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About ATTR-CMAbout

Learn about ATTR-CM and uncover the differences between hereditary and wild-type ATTR-CM

Types of ATTR-CM

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Click here for Vyndaqel®▼ (tafamidis) Prescribing Information.

Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

Transthyretin amyloidosis cardiomyopathy (ATTR-CM) is a life-threatening, under-recognised and under-diagnosed condition that mostly affects older adults.1,2

Navigate the site to increase your understanding of the causes of the disease, signs and symptoms, diagnostic tools, and a current treatment option, which can help to reduce the delay in the diagnosis and subsequent treatment of this ultimately fatal disease.

You can also visit the Supporting Resources section to watch video content and download resources on ATTR-CM.

Understand ATTR-CM and why it is underdiagnosed

 About ATTR-CM  Loading

Suspect ATTR-CM with clinical clues

 Suspect ATTR-CM Loading

Learn about multimodal imaging tools to diagnose ATTR-CM 

 Detect ATTR-CM Loading

Explore further supporting resources about ATTR-CM

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Learn about the current treatment option for ATTR-CM

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An easy way to connect with a member of the Pfizer team

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ATTR-CM= transthyretin amyloid cardiomyopathy.

References:

Witteles RM, Bokhari S, Damy T, et al. Screening for transthyretin amyloid cardiomyopathy in everyday practice. JACC Heart Fail. 2019;7:709–716;Maurer MS, Hanna M, Grogan M, et al. Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey). J Am Coll Cardiol. 2016;68:161–172.
PP-VYN-GBR-1133. January 2024

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Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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