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Drug Safety-related Labeling Changes (SrLC)

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MAVIK (NDA-020528)

(TRANDOLAPRIL)

Safety-related Labeling Changes Approved by FDA Center for Drug Evaluation and Research (CDER)

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08/02/2017 (SUPPL-25)

Approved Drug Label (PDF)

4 Contraindications

Addition of the following:

MAVIK is contraindicated in combination with a neprilysin inhibitor (e.g., sacubitril). Do not administer MAVIK within 36 hours of switching to or from sacubitril/valsartan, a neprilysin inhibitor.

5 Warnings and Precautions

PRECAUTIONS

Drug Interactions

Mammalian Target of Rapamycin (mTOR) Inhibitors

Addition of the following:

Neprilysin Inhibitor

Patients taking concomitant neprilysin inhibitors (e.g., sacubitril) may be at increased risk for angioedema.

WARNINGS

Head and Neck Angiodema

Additions and/or revisions underlined:

Patients receiving coadministration of an ACE inhibitor with an mTOR (mammalian target of rapamycin) inhibitor (e.g., temsirolimus, sirolimus, everolimus) or a neprilysin inhibitor (e.g., sacubitril) may be at increased risk for angioedema.

01/29/2016 (SUPPL-24)

Approved Drug Label (PDF)

5 Warnings and Precautions

Head and Neck Angioedema

Patients receiving coadministration of an ACE inhibitor with an mTOR (mammalian target of rapamycin) inhibitor (e.g., temsirolimus, sirolimus, everolimus) may be at increased risk for angioedema.

7 Drug Interactions

Mammalian Target of Rapamycin (mTOR) Inhibitors

  • Patients taking concomitant mTOR inhibitor (e.g., temsirolimus, sirolimus, everolimus) therapy may be at increased risk for angioedema (see Warnings – Head and Neck Angioedema).