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. 2019 Mar 7;30(4):641–652. doi: 10.1681/ASN.2018080832

Table 3.

Gastrointestinal AEs

AE category Tenapanor Placebo, n=82 Tenapanor
3 mg Twice Daily, n=74 10 mg Twice Daily, n=73 30 mg Twice Daily Titration, n=71 3 mg Twice Daily, n=25 10 mg Twice Daily, n=23 30 mg Twice Daily Titration, n=34
RTP
 Gastrointestinal disorders 24 (32.4) 35 (47.9) 40 (56.3)
 Gastrointestinal disorders by preferred terma
  Diarrhea 22 (29.7) 30 (41.1) 34 (47.9)
   Mild 9 (12.2) 11 (15.1) 14 (19.7)
   Moderate 12 (16.2) 16 (21.9) 17 (23.9)
   Severe 1 (1.4) 3 (4.1) 3 (4.2)
  Vomiting 2 (2.7) 3 (4.1) 3 (4.2)
  Flatulence 2 (2.7) 3 (4.1) 2 (2.8)
  Abdominal discomfort 1 (1.4) 4 (5.5) 1 (1.4)
  Abdominal distension 0 (0.0) 1 (1.4) 2 (2.8)
  Abdominal pain 0 (0.0) 3 (4.1) 0 (0.0)
  Abdominal pain upper 2 (2.7) 1 (1.4) 0 (0.0)
  Frequent bowel movements 0 (0.0) 3 (4.1) 0 (0.0)
  Nausea 2 (2.7) 1 (1.4) 0 (0.0)
  Defecation urgency 0 (0.0) 2 (2.7) 0 (0.0)
RWP
 Gastrointestinal disorders 4 (4.9) 0 (0.0) 0 (0.0) 2 (5.9)
 Gastrointestinal disorders by preferred terma
  Diarrhea 2 (2.4) 0 (0.0) 0 (0.0) 1 (2.9)
   Mild 1 (1.2) 0 (0.0) 0 (0.0) 1 (2.9)
   Moderate 1 (1.2) 0 (0.0) 0 (0.0) 0 (0.0)
   Severe 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
  Abdominal pain 0 (0.0) 0 (0.0) 0 (0.0) 1 (2.9)
  Food poisoning 0 (0.0) 0 (0.0) 0 (0.0) 1 (2.9)

Data are number of patients experiencing AE (%). AE, adverse event.

a

Data shown for AEs that were experienced by >2% of patients in any group.