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No. However, on rare occasions, negative side effects for a particular drug may become apparent after it’s been approved for the general population and large numbers of patients begin using it. In those cases, the FDA and pharmaceutical companies work together to educate the public about those risks and, on rare occasions, remove the medicine from the marketplace.
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Drug Safety
Prescription and OTC drugs marketed in the United States go through a review and testing process by the Food and Drug Administration (FDA). Dosage, side effects, manufacturing and safety are evaluated through this process. Familia...
rize yourself with drug warnings, drug label changes and any drug shortages, so you can protect and maintain your health.
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Important: This content reflects information from various individuals and organizations and may offer alternative or opposing points of view. It should not be used for medical advice, diagnosis or treatment. As always, you should consult with your healthcare provider about your specific health needs.