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While semaglutide and tirzepatide have helped thousands of patients, some individuals still experience weight plateaus
The FDA may take extra time to evaluate the glucagon-related safety signals, particularly the heart rate increase (up to 6.7 bpm above baseline) and dysesthesia (Nature Medicine, 2024)
After the approved drug is on the market, whether generic or branded, API manufacturers must test each batch of the product according to the identified specifications using validated tests and, with each batch, issue a certificate of analysis (COA) that contains specific test results about the substance
Treat them as refrigerated medications and minimize time at room temperature
