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Table 2 Summary of adverse events

From: A double-blind, randomized, multicenter phase 2 study of prasugrel versus placebo in adult patients with sickle cell disease

 

Prasugrel

Placebo

 

(n = 41)

(n = 19)

Any hemorrhagic event, n (%)

  

Required medical attention

0

0

Treatment-emergent

8 (19.5)

1 (5.3)

Possibly related to study drug

6 (14.6)

1 (5.3)

Any non-hemorrhagic event, n (%)

  

Serious

8 (19.5)

4 (21.1)

Study drug discontinuation

2 (4.9)

0

Treatment-emergent

31 (75.6)

17 (89.5)

Possibly related to study drug

2 (4.9)

0

Any event, n (%)

  

Serious

8 (19.5)

4 (21.1)

Study drug discontinuation

2 (4.9)

0

Treatment emergent

34 (82.9)

17 (89.5)

Possibly related to study drug

8 (19.5)

1 (5.3)