Texas SB269 mandates reporting of certain vaccine-related and drug-related adverse events.

Texas SB269 requires physicians to report to the federal Vaccine Adverse Event Reporting System any serious adverse events related to vaccines that are experimental, investigational, or approved for emergency use by the FDA, excluding those administered as part of a clinical trial. It also mandates reporting to the FDA's MedWatch program for drugs that are experimental, investigational, or approved for emergency use by the FDA, excluding those used as part of a clinical trial.

Texas SB269 mandates reporting of certain vaccine-related and drug-related adverse events.

Texas SB269 requires physicians to report to the federal Vaccine Adverse Event Reporting System any serious adverse events related to vaccines that are experimental, investigational, or approved for emergency use by the FDA, excluding those administered as part of a clinical trial. It also mandates reporting to the FDA's MedWatch program for drugs that are experimental, investigational, or approved for emergency use by the FDA, excluding those used as part of a clinical trial.