Dose: 100 ug
Single Dose: 100 (100)
Frequency: 24 hourly
Route: PO
Instructions: In the evening, initially.

is the derivative of Cerivastatin Sodium. It is of Synthetic origin and belongs to Anti-hyperlipidimic. It belongs to dyslipidaemic agent pharmacological group on the basis of mechanism of action. The Molecular Weight of Cerivastatin Sodium is 481.50.

Cerivastatin Sodium is contraindicated in conditions like Acute liver disease,Porphyria.

The symptomatic adverse reactions produced by Cerivastatin Sodium are more or less tolerable and if they become severe, they can be treated symptomatically, these include Dizziness, Headache, Insomnia, Skin rashes, Blurred vision, Dysgeusia, Skin rashes, dizziness.

Cerivastatin Sodium is primarily indicated in conditions like Hyperlipoproteinaemia, and can also be given in adjunctive therapy as an alternative drug of choice in Hypercholesterolaemia.

No data regarding the interactions of Cerivastatin Sodium was found.

Drug should not be given to Paediatrics, Pregnant Mothers, patients suffering from Kidney dysfunction, patients suffering from Liver Malfunction, and Neonates.If prescribing authority justifies the benefits of the drug against the possible damages he/she should reevaluate them and consult the reference material and previous studies.

Tabs Store in a well closed container, Below 30°C. Protect from Moisture and Heat.

It should be avoided during pregnancy since there is a possibility that it could interfere with fetal sterol synthesis. It should be discontinued if marked or persistant increases in serum aminotransferase or creatine-phosphokinase concentrations occur.It shouls not be given in severe renal impairement and liver function should be monitored