Nisoldipine

(British Approved Name, US Adopted Name, rINN)

Drug Nomenclature

International Nonproprietary Names (INNs) in main languages (French, Latin, Russian, and Spanish):
cCB“>Synonyms: Bay-k-5552; Nisoldipiini; Nisoldipin; Nisoldipino; Nisoldipinum
cCB“>BAN: Nisoldipine
cCB“>USAN: Nisoldipine
cCB“>INN: Nisoldipine [rINN (en)]
cCB“>INN: Nisoldipino [rINN (es)]
cCB“>INN: Nisoldipine [rINN (fr)]
cCB“>INN: Nisoldipinum [rINN (la)]
cCB“>INN: Низольдипин [rINN (ru)]
cCB“>Chemical name: Isobutyl methyl 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)pyridine-3,5-dicarboxylate
cCB“>Molecular formula: C20H24N2O6 =388.4
cCB“>CAS: 63675-72-9
cCB“>ATC code: C08CA07
cCB“>Read code: y09tN

Adverse Effects, Treatment, and Precautions

As for dihydropyridine calcium-channel blockers (see Nifedipine).

Interactions

As for dihydropyridine calcium-channel blockers (see Nifedipine).

Pharmacokinetics

Nisoldipine is well absorbed from the gastrointestinal tract after oral doses but undergoes rapid and extensive first-pass metabolism in the gut wall and liver and bio-availability has been reported to be only about 4 to 8%. About 60 to 80% of an oral dose is excreted in the urine and the remainder in the faeces, mainly as metabolites. The terminal elimination half-life is about 7 to 12 hours. Nisoldipine is more than 99% bound to plasma proteins.

A study in 11 patients given oral nisoldipine 10 mg once or twice daily indicated that the pharmacokinetics of nisoldipine could best be described by an open 2-compartment model. Peak plasma concentrations occurred 1 hour after a single oral dose, and varied greatly between the patients. The mean plasma elimination half-life was 11.4 hours after a single dose and 14.0 hours after repeated dosing, which was longer than had been previously reported perhaps reflecting the greater sensitivity of the assay. In another study oral, but not intravenous, nisoldipine increased liver blood flow in 10 healthy subjects and thus affected its own systemic availability. Variations in liver blood flow may account for the interindividual variation in the pharmacokinetics of nisoldipine.

Uses and Administration

Nisoldipine is a dihydropyridine calcium-channel blocker with actions and uses similar to those of nifedipine. It is used in the management of hypertension and angina pectoris. Nisoldipine is given orally usually as a modified-release preparation. Absorption is affected by food and the modified-release preparation should be taken on an empty stomach; it should not be taken with high fat meals. Doses are similar for both hypertension and angina. The initial dose is 10 mg once daily and the usual maintenance dose is 20 to 40 mg once daily.

Proprietary Preparations

Argentina: Nisodipen †;

Austria: Syscor;

Belgium: Sular; Syscor;

Brazil: Syscor;

Chile: Nivas;

Czech Republic: Syscor †;

Finland: Syscor;

Germany: Baymycard;

Hungary: Baymycard;

Italy: Syscor;

New Zealand: Syscor;

South Africa: Syscor †;

Spain: Cornell; Sular; Syscor;

Switzerland: Syscor †;

United Kingdom (UK): Syscor;

United States of America (US and USA): Sular


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