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Vogdia

Vogdia Dosage/Direction for Use

pravastatin

Manufacturer:

Unison

Distributor:

F.C.P.

Marketer:

B.Grimm Pharma
Full Prescribing Info
Dosage/Direction for Use
Doses should be individualized according to the baseline low-density lipoprotein (LDL)-cholesterol levels, the recommended goal of therapy, and patient response. Adjustments should be made at intervals of 4 weeks or more. Doses may need adjusted based on concomitant medications. Pravastatin sodium tablets are administered orally once daily preferably in the evening with or without food.
Hypercholesterolemia: The recommended dose range is 10-40 mg once daily. The therapeutic response is seen within a week and the full effect of a given dose occurs within four weeks, therefore periodic lipid determinations should be performed and the dosage adjusted accordingly. The maximum daily dose is 40 mg.
Cardiovascular prevention: In all preventive morbidity and mortality trials, the only studied starting and maintenance dose was 40 mg daily.
Dosage after transplantation: Following organ transplantation a starting dose of 20 mg per day is recommended in patients receiving immunosuppressive therapy (see Interactions). Depending on the response of the lipid parameter, the dose may be adjusted up to 40 mg under close medical supervision.
Special population: Children: The documentation on efficacy and safety in patients less than 18 years old is limited, therefore, the use of Pravastatin sodium is not recommended in these patients.
Elderly patients: There is no dose adjustment necessary in these patients unless there are predisposing risk factors.
Renal or hepatic impairment: a starting dose of 10 mg a day is recommended in patients with moderate or severe renal impairment or significant hepatic impairment. The dosage should be adjusted according to the response of lipid parameters and under medical supervision.
Concomitant therapy: The lipid lowing effects of Pravastatin sodium on total cholesterol and LDL-cholesterol are enhanced when combined with a bile acid binding resin (eg. cholestyramine, colestipol). Pravastatin sodium tablets should be given either one hour before or at least four hours after the resin.
For patients taking cyclosporine with or without other immunosuppressive medicinal products, treatment should begin with 20 mg of pravastatin once daily and titration to 40 mg should be performed with caution.
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