INDICATIONS AND USAGE
I. Vasospastic Angina
Nifedipine capsule is indicated for the management of vasospastic angina confirmed by any of the following criteria: 1)...
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NIFEDIPINE Capsules (GREENSTONE LLC)
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NIFEDIPINE Capsules (GREENSTONE LLC) Quick Finder
Dosage and Administration
DOSAGE AND ADMINISTRATION
The dosage of Nifedipine capsules needed to suppress angina and that can be tolerated by the patient must be established by titration. Excessive doses can result in hypotension....
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Contraindications
CONTRAINDICATIONS
Known hypersensitivity reaction to Nifedipine.
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Warnings and Precautions
WARNINGS
Excessive Hypotension
Although, in most patients, the hypotensive effect of Nifedipine is modest and well tolerated, occasional patients have had excessive...
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Adverse Reactions
ADVERSE REACTIONS
In multiple-dose United States and foreign controlled studies in which adverse reactions were reported spontaneously, adverse effects were frequent but generally not serious and rarely required...
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Overdosage
OVERDOSAGE
Experience with nifedipine overdosage is limited. Generally, overdosage with nifedipine leading to pronounced hypotension calls for active cardiovascular support including monitoring of cardiovascular and...
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Description
DESCRIPTION
Nifedipine capsule is an antianginal drug belonging to a class of pharmacological agents, the calcium channel blockers. Nifedipine is 3,5-pyridinedicarboxylic acid, 1,4-dihydro-2, 6-dimethyl-4-(2-nitrophenyl)-,...
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Clinical Pharmacology
CLINICAL PHARMACOLOGY
Nifedipine is a calcium ion influx inhibitor (slow-channel blocker or calcium ion antagonist) and inhibits the transmembrane influx of calcium ions into cardiac muscle and smooth muscle. The contractile...
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How Supplied/Storage and Handling
HOW SUPPLIED
Nifedipine soft gelatin capsules are supplied in:
Bottles of 100: 10 mg (NDC 59762-1004-1)
The capsules should be protected from light...
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Report Adverse Event
To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:
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You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at https://vaers.hhs.gov or call (800) 822-7967.