharged from the hospital to the
[[Page 53944]]
Heritage Village Nursing Home, and that at 9:30 a.m., she was admitted
to the latter. GX 11, at 1; GX 25, at 3; GX 27A, at 70. Yet Respondent
noted in her chart that on the same day, he performed a physical exam
at which he took her blood pressure, palpated her deformities and found
that they were "not as painful," and found that her "hand grip
good," RX 16, at 4; the same day, he also issued her a prescription
for sixty OxyContin 80 mg. See GX 28, at 10. Respondent did not,
however, offer any testimony explaining how he could have performed a
physical exam on E.M. on this day.
Likewise, Respondent noted in E.M.'s chart that on November 17,
2006, her blood pressure was 138/94, she was "[d]oing surprisingly
well today," she "spoke my 1st name," and was "oriented," RX 16,
at 5; he also issued a prescription in her name for sixty OxyContin 80
mg. See GX 14, at 5. However, between October 12 and December 8, 2006,
E.M. was a patient in the Manor Care Nursing Home. GX 21, at 203; GX
27B, at 17, 956. Yet the record (including Respondent's testimony)
establishes that Respondent did not travel to the facilities E.M. was
in. Tr. 547.
The ALJ found that there were "numerous inconsistencies between
the testimonies of [I.S.] and Respondent" and that this led her "to
believe that neither is a credible witness with regard to [E.M.'s]
medication and treatment." ALJ at 54. The ALJ further noted the
extensive amount of time that E.M. was in either a hospital or nursing
home/rehab facility (approximately 290 days during the course of
Respondent's prescribing to her) and found "it difficult to believe
that [E.M.'s] family was able to administer [80 mgs of] OxyContin twice
a day for such an expansive time without ever arousing the suspicion of
the facility staff.\5\" Id. I agree and find Respondent's and I.S.'s
testimony implausible. I also agree with the ALJ's conclusion that the
record supports the conclusion that the OxyContin prescriptions
Respondent issued in the name of E.M. lacked a legitimate medical
purpose and were issued outside of the usual course of professional
practice and thus violated Federal law.\6\ 21 CFR 1306.04(a).
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\5\ Among the implausible testimony I.S. gave was that he or a
family member would take the OxyContin to his mother when she was
institutionalized and give her the drug, which was prescribed to be
taken twice a day. Tr. 685. I.S. also asserted that when he went to
his mother's various institutions, and told them that he had
"supplements [and] medications that I give my mother at home, and I
would like you to administer them, * * * they said we won't do that
* * * unless the doctor orders it. But if you want to come in
yourself, or have somebody come in and give it to your mother, we
haven't got a problem with that, and that's what I did." Id. at
692-93. However, I.S. testified that he did not tell the facilities
that he would be administering OxyContin. Id. Indeed, it seems
strange that the facilities did not ask I.S. what medications he
intended to bring into the facility, and as the ALJ found, this
testimony is patently disingenuous.
\6\ Respondent argues that DEA Investigators "could have easily
secured a blood test of [E.M.] to discern whether she was receiving
OxyContin," and that "[b]y the time Respondent realized the focus
of the investigation centered around this patient and the severity
of the charges against him, it was too late because the patient had
passed away." Exceptions at 12. Respondent further argues that
"even though OxyContin was listed as a home medication and there
was evidence that she was taking the medicine s[u]rreptitiously, Dr.
[S.D., her primary care physician,] never ordered a blood test for
opioid levels." Id. at 13. As for DEA's obligation to secure a
blood test, this is beside the point. Moreover, in his testimony,
Respondent acknowledged that "[i]n retrospect" he should have done
a blood test on E.M. to see if she was actually taking the
OxyContin. Tr. 835. However, he then attempted to shift the blame to
Dr. S.D., asking "[w]hat is [his] excuse?" Id.
Respondent ignores that he was one who prescribed 60 tablets of
OxyContin 80 mg to E.M.--which is the second strongest formulation
available and which just happened to be the same prescription that
he was giving her son--each month, and did this for a period of more
than five and a half years and did so even when he knew she was
being treated by other doctors. At a minimum, this evidence
establishes that Respondent acted with deliberate ignorance as to
the likelihood the drugs were being diverted. See Jeri Hassman,
M.D., 75 FR 8194, 8228 (2010) (citing United States v. Katz, 445
F.3d 1023, 1031 (8th Cir. 2006)).
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Respondent further points to an IDFPR Inspector's Report of an
interview he conducted with E.M. and her son on August 9, 2005. During
this interview, E.M. identified two green tablets, which were
reportedly OxyContin, and stated that they "were to combat pain." RX
10. However, earlier in the interview the Inspector had asked E.M. if
she had pain when she initially went to see Respondent and she answered
"no." Id. I.S. had objected that "the question was unfair as he felt
she did not recall." Id. Moreover, Respondent had previously diagnosed
E.M. as having "senile dementia" nearly two years earlier, RX 16, at
1; and Dr. P. (Dr. S.D.'s partner) had diagnosed E.M. as having
Alzheimer's disease and dementia in June 2005, two months prior to the
interview. Thus, there is ample reason to discount E.M.'s statement
regarding the use of the OxyContin.
Respondent also argues that after the instant hearing, the IDFPR
held a hearing on the "same underlying allegations," at which much of
the same evidence was presented; however, at the state hearing,
Respondent was also able to procure the testimony of C.S. (I.S.'s
wife). Exceptions at 15. Respondent argues that the State ALJ "found
that the State did not prove that any diversion occurred." Id.
Respondent does not, however, argue that C.S. was unavailable to
testify in the DEA proceeding and her testimony does not constitute
newly discovered evidence. Cf. ICC v. Brotherhood of Locomotive
Engineers, 482 U.S. 270, 286 (1987). As for the state ALJ's findings,
DEA was not a party to that proceeding. Moreover, this Agency has long
held that it "maintains a separate oversight responsibility [apart
from that which exists in a state board] with respect to the handling
of controlled substances and has a statutory obligation to make its
independent determination as to whether the granting of [a
registration] would be in the public interest." Mortimer B. Levin,
D.O., 55 FR 8209, 8210 (1990). Accordingly, even if Respondent had
submitted the state ALJ's decision, the state ALJ's finding would not
be entitled to collateral estoppel effect in this proceeding.\7\ Cf.
United States v. Mendoza, 464 U.S. 154 (1984). I therefore reject
Respondent's exception that the evidence in the record of this
proceeding does not demonstrate that he engaged in the diversion of
controlled substances and agree with the ALJ's conclusion that he acted
outside of the usual course of professional practice and lacked a
legitimate medical purpose when he issued OxyContin prescriptions in
E.M.'s name. 21 CFR 1306.04(a). See also George Mathew, M.D., 75 FR
66138, 66146 (2010) (under Federal law, where a physician issues a
prescription in violation of 21 CFR 1306.04(a), the drug is deemed
diverted).
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\7\ The Government also notes that in the IDFPR proceeding, the
State's burden of proof was "clear and convincing evidence," but
in this proceeding the "preponderance of the evidence" standard
applies. Gov. Resp. to Resp. Motion for Rehearing and Exceptions, at
13 (citing Tit. 68, Cp. VII, Subchapter a, Admin. Rule, Part
1110.190).
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Finally, Respondent argues that the proven allegations do not
support the revocation of his registration. Resp. Exc. at 16. Contrary
to Respondent's understanding, DEA has held that proof of a single act
of diversion is sufficient to support the revocation of a registration
and the denial of an application. See Dewey C. MacKay, 75 FR 49956,
49977 (2010); Alan H. Olefsky, 57 FR 928, 928-29 (1992) (revoking
registration based on physician's act of presenting two fraudulent
prescriptions to pharmacy for filling). The ALJ's finding that
Respondent issued prescriptions which lacked a legitimate medical
purpose is sufficient by itself to support the revocation of
Respondent's registration, especially, where, as here, the ALJ
[[Page 53945]]
found that "Respondent has repeatedly failed to accept responsibility
for his misconduct." ALJ at 44. See also Jayam Krishna-Iyer, 74 FR
459, 463 (2009) (quoting Medicine Shoppe--Jonesborough, 73 FR 364, 387
(2008) (DEA "has repeatedly held that where a registrant has committed
acts inconsistent with the public interest, the registrant must accept
responsibility for [his] actions and demonstrate that [he] will not
engage in future misconduct.")); see also Hoxie v. DEA, 419 F.3d 477,
483 (6th Cir. 2005) ("admitting fault" is "properly consider[ed]"
by DEA to be an "important factor[]" in the public interest
determination).\8\
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\8\ In concluding that Respondent has not accepted
responsibility for his misconduct, the ALJ noted that "despite my
previous rulings to the contrary, Respondent continues to assert
that most of the evidence and testimony admitted in the instant
hearing is inadmissible and should not be considered" and that he
"continues to assert that he was 'not afforded a capable attorney'
although he was at any time free to procure the assistance of
counsel [and] was notified of such." ALJ at 44 (citing Resp.
Closing Argument Br. at 10).
To make clear, that Respondent continues to object to the
admission of certain evidence and argues that he was not afforded a
capable attorney is of no relevance in determining whether he
accepts responsibility for his misconduct. I thus reject the ALJ's
reliance on Respondent's legal arguments as a basis for concluding
that he does not accept responsibility. However, the record contains
an ample evidentiary basis for concluding that Respondent does not
accept responsibility for most of his misconduct, and his
explanation of his prescribing to E.M. is utterly implausible. Thus,
I conclude that Respondent has not rebutted the Government's prima
facie case. See Hoxie, 419 F.3d at 483 (upholding Agency's reliance
on registrant's lack of candor in determining whether registration
is consistent with the public interest).
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Moreover, the ALJ found that Respondent had committed additional
acts which support the revocation of his registration, including that
he materially falsified his 2006 renewal application when he failed to
disclose the 1998 probation imposed on his state medical license by the
Illinois Department of Professional Regulation. ALJ at 43. As the ALJ
found, this was a material falsification because the underlying conduct
which gave rise to the State's order was Respondent's prescribing of
Dilaudid, a schedule II controlled substance, to four patients "under
questionable circumstances, i.e., for pain related to old injuries or
for pain in which surgery may have provided relief and that two (2) of
the patients may have sold some of the Dilaudid back to Respondent."
GX 7. This falsification was material because under the public interest
standard, DEA is required to assess an applicant's experience in
dispensing controlled substances and his record of compliance with
state and federal laws related to controlled substances. 21 U.S.C.
823(f) (2) & (4). Accordingly, Respondent's failure to disclose the
1998 probation was capable of influencing the Agency's decision as to
whether to grant his application and was a material falsification.\9\
See The Lawsons, Inc., 72 FR 74334, 74338-39 (2007) (other citations
omitted). Under the CSA, material falsification provides a separate and
independent ground for denying an application. 21 U.S.C. 824(a)(1).
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\9\ In his Exceptions, Respondent also contends that the
Agency's consideration of the 1998 Consent Order violates his right
to due process because due process "requires protection from a
never-ending time limit for the DEA to bring an action." Exceptions
at 3. Respondent, however, makes only a conclusory assertion of
prejudice. Cf. United States v. Brockman, 183 F.3d 891, 895 (8th
Cir. 1999). He likewise ignores that in making the public interest
determination, Congress directed the Agency to consider his
experience in dispensing controlled substances, an inquiry which
necessarily entails review of prior incidents of misconduct.
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Substantial evidence also supports the ALJ's findings that
Respondent committed other acts of misconduct. These included his: (1)
Obtaining Marinol, a schedule III controlled substance, from a patient,
who had been dispensed the drug by another doctor, in violation of 21
U.S.C. 844(a); and his (2) failing to document his receipt of the
Marinol in violation of 21 U.S.C. 827(a)(3). ALJ at 48-49. In addition,
Respondent prescribed controlled substances from a new location at
which he did not hold a registration and did so even after he was told
by DEA personnel to stop doing so. ALJ at 30-31, 52-53 (citing GXs 9,
33, and 34). As the ALJ noted, "Respondent's act of continuing to
handle controlled substances after numerous warnings shows a flagrant
disregard for the requirements of the law governing the handling of
controlled substances." Id. at 53.
Finally, based on a 2003 state proceeding, the ALJ found that
Respondent failed to properly supervise an unlicensed person who
distributed phentermine, a schedule IV controlled substance, to
patients of a weight loss clinic where Respondent worked and which was
owned by the unlicensed person who was a personal friend. ALJ at 46.
According to the record, this occurred when Respondent left his medical
bag (which contained the drugs) at the clinic and the clinic owner
distributed the phentermine to its patients. Notably, five years
earlier--as part of the 1998 Consent Order, which resolved the
allegations pertaining to his handling of Dilaudid--Respondent was
required to take a course in controlled substance management. GX 7, at
3. Yet Respondent then committed additional violations of the CSA.
The numerous acts of misconduct proved on this record, along with
Respondent's unwillingness to accept responsibility for much of it, and
his demonstrated inability to take heed of the laws and regulations
pertaining to controlled substances even after being required to
undergo remedial instruction, make clear that his continued
registration "would be inconsistent with the public interest." 21
U.S.C. 823(f). I therefore reject Respondent's exception that the
evidence does not support the revocation of his registration.
Accordingly, I will adopt the ALJ's recommendation that his
registration be revoked and that his applications to renew and modify
his registration be denied.
Order
Pursuant to the authority vested in me by 21 U.S.C. 823(f) &
824(a), as well as 28 CFR 0.100(b), I order that DEA Certificate of
Registration, BH8738063, issued to Richard A. Herbert, M.D., be, and it
hereby is, revoked. I further order that the applications of Richard A.
Herbert, M.D., to renew and modify his registration be, and they hereby
are, denied. This order is effective September 29, 2011.
Dated: August 12, 2011.
Michele M. Leonhart,
Administrator.
Bryan Bayly, Esq., for the Government.
Richard A. Herbert, M.D., Pro Se, for the Respondent.
Opinion and Recommended Ruling, Findings of Fact, Conclusions of Law
and Decision of the Administrative Law Judge
Mary Ellen Bittner, Administrative Law Judge. This proceeding is an
adjudication pursuant to the Administrative Procedure Act, 5 U.S.C. 551
et seq., to determine whether the Drug Enforcement Administration (DEA)
should revoke a physician's Certificate of Registration as a
practitioner and deny any pending applications for renewal or
modification of that registration. Without this registration the
physician, Respondent Richard A. Herbert, M.D., of Riverside, Illinois,
will be unable to lawfully handle controlled substances in the course
of his practice.
On March 11, 2009, the Deputy Assistant Administrator, Office of
Diversion Control, of the DEA issued an Order to Show Cause to
Respondent, giving Respondent notice to show cause why the DEA should
not revoke his
[[Page 53946]]
DEA Certificate of Registration pursuant to 21 U.S.C. 824(a)(l) and
(a)(4), and deny any pending applications for renewal or modification
of such registration pursuant to 21 U.S.C. 823(f), on grounds that he
materially falsified an application for renewal of his registration and
that his continued registration would be inconsistent with the public
interest as that term is used in 21 U.S.C. 824(a)(4) and 823(f).
In substance, the Order to Show Cause alleges that Respondent holds
a DEA Certificate of Registration that expired on October 31, 2006, and
for which Respondent submitted a timely renewal application on
September 26, 2006; that on that renewal application, Respondent was
required to answer whether a state medical board had taken action
against his state license; that on February 26, 1998, the Illinois
then-Department of Professional Regulation had placed Respondent's
medical license on probation for one year because Respondent issued
unlawful prescriptions for Dilaudid, a brand name product containing
the Schedule II narcotic controlled substance hydromorphone
hydrochloride; that Respondent failed to disclose the 1998 probation on
his September 2006 renewal application; that Respondent obtained
dronabinol, a Schedule III hallucinogenic controlled substance, from a
patient who had acquired it pursuant to a prescription from another
physician but had no record of such receipt, and that on July 21, 2003,
Respondent dispensed that dronabinol to another purported patient but
had no record of such dispensing; that on August 15, 2003, the Illinois
Department of Financial and Professional Regulation (IDFPR) placed
Respondent's medical license on probation for three years because
Respondent failed to supervise an unlicensed employee who illegally
handled phentermine, a Schedule IV stimulant controlled substance; that
Respondent disclosed the 2003 probation on his September 2006 renewal
application; that on July 5, 2005, the Illinois Department of
Professional Regulation served Respondent with an administrative
subpoena seeking to obtain patient records and that Respondent did not
fully comply with the subpoena in that he redacted patient
identification information and all dates of treatment; that on July 28,
2007, the administrative subpoena was re-issued to Respondent; and that
from February 2006 through August 2007, Respondent diverted OxyContin,
a brand name product containing the Schedule II narcotic controlled
substance oxycodone, to a patient by giving the patient a prescription
that Respondent wrote in the name of the patient's mother.
Respondent, through counsel, timely requested a hearing on the
allegations in the Order to Show Cause. On October 9, 2009,
Respondent's counsel requested leave to withdraw as counsel because of
a conflict of representation; I granted counsel's request on October
13, 2009; and sent a copy of the memorandum granting that request to
Respondent by Federal Express that same day. Following prehearing
procedures, a hearing was held in Chicago, Illinois, from November 3
through November 6, 2009, with the Government represented by counsel
and Respondent appearing pro se. Both parties called witnesses to
testify and introduced documentary evidence. After the hearing, both
parties filed proposed findings of fact, conclusions of law, and
argument. All of the evidence and posthearing submissions have been
considered, and to the extent the parties' proposed findings of fact
have been adopted, they are substantively incorporated into those set
forth below.
Issue
Whether a preponderance of the evidence establishes that, pursuant
to 21 U.S.C. 824(a)(l) and (a)(4), Respondent's registration with the
Drug Enforcement Administration should be revoked and any pending
applications for renewal or modification of that registration denied,
because Respondent made material misstatements on an application for
registration and because his continued registration would be
inconsistent with the public interest as that term is used in 21 U.S.C.
823(f).
Findings of Fact
I. Background
Respondent is a physician licensed to practice medicine and to
handle controlled substances in Illinois. He has held a DEA
registration since April 13, 2004, with a registered address at
Oakbrook Center Mall in Oak Brook, Illinois. [GX 1]
II. The Illinois Department of Financial and Professional Regulation
The Illinois Department of Financial and Professional Regulation
(IDFPR) is a state agency that licenses physicians and investigates
complaints regarding licensed physicians. Upon conclusion of an
investigation, the information is forwarded to a medical coordinator,
who is a physician, for review. That individual then determines whether
to recommend the case to the Medical Disciplinary Board. [Tr. 151-152]
D. M., a medical investigator and controlled substance inspector for
the IDFPR, testified that the IDFPR was previously known as the
Department of Professional Regulation but was merged with several
stand-alone agencies to eventually become the IDFPR. [Tr. 155]
III. The Evidence Pertaining to Respondent
A. Respondent's Illinois Department of Professional Regulation 1998
Consent Order
Investigator D.M. testified that he and two representatives of the
DEA were involved in a 1994 investigation of Respondent regarding the
diversion of Dilaudid. [Tr. 154, 733] On February 26, 1998, Respondent
entered into a Consent Order with the Illinois then-Department of
Professional Regulation. The Consent Order stated that Respondent "may
have prescribed Dilaudid to four (4) patients under questionable
circumstances, i.e. for pain related to old injuries or for pain in
which surgery may have provided relief and that two (2) of the patients
may have sold some of the Dilaudid back to Respondent." \10\
Respondent did not admit or deny the allegations but, for the purposes
of the Consent Order only, agreed not to contest the allegations.
Respondent testified in the instant hearing that he does not agree that
his actions were unlawful and that his position is that he acted
lawfully. [Tr.743, GX 2]
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\10\ GX 7.
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Under the terms of the Consent Order, Respondent's Illinois
physician and surgeon and controlled substances licenses were both
placed on probation for one year with several conditions, including
completion of a course in controlled substances management and a
requirement that Respondent make and submit controlled substance logs
to the Department of Professional Regulation for a period of time. [GX
7]
B. Respondent's Illinois Department of Financial and Professional
Regulation 2003 Consent Order
Investigator D.M. testified that another IDFPR investigation of
Respondent began in 1999 and concerned the "aiding and abetting in the
unlicensed practice of medicine." \11\ According to Investigator D.M.,
an A.D. had "dispensed" \12\ to patients in Chicago phentermine that
Respondent
[[Page 53947]]
had ordered and received at his Oakbrook office.
---------------------------------------------------------------------------
\11\ Tr. 157.
\12\ Agent D.M. testified that his use of the term "dispense"
referred to "providing the actual pills." Tr. 159.
---------------------------------------------------------------------------
At the hearing in the instant case, Respondent testified that he
had a "deal for pay" with his friend Mr. D., who owned a weight loss
clinic in Chicago. Pursuant to this agreement, Respondent used his DEA
registration to purchase phentermine at his registered Oakbrook
location and then took the phentermine to Mr. D.'s clinic in a locked
bag that Respondent would sometimes leave at the clinic; Respondent saw
patients and created records at the clinic and sold the phentermine to
Mr. D. who in turn sold the phentermine to the patients at a higher
cost. Respondent testified that one day he left his bag filled with his
stock of phentermine at the clinic although he was not there, and when
patients came in Mr. D. provided them with phentermine from the bag and
instructed them to come back in a few days to see Respondent.\13\
Respondent testified that once he was notified that some of those
patients were state investigators, he immediately resigned from the
clinic and offered to cooperate.
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\13\ Tr. 587.
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Respondent testified that at a state hearing regarding the matter,
he admitted that he had guilt because he technically aided in Mr. D.'s
"practice of medicine by not securing my controlled substances" \14\
but that he "didn't actually aid and abet." \15\ On August 15, 2003,
Respondent entered into a Consent Order with the IDFPR with regard to
Mr. D.'s provision of phentermine from the Chicago clinic. The Consent
Order stated that Respondent failed to supervise an unlicensed employee
and Respondent admitted that the allegations were true. As a result of
the Consent Order, Respondent's Illinois physician and surgeon and
controlled substances licenses were placed on probation for a period of
three years with several conditions, including completion of continuing
medical education in the area of prescribing and dispensing controlled
substances and allowing the IDFPR to inspect Respondent's controlled
substance log book and inventory record book upon request. [GX 8]
---------------------------------------------------------------------------
\14\ Tr. 589.
\15\ Tr. 589.
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C. Respondent's Activity During the 2003-2006 Probation Period
The IDFPR filed a complaint against Respondent on April 5, 2007,
alleging that he violated the terms of his probation as set forth in
the 2003 Consent Order by failing to make available for inspection his
controlled substance log and inventory records; receiving dronabinol, a
Schedule III controlled substance, from a purported patient and re-
dispensing it to another purported patient, and failing to keep any
records of the receipt and dispensing of the dronabinol; providing
incomplete records in response to an IDFPR subpoena issued by the
IDFPR; aiding and abetting the unlicensed practice of medicine relating
to a June 2005 incident; and issuing prescriptions for OxyContin to
patients without examining them and failing to keep and maintain
records of those patients and the controlled substances.
1. The IDFPR Inspection of Respondent's Controlled Substances Log
Investigator D.M. testified that in April 2005 he interviewed
Respondent regarding his controlled substances logs and that Respondent
stated that he did not have any logs for the years 2003, 2004, or 2005
because he had not ordered any controlled substance medications and
therefore had no occasion to dispense \16\ them or maintain a log of
them. [Tr. 194] Investigator D.M. further testified that when he again
met with Respondent in May 2005, Respondent iterated that he did not
have a log because he had not dispensed any controlled substances in
2003, 2004, or 2005. Investigator D.M., however, was aware from the
transcript of a Chicago Police Board hearing held on August 10 and
October 13, 2004, that Respondent had testified in that proceeding
about dispensing dronabinol to a patient on July 21, 2003; this
incident is further discussed below. [Tr. 165] Respondent testified in
the instant hearing that "my assumption when D.M. was in there was
that I knew that I had not ordered anything for years, and not
recalling these three patients, I simply filled out a handwritten log
and zero." \17\
---------------------------------------------------------------------------
\16\ Investigator D.M. stated that in this instance,
"dispensing" means providing or prescribing. Tr. 194. But see
supra note 3. The Illinois Compiled Statutes defines "dispense" as
"the interpretation, evaluation, and implementation of a
prescription drug order, including the preparation and delivery of a
drug or device to a patient or patient's agent in a suitable
container appropriately labeled for subsequent administration to or
use by a patient in accordance with applicable State and federal
laws and regulations." 225 ILCS 85/3.
\17\ Tr. 622.
---------------------------------------------------------------------------
Respondent further stated that at the time he knew that he had not
ordered anything from drug wholesalers for many years and therefore had
not dispensed anything, and that he did not recall that he had made a
controlled substances log for 2003, which included three entries and
had been stored in his sample cabinet; later that evening he realized
his error and notified his attorney, who in turn notified Investigator
D.M. and produced the log that included three entries for 2003. [Tr.
622, RX 2]
2. Respondent's Dispensing of Dronabinol
D.S. was a Chicago police officer who tested positive for
tetrahydrocannabinol \18\ (THC) after a random drug test performed by
the Chicago Police Department on July 24, 2003. [Tr. 163] At Officer
D.S.'s subsequent police board hearing on August 10, 2004, Respondent
testified that he treated Officer D.S. on July 21, 2003, at
Respondent's office and gave him eight 10-milligram gelatin capsules of
Marinol \19\ to control nausea and vomiting; that he did not write a
prescription for Marinol for Officer D.S. but gave him "samples" of
the drug that he had in his office; \20\ [GX 5 at 98] that it is his
practice to ask patients to give him their unused medications, so that
he can "recycle" them "as much as I possibly can"; \21\ [GX 6 at
146] and that when he receives medications from patients, he puts the
medication in a bottle, labels it, and stores it, but does not keep a
record of which patient provided the medication. [GX 6 at145]
---------------------------------------------------------------------------
\18\ THC is a Schedule I controlled substance.
\19\ Marinol is a brand name product containing dronabinol, a
Schedule III controlled substance, the active ingredient of which is
a synthetic form of tetrahydrocannabinol, which naturally occurs in
the Schedule I controlled substance marijuana.
\20\ See GX 5 at 98.
\21\ GX 6 at 146.
---------------------------------------------------------------------------
In a continuation of the police board hearing on October 13, 2004,
Respondent testified that the Marinol he gave to Officer D.S. was not a
manufacturing sample but came from another of Respondent's patients,
although Respondent had no record of who that patient was; [GX 6 at
144] when asked at the police board hearing which patient provided the
Marinol, Respondent replied that "[i]t could be anyone of a number of
patients"; \22\ and that the Marinol "probably came from either a
leukemia or lymphoma treatment patient * * * the other possibility is
this could have come from an AIDS patient." \23\ In response to a
question regarding the frequency with which he had prescribed or given
Marinol to patients, Respondent said: "I have a number of patients
that use chemotherapeutic agents for lymphomas and malignancies,
leukemias. I also have a large number of AIDS patients
[[Page 53948]]
that I use Marinol for." \24\ Respondent then testified, however, that
he had prescribed or given samples of Marinol only a few times in the
last several years and that he had the Marinol in his office because it
might have come from a patient who obtained it pursuant to a
prescription from another doctor.
---------------------------------------------------------------------------
\22\ GX 6 at 144-145.
\23\ Id.
\24\ GX 6 at 146.
---------------------------------------------------------------------------
In the instant hearing, the Government entered into evidence
Respondent's medical record for Officer D.S., which indicates that
Respondent "sampled" Marinol 10 mg to Officer D.S. [GX 4] Respondent
testified that he both received and dispensed the Marinol in a plastic
pill case without a label but that he recognized the pills as Marinol
and used a picture in the Physician's Desk Reference (PDR) to verify
what the pill was. Respondent further testified that he remembered the
patient from whom he had received the Marinol because he had never
received Marinol from a patient before. [Tr. 767] Respondent entered
into evidence an affidavit dated May 2, 2008, and signed by a J.W.;
Respondent testified that Mr. J.W. was a former patient of his who had
AIDS.\25\ Mr. J.W.'s affidavit states that he was HIV positive; that
Respondent was one of several physicians who treated him; and that he
took Marinol to stimulate his appetite but because he did not like the
way it made him feel and he could not control its effects, he stopped
taking the Marinol and gave the remaining pills to Respondent. The
affidavit does not identify Mr. J.W.'s source for the Marinol but
states that the cost is high and that Mr. J.W. did not want to dispose
of the pills by flushing them down the toilet or putting them in the
garbage. [RX 17]
---------------------------------------------------------------------------
\25\ The affidavit is signed by a J.W.; there is no witness
signature and the document is not notarized.
---------------------------------------------------------------------------
Respondent testified that as of the date of the hearing he
understood that he was not authorized to acquire Marinol from a
patient, although he had not thought about it before, and that he was
not authorized to provide that Marinol to Officer D.S.. Respondent
further testified that he did not tell Officer D.S. that he had
acquired the Marinol from another patient rather than as a
manufacturing drug sample. [Tr. 765] Respondent further testified that
he did not keep any record of receipt of the Marinol because at the
time he thought that he was only required to maintain records of drugs
that he purchased.
3. Respondent's Response to the IDFPR Subpoenas
Investigator D.M. testified that the IDFPR Medical Disciplinary
Board issued to Respondent a Subpoena Duces Tecum dated June 15, 2005,
pursuant to the Illinois Medical Practice Act of 1997. [GX 10] The
subpoena commanded Respondent to surrender certain documents and
records concerning his treatment of ten individuals, identified on the
subpoena by name and date of birth. The documents were to be
surrendered on or before June 30, 2005, to one of two identified
individuals for inspection by the medical disciplinary board.
Investigator D.M. prepared and attached to the subpoena an
affidavit advising that, according to a profile received from the
Illinois Department of Human Services, [GX 28] Respondent issued
multiple prescriptions of OxyContin 80 mg to the ten individuals whose
records were requested, and that some of those individuals also were
identified as having received Dilaudid from Respondent in the 1994
investigation. The affidavit states that Respondent issued the
prescriptions in question between January 1, 2004, and April 2005, and,
specifically, that during this period Respondent issued 124
prescriptions for Schedule II controlled substances, 123 of which were
for 60 dosage units each of OxyContin 80 mg.
Investigator D.M. testified that in response to the subpoena,
Respondent's attorney provided records from which the names of the
individuals and the dates of treatment were redacted. [GX 3] Further,
Investigator D.M. stated that the documents provided indicated that one
patient had her records sent to a family doctor who agreed to continue
OxyContin and that Respondent did not have copies of those records, and
that after Respondent advised another patient that the Medical
Disciplinary Board had asked to review the patient's records, the
patient strongly objected to such a review and took the records, and
Respondent did not have copies of them. [Tr. 170]
Investigator D.M. further testified that on June 20, 2007, the
Medical Disciplinary Board issued a second subpoena to Respondent,
again requesting the medical records for the ten previously identified
individuals and requiring that no information other than the patient
identity be removed. [Tr. 171] Investigator D.M. testified that he did
not know whether Respondent had provided that information, [Tr. 311]
but that he had seen documents in the possession of an IDFPR attorney
that appeared to include the dates of treatment and other information
that had been previously redacted. [Tr. 175] Respondent testified that
he eventually complied with the subpoena after the remaining patients
gave him permission to provide copies of their records.\26\
---------------------------------------------------------------------------
\26\ As evidence of his compliance with the subpoena, Respondent
admitted into evidence Respondent Ex. 1, which includes the first
page of multiple patient files that appear to have the patients'
names and dates of birth and dates of treatment redacted, although a
name is handwritten at the top of each page.
---------------------------------------------------------------------------
4. Respondent's Issuance of OxyContin Prescriptions
Investigator D.M. testified that he met with Respondent in June
2005 at Respondent's office and that during that interview Respondent
said that he issued to chronic pain patients prescriptions for 60
OxyContin 80 mg and for Tylenol 3 or Tylenol 4,\27\ and that he
instructed the patients to take a half tablet of OxyContin twice a day.
Respondent further said that he used to prescribe Dilaudid 2 or 4 mg.
[Tr. 198] Investigator D.M. further testified that, at that meeting,
Respondent indicated that a number of his patients were employed at
Balmoral horse racing track and, when Investigator D.M. asked
Respondent whether any of the ten patients listed on the subpoena
discussed above knew one another, Respondent stated that two of the
patients, S.P. and C.G., worked at Balmoral. Respondent did not,
however, mention the relationships among I.S., E.M., and C.G., all of
whom were also identified on the subpoena and who, as discussed below,
shared a household. [Tr. 202] Respondent testified in the instant
hearing that he had a personal relationship with Ms. E.M. and went to
high school with her son, Mr. I.S.; Ms. C.G. was identified as Mr.
I.S.'s girlfriend. [Tr. 485]
---------------------------------------------------------------------------
\27\ I take official notice from the 2007 edition of the
Physicians' Desk Reference that Tylenol 3 and Tylenol 4 are brand
names for products containing acetaminophen with codeine, a Schedule
III controlled substance.
---------------------------------------------------------------------------
Investigator D.M. testified that he and Diversion Investigator C.R.
of the DEA's Chicago office interviewed Mr. I.S. in July 2005. Mr. I.S.
told them that he was on the board of directors for harness racing at
Balmoral Park; that approximately sixty percent of the employees there
had drug abuse and/or dependency problems; that he had sustained some
injuries from horse racing accidents; that he had been friends with
Respondent for about 25 or 30 years; that Respondent issued him
OxyContin prescriptions either at Respondent's office or when they met
for lunch; and that Respondent also
[[Page 53949]]
prescribed OxyContin for Mr. I.S.'s girlfriend, C.G., and his mother,
E.M., who both lived with him. [Tr. 212]
Investigator D.M. testified that at the July 2005 interview, Mr.
I.S. showed him OxyContin vials for Ms. E.M., Ms. C.G., and himself,
all of which indicated that they had contained 60 dosage units of 80 mg
strength and that Respondent issued the prescriptions. The label had
been removed from Mr. I.S.'s vial; he explained that it could be
embarrassing for anyone, particularly at the race track, to know that
he was taking OxyContin inasmuch as he was promoting a program to help
people at the track who might have addiction problems. Mr. I.S. further
told the investigators that he had helped to create rules regarding
drug use in both humans and horses; and that he did not think that he
was abusing the medication because he was able to function and he did
not have needle marks, which he said would be a sign of an addict. [Tr.
224]
Mr. I.S. testified in the instant hearing, however, that he removed
the label from his OxyContin bottle so that "the kids wouldn't know
what was in the bottles"; \28\ [Tr. 721] he received his pain
medication from Respondent, whose office was one hour and 25 minutes
away from Mr. I.S.'s residence, [Tr. 722] and that "if I couldn't get
my pain medication from [Respondent], then I would get medication
wherever I could if I had to, but I don't recall even having to." \29\
Mr. I.S. then testified that "there was a time when [Respondent] was
having a problem with the DEA, and I couldn't get my medication, and at
that time when I was getting medication whatever way I could, and I
went to another doctor once"; \30\ and before Ms. E.M. began getting
the OxyContin prescriptions, he "would take her to the doctors and I
would take her to a clinic" and "[y]ou only had to look at my mother
and write her something right away, because she was crippled." \31\
---------------------------------------------------------------------------
\28\ Tr. 720
\29\ Tr. 715.
\30\ Tr. 715.
\31\ Tr. 716.
---------------------------------------------------------------------------
D. E.M.
1. E.M.'s Medical Conditions
Investigator D.M. testified that he interviewed Mr. I.S. again in
August 2005 at Mr. I.S.'s home. Investigator D.M. testified that Mr.
I.S. advised him that Ms. E.M. had recently suffered a stroke and had
been hospitalized at St. Mary's Hospital and treated by V.P., M.D.;
[Tr. 226] that Respondent was Ms. E.M.'s primary physician prior to her
admission to St. Mary's Hospital and that S.D., M.D., treated Ms. E.M.
while she was at a senior care center. [Tr. 312] Mr. I.S. showed
Investigator D.M. prescriptions that Respondent had issued to Ms. E.M.
for various medications, including Plavix, Micardis, Prevacid, aspirin,
Lipitor, nitroglycerin patches, Remeron, Toprol, and Vicodin \32\ which
Mr. I.S. typically filled near his home at a pharmacy called Doc's
Drugs. Mr. I.S. stated that after the stroke Ms. E.M. had difficulty
getting around and was responding to stimuli differently than before
and was no longer doing household chores.
---------------------------------------------------------------------------
\32\ Lipitor is a brand name product containing atorvastatin
calcium, a non-controlled substance and synthetic lipid-lowering
agent. I take official notice of the following information from the
2007 edition of the Physicians' Desk Reference: Plavix is a brand
name product containing clopidogrel bisulfate, a non-controlled
substance and inhibitor of platelet aggregation that helps protect
against future heart attack or stroke; Micardis is a brand name
product containing telmisartan, a non-controlled substance that is a
nonpeptide name product containing lansoprazole, a non-controlled
substance, the active ingredient of which is a compound that
inhibits gastric acid secretion, typically prescribed to treat and
prevent stomach and intestinal ulcers; nitroglycerin patches contain
an organic nitrate, a non-controlled substance, that helps prevent
chronic chest pain caused by heart disease; Remeron is a brand name
product containing mirtazapine, a non-controlled substance and
tetracyclic antidepressant used primarily in the treatment of
depression; Toprol is a brand name product containing metoprolol
succinate, a noncontrolled substance that is indicated for the
treatment of hypertension; and Vicodin is a brand name drug
containing hydrocodone bitartrate, a Schedule III controlled
substance, and acetaminophen, and is indicated for the relief of
moderate to moderately severe pain.
---------------------------------------------------------------------------
Dr. S.D., an internal medicine physician experienced in treating
geriatric patients and in the medical use of controlled substances,
testified that Ms. E.M. suffered from medical problems such as
tachycardia (an irregular heartbeat), lower back pain, arthritis in
multiple joints, and dementia; [Tr. 79] he also noted that Ms. E.M. had
kyphoscoliosis, which he said was not uncommon for a patient of Ms.
E.M.'s age, and often occurs after a person develops osteoporosis; and
that she had been admitted to the hospital at various times for such
ailments as urinary tract infection, pneumonia, chest pain, and
possible seizure disorder. C.K., a licensed practical nurse
specializing in geriatrics and end-of-life care and employed by Hospice
of Kankakee Valley (Kankakee Hospice), testified that when Ms. E.M. was
admitted to Kankakee Hospice, she suffered from "adult failure to
thrive," \33\ arthritis, a steel rod in her right arm, a hump in her
back, and some dementia, as indicated by her difficulty remembering
people, including her son whom she confused with her husband.
---------------------------------------------------------------------------
\33\ Tr. 34.
---------------------------------------------------------------------------
Respondent testified that Ms. E.M. suffered from vascular dementia,
known as Binswanger's disease, which he characterized as a small vessel
disease of the white matter; and benign myalgic encephalomyelitis,
which causes fatigue, bowel disorders, and cognitive deficits.
Respondent testified that because of the dysfunction of the white
matter in the brain, Ms. E.M. found it difficult to walk and perform
organizational tasks. [Tr. 480] Mr. I.S. testified that Ms. E.M.'s
problems of loss of memory and failure to recognize her family were
caused by and occurred only when Ms. E.M. was taking certain
medication. [Tr. 725]
Respondent testified that he treated Ms. E.M. "in concert with the
whole patient"; \34\ that diabetes affects every organ in the body and
causes kidney failure, high blood pressure, coronary disease,
peripheral artery disease, and cerebral vascular disease; [Tr. 472] and
that Ms. E.M. suffered a series of transient ischemic attacks (TIAs), a
closing of a small blood vessel in the brain, around 2004, and had
elevated blood sugar levels. Respondent testified that all of these
factors taken together led him to "try everything that I could to
reverse the arterial sclerosis in the carotid arteries." \35\
---------------------------------------------------------------------------
\34\ Tr. 472.
\35\ Tr. 486.
---------------------------------------------------------------------------
Respondent testified that he prescribed to Ms. E.M. a combination
of high-dosage drugs, including Actos \36\ and Metformin,\37\ to shut
down her body's glucose production and to re-sensitize the peripheral
resistance to insulin, Lipitor to reverse the arterial sclerotic
changes in the neck, and Lycinapro, Morvasc, and Zetia [Tr. 477] with
Metformin to open up her arteries, all of which was part of an anti-
inflammatory treatment to stop the progression of her carotid artery
disease. [Tr. 600] Dr. S.D., however, testified that if Ms. E.M. had
the blood sugar and glycosulated hemoglobin levels Respondent
described, it would not have been necessary to medicate her for
diabetes, and that the proper treatment would have been to try to
control the condition with diet. Dr. S.D. testified that he has never
prescribed Actos or Metformin for "off-label" use; and that in his
opinion, Actos and Metformin
[[Page 53950]]
have no use other than to treat diabetes. [Tr. 133]
---------------------------------------------------------------------------
\36\ See RX 22. Actos is a brand name product containing
pioglitazone hydrochloride, a non-controlled substance, and is an
oral antidiabetic agent that acts primarily by decreasing insulin
resistance. [GX 40]
\37\ I take official notice that Metformin is a non-controlled
substance.
---------------------------------------------------------------------------
Investigator R. testified that she visited the Kankakee Hospice
central office on April 30, 2009, [Tr. 354] where she spoke to
Executive Director D.L., Patient Care Coordinator P.L., C.K., and C.D.,
another nurse who treated Ms. E.M. Investigator R. testified that none
of the people she interviewed had any knowledge of Ms. E.M. ever having
diabetes [Tr. 355] and there was no record of Ms. E.M. receiving
medication such as Actos and Metformin. [Tr. 356] Investigator R. also
obtained from Doc's Drugs pharmacist E.U. a prescription profile
listing all the prescriptions issued to Ms. E.M. and filled at that
pharmacy from January 1, 2006, through August 29, 2008, [Tr. 347] that
indicates that Respondent wrote prescriptions for Ms. E.M. for Actos,
Metformin, Lipitor, Plavix, and Zetia.\38\ Dr. S.D. testified that a
home health nurse caring for Ms. E.M. once asked him about giving Ms.
E.M. Coumadin and Plavix, both blood thinners, but he advised that Ms.
E.M. should not take either drug because she had suffered multiple
falls and those medications increased the danger of bleeding in the
brain.
---------------------------------------------------------------------------
\38\ Zetia is a brand name product containing ezetimibe, a non-
controlled substance that inhibits the intestinal absorption of
cholesterol. [RX 36]
---------------------------------------------------------------------------
Dr. S.D. testified that he told the nurse that Ms. E.M. should just
continue taking aspirin. [Tr. 87]
2. E.M.'s Treating Physicians
Respondent testified that he began treating Ms. E.M. around 2003,
when she was approximately 92 years old, and that he had "a lot
invested in E.M.," \39\ with whom he had had a personal relationship
since he attended high school with Mr. I.S. [Tr. 485] Mr. I.S.
testified that the hospice to which Ms. E.M. was admitted only allowed
patients to use the hospice doctors; that hospice personnel told him
that the only doctor Ms. E.M. could have was Dr. S.D.,\40\ [Tr. 661]
and that he nonetheless admitted his mother to hospice care because he
needed someone to care for her and he could not afford financially to
provide that care himself. Mr. I.S. further testified that Dr. S.D. was
"strictly a hospice doctor that she saw whenever she was admitted to
the hospital, and he helped her get into hospice"; that Respondent was
Ms. E.M.'s primary doctor, [Tr. 677] and that if another physician
prescribed something for Ms. E.M., Mr. I.S. would discuss the issue
with Respondent and follow his advice as to what medication Ms. E.M.
should be prescribed. [Tr. 730] Mr. I.S. testified that he would have
Ms. C.G. "ask Dr. S.D. to write it, and most of the time he would."
\41\ Mr. I.S. also testified that he took Ms. E.M. to see G.M., M.D.,
or T.M., M.D.\42\ "on an emergency basis, and because we didn't want
to see Dr. S.D."; \43\ and if Ms. E.M. was sick, which, according to
Mr. I.S., occurred "maybe once or twice in her life," \44\ he took
her to see Dr. M. Mr. I.S. initially testified that he believed Dr. M.
was aware that Respondent was treating Ms. E.M., [Tr. 698] but later
said that he did not think that either Dr. T.M. or Dr. G.M. knew that
Respondent was treating Ms. E.M. [Tr. 699]
---------------------------------------------------------------------------
\39\ Tr. 487.
\40\ In his brief, Respondent asserts that the hospice
requirement was to use a doctor located in Kankakee. See
Respondent's Closing Argument Brief at 11.
\41\ Tr. 673.
\42\ G.M. and T.M. are physicians who practice together and
appear to have each treated Ms. M. The testimony is not always clear
as to which Dr. M. the witnesses are referencing.
\43\ Tr. 698.
\44\ Tr. 698.
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Dr. S.D. testified that he, along with Dr. V.P., B.D., M.D., and
M.S., M.D., all treated Ms. E.M. for approximately four years prior to
her death in 2009. Dr. S.D. further testified that Ms. E.M. was
admitted to St. Mary's Hospital in Kankakee, Illinois, several times
and also was a patient at Manor Care Nursing Home in Kankakee and at
times had hospice care and home health care; that he was listed as Ms.
E.M.'s primary care physician at each of those institutions; and that
he does not know Respondent and was never informed that Respondent was
treating Ms. E.M. [Tr. 98] Dr. S.D. further testified that Ms. E.M. was
under hospice care for the last two-and-a-half to three years of her
life, during which time he was her primary care physician; that
although he only saw Ms. E.M. a few times in his office and in the
hospital, he gave telephone orders and communicated with the hospice
nurse regarding Ms. E.M.'s condition; he had no reason to believe that
Ms. E.M. was seen by any other doctor or was taking medications not
included on the medication list that he approved; [Tr. 102] and that
any other physician who was treating Ms. E.M. should have informed him
that he or she was prescribing OxyContin to her. [Tr. 140] Dr. S.D.
testified that it is out of the range of normal practice for a
physician to prescribe medications to a patient without consulting with
other treating physicians of which he is aware. [Tr. 144]
Ms. E.M. was first admitted to Kankakee Hospice, which provides
care in the patient's home, on June 9, 2006.\45\ Ms. C.K. testified
that she cared for Ms. E.M. in her home in late 2007 and early 2008,
seeing her twice per week for approximately one hour per visit. [Tr.
30] At each visit Ms. C.K. performed a physical assessment of Ms. E.M.
(taking her blood pressure, heart and respiration rate; listening for
lung sounds, bowel sounds; assessing her skin, cognition, etc.). [Tr.
32] Ms. C.K. testified that every visit from and telephone call or
other conversation with Kankakee Hospice personnel was recorded and
that the hospice also kept hospital records, laboratory test results,
and records received from the doctor.
---------------------------------------------------------------------------
\45\ See GX 17.
---------------------------------------------------------------------------
Ms. C.K. further testified that Kankakee Hospice needs to know of
every physician "who is on board to treat the patient"; \46\ that
there is a primary physician and usually a secondary physician; and
that Kankakee Hospice prefers to have its personnel accompany the
patient to doctor appointments. Ms. C.K. testified that while she cared
for Ms. E.M., none of her family members ever mentioned that Respondent
was treating her, but the family did mention that Ms. E.M. saw Dr. S.D.
and Dr. M. Ms. C.K. also was not aware of any physicians making home
visits to Ms. E.M., although that information should have been
disclosed to Kankakee Hospice.
---------------------------------------------------------------------------
\46\ Tr. 35.
---------------------------------------------------------------------------
3. Ms. E.M.'s Prescriptions and Treatment
Respondent testified that when he began treating Ms. E.M. in 2003,
she was taking multiple pain medications, such as Tylenol No. 4,
Lorcet,\47\ and Vicodin; that she sometimes took as many as 10 or 12
pills per day; and that he changed her regimen to a more potent and
controlled dosage on a regular schedule. [Tr. 498] Respondent testified
that Ms. E.M. suffered from low back pain; that treatment with
medication on an as-needed basis was not sufficient to relieve her
pain; and that the appropriate treatment was to increase the amount of
opioid medication until either the pain went away or the side effects
became too drastic to continue. [Tr. 514] According to Respondent,
instead of tapering a patient off a drug while he still has symptoms, a
doctor should increase the level of the drug in order to extinguish the
symptoms; tolerance with regard to symptoms requires an increased
dosage that relieves the pain, which is different from increasing
dosage to extinguish pain. [Tr. 517] Respondent testified that all
patients develop dependence, which
[[Page 53951]]
means that if the medicine is abruptly withdrawn, the patients will
become antsy, shaky, and complain of nervousness, and that although
some anti-anxiety agents or antihistamines may be used to treat the
withdrawal symptoms, the best option is to withdraw the medication
slowly over a period of time. Respondent testified that addiction "is
the unworkable lifestyle that is created by a person that escalates the
intake of narcotics and opioids," \48\ and is always exhibited by
anti-social behavior.
---------------------------------------------------------------------------
\47\ I take official notice that Lorcet is a brand name product
containing hydrocodone bitartrate and acetaminophen.
\48\ Tr. 519.
---------------------------------------------------------------------------
Dr. S.D. testified that he never prescribed OxyContin to Ms. E.M.
because he was afraid that she could not handle a strong pain
medication, but that he prescribed Aricept for dementia, Toprol XL and
Micardis for cardiac issues, [Tr. 83] and Tylenol, and that he maybe
prescribed Darvocet, and occasionally Vicodin for pain.\49\ Dr. S.D.
testified that Ms. E.M.'s pain, although chronic, was not so severe
that she needed constant pain medication. [Tr. 89]
---------------------------------------------------------------------------
\49\ I take official notice of the following information from
the 2007 edition of the Physicians' Desk Reference: Aricept is a
brand name product containing donepezil hydrochloride, a non-
controlled substance, indicated for the treatment of mild to
moderate dementia; Tylenol is a brand name over-the-counter
medication containing acetaminophen and is indicated for the
temporary relief of minor aches and pains; propoxyphene and
acetaminophen and is used to relieve mild to moderate pain.
---------------------------------------------------------------------------
Mr. I.S. testified that OxyContin seemed to work better than the
other medications Ms. E.M. had tried, and that before she started
taking OxyContin, Ms. E.M. sometimes took as many as four or five pills
per day" \50\ of Vicodin, Lorcet, or "whatever I had." \51\ Mr. I.S.
testified that Respondent started prescribing OxyContin 80 mg to Ms.
E.M. in 2003, and that Mr. I.S. was not surprised by the high dosage
because he "didn't know much about it." \52\ Mr. I.S. further
testified that Respondent never changed the strength or quantity of
OxyContin he prescribed to Ms. E.M. [Tr. 708]
---------------------------------------------------------------------------
\50\ Mr. I.S. later testified that Ms. E.M.s took "[a]t least
three pills a day," in the range of three to seven pills,
"whatever it took to kill her pain, that is as many pills as I gave
her for the day." Tr. 717.
\51\ Tr. 669.
\52\ Tr. 668.
---------------------------------------------------------------------------
Mr. I.S. testified that he initially filled Ms. E.M.'s OxyContin
prescriptions with the brand name drug but because it was very
expensive, he then tried the generic form. According to Mr. I.S.,
however, Ms. E.M. insisted that she wanted the brand name product"
\53\ and the pharmacist had told him that the "deliver[y] mechanism of
oxycodone was that it delivers all at once, and that the OxyContin was
more of a time release thing over 12 hours." \54\ Mr. I.S. further
testified that because the generic drug was not a time release product
and Ms. E.M. insisted that she wanted "the other one," \55\ [Tr. 695]
he thereafter filled the prescriptions with OxyContin. [Tr. 672]
---------------------------------------------------------------------------
\53\ Investigator D.M. testified that in the August 2005
interview, Mr. I.S. had stated that he filled his mother's
prescriptions with generic drugs because his mother had suffered a
stroke and would not recognize the difference between generic and
brand name drugs. Tr. 244.
\54\ Tr. 671.
\55\ Tr. 671.
---------------------------------------------------------------------------
Investigator R., however, testified that she spoke with Mr. E., the
pharmacist from Doc's Drugs, who informed her that if a patient
presents a prescription written for a brand name drug and requests a
generic, or the prescription allows a generic to be substituted for the
brand name product, then the pharmacist must provide the patient with a
generic medication that has the same properties as the brand name drug,
including any time release effect; and that oxycodone 80 mg is not
available as an immediate release tablet because it could be fatal.
[Tr. 840] The Government offered into evidence copies of prescriptions
Respondent issued to Ms. E.M. that investigators obtained from Doc's
Drugs; [Tr. 340; Tr. 412; Tr. 231] each prescription was written for
OxyContin with substitution permitted. Respondent testified that
breaking an OxyContin tablet in half only somewhat obviates the time
release effect and that the active ingredient may release more quickly.
[Tr. 797]
According to a Physician's Desk Reference excerpt for OxyContin
that the Government offered into evidence, "OxyContin tablets are to
be swallowed whole and are not to be broken, chewed, or crushed. Taking
Broken, Chewed, or Crushed OxyContin tablets leads to rapid release and
absorption of a potentially fatal dose of oxycodone." \56\
---------------------------------------------------------------------------
\56\ GX 40 at 17.
---------------------------------------------------------------------------
Investigator D.M. testified that there is a large price
differential between the brand drug and the generic, and that the
OxyContin brand can sell on the street for approximately one dollar per
milligram. [Tr. 297] Investigator R. testified that Mr. E. told her
that Mr. I.S. always picked up Ms. E.M.'s prescriptions and that
although insurance covered the prescriptions, Mr. I.S. paid the co-pay,
which was sometimes as much as $400 for the brand name drug, in cash.
Mr. E. further told Investigator R. that it was unusual for a customer
to request a brand name with such a high co-pay when a generic
alternative was available; [Tr. 414] and that the time release generic
of OxyContin had been available at relevant times except for a period
of approximately six months around 2007. [Tr. 840] Mr. I.S. testified
that he submitted the insurance claims for the OxyContin prescriptions
to Ms. E.M.'s insurance carrier and that he paid Respondent in cash for
his services to Ms. E.M. [Tr. 695]
4. Administering OxyContin to E.M.
On January 18, 2006, Ms. E.M. was admitted to St. Mary's Hospital;
at that time, a home medication list indicated that she received
OxyContin 80 mg every 12 hours. [GX 21 at 9] Respondent testified that
he arranged to have a family member see that OxyContin was included on
Ms. E.M.'s home medication list because he "wanted somebody to figure
out that she was on pain medication." \57\ Dr. S.D. testified that he
ordered that the OxyContin not be continued and that he was not aware
of OxyContin ever again being listed on Ms. E.M.'s medication lists,
[Tr. 90] but that if Ms. E.M. had been on OxyContin and it was stopped,
she would suffer from withdrawal symptoms such as abdominal pain,
diarrhea, and vomiting. [Tr. 106]
---------------------------------------------------------------------------
\57\ Tr. 821.
---------------------------------------------------------------------------
Dr. S.D. also testified that Ms. E.M. did not receive OxyContin
while in the hospital because family members are not permitted to give
medication to patients, that patients receive only those medications
prescribed by the attending physician, and that he was Ms. E.M.'s
attending physician and did not prescribe OxyContin to her. [Tr. 107]
Dr. S.D. testified that he never spoke with Mr. I.S. but would call
his home and leave messages regarding Ms. E.M.'s condition. Dr. S.D.
testified that Mr. I.S. did not return calls, but that he did speak
with Mr. I.S.'s girlfriend. [Tr. 109] Mr. I.S. testified that although
Dr. S.D. issued prescriptions to Ms. E.M. for Vicodin, he did not fill
those prescriptions because his mother was already taking OxyContin.
Investigator R. testified that on October 23, 2006, she met with
Kankakee Hospice's executive director, D.L., who told her that the
Hospice's policy requires that the nurses be informed of all of a
patient's medications and treating physicians. Investigator R. further
testified that at that meeting she also spoke with other Hospice
personnel who told her that OxyContin did not appear on Ms. E.M.'s
medication list and her Kankakee Hospice records did not mention that
she was in pain or that Respondent
[[Page 53952]]
treated her. [Tr. 352] Ms. C.K. testified that Ms. E.M. complained of
pain in her knees and arm and sometimes had difficulty standing and
some stiffness, but that Mr. I.S. or Ms. C.G. gave her Tylenol to
alleviate the pain and that Mr. I.S. said that the Tylenol worked and
he did not want his mother to have anything else. Ms. C.K. testified
that it seemed unusual for the caregivers to insist that only they
would administer certain medications. [Tr. 40, Tr. 45] Ms. C.K. further
testified that as far as she knew, the only controlled substance that
Ms. E.M. took was Valium \58\ for seizures; and that Ms. E.M.'s family
never mentioned that she was taking OxyContin. Ms. C.K. testified that
she was not aware of any controlled substances that were prescribed to
Ms. E.M. on a chronic or recurring basis; that she never saw any
medications prescribed by Respondent or any OxyContin vials or pills at
Ms. E.M.'s home; and that the only medication that the hospice team
attempted to count was Valium, which they had difficulty accessing from
Ms. E.M.'s family. [Tr. 35; Tr. 42] Mr. I.S. testified that he did not
want to tell the Kankakee Hospice personnel about his mother having
OxyContin because Kankakee Hospice had told him that it must have
control over any controlled substances Ms. E.M. took and thus hospice
personnel must have access to those drugs, but that he did not want to
leave the OxyContin "in a cabinet for some punk or something that may
be coming in my house after school to take or whatever." \59\ Mr. I.S.
also testified that Ms. E.M. did not want anyone to know that she was
on pain medication because "she was very old-fashioned, and * * * she
just didn't think it was anybody else's business." \60\
---------------------------------------------------------------------------
\58\ I take official notice of information in the 2007 edition
of the Physicians' Desk Reference that Valium is a brand name
product containing diazepam, a Schedule IV controlled substance.
\59\ Tr. 697.
\60\ Tr. 680.
---------------------------------------------------------------------------
Investigator R. testified that on October 23, 2008, she interviewed
Ms. D., who had treated Ms. E.M. in her home in 2006-2007. Ms. D. told
Investigator R. that Ms. E.M. complained of mild arthritic pain; that
Ms. D. asked Mr. I.S. whether they should look into getting something
stronger to alleviate the pain; and that Mr. I.S. said that he had
previously given Ms. E.M. one-half tablet of Vicodin, but that that
medicine was too strong for her and she should continue to take
Aleve.\61\ [Tr. 448]
---------------------------------------------------------------------------
\61\ I take official notice from the 2007 edition of the
Physicians' Desk Reference that Aleve is a brand name product
containing naproxen sodium, a non-controlled substance.
---------------------------------------------------------------------------
Mr. I.S. testified that Kankakee Hospice only allowed patients to
use the hospice "system for drugs," \62\ and therefore either he or
someone in his family gave Ms. E.M. OxyContin while she was admitted to
Kankakee Hospice and when she was in St. Mary's Hospital, at Manor Care
Nursing Home, at Heritage Village Nursing Home, and at St. James
Hospital. [Tr. 680] Mr. I.S. testified that Ms. E.M. received one
OxyContin pill in the morning and one at night but for the two weeks
before his mother died he gave her only the nighttime dose because he
worried that she may have been too weak to receive more; [Tr. 682]
OxyContin was the only prescription medication that the family gave to
Ms. E.M.; \63\ and to his knowledge, the hospital never gave Ms. E.M.
any pain medication, not even Aleve, and that he did not know why she
should need Aleve.\64\ [Tr. 668]
---------------------------------------------------------------------------
\62\ Tr. 661.
\63\ But see Section D.1. supra: Respondent prescribed Ms.
E.M.'s Actos, Metformin, Lipitor, Plavix, and Zetia, all of which
appeared on Ms. E.M.'s prescription profile from Doc's Drugs but not
always on her home medication lists. GX 27.
\64\ Ms. E.M. did receive pain medication such as Aleve and
Tylenol.
---------------------------------------------------------------------------
Respondent's patient chart for Ms. E.M. includes treatment notes
for at least one day each month beginning September 15, 2003, and
ending on the date of her death, June 13, 2009, [RX 16] but indicates
that Ms. E.M. "missed appointments" with Respondent on both February
28 and March 28, 2006.\65\ Respondent explained that "at this point in
time when I write missed appointment, that will mean that I did not
give her a prescription for pain medication." \66\ Respondent later
testified that "I may have issued it at their home at a later
appointment, at a later point in time, but I don't think I issued it."
\67\ The Government offered into evidence [GX 14] photocopies of
prescriptions Respondent issued to Ms. E.M. for 80 mg OxyContin and
dated February 28 and March 28, 2006. Respondent's patient chart for
Ms. E.M. indicates, and Respondent testified, that he saw her on
October 20 and November 17, 2006, but records from St. Mary's Hospital
in evidence as a Government exhibit show that Ms. E.M. was admitted to
that hospital on October 7, 2006, that she was discharged on October
12, 2006, [GX 21 at 203] and immediately admitted into Manor Care
Nursing Home, where she remained until December 8, 2006. [GX 21 at 203,
GX 27B at 956, GX 43 at 108]
---------------------------------------------------------------------------
\65\ RX 16 at 5.
\66\ Tr. 787.
\67\ Tr. 787.
---------------------------------------------------------------------------
Respondent testified that he completed the continuing medical
education course required under his 2003 Consent Order and that during
that course he learned that it is unlawful "for a pharmacist to refill
a blank and give two dispenses on the same single blank" \68\ for a
Schedule II controlled substance. Respondent further testified that he
believes that a physician can authorize another prescription without
seeing the patient and that it is "even legal under the information
that I go by that you can even predate a controlled substance
prescription"; \69\ [Tr. 739] but that he has never predated
prescriptions and has never written refills although he has written new
prescriptions without seeing the patient. Respondent testified that he
also learned that a physician should ensure that patients to whom he
prescribes a controlled substance do not obtain controlled substances
from another source and that such patients should be tested to verify
that they are actually taking that medication. [Tr. 740] Respondent had
earlier testified that if the Government suspected diversion of
OxyContin with regard to E.M. then either the Government or Dr. S.D.
should have tested her for it. [Tr. 577]
---------------------------------------------------------------------------
\68\ Tr. 738.
\69\ Tr. 739.
---------------------------------------------------------------------------
Mr. I.S. testified that he discussed with Respondent the concern
that Ms. E.M. receive "her proper pain medicine" \70\ when she was in
a nursing home or hospital. [Tr. 674] Mr. I.S. further testified that
Dr. S.D. prescribed Vicodin for Ms. E.M. but that she never asked for
it because she did not need it; and that when Ms. E.M. was in the
nursing home or hospital he hired his girlfriend's daughter to visit
her twice a day and to give her medication and food and to sit with
her. [Tr. 675] Respondent testified that he had instructed "him" \71\
to be aware of other depressants, sleeping pills, narcotics, and
opioids given Ms. E.M. so as to avoid an overdose. [Tr. 656] Mr. I.S.
testified that in the three or four weeks before his mother died, he
met with the St. Mary's Hospital administrator and asked that no new
medications be given to Ms. E.M. without his knowledge. Mr. I.S.
further testified that prior to that time, the hospital had no
directions not to give pain medication to Ms. E.M. and that he reviewed
her medication charts every day to make sure that she did not receive
pain medication. [Tr. 711] Mr. I.S. testified that he never saw any
pain medication listed in Ms. E.M.'s hospital
[[Page 53953]]
charts, not even over-the-counter medications. [Tr. 714]
---------------------------------------------------------------------------
\70\ Tr. 674.
\71\ Presumably he is referring to Mr. I.S. See Tr. 656.
---------------------------------------------------------------------------
Mr. I.S. later testified that in the thirty days before Ms. E.M.
died, he reviewed the charts as many times as he went to the hospital
and that he "left orders with them to not introduce any new
medications to my mother. * * *" \72\ Mr. I.S. then testified that he
always gave directions to the hospital to not give Ms. E.M. any new
medications, and that he had previously told the DEA that both he and
Ms. E.M. were receiving OxyContin. Mr. I.S. testified that he knew that
DEA personnel could go to the hospital to see whether Ms. E.M. received
any other pain medication, so he made sure that she did not get any.
[Tr. 719] Mr. I.S. also testified that if an emergency arose when Ms.
E.M. was in a hospital or nursing home, such as if she were to fall,
then the hospital or nursing home would call him and he would issue
instructions not to give her any pain medication. [Tr. 728]
---------------------------------------------------------------------------
\72\ Tr. 712.
---------------------------------------------------------------------------
Respondent testified that at times, depending on the conditions, he
would omit or reduce the amount of OxyContin he prescribed to Ms. E.M.
or change the dosing schedule based on her clinical situation, and that
if she was suffering certain symptoms, such as from a stroke, he would
have "them" \73\ withhold the pain medication for up to 24 hours. Mr.
I.S. testified that he did not recall whether Respondent ever asked him
to delay the dosage or to hold back Ms. E.M.'s pain medication when she
was hospitalized.
---------------------------------------------------------------------------
\73\ Tr. 656. Presumably Respondent was referring to Ms. E.M.'s
family.
---------------------------------------------------------------------------
E. Respondent's 2006 DEA Renewal Application and Registered Location
On September 25, 2006, Respondent submitted to the DEA an
application to renew his registration. [Tr. 318; GX 31] Respondent's
registered location on that renewal application was listed as 120
Oakbrook Center Mall, Oakbrook, Illinois.\74\ In response to question
number three of the application, "Has the applicant ever had a state
professional license or controlled substance registration revoked,
suspended, denied, restricted, or placed on probation, or is any such
action pending?", Respondent provided an affirmative answer. In his
explanation for that answer, submitted with the application, Respondent
identified and explained the 2003 IDFPR Consent Order but did not refer
to the 1998 Consent Order. [GX 31] Respondent testified that his
omission of the 1998 order was inadvertent and that he had included the
1998 incident on previous renewal applications. [Tr. 618, GX 18]
---------------------------------------------------------------------------
\74\ GX 31.
---------------------------------------------------------------------------
Investigator R. testified that on March 13, 2009, she and another
diversion investigator served upon Respondent the DEA Order to Show
Cause that gave rise to this proceeding. [Tr. 323] Investigator R.
testified that she served the Order to Show Cause at Respondent's
residence in Riverside, Illinois, because the investigators had not
succeeded in serving it at his registered location, and that when the
investigators went to Respondent's residence and "before we had the
opportunity to identify ourselves, [Respondent] slammed the door in our
face when I said, 'Dr. Herbert, I have something for you,' and he said
that 'I am not Dr. Herbert. I am R.S.' " \75\ Investigator R. further
testified that a few minutes later Respondent telephoned her,
indicating that he was returning one of her earlier calls.
---------------------------------------------------------------------------
\75\ Tr. 327.
---------------------------------------------------------------------------
Investigator R. testified that during that telephone conversation
she arranged to serve the Order to Show Cause through Respondent's
attorney the next day; that Respondent informed her that he had moved
his registered location to 2910 South Harlem Avenue, Riverside,
Illinois; [Tr. 324] that she then advised Respondent that in order to
modify his registered location he needed to submit a modification
request along with a copy of his Illinois controlled substance license
showing the new location; and that she provided him a fax number to use
to send the documents. Investigator R. further advised Respondent that
he needed to wait until his modification was approved before he could
handle controlled substances at the new location. [Tr. 327]
Investigator R. testified that prior to March 13, 2009, the DEA had
not received any notification from Respondent or anyone else that he
had moved his medical practice from his DEA registered location in
Oakbrook to Riverside; [Tr. 326] that she had previously made several
failed attempts to contact Respondent at his registered address (she
went to 120 Oakbrook Center and knocked on Suite 711; telephoned
Respondent's office and left messages requesting a call back; and
identified herself in those messages and indicated that she needed to
deliver something); but that she had never been able to locate
Respondent at his registered location except when she arranged to do so
by appointment. [Tr. 325] Investigator R. testified that on March 26,
2009, the leasing office at the Oakbrook Center Mall informed her that
as of July 31, 2008, the locks had been changed on Respondent's
Oakbrook office because he had abandoned the location. [Tr. 324]
Respondent testified that in July 2008 he moved his office to 2910
Harlem Avenue; [Tr. 577] that the DEA would not send him any address
modification forms; that he could not access the forms on-line; and
that he called the DEA office in Chicago multiple times and left
messages in an attempt to get a change of address form.
Investigator R. testified that Respondent's attorney filed with the
DEA a request dated April 7, 2009, to modify Respondent's registered
location. [RX 15] That same day, counsel for the Government sent a
letter to Respondent indicating that since he had already moved his
office, he was not authorized to handle controlled substances at the
new location until the DEA approved the modification of his address.
[GX 9] Investigator R. testified that she served that letter in person
to Respondent's attorney and left for Respondent a telephone message
summarizing the contents of the letter. [Tr. 331] On June 8, 2009,
counsel for the Government sent another letter to Respondent's attorney
indicating that the registered location modification request had not
yet been approved and that, until it was approved, any controlled
substance prescriptions issued by Respondent would be unlawful. [GX 33]
Investigator R. testified that the letter was personally delivered to
Respondent and was faxed to Respondent's attorney. [Tr. 333]
Investigator R. further testified that she obtained from the
Illinois Department of Human Services Prescription Monitoring Program,
to which Illinois pharmacies are required to report information
pertaining to controlled substance prescriptions, a prescription
profile identifying controlled substance prescriptions that Respondent
issued from June through August 2009. [GX 34] During that period,
according to the prescription profile, Respondent issued 29 controlled
substance prescriptions to 13 different people: 60 dosage units of
OxyContin 80 mg to each of seven different people, one of whom also
received 30 diazepam 10 mg; 40 oxycodone 5 mg and 30 Adderal 30 mg to
one person; 90 hydrocodone 7.5 mg to one person; 10 hydrocodone 5 mg to
one person; 30 phentermine 37.5 mg (via two separate prescriptions
written on the same day) to one person; and 14 phentermine 37.5 mg to
one person. [GX 34]
Respondent testified that Investigator R. had told him on March 13,
2009, that he could not handle controlled
[[Page 53954]]
subscriptions but he "didn't take it all that seriously with the word
handling, because I had not ordered any prescriptions, and I had no
samples" \76\ but he did not ask her what she meant by "handling."
Respondent further testified that he did not see anything about
prescribing until he saw the letters from Government counsel, and that
his attorney reviewed the letters and told him that it appeared that
the DEA did "have the power to withhold the registration" \77\ but he
nonetheless continued to issue original controlled substances
prescriptions until October 2009, "when the gravity of what was going
on here became absolutely clear." \78\ [Tr. 778]
---------------------------------------------------------------------------
\76\ Tr. 779.
\77\ Tr. 777.
\78\ Tr. 778.
---------------------------------------------------------------------------
The Parties' Contentions
I. The Government
The Government contends, in substance, that the Deputy
Administrator should revoke Respondent's DEA registration and that any
pending applications for renewal or modification of that registration
should be denied, "because Respondent made material misstatements on
an application for registration and because his continued registration
would be inconsistent with the public interest as that term is used in
21 U.S.C. 823(f)." \79\
---------------------------------------------------------------------------
\79\ Government's Proposed Findings of Fact, Conclusions of Law
and Argument at 3.
---------------------------------------------------------------------------
The Government contends that Respondent has had controlled
substances violations dating back to 1994 and resulting in consent
orders with the Illinois Medical Board in 1998 and 2003. The 1998
consent order involved the unlawful prescribing of Dilaudid and
required Respondent to complete a course pertaining to the handling of
controlled substances. The Government contends that this course had
little effect on Respondent's prescribing, that he continues to violate
applicable law, and that he is evading the allegations rather than
responding to them candidly.
The Government next asserts that Respondent unlawfully received
dronabinol from a patient's prescription, failed to properly record
that receipt, and maintained a misleading and inaccurate record of his
subsequent dispensing of the dronabinol. Further, the Government argues
that Respondent's 2003 Consent Order with the IDFPR arose because the
unlawful dispensing was inevitable based on the arrangement between
Respondent and the clinic owner and Respondent's conduct therefore
enabled and abetted the clinic owner. As with the 1998 Consent Order,
Respondent was again required to complete a course on proper
prescribing and dispensing of controlled substances but, according to
the Government, Respondent ignored this education and continued to
collect violations.
The Government goes on to contend that Respondent violated state
law when he failed to disclose records demanded in an IDFPR subpoena.
The Government argues that the Illinois Medical Practice Act provides
the IDFPR with the authority to serve an administrative subpoena duces
tecum pursuant to a Medical Board investigation and that the Health
Insurance Portability and Accountability Act (HIPAA) provides an
exception for the disclosure of information that is requested by an
order of an administrative tribunal.
The Government further asserts that Respondent's omission of his
1998 Consent Order from his DEA controlled substances registration
renewal application was a material omission because it involved the
diversion of a Schedule II controlled substance and because Respondent
was conversant with the facts of the Consent Order at the immediate
hearing.
The Government argues that Respondent participated in a scheme that
involved the diversion of OxyContin. It argues that there is a lack of
medical history to justify issuing prescriptions for 80 mg OxyContin to
Ms. E.M. and that Respondent's attempts to provide justification for
prescribing to her are essentially post hoc rationalizations.
Additionally, the Government contends, it is unlikely that someone from
Ms. E.M.'s family was able to secretly administer OxyContin twice per
day during the approximately 290 days that she was in a hospital or in-
patient nursing home. According to the Government, Respondent's
arguments are further diminished by not only the conflicts in testimony
between Respondent and Mr. I.S. but also between the testimony and
institutional records, as well as Respondent's questionable patient
chart for Ms. E.M., which includes dates of Respondent's purported
treatment of her when she was confined to a hospital or nursing home.
The Government contends that if Ms. E.M. had received the OxyContin
that Respondent prescribed, she would likely suffer withdrawal symptoms
when institutionalized, but there is no such record. Also, the
Government contends, Respondent's and Mr. I.S.'s claims regarding the
time release properties of generic oxycodone are not credible because
they were refuted by both the Physician's Desk Reference and a
pharmacist.
The Government also argues that Respondent prescribed other drugs,
in addition to OxyContin, in Ms. E.M.'s name but that these drugs were
never administered to her and were likely diverted. The Government
points out that, although Respondent claims that he prescribed Actos
and Metformin to Ms. E.M. to treat diabetes, her other treating
physicians and hospital records indicate that she did not have diabetes
and Mr. I.S.'s testimony is again in conflict with Respondent's because
he testified that the only prescription drug he or his family
administered to Ms. E.M. was OxyContin. The Government further contends
that Plavix was also diverted, relying again on the conflicting
testimony of Respondent and Mr. I.S. and on the evidence that for some
time both Dr. S.D. and Respondent prescribed Plavix but, although Dr.
S.D. discontinued it because of injury risks, Respondent continued to
prescribe it; and Respondent's patient chart for Ms. E.M. provided no
information regarding such prescriptions.
Finally, the Government asserts that Respondent unlawfully
prescribed controlled substances from an unregistered location because
Respondent failed to timely request a modification of his registered
address and continued to issue controlled substances prescriptions at
his new location even after receiving numerous warnings against such
action.
II. Respondent
Respondent contends that the omission of his 1998 state probation
from his renewal application was not a material falsification because
the omission was inadvertent. Respondent asserts that inasmuch as he
accepted the 1998 state probation related to phentermine dispensing,
the DEA should not "seek additional retribution" \80\ for the
incident. Respondent argues his disclosure of the 1998 probation on
previous DEA applications, the DEA and state investigators' awareness
of both the 1998 and 2003 disclosures, and the previous disclosures'
existence "permanently on the D.E.A. computerized files," "clearly
[indicate] no subterfuge motive." \81\
---------------------------------------------------------------------------
\80\ Respondent's Closing Argument Brief at 8.
\81\ Respondent's Closing Argument Brief at 3.
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Respondent argues that in mid-August 2003, because of his 2003
state probation, he "purposely discontinued all ordering of
medications from wholesale suppliers for the purpose of
[[Page 53955]]
dispensing medications;" \82\ that, in the spring of 2005, when
Investigator D.M. asked to inspect Respondent's controlled substance
logs, Respondent did not recall any ordering or dispensing of
controlled substances in 2003 and created a handwritten log indicating
such; that later that same day, he found a controlled substance log
from the first seven months of 2003 that showed three instances in
which he had dispensed a controlled substance; and that Respondent's
attorney contacted Investigator D.M. to notify him of that log and that
Investigator D.M. was given a copy.
---------------------------------------------------------------------------
\82\ Respondent's Closing Argument Brief at 4.
---------------------------------------------------------------------------
Respondent further contends that his dispensing of dronabinol did
not violate 21 U.S.C. 844(a) because he was "acting in the course of
his professional practice." \83\ Respondent argues that he had a
patient who obtained dronabinol via a prescription issued by another
physician; that the patient "lawfully transferred the medication to me
* * * to be used for the benefit of another patient * * *;" and that
he dispensed the dronabinol to another patient and recorded that action
in the patient's chart and in his 2003 controlled substance log.
Respondent argues that his actions fall under the exception in Sec.
844(a) permitting a physician to possess or obtain a controlled
substance when "acting in the course of his professional practice"
\84\ and that there is no prohibition against obtaining medication from
a patient to use for another patient.
---------------------------------------------------------------------------
\83\ Respondent's Closing Argument Brief at 5.
\84\ Respondent's Closing Argument Brief at 5.
---------------------------------------------------------------------------
Respondent then asserts that this entire proceeding was initiated
against him as a form of revenge by the City of Chicago because
Respondent testified on behalf of Officer D.S. at the Chicago Police
Board hearing. Respondent asserts that his right to due process has
been violated because Illinois and the DEA have violated the Illinois
Medical Practice Act and because he was not represented by counsel at
the instant hearing. Respondent argues that any evidence that was not
"generated by [Investigator] R. alone or directly subpoenaed by D.E.A.
has no place in evidence at this hearing." \85\
---------------------------------------------------------------------------
\85\ Respondent's Closing Argument Brief at 9.
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Respondent contends that the DEA has failed to meet its burden of
proof of showing that he failed to comply with the IDFPR administrative
subpoenas issued in 2005 and 2007; Respondent asserts that he provided
the requested records but redacted all identifying information as
required by 225 ILCS 60/22(A)(38). Respondent argues that because the
statute provides that "all information indicating the identity of the
patient shall be removed and deleted" and that because records of
prescriptions he issued and to which Illinois and the DEA have access
include patient names and the date the prescriptions were issued, he
was required to redact the names and treatment dates in order to allow
Illinois to "review the records without tying a specific chart to a
patient." \86\ Respondent further argues that he complied with the
subpoena prior to March 2009 because his attorney supplied codes
revealing the names and Respondent obtained permission from his
patients to provide the relevant medical charts. Respondent contends
that the allegation that he failed to comply with the subpoenas is
another example of revenge-seeking by Chicago because of Respondent's
testimony in the Police Board hearing; that the DEA and Illinois are
"doing the bidding of the City of Chicago;" \87\ that the records
that were the subject of the subpoenas should not have been available
to the DEA because 225 ILCS 36 bars the DEA from having or using
information compiled by Illinois; that Respondent was not represented
by counsel at the instant hearing; and that Respondent relied on the
advice of his previous counsel with regard to the redacted information
provided in response to the subpoenas.
---------------------------------------------------------------------------
\86\ Respondent's Closing Argument Brief at 9.
\87\ Respondent's Closing Argument Brief at 10.
---------------------------------------------------------------------------
Respondent asserts that there is no evidence of diversion with
regard to his prescribing OxyContin to Ms. E.M.; that he treated her
for more than five and a half years prior to her death; that Ms. E.M.
suffered from multiple medical problems (including severe
kyphoscoliosis, cerebral vascular disease, Binswanger's Disease, and
diabetes); that Ms. E.M. and seven other patients required the
prescriptions he issued them for OxyContin 80 mg because that strength
was not a high dose for them because of the form of chronic pain from
which they suffered; and that he properly treated Ms. E.M. for diabetes
and inflammatory vascular disease by prescribing Actos and Metformin.
Respondent also asserts that Actos and Metformin are not controlled
substances and are therefore outside the DEA's jurisdiction.
Respondent argues that it is not plausible that the OxyContin he
prescribed to Ms. E.M. was diverted because: Respondent and his
patients were aware of the DEA investigation and the patients produced
their current medications when interviewed; the DEA and Dr. S.D. failed
to perform opioid level tests on Ms. E.M., even though they were free
to do so and she showed signs of clinical opioid usage and rarely
complained of pain despite the presence of "multiple and obvious pain
sources;" \88\ if Respondent performed an opioid test on Ms. E.M. it
would not disprove diversion; Mr. I.S. never filled the prescriptions
that Drs. S.D. and V.P. issued to Ms. E.M. for Vicodin; and Respondent
had previously prescribed OxyContin 80 mg to Ms. C.G. and, after
Respondent stopped treating her, a Dr. M. continued the same
prescriptions. Respondent further claims that the failure of the DEA,
Dr. S.D., Dr. V.P., and Dr. M.\89\ to test Ms. E.M. for opioids and
thereby exonerate Respondent, cannot be used against him because, if
they had suspicions of diversion, they should have "[acted] to clear
up this charge." \90\ Respondent contends that Investigator R.
conducted her investigation with "obvious prejudice" \91\ to cast
Respondent in an unfavorable light. Respondent asserts that Drs. S.D.,
P., and M. were aware that Ms. E.M. had pain because they prescribed
pain medicines such as Vicodin and morphine; that Ms. E.M.'s not taking
the pain medication should have alerted these doctors that her family
was medicating her; that Ms. E.M.'s family asked Respondent not to
communicate with her other doctors and he complied to avoid discharge
as her physician; and that Respondent "placed OxyContin on the
record." \92\
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\88\ Respondent's Closing Argument Brief at 14.
\89\ Although he refers to a "Dr. M." in his brief, I presume
that Respondent actually intended to refer to either Dr. G.M. or Dr.
T.M. because there was no evidence presented that Ms. E.M. was ever
treated by a Dr. M.
\90\ Respondent's Closing Argument Brief at 15.
\91\ Respondent's Closing Argument Brief at 15.
\92\ Respondent's Closing Argument Brief at 17.
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Respondent contends that the DEA acted "capriciously and in bad
faith" \93\ by invalidating his DEA registration when he moved his
office from his registered location and by refusing to reinstate his
license pending the instant proceedings. Respondent argues that he was
not permitted access to forms or other communication methods on the DEA
Web site and that none of his calls to Investigator R. and the DEA's
Chicago office were returned; that the DEA refused to transfer
Respondent's registration to his new office after "the D.E.A. finally
figured out I moved"; \94\ that Respondent sent a letter to the DEA
advising it of his move in lieu of the forms he "was not allowed to
fill
[[Page 53956]]
out"; \95\ that Respondent "essentially stopped practicing medicine"
\96\ after he received a second letter from Government counsel; and
that the DEA allowed his registration to remain active on its website
even though it had the power to "shut off [his] registration by
pulling it from the active list on their pharmacy access Web site,"
\97\ thereby creating "an incident and another charge against me"
\98\ that occurred for no reason other than harassment. Respondent
further claims that the cases counsel for the Government cited in his
letter to Respondent regarding his change of address are not applicable
in this situation because those cases involved "two meth suppliers to
convenience stores, a pharmacy, and a doctor whose state license had
already been revoked" \99\ and Respondent,\100\ as a "practicing MD
with no criminal complaint" \101\ does not fit into any of those
categories. Respondent further argues that the DEA had the power to
deactivate his controlled substance license on the DEA Web site,
thereby "shutting down [his] ability to issue any controlled
substances" \102\ and that because the DEA's failure to do so was more
harassment which was "clearly unethical if not illegal," \103\
Respondent should not be held responsible.
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\93\ Respondent's Closing Argument Brief at 17.
\94\ Respondent's Closing Argument Brief at 17.
\95\ Respondent's Closing Argument Brief at 17.
\96\ Respondent's Closing Argument Brief at 17.
\97\ Respondent's Closing Argument Brief at 17.
\98\ Respondent's Closing Argument Brief at 18.
\99\ Respondent's Closing Argument Brief at 18.
\100\ Respondent's Closing Argument Brief at 18.
\101\ Respondent's Closing Argument Brief at 18.
\102\ Respondent's Closing Argument Brief at 18.
\103\ Respondent's Closing Argument Brief at 18.
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Discussion and Conclusions
I. The Applicable Statutory and Regulatory Provisions
The Controlled Substances Act provides that any person who
dispenses (including prescribing) a controlled substance must obtain a
registration issued by the DEA in accordance with applicable rules and
regulations.\104\ "A separate registration shall be required at each
principal place of business or professional practice where the
applicant * * * dispenses controlled substances." \105\ DEA
regulations provide that any registrant may apply to modify his
registration to change his address but such modification shall be
handled in the same manner as an application for registration." \106\
---------------------------------------------------------------------------
\104\ 21 U.S.C. 822(a)(2).
\105\ 21 U.S.C. 822(e).
\106\ 21 CFR 1301.51.
---------------------------------------------------------------------------
It is unlawful for any person to possess a controlled substance
unless that substance was obtained pursuant to a valid prescription
from a practitioner acting in the course of his professional
practice.\107\ A registered individual practitioner is required to
maintain records of controlled substances in Schedules II through V
that are dispensed and received, including the number of dosage units,
the date of receipt or disposal, and the name, address, and
registration number of the distributor.\108\
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\107\ 21 U.S.C. 844(a).
\108\ 21 CFR 1304.03(b), 1304.22(a)(2)(ix), 1304.21(a),
1304.22(c), and 1304.22(a)(2)(iv).
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A. Revocation of DEA Registrations
The Controlled Substances Act, at 21 U.S.C. 824(a), provides,
insofar as pertinent to this proceeding, that the Deputy Administrator
may revoke a registration if she finds that the registrant has
materially falsified an application for registration or renewal of
registration \109\ and/or if she finds that the continued registration
would be inconsistent with the public interest as that term is used in
21 U.S.C. 823(f).\110\
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\109\ 21 U.S.C. 824(a)(1).
\110\ 21 U.S.C. 824(a)(4).
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B. The Public Interest Standard
Pursuant to 21 U.S.C. 823(f), the Deputy Administrator may deny an
application for a DEA Certificate of Registration if she determines
that such registration would be inconsistent with the public interest.
In determining the public interest, the Deputy Administrator is
required to consider the following factors:
(1) The recommendation of the appropriate state licensing board or
professional disciplinary authority.
(2) The applicant's experience in dispensing, or conducting
research with respect to controlled substances.
(3) The applicant's conviction record under Federal or State laws
relating to the manufacture, distribution, or dispensing of controlled
substances.
(4) Compliance with applicable State, Federal, or local laws
relating to controlled substances.
(5) Such other conduct which may threaten the public health and
safety.
As a threshold matter, it should be noted that the factors
specified in section 823(f) are to be considered in the disjunctive:
The Deputy Administrator may properly rely on any one or a combination
of those factors, and give each factor the weight she deems
appropriate, in determining whether a registration should be revoked or
an application for registration denied.\111\
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\111\ See Henry J. Schwarz, Jr. M.D., 54 FR 16,422 (DEA 1989).
---------------------------------------------------------------------------
II. The Factors To Be Considered
A. Renewal of Respondent's DEA Registration
1. Material Falsification of a Renewal Application
Respondent materially falsified his 2006 renewal application for a
DEA registration when he failed to disclose any information regarding
his 1998 state probation, even though he did disclose his 2003 state
probation. I find unpersuasive Respondent's argument that the omission
is irrelevant due to the DEA's awareness of and Respondent's previous
disclosure of the 1998 probation: The DEA has repeatedly held that "
'[t]he provision of truthful information on applications is absolutely
essential to effectuating [the] statutory purpose' of determining
whether the granting of an application is consistent with the public
interest." \112\ A false statement is material if it "has a natural
tendency to influence, or was capable of influencing, the decision of
the decisionmaking body to which it was addressed." \113\ While the
evidence must be "clear, unequivocal, and convincing," the "ultimate
finding of materiality turns on an interpretation of the substantive
law." \114\ The Deputy Administrator has also previously held that
"[t]he explanation given by an applicant who has affirmatively
answered a liability question is * * * material because the public
interest inquiry under section 303(f) requires, inter alia, that the
Agency examine '[t]he applicant's experience in dispensing * * *
controlled substances,' and its [c]ompliance with applicable State,
Federal, or local laws relating to controlled substances.' " \115\
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\112\ The Lawsons, 72 FR at 74338 (quoting Peter H. Ahles, 71 FR
50097, 50098 (2006)). See also Hoxie v. DEA, 419 F.3d 477, 483 (6th
Cir. 2005) ("Candor * * * is considered by the DEA to be an
important factor when assessing whether a * * * registration is
consistent with the public interest.").
\113\ Kungys v. United States, 485 U.S. 759, 770 (1988) (int.
quotation and other citations omitted).
\114\ Id. at 772 (int. quotation and other citations omitted).
\115\ The Lawsons, 72 FR at 74338 (citing 21 U.S.C. 823(f)).
---------------------------------------------------------------------------
Although Respondent claims that his omission of the 1998 probation
from his registration renewal application was inadvertent, that is
irrelevant because the Government only needs to show that the applicant
"knew or should have known that the response given to the liability
question was false," not that the material falsification was
intentional.\116\ It is apparent that Respondent was aware of his 1998
probation because he
[[Page 53957]]
admittedly disclosed it on previous DEA registration applications and
because he entered into a consent order with the IDFPR and purportedly
completed the required conditions. Respondent therefore knew or should
have known that his response to the liability question was false.
---------------------------------------------------------------------------
\116\ The Lawsons, 72 FR at 74339; Samuel Arnold, 63 FR 8687 at
8688 (1998).
---------------------------------------------------------------------------
Respondent's omitted 1998 probation was related to Respondent's
handling of Dilaudid, which is directly related to the second and
fourth factors listed in 21 U.S.C. 823(f). Regardless of whether DEA
and Illinois had prior knowledge of that probation, the omission of an
offense related to the handling of a schedule II controlled substance
would certainly have a natural tendency to influence the decision of
whether to grant Respondent's application when considering the
applicant's experience in handling controlled substances and compliance
with applicable State, Federal, and local laws relating to controlled
substances. I thus conclude that Respondent's failure to disclose the
1998 state probation was a material misrepresentation because it
"ha[d] a natural tendency to influence the * * * decision" of the DEA
as to whether to grant his application for a new registration. Under
DEA precedent, a material falsification "provides an independent and
adequate ground for denying" Respondent's application.\117\
---------------------------------------------------------------------------
\117\ The Lawsons, 72 FR at 74338; Cf Bobby Watts, 58 FR 46997
(1993).
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2. Candor and Admission of Fault
The DEA properly considers the candor of the physician and his
forthrightness in assisting in the investigation and admitting fault
important factors in determining whether the physician's registration
should be revoked.\118\ I find that Respondent has repeatedly failed to
accept responsibility for his misconduct. This failure is evidenced by
Respondent's consistent denial of any wrongdoing: Respondent asserts
that his actions leading to his 1998 state probations were lawful even
after he agreed to enter into a consent order with the IDFPR; with
regard to his 2003 state probation, Respondent asserts (1) that his
only blame was in leaving his bag, without a secure lock, at the clinic
when he was not present and that he clearly "could not prevent the
owner's actions once I left medicine (Phentermine) in my locked bag"
and (2) that the DEA should not "seek additional retribution" with
regard to the incident because he accepted the state probation;
Respondent repeatedly claims that the immediate hearing is the result
of a "vendetta" against him instigated by the City of Chicago;
despite my previous rulings to the contrary, Respondent continues to
assert that most of the evidence and testimony admitted in the instant
hearing is inadmissible and should not be considered; and Respondent
continues to assert that he was "not afforded a capable attorney"
\119\ although he was at any time free to procure the assistance of
counsel, was notified of such, and he did not request a postponement of
the instant hearing prior to its commencement in order to do so.\110\
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\118\ Hoxie v. DEA, 419 F.3d 477, 483 (6th Cir. 2005).
\119\ Respondent's Closing Argument Brief at 10.
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B. The Public Interest Standard
As noted above, Respondent submitted a request to modify his
registration, which is still pending. Pursuant to 21 CFR 1301.51, a
request for a modification shall be handled in the same manner as an
application for registration. Pursuant to 21 U.S.C. 823(f), the Deputy
Administrator may deny an application for a DEA Certificate of
Registration if she determines that such registration would be
inconsistent with the public interest, consistent with the five factors
described above.
In light of the circumstances of this case, I will consider
Respondent's compliance with applicable law and experience in handling
controlled substances together below.
1. The Recommendation of the Appropriate State Licensing Board
It is undisputed that Respondent is currently licensed as a
physician and to handle controlled substances in Illinois. Inasmuch as
Respondent is currently authorized to handle controlled substances in
Illinois, I find that this factor weighs in favor of a finding that
Respondent's registration would not be inconsistent with the public
interest. However, I note that state licensure is a necessary but not
sufficient condition for DEA registration, and I therefore find that
this factor is not dispositive.
2. Respondent's Experience in Handling Controlled Substances and
Compliance With Applicable State, Federal, or Local Laws Relating to
Controlled Substances
I conclude that Respondent's experience in handling controlled
substances and Respondent's compliance with applicable State, Federal,
or local laws relating to controlled substances weighs in favor of a
finding that his registration would not be consistent with the public
interest.
(a) Respondent's Prior State Disciplinary Actions
In the previously discussed 1998 Consent Order, the then IDPR
alleged that Respondent "may have prescribed Dilaudid to four (4)
patients under questionable circumstances"; \120\ Respondent did not
admit or deny the allegations but did agree not to contest them. As a
condition of his probation, Respondent was required to complete a
remedial education course in controlled substance management. In his
Closing Argument Brief, Respondent asserts that there was never any
finding that the probation came about as a result of unlawful
prescribing of Dilaudid, and in the instant hearing Respondent
testified that his actions related to the incident were lawful.
---------------------------------------------------------------------------
\120\ GX 7 at 2.
---------------------------------------------------------------------------
In the 2003 Consent Order the IDFPR alleged, and Respondent
admitted, that he failed to supervise an unlicensed employee. In the
instant hearing and in his Closing Argument Brief, however, Respondent
asserts that he was the employee and that he was unable to prevent the
clinic owner from removing the phentermine from Respondent's locked
bag, but that he accepted the probation because he should not have left
the bag at the clinic when he was not there. As a condition of his
probation, Respondent was required to complete ten hours of continuing
education in the area of prescribing and dispensing controlled
substances. I find that Respondent's conduct leading to the 2003
Consent Order and his apparent lack of understanding of proper methods,
even after completing several hours of controlled substance handling
education, weigh in favor of a finding that his continued registration
would be inconsistent with the public interest.
(b) Respondent's Receipt and Dispensing of Marinol
I find no merit to Respondent's assertions that he lawfully
received Marinol from a patient and also lawfully provided it to
another patient. Pursuant to 21 U.S.C. 844(a), "[i]t shall be unlawful
for any person knowingly or intentionally to possess a controlled
substance unless such substance was obtained directly, or pursuant to a
valid prescription or order, from a practitioner, while acting in the
course of his professional practice * * *" except as otherwise
authorized by the Controlled Substances Act.
Respondent's interpretation of 21 U.S.C. 844(a) is mistaken;
Respondent apparently believes that, because he is
[[Page 53958]]
a practitioner who was purportedly acting in the course of his
professional practice at the time he received the Marinol, this section
permitted him to receive the Marinol from a patient. Respondent,
however, fails to recognize that 21 U.S.C. 844(a) requires that the
controlled substance be obtained directly or pursuant to a prescription
from a practitioner, not provided to a practitioner acting in the
course of his professional practice. Respondent has made no assertion
and provided no evidence that Mr. J.W., from whom Respondent admittedly
obtained the Marinol, was a practitioner \121\ acting in the course of
his professional practice or that Mr. J.W. possessed the proper DEA
registration to dispense or distribute controlled substances, as
required by 21 U.S.C. 822(a)(1) and 21 CFR 1307.11(a)(1),\122\ when he
provided Respondent with the Marinol. Pursuant to 21 CFR 1307.12,
however, a person in lawful possession of a controlled substance may,
without a registration to do so, distribute such substance to the
person from whom it was obtained or to the manufacturer of the
substance. Respondent, however, testified at a police board hearing
that the Marinol likely came from the prescription of another doctor,
not Respondent. Mr. J.W., therefore, did not obtain the Marinol
directly from or pursuant to a prescription from Respondent and there
is no evidence indicating that Mr. J.W. possessed a DEA registration to
distribute or dispense controlled substances so Respondent was
subsequently not authorized to receive the Marinol from Mr. J.W. under
21 CFR 1307.12.
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\121\ "Practitioner" is defined in 21 U.S.C. 802(21) as: "a
physician, dentist, veterinarian, scientific investigator, pharmacy,
hospital, or other person licensed, registered, or otherwise
permitted, by the United States or the jurisdiction in which he
practices or does research, to distribute, dispense, conduct
research with respect to, administer, or use in teaching or chemical
analysis, a controlled substance in the course of professional
practice or research."
\122\ 21 CFR 1307.11(a)(1) generally provides that a
practitioner who is registered to dispense a controlled substance
may distribute a quantity of such substance to another practitioner
for the purpose of general dispensing to patients provided that both
the distributing and the receiving practitioners record the
distribution in accordance with 21 CFR 1304.22(c).
---------------------------------------------------------------------------
Respondent apparently recognizes, as indicated in his Closing
Argument Brief, that he is required to record the receipt and
subsequent dispensing of controlled substances. Pursuant to 21 CFR
1304.03(b), 1304.22(a)(2)(ix), 1304.21(a), 1304.22(c), and
1304.22(a)(2)(iv), a registered individual practitioner is required to
maintain records of controlled substances in Schedules II-V that are
dispensed and received, including the number of dosage units, the date
of receipt or disposal, and the name, address, and registration number
of the distributor. In his brief, Respondent asserts that he has a "
'non monetary' receipt supplied by Mr. J.W." \123\ The only document
admitted into evidence that relates to the receipt of the Marinol,
however, is an affidavit \124\ with a signature reading "J.W." and
dated May 2, 2008, nearly five years after Respondent purportedly
received and subsequently dispensed the Marinol. Not only is the
general authenticity of that document suspect, but it also can not
reasonably be viewed as a proper record of receipt, particularly
considering that it was prepared nearly five years after the event and
that Respondent previously claimed to have no recollection of the
details of obtaining the Marinol. Respondent also entered into evidence
a controlled substances log dated January 2003 through August 14, 2004,
indicating that on July 21, Respondent dispensed 8 Marinol 10mg to
Officer D.S., which, despite the questionable circumstances under which
it was presented to the IDFPR investigator, may arguably be considered
a record of dispensing.
---------------------------------------------------------------------------
\123\ Respondent's Closing Argument Brief at 5.
\124\ Although the document is signed, it is neither witnessed
nor notarized, and when the document was admitted, no witness was
presented to verify the document's authenticity.
---------------------------------------------------------------------------
Accordingly, I find that Respondent's receipt of the Marinol was
unlawful under 21 U.S.C. 844(a) and 21 CFR 1304.03(b), 1304.21(a),
1304.22(c), 1304.22(a)(iv), 1304.22(a)(2)(ix), 1307.11, and 1307.12 because Respondent did not receive the Marinol directly from or
pursuant to a prescription or order from a practitioner acting in the
course of his professional practice or from a person who was in lawful
possession of and originally obtained the Marinol from Respondent, or
as otherwise authorized by the Controlled Substances Act, and because
the receipt of the Marinol was not properly recorded. Additionally, as
the Government points out, Respondent testified in the instant hearing
that he has also in the past provided to patients Tylenol III and
Tylenol IV that he had obtained from other patients to whom it had been
prescribed by other physicians. I find that Respondent's unlawful
receipt of a Schedule III controlled substance and failure to properly
record such receipt weigh in favor of a finding that Respondent's
continued registration would be inconsistent with the public interest.
(c) IDFPR Administrative Subpoenas
I find that the Government has not provided sufficient evidence to
indicate that Respondent violated state law when he failed to comply
with a subpoena duces tecum issued by the IDFPR requesting copies of
patient records.
The Government correctly asserts that the IDFPR has the authority
to "subpoena the medical and hospital records of individual patients
of" \125\ licensed physicians. Respondent, however, is essentially
correct in his assertion that all information provided pursuant to such
a subpoena and which indicates the identity of the patient, shall be
removed and deleted prior to submission to the disciplinary board or
department. Respondent further correctly asserts that the term "all
information indicating the identity of the patient" includes patient
names and dates of treatment because the IDFPR and the DEA have the
ability to match that information with prescription records. Respondent
also testified at the instant hearing that disclosure of the requested
information, without first obtaining patient permission, would violate
the federal Health Insurance Portability and Accountability Act
(HIPAA).
---------------------------------------------------------------------------
\125\ 225 ILCS 60/38.
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Although neither party has submitted any relevant case law on the
topic, the Illinois Supreme Court has provided some guidance regarding
the disclosure of confidential patient information pursuant to an
administrative subpoena. In People v. Manos, the court held that the
Illinois legislature did not expressly provide for the investigatory
power provided to the IDFPR to override the physician-patient privilege
as codified in 735 ILCS 5/8-802. The IDFPR, therefore, cannot require a
physician under an administrative investigation to produce confidential
patient medical records unless one of the statutory exceptions set
forth in 735 ILCS 5/8-802 applies.\126\ Additionally, the court adopted
a finding that the mere deletion of patient names and identifying
information does not remove the records from protection under the
physician-patient privilege when the department that issued the
subpoena knows the names of the patients whose records were sought,
those patients are not parties to the investigatory proceedings, and
matching the records to the names would not be difficult even if the
names and other identifying information were redacted.\127\ I note that
at the time that
[[Page 53959]]
the IDFPR issued the subpoenas to Respondent on June 15, 2005, and June
20, 2007, no applicable exception applied under 735 ILCS 5/8-802.\128\
An exception for subpoenas issued pursuant to the Medical Practice Act
is now included in 735 ILCS 5/8-802,\129\ however, that exception did
not become effective until August 27, 2007 and is therefore not
applicable.
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\126\ People v. Manos, 202 Ill. 2d 563 (2002).
\127\ People v. Manos, 202 Ill. 2d 563 (2002) (citing Parkson v.
Central DuPage Hospital, 105 Ill. App. 3d 850 (1982)).
\128\ The exceptions in effect during the applicable period are
as follows: "* * * (1) in trials for homicide when the disclosure
relates directly to the fact or immediate circumstances of the
homicide, (2) in actions, civil or criminal, against the healthcare
practitioner for malpractice * * *, (3) with the expressed consent
of the patient * * *, (4) in all actions brought by the patient, his
or her personal representative, a beneficiary under a policy of
insurance, or the executor or administrator of his or her estate
wherein the patient's physical or mental condition is an issue * *
*, (4.1) in all actions brought against the patient, his or her
personal representative, a beneficiary under a policy of insurance,
or the executor or administrator of his or her estate wherein the
patient's physical or mental condition is an issue, (5) upon an
issue as to the validity of a document as a will of the patient, (6)
in any criminal action where the charge is either first degree
murder by abortion, attempted abortion or abortion, (7) in actions,
civil or criminal, arising from the filing of a report in compliance
with the Abused and Neglected Child Reporting Act [325 ILCS 5/1 et
seq.], (8) to any department, agency, institution or facility which
has custody of the patient pursuant to State statute or any court
order of commitment, (9) in prosecutions where written results of
blood alcohol tests are admissible pursuant to Section 11-501.4 of
the Illinois Vehicle Code [625 ILCS 5111-501.4], (10) in
prosecutions where written results of blood alcohol tests are
admissible under Section 5-lla of the Boat Registration and Safety
Act [625 ILCS 45/5-11a], or (11) in criminal actions arising from
the filing of a report of suspected terrorist offense in compliance
with Section 29D-10(p)(7) of the Criminal Code of 1961 [720 ILCS 5/
29D-l0].
\129\ "No physician or surgeon shall be permitted to disclose
any information he or she may have acquired in attending any patient
in a professional character, necessary to enable him or her
professionally to serve the patient, except only * * * (12) upon the
issuance of a subpoena pursuant to Section 38 of the Medical
Practice Act of 1987 [225 ILCS 60/38]. * * *" 735 ILCS 5/8-802.
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I agree with the Government's assertion that Respondent's argument
that compliance with the subpoenas would violate HIPAA is baseless
because the subpoena was issued as an order of an administrative
tribunal.\130\ Nonetheless, I further find that because of the Illinois
Supreme Court decision in Manos, it does not matter whether the
disclosure would violate HIP AA because it was not disclosable under
the physician-patient privilege law in effect in Illinois at the time
of the issuance of the subpoena.\131\ Accordingly, I find that the
Government has not met its burden of proof that Respondent violated
state law in failing to comply with a subpoena duces tecum issued by an
administrative tribunal.
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\130\ See 45 CFR 164.512(e)(1), (2), and (3).
\131\ I also find no merit to Respondent's argument that he
relied on the advice of counsel when he provided the redacted
patient files to the IDFPR. Respondent has cited no relevant law to
indicate that reliance on counsel would relieve him of
responsibility for failing to comply with a subpoena.
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I note that I have already found no merit to Respondent's argument
that the patient files and the testimony of Investigator D.M. in the
immediate hearing are inadmissible in this proceeding and should not be
available to the DEA.\132\ Because Respondent is likely to present this
argument again, however, I will add that, in addition to the reasons
previously stated in my Memorandum to Parties and Rulings, dated
February 12, 2010 and Memorandum to Parties and Ruling, dated April 9,
2010, the section of this opinion regarding the IDFPR subpoena duces
tecum cannot provide the basis for an argument that the relevant
patient files are inadmissible because Respondent obtained permission
to provide the files, thereby waiving the physician-patient privilege.
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\132\ See Memorandum to Parties and Rulings, dated February 12,
2010 and Memorandum to Parties and Ruling, dated April 9, 2010.
(Respondent relied on 225 ILCS 60/22(A)(5) and 60/23(B) to exclude
the testimony of IDFPR Investigator D.M. and to exclude all evidence
relating to Respondent's dispensing of Marinol to D.S. I denied
Respondent's request and found that Section 60/23(B)'s constraint on
the Medical Disciplinary Board's ability to further disclose
reported information is limited to the confidentiality of medical
reports and committee reports as otherwise protected by law.)
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(d) Prescribing From an Unregistered Location
I find that Respondent violated federal law by prescribing
controlled substances from his new location without a valid
registration. As provided in 21 U.S.C. 822(e), "[a] separate
registration shall be required at each principal place of business or
professional practice where the applicant * * * dispenses controlled
substances." Additionally, pursuant to 21 CFR 1301.51, any registrant
may apply to modify his registration to change his address but such
modification shall be handled in the same manner as an application for
registration. Unlike a renewal application, which, when timely filed,
remains in effect past the registration expiration date while the DEA
makes a final determination on the application,\133\ a request for a
modification is treated as a new application; a registrant, therefore,
is not authorized to dispense or prescribe controlled substances at his
new location pending approval of a modification request to change a DEA
registered address.\134\
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\133\ See 5 U.S.C. 558(c).
\134\ See John J. Fotinopoulos, 72 FR 24602 (2007).
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The record demonstrates that even though Respondent moved from his
registered address to a new location in July 2008, he failed to notify
the DEA of this change until at least April 7, 2009,\135\ after a DEA
diversion investigator was unable to locate Respondent at his
registered address and eventually located him at his residence.
Additionally, Respondent admittedly continued to handle controlled
substances not only while that modification was pending but after the
DEA had notified him in writing at least two times, and Respondent's
own attorney confirmed at least once, that he was not permitted to do
so. Respondent's argument that the DEA actively prevented him from
submitting a request for modification of his registered location is
unconvincing, particularly considering that Respondent failed to
provide any evidence indicating he ever attempted to submit the
request.\136\
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\135\ RX 15.
\136\ Respondent submitted several documents with his brief,
marked as "Brief Exhibits." I have not considered these documents
in reaching my findings and conclusions, however, because they were
not offered or admitted into evidence. See 21 CFR 1316.57.
Respondent also makes several references to testimony that was
offered in related state proceedings; that information also will not
be considered here for the same reason.
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Respondent's act of continuing to handle controlled substances
after numerous warnings shows a flagrant disregard for the requirements
of the law governing the handling of controlled substances.
Additionally, Respondent not only refuses to accept any blame
whatsoever for failing to properly notify the DEA of his change of
address but also claims that the DEA is responsible for him continuing
to issue prescriptions for controlled substances and for pharmacies
continuing to fill those prescriptions. I therefore find that
Respondent's failure to comply with federal law regarding modification
of his controlled substances registration and his additional refusal to
accept responsibility for his actions strongly support a finding that
Respondent's continued registration would be inconsistent with the
public interest.
(e) Diversion of OxyContin
I find that the Government has met its burden in establishing
diversion by a preponderance of the evidence and the Government has
also shown that even if Respondent was unaware of the diversion,
Respondent was involved in a scheme that created the opportunity for
diversion of a Schedule II controlled substance.
[[Page 53960]]
The DEA has held that a finding that a practitioner is reckless or
negligent in ignoring the warning signs that a patient is either
personally abusing controlled substances or diverting them to others is
an indication that the practitioner's registration would be
inconsistent with the public interest; misconduct that is
"unintentional, innocent or devoid of improper motivation * * *
creates the opportunity for diversion and could justify revocation or
denial." \137\
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\137\ See Paul J. Caragine, Jr., 63 FR 51592 (DEA 1998).
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The evidence in this case clearly demonstrates that Respondent
knowingly and willingly participated in a scheme to deceive other
healthcare providers with regard to Ms. E.M.'s use of a Schedule II
controlled substance and was at the very least reckless or negligent in
ignoring the possibility of diversion and thereby created the
opportunity for diversion of OxyContin. The record establishes that
Respondent willingly agreed to continue to treat and to prescribe
controlled substances to Ms. E.M. and to refrain from revealing his
involvement to anyone other than Ms. E.M.'s family, even while Ms. E.M.
was institutionalized and while she was being treated by other
physicians. The numerous inconsistencies between the testimonies of Mr.
I.S. and Respondent lead me to believe that neither is a credible
witness with regard to Ms. E.M.'s medication and treatment and raises
the questions of whether Respondent actually even treated Ms. E.M. and
whether she received OxyContin.
The evidence shows that each month for several years, Respondent
provided prescriptions for 60 OxyContin 80 mg tablets to three members
of the same household, including Ms. E.M., who was over 90 years old
and purportedly frail. As the Government points out, Ms. E.M. was
confined to a hospital or nursing home for a total of approximately 290
days during that period.
I first find it difficult to believe that Ms. E.M.'s family was
able to administer OxyContin twice a day for such an expansive time
without ever arousing the suspicion of the facility staff. I also find
it difficult to believe that for each of those approximately 290 days,
although Ms. E.M. was purportedly receiving a total of 160 mg of
OxyContin per day, two doses of 80 mg each,\138\ Ms. E.M.'s family was
able to prevent the possibility of an overdose simply by reviewing her
daily charts (with the exception of the last three or so weeks of Ms.
E.M.'s life when Mr. I.S. claims that he prohibited the facility from
providing any type of pain medication to her).
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\138\ According to the Physician's Desk Reference, 80 mg is the
second-highest dosage of OxyContin available in a single pill.
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Respondent ignored the warning signs of diversion by assisting in
the family's scheme to conceal Ms. E.M.'s OxyContin prescriptions and
by failing to test Ms. E.M.'s opioid levels to ensure that she actually
received the drug. I find that Respondent was at least reckless or
negligent in ignoring the warning signs of diversion with regard to the
OxyContin he prescribed to Ms. E.M. and his conduct, intentional or
not, thereby created the opportunity for diversion.
I find that Respondent did not issue OxyContin prescriptions for a
legitimate medical purpose while acting in the scope of his
professional practice. While I agree with Respondent that the DEA's
governing regulations do not require him to perform a physical
examination of a patient before providing each prescription, 21 CFR
1306.04(a), requires that controlled substance prescriptions be issued
for a legitimate medical purpose by a practitioner acting in the scope
of his professional practice.
The evidence also does not support a finding that Respondent issued
OxyContin prescriptions to Ms. E.M. pursuant to 21 CFR 1306.12(b)(1),
1306.05, or 1306.04(a). What constitutes bona fide "medical practice"
by a physician dispensing narcotic drugs must be determined upon
consideration of the evidence and attending circumstances.\139\ The
Supreme Court of the United States clarified this issue in Gonzales v.
Oregon: \140\
Under DEA regulations, a prescription for a controlled substance
is not "effective" unless it is "issued for a legitimate medical
purpose by an individual practitioner acting in the usual course of
his professional practice." 21 CFR 1306.04(a). This regulation
further provides that "an order purporting to be a prescription
issued not in the usual course of professional treatment * * * is
not a prescription within the meaning and intent of [21 U.S.C. 829]
and * * * the person issuing it, shall be subject to the penalties
provided for violations of the provisions of law related to
controlled substances." Id. As the Supreme Court explained, "the
prescription requirement * * * ensures patients use controlled
substances under the supervision of a doctor so as to prevent
addiction and recreational abuse. As a corollary, [it] also bars
doctors from peddling to patients who crave the drugs for those prohibited uses." (Emphasis added).
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\139\ Moore v. U.S., 128 F.2d 887 (1942).
\140\ 126 S.Ct. 904, 925 (2006) (citing Moore, 423 U.S. 122, 135
(1975)).
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Contrary to Respondent's assertions, the evidence does not support
a finding that Respondent regularly saw Ms. E.M. as a patient; she
therefore did not use controlled substances under his supervision. Mr.
I.S.'s testimony combined with the discrepancies between Respondent's
own records for Ms. E.M. and the admission and treatment dates for Ms.
E.M. from hospice and treating hospitals indicate that it is unlikely
that Respondent saw Ms. E.M. as a patient as frequently as he claims.
Respondent even admitted that he relied on reports from Ms. E.M.'s
family to determine the course of her treatment. Additionally,
Respondent knowingly participated in a scheme to conceal Ms. E.M.'s
alleged use of OxyContin from her treating physicians and other
caregivers. Such actions certainly do not "ensure patients use
controlled substances under the supervision of a doctor," as explained
by the Supreme Court. Because Ms. E.M. was not using OxyContin under
the supervision of Respondent and Respondent's actions contributed to
the prevention of her other physicians to supervise her use, Respondent
did not issue OxyContin prescriptions to Ms. E.M. for a legitimate
medical purpose while acting in the scope of his professional practice.
I therefore find that the prescriptions that Respondent issued to E.M.
for OxyContin were not issued for a legitimate medical purpose.
Accordingly, I find that Respondent was at least reckless or
negligent in ignoring the warning signs of diversion and issued
prescriptions for other than a legitimate medical purpose and that this
conduct weighs in favor of a finding that Respondent's registration
would not be consistent with the public interest.
3. Respondent's Conviction Record
There is no evidence that Respondent has ever been convicted under
any federal or state laws relating to the manufacture, distribution, or
dispensing of controlled substances. I therefore find that this factor,
although not dispositive, weighs against a finding that his continued
registration would be inconsistent with the public interest.
4. Other Conduct
In light of my findings discussed above, I find it unnecessary to
determine whether Respondent's prescribing of various noncontrolled
substances to Ms. E.M. should weigh in favor of a finding that his
continued registration would be inconsistent with the public interest.
[[Page 53961]]
Conclusion
I conclude that Respondent's registration with the DEA would be
inconsistent with the public interest.
Recommended Decision
I recommend that Respondent's controlled substances registration be
revoked and his application for renewal and modification of his DEA
registration be denied.
Dated: June 15, 2010.
Mary Ellen Bittner,
Administrative Law Judge.
[FR Doc. 2011-22093 Filed 8-29-11; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an unofficial version. An official version of this publication may be obtained
directly from the Government Printing Office (GPO).
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