Veterinarians and animal owners are encouraged to report adverse experiences and product failures to the government Agency that regulates the product.| U.S. Food and Drug Administration
Reporting on prescription/OTC medicines, non-vaccine biologicals, medical devices, special nutritional products, cosmetics and non-prescription human drug.| U.S. Food and Drug Administration
Testimony: Amy Abernethy, Md, Phd., FDA Office of the Commissioner, Before the Senate Committee on Agriculture, Nutrition, and Forestry, 7/25/19| U.S. Food and Drug Administration
FDA approved Epidiolex (cannabidiol) oral solution, the first drug comprised of an active ingredient derived from marijuana, to treat two rare and severe forms of epilepsy.| U.S. Food and Drug Administration
Delta-8 THC products are not approved by the FDA and may put you at risk.| U.S. Food and Drug Administration
Health professionals, consumers and patients can voluntarily report observed or suspected adverse events for human medical products to FDA. Voluntary reporting can help FDA identify unknown risk for approved medical products. Reporting can be done through our online reporting portal or by downloading, completing and then submitting FDA Form 3500 (Health Professional) or 3500B (Consumer/Patient) to MedWatch: The FDA Safety Information and Adverse Event Reporting Program.| www.accessdata.fda.gov