United States v. Ray RoyaUnited States v. Ray Roya
Appellant, Dr. Ray Roya, was convicted after a bench trial on all counts of a 24 count indictment which charged him with dispensing and attempting to dispense
The Government’s evidence included the testimony of eight agents from the Illinois Bureau of Investigation who, over a 63-day period, obtained 24 prescriptions from Roya for either Preludin or Tuinal. The testimony was similar for each of the counts, so we will summarize the testimony of one of the agents to provide the flavor of Dr. Roya’s practice insofar as it related to his contacts with the agents.
On February 21,1975, agent Paula Riccio telephoned Roya for an appointment, and then went to his office. The office consisted of a large waiting room with 20 to 25 chairs for patients. While she waited, she observed other people enter Roya’s inner office and emerge five to ten minutes later holding a white piece of paper. When she entered the inner office for her appointment she observed no examining table or weight scale. After a brief conversation she told Roya that she wanted a prescription for Preludin. She also said that her boyfriend would share the Preludin with her and that he would pay for the prescription. She did not indicate to him that she desired to reduce her weight, a recognized legitimate medical use for Preludin. Roya asked her no questions about her medical history, did not take her blood pressure, and did not listen to her heartbeat; he conducted no physical examination. He wrote and gave her a prescription for 30 Preludin tablets (Count 5), a normal monthly supply. She paid him $10.00 and left.
Three days later, she returned and told him that she had shared the Preludin tablets with her boyfriend over the weekend and had used all 30 tablets. She asked for another prescription. He told her he could not write another prescription in her own name because the authorities were closely monitoring usage of the drug. He agreed instead to write a prescription in the name of her boyfriend, Steve Miller (Count 6). Riccio paid $10.00 for the prescription and left. During the interview, Roya did not refer to a patient file, again asked no questions about her medical history, and again failed to give her a physical examination. Obviously, he made no clinical determination as to Steve Miller.
On March 1,1975, Riccio and agent Steve Miller visited Roya’s office. Miller requested a prescription for Tuinal. Although Miller did not indicate that he was having difficulty sleeping, Roya wrote and gave a prescription to him for 30 Tuinal capsules (Count 1). He asked Miller no questions about his medical history and conducted no physical examination. Riccio asked for another Preludin prescription. She was given the prescription after she gave Roya the name of someone over 30 years of age to place on the prescription. She chose “Joyce Jones” (Count 8). They paid Roya $20.00 for the two prescriptions and left.
In this appeal, Roya argues that the district court erred in not dismissing the indictment in its entirety or at least as to the counts dealing with Preludin. He also contends that the Government’s evidence was insufficient to sustain his conviction on Counts 1, 2, 3, 4, 5, 7, 9,10, 11,14,15, 20, 21, and 22.
I. THE INDICTMENT
Roya argues that the indictment was vague, uncertain, and failed to inform him of the nature and cause of the accusations
Appellant’s first argument to support the vagueness of the indictment is that each count fails to cite the regulation which proscribed the conduct for which he was charged. The 24 count indictment consisted of four counts charging him with violations of
A prescription for a controlled substance to be effective must be issued for a legitimate medical purpose by an individual practitioner acting in the usual course of his professional practice . . . . 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 section 309 . . 5 and the . person issuing it, shall be subject to the penalties provided for violations of the law relating to controlled substances.
[Emphasis added.] Because the indictment failed to include a reference to this regulation, appellant argues that the indictment failed to inform him with sufficient clarity of the charges against him.
It is true that the disputed language tracks some of the language in the regulation. This regulation, however, has been held by this court in
United States v. Green,
In any event, looking at the indictment here involved we note that it clearly stated the essential elements of the offense and that the disputed language merely clarified the grand jury’s position that the ac
In any event, the disputed language, in our opinion, was not essential to a properly drawn indictment. An indictment founded on a general provision of a statute need not negative an exception made by a proviso or other distinct clause, whether in the same section or elsewhere.
McKelvey v. United States,
The appellant also argues that the indictment should have been dismissed because it failed to contain the essential element of the regulation that the dispensing was without “a legitimate medical purpose.” Because of our holding that neither citation to the regulation nor inclusion of its language was necessary to charge the defendant with a violation of
Roya also argues that the district court should have dismissed the indictment because of its failure to state in each count the names and addresses of persons to whom he allegedly dispensed or attempted to dispense controlled substances. The test is whether the indictment sets forth the elements of the offense charged and sufficiently apprises the defendant of the charges to enable him to prepare for trial.
United States v. Jeffers,
Roya here also complains of the denial of his motion for a bill of particulars as to the names and addresses. The denial of a motion for a bill of particulars does not constitute an abuse of discretion “unless the deprivation of the information sought leads to the defendant’s inability adequately prepare his case, to avoid surprise at trial, or to avoid the later risk of double jeopardy.”
United States v. Addonizio,
The record indicates that the Government provided the defendant with Illinois Bureau of Investigation reports pursuant to
In our opinion, the deprivation of this information linking specific agents to specific counts did not lead to defendant’s inability to prepare his case adequately, or cause him surprise at trial, or place him in risk of double jeopardy.
See United States v. Rimanich,
Appellant next challenges the sufficiency of the indictment on the ground that the Attorney General’s addition and reclassification of Tuinal and Preludin as Schedule II controlled substances was void because the Attorney General’s authority, although derived from the statute,
It is well-established constitutional doctrine that Congress may enact legislation which prescribes essential standards and basic legislative policy within which a designated administrator may promulgate rules and regulations. The standards need only be “sufficiently definite and precise to enable Congress, the courts and the public to ascertain whether the Administrator . . . has conformed to those standards.”
Yakus
v.
United States,
Alternatively, appellant argues that even if the delegation was valid, the fourteen counts of the indictment that involved Preludin (phenmetrazine) were invalid because the Attorney General failed to make the requisite findings when he transferred it from Schedule III to Schedule II. The findings necessary for such a transfer are: (1) the drug or other substance has a high potential for abuse; (2) the drug or other substance has a currently accepted medical use in treatment in the United States or a currently accepted medical use with severe restrictions; and (3) abuse of the drug or other substance may lead to severe psychological dependence.
On July 7, 1971, the Director of the Bureau of Narcotics and Dangerous Drugs, on behalf of the Attorney General,
6
made findings that amphetamines and methampheta
[I]n view of the order transferring amphetamines and methamphetamine to schedule II published in the Federal Register of July 7, 1971 (36 F.R. 12734), and the resulting strict production and distribution controls imposed upon amphetamines and methamphetamine by this transfer, finds that persons disposed to abuse amphetamines and methamphetamine now may direct their attention to methylphenidate and phenmetrazine, drugs which presently are not known to be the subject of substantial abuse in the United States. Further, there is no evidence to indicate that there is any abuse of methylphenidate and phenmetrazine when administered with proper medical supervision.
36 Fed.Reg. 20686 (Oct. 28,1971). [Emphasis added.] We are satisfied that this language indicates that the Director incorporated the findings of July 7, 1971 into his decision to transfer Preludin to Schedule II, and thus made the requisite factual findings. Therefore, we reject the premise of appellant’s argument and accordingly do not find the fourteen counts concerning Preludin to be invalid.
II. SUFFICIENCY OF THE EVIDENCE
Roya challenges the sufficiency of the evidence for the first four counts on the ground that the Government failed to prove that he “dispensed” controlled substances as required by the statute. 7 The definitional section of the statute defines “dispense” as:
to deliver a controlled substance to an ultimate user or research subject by, or pursuant to the lawful order of a practitioner, including the prescribing and administering of a controlled substance and the packaging, labeling, or compounding necessary to prepare the substance for' such delivery.
a prescription for a substance cannot be regarded as less than the constructive or attempted transfer of the substance itself, since a prescription is the written representation of the drug and enables its possessor to claim physical custody and control over the drug prescribed.
United States v. Tighe,
Appellant challenges his conviction on Counts 5, 7, 9, 10, 11, 14, 15, 20, 21, and 22 on the ground of insufficiency of the evidence. He argues that the Government’s evidence was insufficient to prove that he dispensed the controlled substance for other than a legitimate medical purpose
We find the evidence clearly sufficient under our standard of review to sustain the conviction. The agents for whom appellant prescribed the controlled substance all testified that appellant did not ask for a medical history during any of the interviews; nor did he conduct a single physical examination of any of the agents. Furthermore, the testimony of expert witnesses indicated that these actions were outside the course of professional practice.
For the reasons stated herein, we affirm the conviction on all counts.
AFFIRMED.
Notes
. The controlled substances were Preludin, a brand name for phenmetrazine, and Tuinal, a brand name for sodium amobarbital and sodium secobarbital. We will refer to these substances by their commercial names.
.
Except as authorized by this subchapter, it shall be unlawful for any person knowingly or intentionally to manufacture, distribute, or dispense, or possess with intent to manufacture, distribute, or dispense, a controlled substance.
Section 846 provides:
Any person who attempts or conspires to commit any offense defined in this subchap-ter is punishable by imprisonment or fine or both which may not exceed the maximum punishment prescribed for the offense, the commission of which was the object of the attempt or conspiracy.
. The first four counts of the indictment read as follows:
On or about . ., at Chicago, in the Northern District of Illinois, Eastern Division, RAY ROYA, defendant herein, knowingly and intentionally dispensed 30 Preludin [or Tuinal] tablets (phenmetrazine), a Schedule II Controlled Substance pursuant to a prescription not written in the course of professional practice; In violation of Title21, United States Code, Section 841(a)(1) .
Counts Five through 24 read as follows:
On or about . ., at Chicago, in the Northern District of Illinois, Eastern Division, RAY ROYA, defendant herein, knowingly and intentionally attempted to dispense 30 Tuinal [or Preludin] capsules (sodium amo-barbital and sodium secobarbital), a Schedule II Controlled Substance pursuant to a prescription not written in the course of professional practice, in violation of Title21, United States Code, Section 841(a)(1) ; In violation of Title21, United States Code, Section 846 .
. At the time the indictment was issued the regulation was designated
. Section 309, or more fully, Pub.L. 91-513, Title II, § 309, is codified as
Except when dispensed directly by a practitioner, other than a pharmacist, to an ultimate user, no controlled substance in schedule II, which is a prescription drug as determined under the Federal Food, Drug, and Cosmetic Act, may be dispensed without the written prescription of a practitioner,-’ . . .
. The Attorney General is not required to act personally to add a new drug to Schedule III.
United States v. Benish,
. The remaining 20 counts charged appellant with an attempt to dispense. Appellant challenged ten of these counts on the ground of insufficiency of evidence. These arguments will be addressed in the text infra.