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Table 3 Summary of treatment-emergent adverse events in all treated Chinese participants

From: Rimegepant orally disintegrating tablet 75 mg for acute treatment of migraine in adults from China: a subgroup analysis of a double-blind, randomized, placebo-controlled, phase 3 clinical trial

TEAE, n (%)

Rimegepant 75 mg

n = 538

Placebo

n = 537

Any TEAE

82 (15.2)

88 (16.4)

Serious TEAE

1 (0.2)a

2 (0.4)

Most common TEAEsb

  

 Protein urine present

8 (1.5)

7 (1.3)

 Nausea

6 (1.1)

14 (2.6)

 Urinary tract infection

5 (0.9)

8 (1.5)

 Blood creatine phosphokinase increased

5 (0.9)

3 (0.6)

 Proteinuria

4 (0.7)

1 (0.2)

 Photophobia

4 (0.7)

3 (0.6)

 Upper respiratory tract infection

3 (0.6)

4 (0.7)

 Blood urine present

3 (0.6)

2 (0.4)

 Blood glucose increased

3 (0.6)

1 (0.2)

 Urine leukocyte esterase positive

3 (0.6)

1 (0.2)

Study drug-related

  

Any TEAE

45 (8.4)

43 (8.0)

Serious TEAE

0

1 (0.2)

  1. MedDRA, ODT Orally disintegrating tablet, TEAE Treatment emergent adverse event
  2. aThis serious TEAE was classified using the MedDRA (version 23.0) preferred term “infection”
  3. bTEAEs occurring in ≥0.5% of participants in the rimegepant ODT 75 mg group