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It should be noted that the FDA did not say whether the deaths or adverse side effects were specifically caused by the drugs.The pharmaceutical giant didnt report the deaths to the agency within the FDAs required timeframe, according to the letter.In a statement released March 10, Novo Nordisk said it initially received inspectional observations from the FDA in February 2025, and that it has been working diligently to address those observations ever since.In the statement on Tuesday, the drugmaker acknowledged it received the warning letter and that it welcomes further dialogue with the US FDA. The company said it is working diligently to address the concerns of the FDA.The drugmaker noted that the FDAs warning letter acknowledges the significant measures Novo Nordisk has taken over the past year meant to ensure full compliance with reporting requirements

The seizures associated with bupropion XL overdose may be single or multiple but are usually quick in onset and only last a short time

Refrigeration slows degradation