Lipidof 200 mg is a potent lipid-lowering medication belonging to the fibrate class, designed to manage various types of hyperlipidemia, including type IIa, IIb, III, IV, and V, especially in patients who have not responded adequately to dietary measures and other therapies. Its active component, fenofibric acid, is a fibric acid derivative that works by modulating lipid metabolism to lower triglycerides, reduce LDL cholesterol, and increase HDL cholesterol.
Lipidof 200 mg is a prodrug administered orally as a 200 mg capsule, which is rapidly converted to fenofibric acid after ingestion. By targeting multiple lipid pathways, Lipidof helps reduce atherogenic lipoproteins, improving cardiovascular health while also lowering serum uric acid levels in hyperuricemic individuals.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Fibrates – Lipid-Lowering Agent
Lipidof 200 mg is indicated for the treatment of:
Hyperlipidemia: Types IIa, IIb, III, IV, and V
Patients unresponsive to diet and lifestyle modifications
Mixed hyperlipidemia where triglycerides and LDL cholesterol are elevated
As part of a comprehensive approach to cardiovascular risk reduction in high-risk patients
Before starting Lipidof 200 mg, patients should maintain a triglyceride-lowering diet and continue it during therapy to maximize effectiveness.
Mechanism of Action:
Lipidof 200 mg is rapidly hydrolyzed to fenofibric acid, the active form
Activates peroxisome proliferator-activated receptor alpha (PPARα)
Increases lipoprotein lipase activity, enhancing triglyceride breakdown
Reduces apolipoprotein CIII, a natural inhibitor of lipoprotein lipase
Converts small, dense LDL particles into larger, less atherogenic particles
Increases HDL cholesterol by raising apolipoproteins AI and AII
Reduces serum uric acid by increasing urinary excretion
Clinical Effects:
Lowers triglycerides, total cholesterol, VLDL, and LDL cholesterol
Raises HDL cholesterol
Improves overall lipid profile and cardiovascular risk
Adults: 1 capsule (200 mg) once daily with meals to optimize absorption
Dosage should be individualized based on patient response, with follow-up lipid testing every 4–8 weeks
For hypertriglyceridemia, doses may range from 67–200 mg daily based on severity
Continue dietary and lifestyle interventions while on treatment
May potentiate the effects of warfarin; monitor INR
May improve glucose tolerance when used with antidiabetic medications
Caution with HMG-CoA reductase inhibitors due to increased risk of rhabdomyolysis
May increase nephrotoxicity of cyclosporine
Hypersensitivity to fenofibric acid or fibrates
Severe renal or hepatic impairment
Existing gallbladder disease
Nursing mothers
Photosensitivity to ketoprofen
Gastrointestinal: nausea, anorexia, gastric pain
Skin: pruritus, urticaria
Nervous system: headache, dizziness, vertigo
Musculoskeletal: myotoxicity
Other: fatigue, hair loss, impotence
Pregnancy Category C: Use only if benefits outweigh risks
Not recommended for breastfeeding due to potential tumorigenicity observed in animals
Monitor renal function, especially in elderly or those with pre-existing renal disease
Liver function tests recommended every 3 months during the first year of therapy
Discontinue if signs of myotoxicity or elevated creatinine kinase levels are observed
No specific antidote; supportive care and monitoring of vital signs recommended
Hemodialysis is ineffective due to high plasma protein binding
Store below 30°C in a dry place, protected from light. Keep out of reach of children.
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