Bill > SSB3115

Introduced Session

S.F. _____ This bill relates to abortions, including informed consent, dispensing of abortion-inducing drugs, and reporting abortion-inducing drug complications. DIVISION I —— INFORMED CONSENT. Under the bill, a physician, prior to performing or attempting to perform an abortion, is required to perform an in-person examination of the woman seeking an abortion, including screening for indicia of coercion or abuse; if necessary, the physician shall make a referral to an appropriate health care provider consistent with the examination results. The bill requires a physician, prior to prescribing or dispensing an abortion-inducing drug, to do all of the following: have the woman being prescribed or dispensed the drug sign a patient agreement form, obtain written confirmation that the physician has informed the woman of specific health and safety information related to abortion-inducing drugs as detailed in the bill, and advise the pregnant woman how to access emergency surgical intervention in cases of an incomplete abortion, severe bleeding, or other medical complications. The bill specifies that these requirements shall not apply to a chemical abortion performed in response to a medical emergency. The bill provides that the prohibition on dispensing of abortion-inducing drugs shall not be construed to impose civil or criminal liability on a woman upon whom a chemical abortion has been performed. Under the bill, a physician who fails to comply with the informed consent requirements is subject to licensee discipline. The bill requires the board of medicine to adopt rules to administer this division of the bill. The bill defines “abortion-inducing drug”, “chemical abortion”, “dispense”, “medical emergency”, and “pregnant” or “pregnancy”. The bill requires the department of health and human services (HHS) to publish on HHS’s internet site notice that it may be possible to reverse the effects of a chemical abortion, and information and resources on reversing the effects of a S.F. _____ chemical abortion. DIVISION II —— DISPENSING AND REPORTING —— ABORTION-INDUCING DRUGS. The bill defines “abortion-inducing drug”, “abortion-inducing drug complication”, “chemical abortion”, “dispense”, “interested party”, “medical emergency”, “physician”, “postfertilization age”, and “rural emergency hospital”. The bill prohibits a person from dispensing an abortion-inducing drug in this state unless the drug is dispensed in a health care setting directly to the woman prescribed the drug, and the person dispensing the drug is authorized to do so pursuant to Code section 147.107 (drug dispensing, supplying, and prescribing —— limitations). These requirements do not apply to a medical emergency. The bill requires a hospital, rural emergency hospital, or the attending physician to file a report with HHS using a prescribed form within 30 days of discharge or death of a woman who presented with or was treated for an abortion-inducing drug complication. The form must be signed and completed by the attending physician and contain the age of the woman experiencing the abortion-inducing drug complication, the woman’s state and county of residence, the date the abortion-inducing drug was used by the woman, and the probable postfertilization age of the unborn child at the time of the abortion-inducing drug complication. The report must identify the physician who performed the chemical abortion, the facility where the chemical abortion was performed, the referring physician, agency, or service, if any, and the specific complication or complications that led to the treatment performed along with the most recent international classification of diseases code for each, if applicable. The report shall be confidential and not subject to disclosure under Code chapter 22 (open records). The bill also requires HHS to prepare annually on or before December 31 a comprehensive statistical report based S.F. _____ upon the aggregated data gathered from the reports filed on abortion-inducing drug complications. Under the bill, the data gathered by HHS must be anonymized to prevent public disclosure of either the physician or hospital that filed a report, or the woman about whom a report is filed. HHS is required to make the anonymized data publicly available in a downloadable format on its internet site. This division of the bill creates a private cause of action against any person who dispenses an abortion-inducing drug in violation of this division of the bill for all damages caused by the abortion-inducing drug suffered by a woman upon whom a chemical abortion was performed or was attempted; the biological father of the unborn child who was or was attempted to be aborted through a chemical abortion; or the grandparent, parent, sibling, child, legal guardian, or conservator of the woman upon whom a chemical abortion was performed or was attempted. A prevailing plaintiff in an action brought under this division of the bill, in addition to compensatory and punitive damages, is entitled to statutory damages in the amount of $50,000, court costs, and reasonable attorney fees. In an action brought under this division of the bill, the name and other identifying characteristics of a woman who sought or obtained an abortion-inducing drug shall be redacted from all pleadings and documents filed in the action without a court order, and the court may make further orders as necessary to protect the identity and privacy of the woman who sought or obtained an abortion-inducing drug. This division of the bill is not to be construed to impose civil or criminal liability upon a woman upon whom a chemical abortion is performed. Under the bill, a licensee that fails to comply with this division of the bill is subject to licensee discipline. DIVISION III —— ABORTION-RELATED PROVISIONS. The bill amends Code section 144.29A (termination of pregnancy reporting —— legislative intent) to require a health care provider that diagnoses or induces a spontaneous termination of pregnancy S.F. _____ to include in the required report to HHS if mifepristone or misoprostol was used to induce a spontaneous termination of pregnancy. Current law requires the health care provider to only disclose if mifepristone was used to induce a spontaneous termination of pregnancy. The bill also requires the health care provider to disclose whether mifepristone or misoprostol were ingested by the patient within 14 days prior to the spontaneous termination of pregnancy. The bill excludes a spontaneous termination from the definition of abortion for the purpose of the reporting requirements and penalties on abortions under Code chapter 146B (abortion —— postfertilization age).

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Other Sponsors (1)

Senate Judiciary Committee (16:00:00 2/18/2026 RM 116) (on 02/18/2026)

Official Document