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NITROCARD

Nitroglycerin

Composition:

Each sustained release tablet contains Nitroglycerin USP 2.6 mg.

Pharmacology:

Nitroglycerin relaxes the vascular smooth muscle. Although the precise details remain unclear, the direct effect on vascular smooth muscle appears to be the result of liberation of free radicals of nitric oxide (NO) which activates guanylate cyclase, resulting in increased synthesis of cyclic GMP. It is possible that NO combines with sulfhydryl groups in the endothelium and produces S-nitrosothiols that stimulate guanylate cyclase production. This is enhanced by N-acetylcysteine, which provides a source of sulfhydryl groups. Cyclic GMP reduces stored calcium and thus interferes with calcium-activated smooth muscle contraction.

Indications:

Nitroglycerin is used for the prophylaxis and long term management of angina pectoris, heart failure and myocardial infarction.

Dosage & administration:

The dosage is determined on the basis of individual requirement depending on the severity of the disease, response to nitrglycerol and development of side-effects. The usual daily dose initially 1 tablet twice daily. The dose may be gradually increased to 2-3 tablets twice daily.

Side-effects:

Headache, flushing, dizziness, postural hypotension, tachycardia may occur.

Contraindications:

Hypersensitivity to nitrates. Obstructive hypertrophic cardiomyopathy. Low cardiac output secondary to hypovolemia. Inferior myocardial infarction with right ventricular involvement. Raised intracranial pressure. Mitral valve propalpse. Glaucoma.

Drug interactions:

Pharmacodynamic interactions: Orthostatic hypotension may occur with the combined use of calcium channel blockers, antihypertensive agents, phenothiazine, and tricyclic antidepressants. Use of alcohol with nitroglycerin may produce severe hypotension and collapse.

Pharmacokinetic interactions: Oral nitroglycerin may enhance the bioavailability of dihydroergotamine.

Use in special groups:

Neonates: Safety and efficacy for use in infants and children have not been established.

Children: Safety and efficacy for use in children has not been established.

Breast milk: Safety and efficacy for use in nursing mother has not been established.

Pregnant women: Safety for use during pregnancy has not been established. Use only when clearly needed and when the potential benefits outweigh the unknown potential hazards to the foetus.

The elderly: Symptoms of cerebral ischaemia due to postural hypotension may develop with rapidly acting formulations.

Packing:

Each box contains 5´10's SR Tablets.

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