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Table 3 Summary of adverse events

From: Risedronate therapy in patients with mild-to-moderate chronic kidney disease with osteoporosis: post-hoc analysis of data from the risedronate phase III clinical trials

 

eGFR (mL/min/1.73 m2)

90

60 to <90

30 to <60

P value

Number of subjects

99

525

228

 

All adverse events

82 (82.8%)

462 (88.0%)

198 (86.8%)

0.3609*

gastrointestinal symptoms–relate adverse events

33 (33.3%)

192 (36.6%)

88 (38.6%)

0.6631*

 Abdominal pain upper

4 (4.0%)

31 (5.9%)

7 (3.1%)

NT

 Constipation

4 (4.0%)

37 (7.0%)

19 (8.3%)

NT

 Diarrhoea

4 (4.0%)

17 (3.2%)

12 (5.3%)

NT

 Stomach discomfort

11 (11.1%)

44 (8.4%)

14 (6.1%)

NT

Urinary- and kidney function-related adverse events

2 (2.0%)

11 (2.1%)

7 (3.1%)

0.6295*

Osteonecrosis of the jaw

0 (0.0%)

0 (0.0%)

0 (0.0%)

NT

Atypical femoral fractures

0 (0.0%)

0 (0.0%)

0 (0.0%)

NT

  1. NT not test
  2. * Fisher’s exact test