Pravastatin (Na)
Also known as: Eptastatin Na
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).

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
Pravastatin (Na) is primarily indicated in conditions like Gastro-oesophageal reflux disease (refractory to other treatment), Hypercholesterolaemia, Induction and maintenance of anaesthesia.
Contraindications
Pravastatin (Na) is contraindicated in conditions like Hepatic disease.
Dosage
Pravastatin (Na)'s dosage details are as follows:
| Dose | Single Dose | Frequency | Route | Instructions |
|---|---|---|---|---|
| Adult Dosage | ||||
| 25 mg | 25 mg | Every 24h | PO | At night. |
| Paediatric Dosage (20kg) | ||||
| 0 – 0 | — | — | Not recommended in this age group | |
| Neonatal Dosage (3kg) | ||||
| 0 – 0 | — | — | Not recommended in this age group | |
Drug Interactions
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
Available Brands
Storage Conditions
Drug Classification
- 1.12.6 — Lipid-regulating drugs /Anti-atheromas