Nevada
AB346
AB346 - Establishes provisions governing the prescribing, dispensing and administering of medication designed to end the life of a patient. (BDR 40-600)
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(Reprinted with amendments adopted on April 15, 2025)
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A.B. 346
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*AB346_R1*
ASSEMBLY BILL NO. 346–ASSEMBLYMEMBERS
DALIA AND GALLANT
MARCH 3, 2025
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JOINT SPONSOR: SENATOR FLORES
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Referred to Select Committee on End-of-Life Care
SUMMARY—Establishes provisions governing the prescribing,
dispensing and administering of medication designed
to end the life of a patient. (BDR 40-600)
FISCAL NOTE: Effect on Local Government: No.
Effect on the State: Yes.
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EXPLANATION – Matter in bolded italics is new; matter between brackets [omitted material] is material to be omitted.
AN ACT relating to health care; revising provisions concerning
medical certificates of death of persons who self-administer
a medication that is designed to end the life of the person;
authorizing a physician or advanced practice registered nurse
to prescribe a medication that is designed to end the life of a
patient under certain circumstances; prohibiting persons
other than a patient from administering a medication that is
designed to end the life of the patient; imposing
requirements relating to the medical records of a patient who
requests a medication that is designed to end the life of the
patient; providing immunity to certain providers of health
care and health care facilities for certain actions relating to
prescribing or dispensing a medication that is designed to
end the life of a patient; authorizing the owner or operator of
a health care facility to prohibit the provision of certain
services relating to a medication that is designed to end the
life of a patient; prohibiting a person from including certain
provisions in a will, contract, agreement or policy of life
insurance; prohibiting certain actions on a policy of life
insurance because the insured requested or revoked a request
for a medication that is designed to end the life of the
insured; and providing other matters properly relating
thereto.
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*AB346_R1*
Legislative Counsel’s Digest:
Existing law authorizes a patient who has been diagnosed with a terminal
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condition to refuse life-resuscitating or life-sustaining treatment in certain
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circumstances. (NRS 449A.400-449A.581, 450B.400-450B.590) Sections 5-33 of
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this bill authorize a patient, under certain circumstances, to self-administer a
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medication that is designed to end the life of the patient. Section 14 defines
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“practitioner” to mean a physician, osteopathic physician or advanced practice
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registered nurse. Sections 6-13, 15 and 16 define other relevant terms. Section 17
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authorizes a patient to request that his or her attending practitioner prescribe a
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medication that is designed to end his or her life if the patient: (1) is at least 18
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years of age; (2) has been diagnosed with a terminal condition by at least two
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practitioners; (3) has made an informed and voluntary decision to end his or her
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own life; (4) is mentally capable of making such a decision; and (5) is not
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requesting the medication because of coercion, deception or undue influence.
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Section 18 prescribes certain requirements concerning the manner in which a
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patient may request a medication that is designed to end the life of the patient,
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including that the patient make two verbal requests and one written request for the
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medication, and that the written request for the medication be signed by a witness.
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Section 19 prescribes the form for the written request for the medication. Section
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20 imposes certain requirements before a practitioner is authorized to prescribe a
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medication that is designed to end the life of a patient, including that the
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practitioner: (1) inform the patient of his or her right to revoke a request for the
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medication at any time; (2) determine and verify that the patient meets
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the requirements for making such a request; (3) discuss certain relevant factors with
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the patient, including the diagnosis and prognosis of the patient and alternative
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options for care; (4) refer the patient to a consulting practitioner who can confirm
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the diagnosis, prognosis and mental capability of the patient and that the patient has
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not been coerced or unduly influenced; and (5) instruct the patient against self-
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administering the medication in public. Section 21 requires a practitioner who
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determines that a patient who has requested a prescription for a medication that is
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designed to end his or her life may not be mentally capable to refer the patient to a
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qualified mental health professional and to receive confirmation about the patient’s
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mental capability.
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Section 22: (1) prescribes procedures for the issuance of a prescription for a
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medication that is designed to end the life of the patient; and (2) provides that only
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an attending practitioner or a pharmacist may dispense such a medication. Section
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22.5 of this bill prescribes the manner in which the attending practitioner may bill
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the patient or the insurer of the patient for diagnosing the condition of the patient
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and prescribing the medication. Section 23 prohibits an attending practitioner from
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prescribing a medication that is designed to end the life of a patient based solely on
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the age or disability of the patient. Section 24 requires certain providers of health
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care to include certain information concerning requests and prescriptions for and
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the dispensing of a medication that is designed to end the life of a patient in the
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medical record of the patient. If a patient who has requested a medication that is
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designed to end the life of a patient transfers care to another practitioner or health
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care facility, sections 24 and 31 require the practitioner or health care facility that
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previously provided care to the patient to forward the patient’s medical records to
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the new practitioner or health care facility. Section 27 prescribes certain
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information that must be reported by an attending practitioner to the Division of
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Public and Behavioral Health of the Department of Health and Human Services
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relating to a patient who has been prescribed or self-administered such a
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medication. Section 28 requires the Division to compile an annual report
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concerning the implementation of the provisions of this bill authorizing a patient to
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request a prescription for a medication that is designed to end the life of the patient.
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*AB346_R1*
Sections 27, 40 and 43 of this bill provide that such information is otherwise
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confidential when reported to the Division.
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Section 25 authorizes a patient, at any time, to revoke a request for a
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medication that is designed to end his or her life. Sections 26 and 35 of this bill
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provide that only the patient to whom a medication that is designed to end his or
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her life is prescribed may administer the medication. Section 26 establishes
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requirements for the disposal of any unused portion of the medication.
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Section 33 makes certain persons exempt from professional discipline and
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immune from civil and criminal penalties and provides that such persons do not
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violate any applicable standard of care for taking actions authorized by this bill to
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assist a patient in acquiring a medication that is designed to end the life of the
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patient. Section 33.3 of this bill requires a person who administers emergency
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medical services to treat a prescription for a medication that is designed to end the
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life of a patient as a written do-not-resuscitate order for the purpose of withholding
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life-sustaining treatment. Section 33.6 of this bill requires a person who administers
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emergency medical services who responds to a person who has self-administered a
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medication that is designed to end his or her life to indicate “medical aid in dying”
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in any report concerning the incident. Section 33.1 of this bill makes a conforming
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change to include a patient who has self-administered a medication designed to end
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his or her life in the definition of “qualified patient” for the purpose of provisions
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governing the withholding of life-sustaining treatment. Section 29 provides that a
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death resulting from the self-administration of a medication that is designed to end
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the life of a patient is not mercy killing, euthanasia, assisted suicide, suicide or
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homicide when done in accordance with the provisions of this bill, and section 2 of
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this bill requires a death certificate to list the terminal condition of the patient as the
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cause of death of the patient. However, section 1.5 of this bill requires a death
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certificate to include a box that may be marked to indicate that a patient died from
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the self-administration of a medication that is designed to end the life of a patient,
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and section 2 requires the death certificate of such a patient to indicate that the
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patient died in that manner through a mark in that box. Sections 1 and 3 of this bill
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provide that a coroner, coroner’s deputy or local health officer is not required to
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certify the cause of such a death. Section 42 of this bill: (1) authorizes a coroner to
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make an appropriate investigation after discovering that a person has self-
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administered a medication designed to end the life of the person, to the extent
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necessary to determine the cause of the terminal condition with which the person
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was diagnosed; and (2) requires a coroner to cease such an investigation after
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determining that the terminal condition resulted from a natural cause. Section 41 of
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this bill makes a conforming change to revise certain internal references.
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Sections 30 and 38 of this bill prohibit a person from preventing or requiring a
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person to make or revoke a request for a medication that is designed to end the life
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of the person as a condition to receiving health care or as a condition in an
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agreement, contract or will.
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Section 31 clarifies that a practitioner is not required to prescribe a medication
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that is designed to end the life of a patient and remains responsible for treating the
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patient’s pain. However, if a patient who is diagnosed with a terminal condition
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requests information concerning the prescription and self-administration of a
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medication that is designed to end the life of the patient, section 31 requires a
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practitioner to provide that information or facilitate the transfer of the patient to
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another provider of health care. Section 31 also provides that a pharmacist is not
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required to fill a prescription for or dispense such a medication. Section 32
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authorizes the owner or operator of a health care facility to prohibit an employee or
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independent contractor of the health care facility or any person who provides
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services on the premises of the health care facility from providing any services
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relating to prescribing a medication that is designed to end the life of a patient
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while acting within the scope of his or her employment or contract with the facility
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*AB346_R1*
or while on the premises of the facility. Section 33 prohibits a health care facility or
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provider of health care from taking certain actions against an employee or
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independent contractor who: (1) provides accurate, scientific information
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concerning end-of-life care to a patient; or (2) facilitates the prescription or self-
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administration of a medication that is designed to end the life of the patient.
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Sections 34-37 of this bill make conforming changes to clarify that a practitioner or
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pharmacist is authorized to dispense a medication that is designed to end the life of
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a patient that is a controlled substance or dangerous drug and a patient may self-
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administer such a medication in accordance with other provisions governing
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medications designed to end the life of a patient.
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Section 39 of this bill provides that a proposed protected person shall not be
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deemed to be in need of a general or special guardian solely because the proposed
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protected person requested a medication that is designed to end his or her life or
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revoked such a request.
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Sections 44 and 45 of this bill prohibit insurers from conditioning life
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insurance benefits, group life insurance benefits or the payment of claims on
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whether the insured makes, fails to make or revokes a request for a medication that
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is designed to end the life of the insured or self-administers such a medication.
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Section 46 of this bill makes a conforming change to reflect this prohibition on a
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policy of group life insurance.
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WHEREAS, A mentally capable adult patient should have the
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right to self-determination concerning his or her health care
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decisions based on his or her values, beliefs or personal preferences;
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and
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WHEREAS, It is important that patients have the full range of
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options for their care, especially at the end of their lives; and
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WHEREAS, Patients with a terminal illness may undergo
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unremitting pain, agonizing discomfort and a sudden, continuing
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and irreversible reduction in their quality of life; and
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WHEREAS, The availability of medical aid in dying provides an
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additional palliative care option for persons with a terminal illness
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who seek to retain their autonomy and some level of control over
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the progression of their disease or ease unnecessary pain and
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suffering; and
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WHEREAS, The integration of medical aid in dying into standard
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end-of-life care has demonstrably improved such care by
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contributing to better conversations between providers of health care
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and patients, earlier and more appropriate enrollment in hospice care
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and better training concerning palliative care for providers; and
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WHEREAS, Patient-directed care respects and responds to the
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decisions, preferences, needs and values of individual patients,
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ensures that the values of patients direct all clinical decisions
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concerning their care and ensures that patients are fully informed of
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and able to access the options for care that they desire; now,
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therefore,
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*AB346_R1*
THE PEOPLE OF THE STATE OF NEVADA, REPRESENTED IN
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SENATE AND ASSEMBLY, DO ENACT AS FOLLOWS:
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Section 1. Chapter 440 of NRS is hereby amended by adding
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thereto a new section to read as follows:
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1. A coroner, coroner’s deputy or local health officer is not
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required to certify the cause of death of a patient who dies after
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self-administering a medication that is design
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