Relating to required reports of certain vaccine-related or drug-related adverse events.

SB 269 requires physicians to report certain serious adverse reactions to federal systems (VAERS for vaccines, MedWatch for drugs) when patients receive experimental/investigational vaccines or drugs approved for emergency use by the FDA. It defines "serious adverse events" as those causing death, life-threatening conditions, hospitalization, or significant disability. Physicians must report within one year of vaccination/drug administration if they diagnose the condition and know the patient received a covered vaccine or drug. Violations may result in non-disciplinary corrective action for first offenses or disciplinary measures by the Texas Medical Board for repeat failures. The law applies only to non-routine vaccines/drugs, excluding standard vaccines and clinical trial uses.