Adverse events ‐ number of deaths (during intervention) Â · people with dementia and their carers
1 finding from 1 review
acceptability and safety of treadmill training ‐ Active control group (co‐interventions were similar in both groups) Number of adverse events and drop‐outs · people with Parkinson's disease
1 finding from 1 review
Dropouts, adverse events and deaths during intervention phase Numbers of dropouts, adverse events and deaths from all causes · people with stroke
tDCS showed no clear difference in secondary outcome measure: dropouts, adverse events and deaths… compared with any type of active control intervention (moderate certainty).
1 finding from 1 review
acceptability and safety of treadmill training ‐ No intervention control group (co‐interventions were not similar in both groups) Number of adverse events and drop‐outs · people with Parkinson's disease
1 finding from 1 review
Dropouts, adverse events and deaths during intervention phase Numbers of dropouts, adverse events and deaths from all causes · people with stroke
tDCS showed no clear difference in secondary outcome measure: dropouts, adverse events and deaths… compared with any type of placebo or passive control intervention (moderate certainty).
1 finding from 1 review
Adverse events Post‐intervention · adults with neuropathic pain
It is very uncertain whether herbal treatment changes adverse events Post‐intervention compared with placebo (very low certainty).
1 finding from 1 review
Intervention not reported
Adverse events Post‐intervention · adults with stroke
1 finding from 1 review
Adverse events ‐ death from suicide during intervention (RR > 1 denotes greater risk)Â · people with severe mental disorders
It is very uncertain whether lay health worker‐ changes adverse events ‐ death from suicide during intervention (RR > 1… compared with specialist‐led care (very low certainty).
1 finding from 1 review
Minor adverse events Defined as any adverse event within 8 weeks of surgery that does not require further intervention · people with intermittent exotropia, aged less than 11 years
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Minor adverse events Defined as any adverse event within 8 weeks of surgery that does not require further intervention · people with intermittent exotropia, aged 5 to 49 years
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Minor adverse events Defined as any adverse event within 8 weeks of surgery that does not require further intervention · people with intermittent exotropia, aged over 6 years
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Minor adverse events Defined as any adverse event within 8 weeks of surgery that does not require further intervention · people with intermittent exotropia, aged 3 to < 11 years
Bilateral lateral rectus recession showed no clear difference in minor adverse events Defined as any adverse event within 8 weeks of… compared with unilateral lateral rectus recession with medial rectus resection (low certainty).
1 finding from 1 review
Adverse events 12 months postintervention · adults with refractory glaucoma
1 finding from 1 review
Intervention not reported
Adverse events 12 months postintervention · adults with refractory glaucoma
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Adverse events 12 months postintervention · adults with refractory glaucoma
1 finding from 1 review
Adverse events 12 months postintervention · adults with refractory glaucoma
1 finding from 1 review
Adverse events post‐intervention ‐ not reported · patients with fibromyalgia
The review found no eligible studies for this question.
1 finding from 1 review
Adverse events post‐intervention ‐ not reported · patients with fibromyalgia
The review found no eligible studies for this question.
1 finding from 1 review
Adverse events post‐intervention ‐ not reported · patients with fibromyalgia
The review found no eligible studies for this question.
1 finding from 1 review
Adverse events Adverse events due to study interventions · adults with chronic low‐back pain
1 finding from 1 review