HB 739 -- Women's Pregnancy Education Information Act Co-Sponsors: Phillips, Barry, Marble, Portwood, Cunningham This bill revises the Women's Pregnancy Education Information Act. Beginning January 1, 2002, a prescribing physician is required to confer with a patient at least 24 hours before a prescription is delivered to the patient, a pharmacy, or pharmacist about the indicators or contra-indicators concerning the use of mifepristone (RU-486), misoprostol (only if prescribed in connection with inducing an abortion), or any combination of drugs which are intended to induce an abortion. A physician is required to consider a patient's medical history and medical condition during the discussion. Prior to or during the physician's discussion, a patient is required to be screened for physical, psychological, and situational risk factors which would predispose the patient to or increase the risk of experiencing one or more emotional or physical reactions to the use of the drug or drugs. Prior to the delivery of the prescription, a prescribing physician and the patient are required to sign a written statement which certifies that the screening and discussion have been completed and that the woman has given her informed consent, freely and without coercion. All executed statements will be maintained in the patient's medical file and are subject to confidentiality rules and laws.Copyright (c) Missouri House of Representatives