Trandolapril indications and usage: Difference between revisions

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====Hypertension====
====Hypertension====
MAVIK is indicated for the treatment of [[hypertension]]. It may be used alone or in combination with other antihypertensive medication such as [[hydrochlorothiazide]].
MAVIK is indicated for the treatment of [[hypertension]]. It may be used alone or in combination with other antihypertensive medication such as [[hydrochlorothiazide]].


====Heart Failure Post Myocardial Infarction or Left-Ventricular Dysfunction Post Myocardial Infarction====
====Heart Failure Post Myocardial Infarction or Left-Ventricular Dysfunction Post Myocardial Infarction====

Revision as of 22:14, 18 February 2014

Trandolapril
MAVIC® FDA Package Insert
Indications and Usage
Dosage and Administration
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Overdosage
Description
Clinical Pharmacology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
Clinical Trials on Trandolapril
ClinicalTrials.gov

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Amr Marawan, M.D. [2]

Indications and Usage

Hypertension

MAVIK is indicated for the treatment of hypertension. It may be used alone or in combination with other antihypertensive medication such as hydrochlorothiazide.

Heart Failure Post Myocardial Infarction or Left-Ventricular Dysfunction Post Myocardial Infarction

MAVIK is indicated in stable patients who have evidence of left-ventricular systolic dysfunction (identified by wall motion abnormalities) or who are symptomatic from congestive heart failure within the first few days after sustaining acute myocardial infarction. Administration of trandolapril to Caucasian patients has been shown to decrease the risk of death (principally cardiovascular death) and to decrease the risk of heart failure-related hospitalization.[1]

References

  1. "MAVIK (TRANDOLAPRIL) TABLET [ABBVIE INC.]".

Adapted from the FDA Package Insert.