Category: Drug stability

Reports from the FDA highlight significant concerns regarding the quality of compounded drugs, including semaglutide, with some batches containing incorrect dosages or ingredients. This raises the critical question: Does compounded semaglutide lose its potency over time, and what factors contribute to its stability?

Multiple studies have shown that atorvastatin, a widely prescribed cholesterol-lowering medication, is susceptible to degradation when exposed to light, heat, and moisture. Understanding whether **is atorvastatin light sensitive** is crucial for ensuring the drug maintains its therapeutic efficacy and for patient safety.

According to one study, tablets of amine salts combined with lactose can darken with age due to a reaction accelerated by temperature and high humidity. Understanding why pills turn brown? is critical for patient safety, as this visual change can signal a loss of potency or even the creation of harmful byproducts.

Up to 90% of patients carry genetic variants influencing drug response, a key aspect of medication lability. Understanding **what determines lability** is crucial, as it involves both the inherent instability of the drug molecule and external factors affecting its behavior.