GLP-1 Drugs Show Weight Loss Potential but Raise Safety Concerns

Published
November 17, 2025
Category
Science & Health
Word Count
280 words
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GLP-1 drugs, such as Ozempic, have shown significant potential for weight loss, according to recent research compiled in three Cochrane reviews. These studies indicate that GLP-1 receptor agonists, including tirzepatide, semaglutide, and liraglutide, produce clinically meaningful weight loss when compared to placebo, with tirzepatide leading to an average reduction of approximately 16% over 12 to 18 months.

Semaglutide and liraglutide also yielded substantial weight loss, averaging 11% and 4-5% respectively, over varying durations. However, the reviews raise critical questions regarding the long-term safety and side effects of these medications.

For instance, participants reported higher instances of mild-to-moderate gastrointestinal issues, leading some to discontinue treatment. Despite the promising short-term results, the lack of robust long-term safety data remains a concern, with indications that effects may diminish after treatment cessation.

The reviews emphasize the need for independent research to address potential conflicts of interest, as many studies were funded by the pharmaceutical companies that manufacture these drugs. The authors highlighted the importance of understanding GLP-1 drugs in diverse populations, given the limited representation in clinical trials from lower-income countries.

The potential for weight regain post-treatment also poses a challenge to the sustainability of the observed benefits. With obesity affecting millions, the findings from these reviews will contribute to future World Health Organization guidelines on the use of GLP-1 receptor agonists for obesity treatment.

Experts underscore the necessity of viewing these medications within a broader health context, addressing issues like access and affordability to avoid worsening health inequities. As the medical community navigates the challenges presented by obesity treatment, the efficacy of these GLP-1 drugs must be balanced against the pressing need for comprehensive safety evaluations to guide clinical practice and policy decisions.

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