Clinical review report: Tafamidis (Vyndaqel) (Pfizer Canada ULC) indication: for the treatment of adult patients with cardiomyopathy due to transthyretin-mediated amyloidosis, wild-type or hereditary, to reduce cardiovascular mortality and cardiovascular-related hospitalization

The objective of this report was to perform a systematic review of the beneficial and harmful effects of tafamidis meglumine 80 mg for the treatment of adult patients with cardiomyopathy due to wild-type or hereditary transthyretin-mediated amyloidosis (hATTR)

Bibliographic Details
Corporate Author: Canadian Agency for Drugs and Technologies in Health
Format: eBook
Language:English
Published: Ottawa (ON) Canadian Agency for Drugs and Technologies in Health 2020, April 2020
Series:CADTH common drug review
Online Access:
Collection: National Center for Biotechnology Information - Collection details see MPG.ReNa
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245 0 0 |a Clinical review report: Tafamidis (Vyndaqel) (Pfizer Canada ULC)  |h Elektronische Ressource  |b indication: for the treatment of adult patients with cardiomyopathy due to transthyretin-mediated amyloidosis, wild-type or hereditary, to reduce cardiovascular mortality and cardiovascular-related hospitalization 
246 3 1 |a Clinical review report for Tafamidis (Vyndaqel) 
246 3 1 |a Tafamidis (Vyndaqel) (Pfizer Canada ULC) 
260 |a Ottawa (ON)  |b Canadian Agency for Drugs and Technologies in Health  |c 2020, April 2020 
300 |a 1 PDF file (80 pages) 
505 0 |a Includes bibliographical references 
710 2 |a Canadian Agency for Drugs and Technologies in Health 
041 0 7 |a eng  |2 ISO 639-2 
989 |b NCBI  |a National Center for Biotechnology Information 
490 0 |a CADTH common drug review 
500 |a "Final (with redactions)." 
856 4 0 |u https://www.ncbi.nlm.nih.gov/books/NBK563057  |3 Volltext 
082 0 |a 610 
520 |a The objective of this report was to perform a systematic review of the beneficial and harmful effects of tafamidis meglumine 80 mg for the treatment of adult patients with cardiomyopathy due to wild-type or hereditary transthyretin-mediated amyloidosis (hATTR)