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AboutAboutAbout ATTR-CMMOD/MOAStudy DesignDosingEfficacy & SafetyAccess & SupportAccess & SupportAccess & Patient SupportEventsMaterialsVideos
Prescribing InformationPatient InformationIndication Patient Site
VYNDAMAX® (tafamidis) for transthyretin amyloid cardiomyopathy (ATTR-CM)​​​​​​​Approved to reduce CV mortality and CV-related hospitalization Efficacy and safety profile Learn more Loading Dosing Learn more Loading Study design Learn more Loading VYNDAMAX resources

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CV=cardiovascular.

VYNDAMAX® AND VYNDAQEL® are registered trademarks of Pfizer Inc.

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INDICATION AND LIMITATIONS OF USEVYNDAQEL and VYNDAMAX are indicated for the treatment of the cardiomyopathy of wild-type or hereditary transthyretin-mediated amyloidosis in adults to reduce cardiovascular mortality and cardiovascular-related hospitalization.Please see Full Prescribing Information including Patient Information.
Important Safety Information

Adverse Reactions

In studies in patients with ATTR-CM, the frequency of adverse events in patients treated with VYNDAQEL® (tafamidis meglumine) was similar to placebo.

Specific Populations​​​​​​​

Pregnancy: Based on findings from animal studies, VYNDAQEL and VYNDAMAX may cause fetal harm when administered to a pregnant woman.

Lactation: There are no available data on the presence of tafamidis in human milk, the effect on the breastfed infant, or the effect on milk production. Tafamidis is present in rat milk. When a drug is present in animal milk, it is likely the drug will be present in human milk. Breastfeeding is not recommended during treatment with VYNDAQEL and VYNDAMAX.

Indication VYNDAQEL and VYNDAMAX are indicated for the treatment of the cardiomyopathy of wild-type or hereditary transthyretin-mediated amyloidosis in adults to reduce cardiovascular mortality and cardiovascular-related hospitalization.

Please see Full Prescribing Information including Patient Information.

Please see full Prescribing Information.

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