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. 2012 Jun;23(6):1108–1116. doi: 10.1681/ASN.2011111112

Table 2.

Adverse events reported in the included RCTs

Adverse Events Studies Reporting (n) Steroid Group (n/n) Control Group (n/n) RR (95% CI) P Value
Total patients with adverse events 8 60/245 34/243 1.55 (1.09–2.21) 0.02
Specific adverse events
 diabetes mellitus/impaired glucose intolerance 3 4/108 1/110 2.55 (0.51–12.72) 0.26
 hypertension 3 12/93 15/90 0.78 (0.39–1.54) 0.48
 insomnia, palpitations, increased perspiration, headache 4 7/104 1/103 2.72 (0.60–12.44) 0.20
 gastrointestinal bleeding 1 1/17 0/17 3.00 (0.13–68.84) 0.49
 cushingoid features 3 9/82 0/84 7.18 (1.34–38.42) 0.02
 weight increase 1 22/33 13/31 1.56 (0.98–2.57) 0.06
 cough 2 2/81 3/79 0.75 (0.09–6.28) 0.79