DrugInfoSys

Pravastatin (Na)

Also known as: Eptastatin Na

Drug #594

Pravastatin (Na) is a lipid-lowering agent, belongs to the group of drugs known as HMG-CoA reductase inhibitors which includes fluvastatin, lovastatin and simvastatin. More hydrophilic than the other members of this group unlike the others, pravastatin does not require hydrolysis for activation.Pravastatin (Na) is used for the treatment of primary hypercholesterolemia, and for primary prophylaxis of a myocardial infarction in patients with hypercholesterolemia who are at risk of a myocardial infarction. It was approved by the FDA in October 1991. It exerts it slipid lowering effects by inhibiting hydroxymethylglutaryl-CoA (HMG-CoA) reductase, an enzyme necessary for the intracellular synthesis of cholesterol. As a consequence of inhibiting HMG-CoA reductase, intracellular synthesis of cholesterol is impaired. This, in turn, increases the clearance of circulating LDL. In addition, pravastatin inhibits hepatic synthesis of VLDL, the precursor for LDL. The result is a reduction of circulating total cholesterol and LDL cholesterol.

Primary Characteristics

Pravastatin (Na) is also known as Eptastatin Na.

It is of Semi Synthetic origin and belongs to Naphalene.

It belongs to HMGCoA reductase inhibitor pharmacological group on the basis of mechanism of action and also classified in Antilipemic Agent pharmacological group.

Molecular Weight: 466.5 · Solubility in Water: readily soluble · Solubility in Alcohol: readily soluble · Non-proprietary name: Pravastatin (Na).

Molecular structure of Pravastatin (Na)

Pharmacokinetics

Absorption: Pravastatin (Na) has an oral bioavailability is 34%.

Distribution: Pravastatin (Na) has a volume of distribution is 0.5 - 1 l/kg. plasma protein binding is 50 %.

Elimination: it is metabolised via Hepatic, plasma half-life is 1.5 - 2 hr, renal excretion is 20 %.

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Indications

Contraindications

Pravastatin (Na) is contraindicated in conditions like Hepatic disease.

Dosage

Pravastatin (Na)'s dosage details are as follows:

DoseSingle DoseFrequencyRouteInstructions
Adult Dosage
25 mg25 mgEvery 24hPOAt night.
Paediatric Dosage (20kg)
0 – 0Not recommended in this age group
Neonatal Dosage (3kg)
0 – 0Not recommended in this age group

Drug Interactions

Unknown2 interactions
1 interaction

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

Side Effects

Pravastatin (Na) in overdosage may give rise to further complications which include Cataract.

Pravastatin (Na) is known to cause more or less tolerable side effects which are usually transient. These include Elevation of CPK , Myositic syndrome .

Warnings / Precautions

Pravastatin should be used with caution in patients with any liver, kidney or heart disease, history of alcoholism, hypothyroidism or any allergy, especially drug allergies. Limit alcohol intake this may aggravate drug side effects. This drug should not be used during pregnancy or lactation.

Available Brands

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Single Ingredient

Storage Conditions

Pravastatin (Na) should be stored Tab.

Drug Classification

  1. 1.12.6Lipid-regulating drugs /Anti-atheromas

Manufacturers

Manufacturers of Pravastatin (Na) in Pakistan: