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Adverse Event Reporting
Although The Merck Manuals are published by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., the Merck Manuals are not connected in any way with Merck's line of pharmaceutical products.
To report an adverse experience with a specific Merck product, please call the Merck National Service Center at 800-444-2080. You may also report an adverse event directly to your healthcare provider or to the U.S. Food and Drug Administration (FDA) by calling 1-800-FDA-1088 or visiting http://www.fda.gov/Safety/MedWatch.
Non-U.S. residents: countries outside the United States may have specific procedures in place to address reports of adverse events. Please ask your healthcare provider for more information or contact your local health authority.
If you have questions relating to Merck prescription products, your medical condition or personal health matters, please contact your physician or healthcare provider since he or she is most familiar with your medical condition. Merck cannot respond to questions about general medical information or information regarding your specific condition.