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Information relating to specific disease areas aligned to Pfizer’s portfolio and other resources designed for Pfizer medicines.

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

Learn about the red flags that may raise suspicion of and techniques used to diagnose ATTR-CM

Explore a range of educational resources to support the diagnosis of ATTR-CM

Click here for Vyndaqel®▼ (tafamidis) Prescribing Information. Adverse event reporting information can be found at the bottom of the page.

Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

Transthyretin amyloid cardiomyopathy (ATTR-CM) is a life-threatening, under-recognised, and underdiagnosed condition that mostly affects older adults1,2 and there could be one patient in every heart failure clinic3.
Navigate the site to increase your understanding of the causes of the disease, signs and symptoms, diagnostic tools, and current and emerging treatment strategies, which can help to reduce the delay in the diagnosis and subsequent treatment of this ultimately fatal disease.
You can also visit the Educational Resources section to sign up to a virtual event or watch an expert speaker video.

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What is ATTR-CM?

Understand ATTR-CM and why it is underdiagnosed

Understand ATTR-CM

The different types of ATTR-CM

Uncover the differences between hereditary and wild-type ATTR-CM

Uncover ATTR-CM

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Diagnosis of ATTR-CM

Learn about techniques used to diagnose ATTR-CM, such as endomyocardial biopsy and nuclear scintigraphy

Diagnose ATTR-CM

Current standard of care and emerging treatment strategies

Learn about current and emerging therapies for ATTR-CM

Discover emerging therapies

ATTR-CM Educational Resources

Explore educational resources surrounding ATTR-CM​​​​​​​

Explore educational resources

Contact a Pfizer representative

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

Contact us​​​​​​​


References:

1. Witteles RM, Bokhari S, Damy T et al.  Screening for Transthyretin Amyloid Cardiomyopathy in Everyday Practice. JACC Heart Fail. 2019; 7(8): 709–716
2. Lane T, Fontana M, Martinez-Naharro A et al. Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis. Circulation. 2019; 140: 16–26
​​​​​​​3. Pfizer Data on File PP-VYN-GBR-0145 2020

PP-VYN-GBR-0945. January 2022

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