Full Generic Medicine Info
Dosage/Direction for Use

Angina pectoris, Hypertension
Adult: Immediate-release: Initially, 5 or 10 mg bid increased if necessary at intervals of no less than 1 wk to max of 20 mg bid. Modified-release: Initially, 17 mg once daily, increased by 8.5 mg/wk (or longer intervals). Max: 34 mg once daily.
Elderly: Immediate-release: Initially, 5 or 10 mg once daily. Modified-release: Initially, 8.5 mg once daily.
Hepatic impairment: Immediate-release: Initially, 5 or 10 mg once daily. Modified-release: Initially, 8.5 mg once daily.
Concomitant use w/ CYP3A4 inducers.
Special Precautions
Patients w/ severe aortic stenosis, heart failure, hypertrophic cardiomyopathy (HCM) w/ outflow tract obstruction. Hepatic impairment. Elderly. Pregnancy and lactation. Monitoring Parameters Monitor BP carefully during the initial admin or if there is subsequent upward dose adjustment.
Adverse Reactions
Dizziness, headache, peripheral oedema, chest pain, angina exacerbation, palpitations, vasodilation, pharyngitis, sinusitis, nausea, rash.
Symptoms: Hypotension. Management: Symptomatic and supportive treatment. Monitor CV and resp function. Elevation of extremities, use of calcium infusion, pressor agents and fluid may be necessary.
Drug Interactions
May increase serum levels w/ CYP3A4 inhibitors. Increased levels w/ cimetidine. Increased antihypertensive effect w/ atenolol. Propranolol attenuated heart rate increase following intake of immediate-release nisoldipine. Reduced bioavailability w/ quinidine. Increased quinidine levels w/ immediate-release nisoldipine.
Potentially Fatal: Concomitant use w/ potent CYP3A4 inducers (e.g. phenytoin) may decrease nisoldipine plasma concentration to undetectable levels.
Food Interaction
High-fat food increases peak concentration. Avoid grapefruit-containing foods and beverages as it increases peak concentrations and oral bioavailability of nisoldipine. Levels may be reduced w/ St John's wort.
Nisoldipine is a dihydropyridine Ca channel blocker. It inhibits the movement of Ca ions into vascular smooth muscle and cardiac muscle. It reversibly competes w/ other dihydropyridines for binding to the Ca channel.
Duration: >24 hr.
Absorption: Well absorbed from the GI tract. High-fat food increases peak concentration. Bioavailability: Approx 4-8%.
Distribution: Plasma protein binding: >99%.
Metabolism: Undergoes rapid and extensive first-pass metabolism in the gut wall and liver.
Excretion: Via urine (approx 60-80%) and faeces (remaining dose as metabolites). Terminal elimination half-life: Approx 7-12 hr.
Oral: Store between 20-25°C. Protect from light and moisture.
CIMS Class
Calcium Antagonists
ATC Classification
C08CA07 - nisoldipine ; Belongs to the class of dihydropyridine derivative selective calcium-channel blockers with mainly vascular effects. Used in the treatment of cardiovascular diseases.
Disclaimer: This information is independently developed by CIMS based on nisoldipine from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to CIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, CIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2021 CIMS. All rights reserved. Powered by
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