International Task Force
on Euthanasia and Assisted Suicide
Ashcroft Directive
In November 2001, Attorney General John Ashcroft issued a Directive which stated that prescribing federally controlled substances to assist suicide violates the federal Controlled Substances Act (CSA). In conjuction with the Directive, Ashcroft also sent a letter to leaders of major organizations of health professionals in which he made it clear that the use of federally controlled substances for pain management is encouraged. Ashcroft Directive Letter to Health Professionals November 6, 2001 MEMORANDUM: ASA HUTCHINSON, ADMINISTRATOR FROM: John Ashcroft, Attorney General SUBJECT: Dispensing of Controlled Substances to Assist Suicide As you are aware, the Supreme Court reaffirmed last term that the application of federal law regulating controlled substances is uniform throughout the United States and may not be nullified by the legislative decisions of individual States. See United States v. Oakland Cannabis Buyers' Coop., 532 U.S. 483 (2001). In light of this decision, questions have been raised about the validity of an Attorney General letter dated June 5, 1998, which overruled an earlier Drug Enforcement Administration (DEA) determination that narcotics and other dangerous drugs controlled by federal law may not be dispensed consistently with the Controlled Substances Act, 21 U.S.C. §§ 801-971 (1994 & Supp.II 1996) (CSA), to assist suicide in the United States. Upon review of the Oakland Cannabis decision and other relevant authorities, I have concluded that the DEA's original reading of the CSA that controlled substances may not be dispensed to assist suicide was correct. I therefore advise you that the original DEA determination is reinstated and should be implemented as set forth in greater detail below. The attached Office of Legal Counsel opinion, entitled "Whether Physician-Assisted Suicide Serves a 'Legitimate Medical Purpose' Under The Drug Enforcement Administration's Regulations Implementing the Controlled Substances Act" (June 27, 2001) ("OLC Opinion") (attached) sets forth the legal basis for my decision. 1. Determination on Use of Federally Controlled Substances to Assist Suicide. For the reasons set forth in the OLC Opinion, I hereby determine that assisting suicide is not a "legitimate medical purpose" within the meaning of 21 C.F.R. § 1306.04 (2001), and that prescribing, dispensing, or administering federally controlled substances to assist suicide violates the CSA. Such conduct by a physician registered to dispense controlled substances may "render his registration inconsistent with the public interest" and therefore subject to possible suspension or revocation under 21 U.S.C. § 824(a)(4). This conclusion applies regardless of whether state law authorizes or permits such conduct by practitioners or others and regardless of the condition of the person whose suicide is assisted. I hereby direct the DEA, effective upon publication of this memorandum in the Federal Register, to enforce and apply this determination, notwithstanding anything to the contrary in the June 5, 1998, Attorney General's letter. 2. Use of Controlled Substances to Manage Pain Promoted. Pain management, rather than assisted suicide, has long been recognized as a legitimate medical purpose justifying physicians' dispensing of controlled substances. There are important medical, ethical, and legal distinctions between intentionally causing a patient's death and providing sufficient dosages of pain medication necessary to eliminate or alleviate pain. 3. No Change in Current DEA Policies and Enforcement Practices Outside Oregon. The reinstated determination makes no change in the current standards and practices of the DEA in any State other than Oregon. Former Attorney General Janet Reno's June 5, 1998, letter relating to this matter emphasized that action to revoke the DEA registration of a physician who uses federally controlled substances to assist a suicide "may well be warranted where a physician assists in a suicide in a state that has not authorized the practice under any conditions." The reinstated determination does not portend any increase in investigative activity or other change from the manner in which the DEA presently enforces this policy outside of Oregon. 4. Enforcement in Oregon. Under 3 Oregon Revised Statutes (O.R.S.) § 127.855 (1999), an attending physician who writes a prescription for medication to end the life of a qualified patient must document the medication prescribed. Under 3 O.R.S. § 127.865(1)(b) (1999), the State of Oregon's Health Division must require any health care provider upon dispensing medication pursuant to the Death with Dignity Act to file a copy of the dispensing record with the Division. Those records should contain the information necessary to determine whether those holding DEA registrations who assist suicides in accordance with Oregon law are prescribing federally controlled substances for that purpose in violation of the CSA as construed by this Memorandum and the attached OLC Opinion. The Department has the authority to take appropriate measures to obtain copies of any such reports of records sent to the Oregon State Registrar. See 21 U.S.C. § 876. When inspection of these documents discloses prohibited prescription of controlled substances to assist suicide following the effective date of this memorandum, then appropriate administrative action may be taken in accordance with 21 C.F.R. §§ 1316.41 to 1316.68 (2001). Thus, it should be possible to identify the cases in which federally controlled substances are used to assist suicide in Oregon in compliance with Oregon law by obtaining reports from the Oregon State Registrar without having to review patient medical records or otherwise investigate doctors. Accordingly, implementation of this directive in Oregon should not change the DEA's current practices with regard to enforcing the CSA so as materially to increase monitoring or investigation of physicians or other health care providers or to increase review of physicians' prescribing patterns of controlled substances used for pain relief. 5. Distribution. Please ensure that this Memorandum and the OLC opinion on which it is based are promptly distributed to appropriate DEA personnel, especially those with authority over the enforcement of the CSA in Oregon. Attachment [The above Directive was published in the Federal Register on November 9, 2001 at 66 Federal Register 56607-56608.] Text of Ashcroft Letter to Health Professionals The following is the text of a November 6, 2001 letter sent by Attorney General John Ashcroft to Richard Corlin, President of the American Medical Association. November 6, 2001 Richard F. Corlin, M.D. Dear Dr. Corlin: I am today restoring a judgment originally made by the Drug Enforcement Administration (DEA) that narcotics and other dangerous drugs controlled by federal law may not legally be used to assist suicide or for euthanasia in any part of our nation. This decision will be applied prospectively only. The American Medical Association has long taken the position that physician-assisted suicide is not a legitimate medical practice. At the same time, the AMA has been rightly concerned to ensure that efforts to prevent the misuse of controlled substances to assist suicide do not deter physicians from prescribing controlled substances to alleviate pain. I want the nation's doctors to know that under this decision they will have no reason to fear that prescription of controlled substances to control pain will lead to increased scrutiny by the DEA even when high doses of painkilling drugs are necessary and even when dosages needed to control pain may increase the risk of death. My decision today makes no change in the current standards and practices of the DEA in any state other than Oregon. Former Attorney General Janet Reno's June 5, 1998, letter emphasized that action to revoke the DEA registrations of physicians who dispense federally controlled substances to assist suicides "may well be warranted where a physician assists in a suicide in a state that has not authorized the practice under any conditions." Today's decision does not portend an increase in investigative or enforcement activity in any part of the nation outside of Oregon. Even in Oregon, enforcement of today's decision will not increase DEA scrutiny of physicians' prescription of controlled substances for pain relief. Under Oregon law, a report that identifies the precise drugs used in every case of assisted suicide must be made to state authorities. The DEA has statutory authority to obtain these reports. Thus, it should be possible to identify the cases in which federally controlled substances are used to assist suicide in Oregon in compliance with Oregon law by obtaining reports from the Oregon State Registrar without having to review patient medical records or otherwise investigate doctors. Accordingly, implementation of this directive in Oregon should not change the DEA's current practices with regard to enforcing the Controlled Substances Act so as materially to increase monitoring or investigation of physicians or other health care providers or to increase review of physicians' prescribing patterns of controlled substances used for pain relief. I am therefore requesting that the AMA take all appropriate measures to inform and reassure its membership and other physicians that there will be no increase in DEA scrutiny of physicians' prescription of controlled substances to control pain in any state, including Oregon, as a consequence of today's decision. Consequently, physicians throughout the country should feel confident that they may prescribe federally controlled drugs to the full extent desirable to relieve pain without any fear that their prescriptions will be questioned or investigated as a result of today's action. Sincerely, John Ashcroft On November 6, 2001, Ashcroft also sent the above assurances to: Back to Oregon v. Ashcroft page
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