fda warning letters glp-1 september 2025 The U.S. Food and Drug Administration (FDA) has issued a to Novo Nordisk over its alleged failure to report adverse side effects, including death, in patients who took its medications Targeting Hims & Hers, F.D.A.

In the future, patients using GLP-1 patches with GLP-1 or GIP/GLP-1 molecules may experience the side effects of GLP-1 agonist drugs, such as constipation, diarrhea, vomiting, abdominal pain, gallbladder disease, pancreatitis, kidney injury, and hypoglycemia

Programs were filtered against four criteria: clinician oversight (real review, not rubber-stamping), pharmacy quality (state-licensed, ideally 503(a) or 503B disclosure), pricing transparency (no surprise dose escalation), and refund-policy clarity (terms readable before paying)

Blue Cross Blue Shield (BCBS) coverage for GLP-1 medications like Wegovy and Ozempic remains inconsistent across state plans and employer groups

Individualized medication: Study the pharmacokinetic differences of IGF-1 LR3 in patients with different genotypes (such as IGF1R polymorphism)

This leads scientists to hypothesize that increased food intake may be a factor in the observed weight gain among the Ipamorelin groups

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