Mode
Text Size
Log in / Sign up

Pharmacovigilance analysis identifies 25 drug safety signals for cachexia in 4,878 FAERS reportsAnalysis identifies drugs linked to muscle and weight loss

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Note that 25 drugs, including nivolumab and paclitaxel, show safety signals for cachexia in pharmacovigilance data.

This systematic review analyzes pharmacovigilance data from the U.S. FDA Adverse Event Reporting System (FAERS) between 2004 and 2025 to identify medications associated with cachexia. The analysis included 4,878 individual case safety reports. The study identified 25 drug safety warning signals for cachexia, suggesting a need for regulatory review and potential label updates.

Key findings include a mortality rate of 25.6% among the reported cases. Specific drugs showed positive signals through disproportionality analysis: low calcium peritoneal dialysis solution lactate G15 (ROR 495.67; 95% CI 336.94-729.18), nivolumab (ROR 15.29; 95% CI 13.65-17.13; 319 cases), and Kaletra (ROR 10.44; 95% CI 7.98-13.65). The median time-to-onset (TTO) for cachexia was 31 days, with more than half of cases occurring within the first 120 days.

A primary limitation of this study is that the data source consists of self-reported adverse events in a pharmacovigilance database. These findings represent signals of association rather than confirmed causation. Clinical application is currently limited by the nature of the data source, but the findings may inform future regulatory monitoring of these agents.

How this fits prior evidence

This pharmacovigilance analysis identifies specific drug signals for cachexia, a condition that may impact the clinical management of patients on various therapies. The review identifies signals for nivolumab and paclitaxel. These findings relate to prior coverage of nivolumab in melanoma and paclitaxel in nasopharyngeal carcinoma, though the current study focuses specifically on the safety signal of cachexia rather than efficacy outcomes.

When a patient undergoes intensive treatment, they may experience cachexia. This is a condition where the body loses significant muscle mass and weight, often making it harder for patients to maintain their strength. New research looked at thousands of safety reports to see which medications might be linked to this issue.

The study looked at 4,878 reports and found 25 different drug signals for cachexia. Some specific medications, like low calcium peritoneal dialysis solution lactate G15, nivolumab, and Kaletra, showed stronger signals for being associated with the condition. In many cases, the symptoms appeared quickly, with more than half of the cases starting within the first 120 days.

It is important to remember that these results come from a database of self-reported events. This means the study shows a statistical link, not a proven cause. Because the data is based on reports rather than controlled trials, the exact strength of these links is still being evaluated by experts.

What this means for you:
Analysis of safety reports identified 25 drugs that may be linked to muscle wasting and weight loss.

Common questions

What is cachexia?

Cachexia is a condition where a person experiences significant weight loss and muscle wasting. It often happens during serious illnesses. This study looked at how certain medications might be linked to this condition in patients.

Which specific drugs showed a link to muscle loss?

The study identified 25 drug signals. Specific medications that showed a positive signal for cachexia included low calcium peritoneal dialysis solution lactate G15, Kaletra, and nivolumab. These results suggest a need for further review of these labels.

How quickly do these symptoms typically appear?

The study found that the median time to onset was 31 days. More than half of the cases of cachexia occurred within the first 120 days of treatment. You should talk to your doctor about your specific treatment timeline.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedSep 2026
View Original Abstract ↓
BackgroundCachexia is a devastating metabolic syndrome that has a profound impact on survival rate and quality of life. Currently, there is still a scarcity of systematic evidence regarding drug-induced cachexia. This study aims to identify drugs associated with cachexia through the first large-scale pharmacovigilance analysis, and to characterize their risk features using real-world data.MethodsData from the U.S. FDA Adverse Event Reporting System (FAERS) from January 2004 and March 2025 were analyzed. Reports listing cachexia as an adverse event were extracted. Disproportionality analysis was performed on the top 50 most frequently reported drugs using reporting odds ratio (ROR), proportional reporting ratio, Bayesian Confidence Propagation Neural Network, and Multi-item Gamma Poisson Shrinker. A drug was considered a positive signal only if it met the threshold across all four methods. The Weibull shape parameter test was used to analyze the time-to-onset (TTO) profile.ResultsAmong 4,878 individual case safety reports of drug-related cachexia, the mortality rate was 25.6%. Disproportionality analysis identified 25 drugs with consistent positive signals across all four algorithms. These drugs spanned nine categories, with antineoplastic and immunomodulating agents being the most common. The drugs with stronger signals were low calcium peritoneal dialysis solution lactate G15 (ROR 495.67, 95% CI 336.94–729.18), Kaletra (ROR 10.44, 95% CI 7.98–13.65), and nivolumab (ROR 15.29, 95% CI 13.65–17.13). The drugs with a higher number of reported cases were nivolumab (319 cases), paclitaxel (160 cases), and Zometa (131 cases). The median TTO was 31 days, and more than half of cases occurred within the first 120 days, presenting an “early failure” pattern.ConclusionThis study identified 25 drug safety warning signals that are significantly associated with the occurrence of cachexia. Cachexia is more likely to occur in the initial stage of drug treatment and has a high mortality rate. Continuous regulatory review and label updates of the safety information of relevant medications should be promoted.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.