by The ongoing supply shortages of brand-name drugs such as Ozempic and Wegovy have led many consumers to explore alternative options. These alternatives come in the form of compounded drugs produced by specialized pharmacies known as compounding pharmacies. However, the legality and safety of these alternatives have raised concerns, according to Kelly Ann Barnes, a professor of pharmacy law at Northeastern University.
The U.S. Compounding Pharmacies are authorized by the U.S. Food and Drug Administration (FDA) to manufacture off-label versions of pharmaceutical products that are in short supply. Semaglutide, the active ingredient in Ozempic and Wegovy, is currently in high demand due to its effectiveness in weight loss and diabetes management. As a result, compounding pharmacies have stepped in to meet the demand.
However, recent FDA warnings highlight the potential risks associated with these alternatives. Some compounded semaglutide products have been identified as counterfeit or improperly formulated, posing a threat to consumer safety. Barnes advises consumers to exercise caution when considering compounded drugs as alternatives to brand-name medications.
The FDA’s role in regulating compounded drugs is limited, as they are considered individualized treatments. The agency can only take action if it identifies a clear and present danger to public health. In the meantime, consumers are encouraged to consult their healthcare providers for guidance on safe and effective alternatives to Ozempic and Wegovy.
While compounded drugs may offer a solution to the current shortages of brand-name semaglutide medications, consumers must exercise caution and consult their healthcare providers to ensure their safety. The FDA’s limited regulatory oversight of compounded drugs highlights the importance of individualized consultations and careful consideration before opting for these alternatives.
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1. Source: Coherent Market Insights, Public sources, Desk research
2. We have leveraged AI tools to mine information and compile it
