Leqvio Clinical Trial Adverse Events by Incidence Rate
Injection-site reactions were most common (8.2% vs 1.8% placebo) across ORION-9/10/11. No significant liver, kidney, or muscle toxicity signals emerged.
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Injection-site reactions were most common (8.2% vs 1.8% placebo) across ORION-9/10/11. No significant liver, kidney, or muscle toxicity signals emerged.
Injection-site reactions affect about 8.2% of Leqvio users and are usually mild. No withdrawal syndrome exists, but LDL-C rebounds within 6-12 months of stopping.
Most Leqvio side effects are mild injection-site reactions (8.2% vs 1.8% placebo); permanent effects remain unconfirmed in trial data. See what to monitor.
A guide to the rare but serious adverse events linked to Leqvio (inclisiran), covering trial data, FDA labeling, post-market reports, and how to monitor patients on twice-yearly PCSK9i injections.
Leqvio's long-term side effects are mostly mild injection-site reactions (8.2%); serious events match placebo, except in severe renal or hepatic impairment.