Serious adverse events · postmenopausal women at lower risk of fractures1
It is very uncertain whether risedronate 5 mg/day changes serious adverse events compared with placebo (very low certainty).
1 finding from 1 review
RR 0.74 [0.42, 1.3]
Studies not reported
Very low
Serious adverse events · children with acute asthma
1 finding from 1 review
Intervention not reported
Serious adverse events · adults with complex regional pain syndrome type 1 (lower limb)
1 finding from 1 review
no estimate extracted
20 participants
Very low
Proportion of participants with 1 or more serious adverse events according to International Conference on Harmonisation Good Clinical Practice (ICH‐GCP) · adults admitted to the ICU
It is very uncertain whether higher changes proportion of participants with ≥ 1 serious adverse events according… compared with lower FiO2 or targets of arterial oxygenation (very low certainty).
1 finding from 1 review
Serious adverse events (N) · people at increased risk for developing type 2 diabetes
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Adverse events ‐ not reported · subfertile women undergoing IVF or IVF/ICSI
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Adverse events (minor bleeding) · people hospitalised with COVID‐19
Higher‐dose anticoagulants leads to higher adverse events (minor bleeding) compared with lower‐dose anticoagulants (high certainty).
1 finding from 1 review
Major adverse events
It is very uncertain whether PAE changes major adverse events compared with TURP (very low certainty).
1 finding from 1 review
Major adverse events
It is very uncertain whether PUL changes major adverse events compared with sham (very low certainty).
1 finding from 1 review
Major adverse events
It is very uncertain whether PUL changes major adverse events compared with TURP (very low certainty).
2 findings from 1 review
Major adverse events · men with benign prostatic hyperplasia
It is very uncertain whether aquablation changes major adverse events compared with transurethral resection of the prostate (very low certainty).
1 finding from 1 review
Withdrawals due to adverse events · postmenopausal women at lower risk of fractures1
Intermittent/cyclic etidronate 400 mg/day showed no clear difference in withdrawals due to adverse events compared with placebo (low certainty).
1 finding from 1 review
RR 1.41 [0.81, 2.47]
Studies not reported
Low
Withdrawals due to adverse events · postmenopausal women at lower risk of fractures1
Risedronate 5 mg/day showed no clear difference in withdrawals due to adverse events compared with placebo (low certainty).
1 finding from 1 review
RR 0.67 [0.38, 1.18]
Studies not reported
Low
Sexual adverse events
Naftopidil probably leads to lower sexual adverse events compared with silodosin (alpha‐blocker) (moderate certainty).
1 finding from 1 review
Sexual adverse events
Naftopidil showed no clear difference in sexual adverse events compared with tamsulosin (alpha‐blocker) (low certainty).
1 finding from 1 review
Sexual adverse events
Silodosin probably leads to higher sexual adverse events compared with tamsulosin (moderate certainty).
1 finding from 1 review
Sexual adverse events
Silodosin probably leads to higher sexual adverse events compared with naftopidil (moderate certainty).
1 finding from 1 review
Sexual adverse events
Silodosin probably leads to higher sexual adverse events compared with alfuzosin (moderate certainty).
1 finding from 1 review
Sexual adverse events
Silodosin probably leads to higher sexual adverse events compared with placebo (moderate certainty).
1 finding from 1 review
Sexual adverse events
1 finding from 1 review