FDA label 547aacb1-dd90-4934-80ff-6b3db422175a

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID
c84cda13-e2fb-46d6-a9a2-5a3311387ff8
SPL ID
547aacb1-dd90-4934-80ff-6b3db422175a
Version
4
Effective date
2011-07-13
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:42:43

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: Use In Patients With Angina: Increases in frequency, duration, or severity of angina have been seen in chronic oral therapy with oral nicardipine. Induction or exacerbation of angina has been seen in less than 1% of coronary artery disease patients treated with nicardipine hydrochloride injection. The mechanism of this effect has not been established. Use In Patients With Heart Failure: Titrate slowly when using nicardipine hydrochloride injection, particularly in combination with a beta-blocker, in patients with heart failure or significant left ventricular dysfunction because of possible negative inotropic effects. Intravenous Infusion Site To reduce the possibility of venous thrombosis, phlebitis, local irritation, swelling, extravasation, and the occurrence of vascular impairment, administer drug through large peripheral veins or central veins rather than arteries or small peripheral veins, such as those on the dorsum of the hand or wrist. To minimize the risk of peripheral venous irritation, change the site of the drug infusion every 12 hours.

Adverse reactions cross-check#

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Adverse reactions sections page 1 of 1 · 2 matching rows.

adverse reactions

ADVERSE REACTIONS: Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The adverse reaction information from clinical trials does, however, provide a basis for identifying the adverse events that appear to be related to drug use and for approximating rates. Two hundred forty-four patients participated in two multicenter, double-blind, placebo controlled trials of nicardipine hydrochloride injection. Adverse experiences were generally not serious and most were expected consequences of vasodilation. Adverse experiences occasionally required dosage adjustment. Therapy was discontinued in approximately 12% of patients, mainly due to hypotension, headache, and tachycardia. The table below shows percentage of patients with adverse events where the rate is >3% more common on nicardipine hydrochloride injection than placebo. Adverse Experience Nicardipine HCl (n=144) Placebo (n=100) Body as a Whole Headache, n (%) 21 (15) 2 (2) Cardiovascular Hypotension, n (%) 8 (6) 1 (1) Tachycardia, n (%) 5 (4) 0 Digestive Nausea/vomiting, n (%) 7 (5) 1 (1) Other adverse events have been reported in clinical trials or in the literature in association with the use of intravenously administered nicardipine. Body as a Whole: fever, neck pain Cardiovascular: angina pectoris, atrioventricular block, ST segment depression, inverted T wave, deep-vein thrombophlebitis Digestive: dyspepsia Hemic and Lymphatic: thrombocytopenia Metabolic and Nutritional: hypophosphatemia, peripheral edema Nervous: confusion, hypertonia Respiratory: respiratory disorder Special Senses: conjunctivitis, ear disorder, tinnitus Urogenital: urinary frequency Sinus node dysfunction and myocardial infarction, which may be due to disease progression, have been seen in patients on chronic therapy with orally administered nicardipine.

adverse reactions table

<table cellspacing="0" cellpadding="0" border="0" width="100%"> <tbody> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule" colspan="3" align="center"> The table below shows percentage of patients with adverse events where the rate is &gt;3% more common on nicardipine hydrochloride injection than placebo. <content styleCode="bold"/> </td> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule"> <content styleCode="bold">Adverse Experience </content> </td> <td valign="top" styleCode="Rrule"> <content styleCode="bold">Nicardipine HCl (n=144) </content> </td> <td valign="top" styleCode="Rrule"> <content styleCode="bold">Placebo (n=100) </content> </td> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule"> <content styleCode="bold">Body as a Whole </content> </td> <td valign="top" styleCode="Rrule"/> <td valign="top" styleCode="Rrule"/> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule">Headache, n (%) </td> <td valign="top" styleCode="Rrule">21 (15) </td> <td valign="top" styleCode="Rrule">2 (2) </td> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule" colspan="3"> <content styleCode="bold">Cardiovascular </content> </td> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule">Hypotension, n (%) </td> <td valign="top" styleCode="Rrule">8 (6) </td> <td valign="top" styleCode="Rrule">1 (1) </td> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule">Tachycardia, n (%) </td> <td valign="top" styleCode="Rrule">5 (4) </td> <td valign="top" styleCode="Rrule">0 </td> </tr> <tr styleCode="Botrule"> <td valign="top" styleCode="Lrule Rrule" colspan="3"> <content styleCode="bold">Digestive </content> </td> </tr> <tr> <td valign="top" styleCode="Lrule Rrule">Nausea/vomiting, n (%) </td> <td valign="top" styleCode="Rrule"> 7 (5) </td> <td valign="top" styleCode="Rrule">1 (1) </td> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.