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Nexletol may affect the way other medicines work, and other medicines may affect how nexletol works The fda approved nexletol based on evidence from two clinical trials (trial 1/ nct02666664 and trial 2/nct02991118) of 3009 patients with high ldl cholesterol and known atherosclerotic. Fda approval history for nexletol (bempedoic acid) used to treat high cholesterol, familial heterozygous, cardiovascular risk reduction
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Supplied by esperion therapeutics, inc. The fda has expanded the approval of nexletol and nexlizet to prevent myocardial infarction and coronary revascularization in both primary and secondary prevention patients. Nexletol by is a prescription medication manufactured, distributed, or labeled by esperion therapeutics, inc.
Drug facts, warnings, and ingredients follow.
The fda has approved broad new label expansions for bempedoic acid (nexletol Esperion therapeutics, inc) to reduce the risk of myocardial infarction and coronary revascularization in adults with established cardiovascular disease (cvd) or a high risk for a cvd event who are unable to use statin therapy The medication is also approved as an adjunct to diet, alone or in combination with other. Espr) today announced that the united states food and drug administration (fda) has approved broad new label expansions for nexletol ® (bempedoic acid) tablets and nexlizet ® (bempedoic acid and ezetimibe) tablets based on positive clear outcomes data that include indications for cardiovascular risk reduction and expanded.
To reduce the risk of myocardial infarction and coronary revascularization in adults who are unable to take recommended statin therapy (including those not taking a.
