Sandbox Lopressor

Sandbox Lopressor®
Black Box Warning
Adult Indications and Dosage   FDA-Labeled Use   Off-Label Use
Pediatric Indications and Dosage   FDA-Labeled Use   Off-Label Use
Contraindications
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Patient Information   Patient Information from FDA   Patient Information from NLM
Combined Alcohol Use
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

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Black Box Warning

WARNING See full prescribing information for complete boxed warning. Ischemic Heart Disease: Following abrupt cessation of therapy with certain beta-blocking agents, exacerbations of angina pectoris and, in some cases, myocardial infarction have occurred. When discontinuing chronically administered Lopressor, particularly in patients with ischemic heart disease, the dosage should be gradually reduced over a period of 1-2 weeks and the patient should be carefully monitored. If angina markedly worsens or acute coronary insufficiency develops, Lopressor administration should be reinstated promptly, at least temporarily, and other measures appropriate for the management of unstable angina should be taken. Patients should be warned against interruption or discontinuation of therapy without the physician’s advice. Because coronary artery disease is common and may be unrecognized, it may be prudent not to discontinue Lopressor therapy abruptly even in patients treated only for hypertension.

Pricing

Black box warning Dosing information Mechanism of action Indications Contraindications Warnings and Precautions Adverse reactions Drug Interactions Overdosage Pharmacology Clinical studies Patient counseling information Pill images and characteristics