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Table 2 Summary of safety data

From: A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis

AE

Total population (n = 27) n (%)

Summary of AEs

 Any AE

26 (96)

 Any AE related to study drug

16 (59)

 Any serious AE

7 (26)

 Any study drug-related serious AE

0

 Death

2 (7)

 Any AE leading to discontinuation

2 (7)

Common AEs (occurring in > 15% of patients)

 Flushing

7 (26)

 Diarrhea

6 (22)

 Infusion-related reaction

6 (22)

 Nasopharyngitis

6 (22)

 Urinary tract infection

6 (22)

 Vomiting

6 (22)

 Wound

6 (22)

 Nausea

5 (19)

AEs related to study drug in > 2 patients

 Infusion-related reaction

6 (22)

 Flushing

6 (22)

 Diarrhea

3 (11)

  1. Abbreviation: AE adverse event