- March 15, 2022
- Newsletter
- 617-430-5616
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Brand Name :
Mavik
Synonyms :
trandolapril
Class :
ACE Inhibitors
Dosage Forms & Strengths
Tablet
1mg
2mg
4mg
Nonblack patients:
1
mg
orally
every day
black patients: 2 mg orally every day
Maintenance dose
2-4 mg orally every day or divided in every 12 hours
congestive Heart Failure (CHF)
1
mg
orally
daily
or may be increased up to 4 mg
left Ventricular Dysfunction Following Myocardial Infarction
1
mg
orally
daily or may be increased up to 4 mg
Note: Indicated for Left Ventricular Dysfunction Post-MI
may increase the toxic effect of angiotensin receptor II blockers
may enhance the hypotensive effect when combined with sparsentan
may diminish the serum concentration when combined with angiotensin-converting enzyme inhibitors
May diminish the effects of ketoprofen by pharmacodynamic antagonism
may diminish the effects of indomethacin by pharmacodynamic antagonism
May increase the adverse/toxic effect of NSAIDs
May increase the adverse/toxic effect of NSAIDs
May increase the adverse/toxic effect of NSAIDs
May increase the adverse/toxic effect of NSAIDs
May increase the adverse/toxic effect of NSAIDs
choline magnesium trisalicylate
may enhance the nephrotoxic effect of ACE inhibitors
may enhance the bradycardic effect of beta-blockers
may enhance the bradycardic effect of beta-blockers
may enhance the bradycardic effect of beta-blockers
may enhance the bradycardic effect of beta-blockers
may enhance the bradycardic effect of beta-blockers
ACE Inhibitors may enhance the potential for allergic or hypersensitivity reactions to allopurinol
icatibant may reduce the antihypertensive effect of ACE inhibitors
may increase the nephrotoxic effect of salicylates
may decrease the antihypertensive effect when combined with angiotensin-converting enzyme inhibitors
may have an increased hyperkalemic effect when combined with angiotensin-converting enzyme inhibitors
drospirenone/ethinyl estradiol/levomefolate
may increase the hyperkalemic effect of Drospirenone-Containing Products
Adverse drug reactions
Frequency Defined
>10%
Hypotension (1-11%)
Elevated Uric Acid (15%)
Cough (1.9-35%)
1-10%
Hyperkalemia (5.3%)
Syncope (5.9%)
Dizziness (1.3-2.3%)
Hypocalcemia (4.7%)
Bradycardia (1-5%)
Stroke (3.8%)
Frequency Not Defined
ARF if renal artery stenosis
Angioedema
Pregnancy warnings:
AU TGA pregnancy category: D
US FDA pregnancy category: D
Lactation:
Excreted into human milk is unknown
Pregnancy Categories:
Category A: Satisfactory and well-controlled studies show no risk to the fetus in the first or later trimester.
Category B: No evidence shown of risk to the fetus found in animal reproduction studies, and there are not enough studies on pregnant women
Category C: Adverse effects on the fetus found with evidence in animal reproduction studies and no adequate evidence for a result in humans must take care of potential risks in pregnant women
Category D: adequate data available with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.
Category N: There is no data available for the drug under this category
Patient Information Leaflet
Generic Name: trandolapril
Why do we use trandolapril?
trandolapril is an ACE Inhibitors used to treat Post MI, Hypertension, and CHF.