Adverse events Self‐reported outcomes
Psychological interventions showed no clear difference in adverse events Self‐reported outcomes compared with usual care (low certainty).
1 finding from 1 review
Adverse events other than hypoglycaemia
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 other than hypoglycaemia
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 other than hypoglycaemia
1 finding from 1 review
Grades 3 and 4 adverse events · hospitalised individuals with COVID‐19 (moderate to severe disease)
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: death ‐ at end of treatment (secondary outcome) · people with depression after stroke
It is very uncertain whether pharmacological intervention and non‐invasive brain stimulation… changes adverse events: death (secondary outcome) compared with a pharmacological intervention and sham stimulation or usual care… (very low certainty).
1 finding from 1 review
Adverse events Length of · and
1 finding from 1 review
Adverse events Falls while switching glasses · Older people living in the community
Assistive technology for vision improvement interventions showed no clear difference in adverse events Falls while switching glasses compared with usual care or attention control (low certainty).
1 finding from 1 review
Serious adverse events, i.e. serious enough to require withdrawal of the treatment · children and adults with SMA type 3
1 finding from 1 review
Adverse events (e.g. skeletomuscular injury) · patients with stable angina pectoris
1 finding from 1 review
Discontinuation of medication due to adverse events · Women of reproductive age seeking to avoid pregnancy
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 (treatment related) To discharge · newborn infants with opioid withdrawal
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 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 related to taking of blood samples · children aged 6 to 12 years
1 finding from 1 review
Serious adverse events Duration 3 days to 3 weeks · acute asthma exacerbation
Antibiotics showed no clear difference in serious adverse events Duration 3 days to 3 weeks compared with placebo or usual care (low certainty).
1 finding from 1 review
Number experiencing adverse effects · the management of chronic obstructive pulmonary disease
It is very uncertain whether multi‐component intervention changes adverse events: number of people experiencing an AE compared with other intervention or routine, usual care or control treatment (very low certainty).
1 finding from 1 review
Rate of discontinuation due to all other adverse events · Women of reproductive age seeking to avoid pregnancy
Intensive counseling showed no clear difference in rate of discontinuation due to all other adverse events compared with usual family planning care (low certainty).
1 finding from 1 review
Serious adverse events at time point closest to 90 days · participants with internal medicine diseases and conditions
It is very uncertain whether short‐stay unit hospitalisation changes serious adverse events at time point closest to 90 days compared with usual care (very low certainty).
1 finding from 1 review
RR 0.95 [0.59, 1.54]
1907 participants
Very low