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Generic Nexletol ( Bempedoic acid )
Nexletol (bempedoic acid) is a lipid‑lowering agent indicated as an adjunct to diet and maximally tolerated statin therapy in adults with heterozygous familial hypercholesterolemia or established atherosclerotic cardiovascular disease who require additional lowering of low‑density lipoprotein cholesterol (LDL‑C). It is a first‑in‑class adenosine triphosphate‑citrate lyase (ACL) inhibitor that acts in the liver, upstream of HMG‑CoA reductase, to reduce cholesterol synthesis and upregulate LDL receptors, thereby increasing LDL clearance from the blood. Bempedoic acid is a prodrug that is activated to its CoA ester solely in the liver, minimizing potential off‑target effects in skeletal muscle. Nexletol is not a statin and does not replace the need for lifestyle modifications.
Usual adult dose: The recommended dose is 180 mg taken orally once daily, with or without food. Tablets should be swallowed whole. No dose adjustment is required on the basis of age, mild‑to‑moderate renal impairment, or mild hepatic impairment. The safety and efficacy of Nexletol have not been established in patients with severe renal impairment or end‑stage renal disease, or in those with moderate or severe hepatic impairment; its use in these populations is not recommended. The lipid‑lowering effect should be evaluated after 4 weeks of treatment, and the dose should be maintained at 180 mg once daily; there is no additional benefit from higher doses.
Dosage form: Film‑coated tablets: 180 mg (white to off‑white, oval, debossed with “180” on one side and “ESP” on the other). Available in blister packs of 30 tablets.
Onset of action: Significant reductions in LDL‑C are observed within 4 weeks of initiating once‑daily therapy, with the full lipid‑modulating effect generally achieved by 12 weeks of continuous treatment.
Duration of action: The therapeutic effect is maintained over a 24‑hour dosing interval with once‑daily administration. The elimination half‑life of bempedoic acid is approximately 21 hours.
Alcohol recommendation: No direct pharmacokinetic interaction between bempedoic acid and alcohol is known. However, excessive alcohol consumption can adversely affect liver function and lipid metabolism, potentially reducing the effectiveness of lipid‑lowering therapy and increasing the risk of hepatic adverse events. Moderation is strongly advised, and patients with pre‑existing liver disease should exercise caution.
Most common side effects: Upper respiratory tract infection, muscle spasms, back pain, abdominal pain or discomfort, bronchitis, pain in extremities, anemia, and hyperuricemia. Hyperuricemia is a class effect of ACL inhibitors; serum uric acid levels may rise within the first 4 weeks and stabilize thereafter; gout may develop in predisposed patients. Mild, reversible increases in serum creatinine and blood urea nitrogen have been observed. Because bempedoic acid may increase the risk of tendon injury or rupture, patients should discontinue therapy and seek medical attention at the first sign of tendon pain, swelling, or inflammation. Nexletol is not associated with statin‑type myopathy but may still cause muscle spasms; patients should report any new or worsening muscle symptoms. Concomitant use with statins may amplify the risk of statin‑related muscle effects; routine monitoring of lipid levels and clinical assessment for adverse events are recommended.
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+ Next orders 10% discount
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+ Next orders 10% discount
+ Package delivery insurance
+ Next orders 10% discount
