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Bill

HSB 186

A bill for an act relating to medication abortions including required informed consent and the dispensing of abortion-inducing drugs to patients within the state.

2025-2026 Regular Session

Imposes written, time‑sensitive informed consent and discharge instructions for medication abortion, restricts mifepristone dispensing to clinical settings, and funds reversal info

Committee report approving bill, renumbered as HF 775.
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Bill Summary · HSB 186

Summary: HSB 186 (renumbered HF 775) — Medication Abortion, Informed Consent, and Mifepristone Dispensing

Status and timeline
- Introduced: February 17, 2025
- Committee action: Subcommittee recommended passage (Feb 25, 2025); Committee report recommending passage (Feb 26, 2025)
- Renumbered: HF 775 (Committee report approving bill, renumbered)
- Additional action: Committee report approving bill (March 5, 2025)
- Classification: Proposed bill; subject to Health and Human Services committee action

Purpose and intent
- Establish enhanced informed-consent requirements for medication abortions and regulate the dispensing of abortion-inducing drugs (notably mifepristone) within the state.
- Require explicit, written confirmation from pregnant patients that they were informed of risks, including the potential (if applicable) to reverse effects and that time is critical.
- Promote access to information and resources about reversing a medication abortion through the state health department’s materials.

Key provisions

1) Informed consent and certification
- For a medication abortion, except in a medical emergency, a physician (or the referring physician or an agent) must obtain written certification from the pregnant woman.
- The certification must show that the woman has been informed, prior to the abortion, of all risks commonly associated with medication abortion.
- The certification must acknowledge that it may be possible to reverse the intended effects if the patient changes her mind, but that time is of the essence.
- Information about reversing the effects and assistance/resources available to reverse are provided on the Department of Health and Human Services (HHS) website.

2) Post-dispensing discharge instructions
- After dispensing an abortion-inducing drug, the attending physician or the physician’s agent must provide written discharge instructions that include the specified statements regarding risks and reversal information.

3) State information dissemination
- HHS is required to publish and maintain on its website materials informing women about the possibility of reversing a medication abortion and the resources available to assist.

4) Mifepristone dispensing restrictions
- It is prohibited to dispense mifepristone to a patient in the state for use in inducing a medication abortion unless it is dispensed directly to the patient in a healthcare setting.

5) Enforcement and discipline
- Failure by a physician to comply with these provisions is grounds for licensee discipline.

6) Emergency exception
- The consent and information requirements do not apply in cases of medical emergencies.

Affected parties and impacts
- Physicians and healthcare providers: Additional written consent requirements, discharge instructions, and potential licensure discipline for noncompliance.
- Patients seeking medication abortions: New informed-consent disclosures, explicit information on reversal options, and requirement that mifepristone be dispensed in specific settings.
- Health care settings and dispensing sites: Compliance with dispensing location restrictions for mifepristone.
- State agencies (HHS): Responsible for developing and publishing informational materials and maintaining resources on reversal options.

Notes
- The bill emphasizes patient information, time-sensitive reversal considerations, and stricter dispensing controls, alongside professional-licensing oversight.

Compiled from official sources — confirm details with the bill’s official record.

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