DrugInfoSys

Gemfibrozil

Drug #335

Gemfibrozil is antihyperlipidimic agent and reduces high levels of blood cholesterol. Gemfibrozil is the congener of the first generation fibric acid derivative clofibrate. It differs from clofibrate in its aliphatic chain and has two methyl groups rather than a chlorine atom on the phenoxy group.

Primary Characteristics

It is of Synthetic origin and belongs to Fibrates.

It belongs to Lipid lowering agents pharmacological group on the basis of mechanism of action and also classified in Antilipemic Agent pharmacological group.

Molecular Weight: 250.4 · pKa: 4.7 · Solubility in Water: InSoluble · Solubility in Alcohol: Slouble · Non-proprietary name: Gemfibrozil.

Molecular structure of Gemfibrozil

Pharmacokinetics

Absorption: Gemfibrozil has an oral bioavailability is 100%.

Distribution: Gemfibrozil has a volume of distribution is 0.14l/kg. plasma protein binding is 95%.

Elimination: plasma half-life is 1.5 hr, renal excretion is 70%.

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Indications

Contraindications

Gemfibrozil is contraindicated in conditions like Gall stones, Hepatic disease.

Dosage

Gemfibrozil's dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
0.9 – 1.2 gPOIn two divided doses given 30 min before the morning and evening meals
Paediatric Dosage (20kg)
0 – 0Not Recommended in this Age Group
Neonatal Dosage (3kg)
0 – 0Not recommended in this age group

Drug Interactions

Unknown5 interactions
6 interactions
Major2 interactions

Always consult your physician for the change of dose regimen or an alternative drug of choice that may strictly be required.

Side Effects

Gemfibrozil in overdosage may give rise to further complications which include Myositic syndrome .

Gemfibrozil produces potentially life-threatening effects which include Arrhythmias, Hypokalemia, Hypokalemia. Careful monitoring is needed with proper medical management.

Gemfibrozil is known to cause more or less tolerable side effects which are usually transient. These include Dermatitis, Gall stones, GI symptoms, Headache, Impotence, Nausea.

Warnings / Precautions

Obtain periodic determination of serum lipid during administration of gemfibrozil. Withdraw the drug after 3 months if adequate response is not achieved. Perform periodic blood count during first 12 months of administration. Carefully monitor blood glucose level during therapy because it has a hyperglycemic effect. Avoid if creatinine clearance less than 30 ml/min.

Interference in Pathology

Gemfibrozil may interfere in the diagnosis of High level of Aaminotransfraces, Decrease in WBC or hemotocnt.

Available Brands

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Single Ingredient

Storage Conditions

Gemfibrozil should be stored Tab, Caps .

Drug Classification

  1. 1.12.6Lipid-regulating drugs /Anti-atheromas

Manufacturers

Manufacturers of Gemfibrozil in Pakistan: