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Current data from clinical trials indicate that retatrutide, administered via subcutaneous injection, demonstrates a predictable and manageable safety profile, consistent with other incretin-based therapeutics

Patients and health care professionals should report any adverse reactions to FDAs MedWatch program: Complete and submit the report online at www.fda.gov/medwatch/report.htm Download and complete the appropriate form, then submit it via fax at 1-800-FDA-0178

Not everyone who develops a PE has symptoms of DVT