Withdrawals due to adverse events · induction of remission in Crohn's disease
It is very uncertain whether elemental changes withdrawal due to adverse events compared with non‐elemental enteral feeds (very low certainty).
1 finding from 1 review
Withdrawals due to adverse events · induction of remission in Crohn's disease
It is very uncertain whether enteral nutrition changes withdrawal due to adverse events compared with corticosteroids (very low certainty).
1 finding from 1 review
Intervention not reported
Adverse events: hypersensitivity · People with AML in first complete remission
It is very uncertain whether the intervention changes adverse events: hypersensitivity (very low certainty).
1 finding from 1 review
Intervention not reported
Withdrawal due to adverse events · patients with rheumatoid arthritis pain
The intervention showed no clear difference in withdrawal due to adverse events (low certainty).
1 finding from 1 review
Adverse events Respiratory infection (pneumonia) Nasal mucosa or skin trauma · adults in the ICU, requiring respiratory support
HFNC showed no clear difference in adverse events Respiratory infection (pneumonia) Nasal mucosa or… compared with standard oxygen therapy (moderate certainty).
1 finding from 1 review
Adverse events (episodes of peritonitis) ‐ not treated with an aminoglycoside · patients receiving PD
Angiotensin‐converting enzyme inhibitors (ACEi) showed no clear difference in adverse events (episodes of peritonitis) ‐ not treated with an… compared with conventional therapy (moderate certainty).
1 finding from 1 review
Treatment related adverse events, · people with dry eye
1 finding from 1 review
Withdrawals due to adverse events · adults with fibromyalgia
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
Severe adverse events (≥ grade 3) · women withe low‐risk GTN
The intervention showed no clear difference in severe adverse events (≥ grade 3) (low certainty).
1 finding from 1 review
Treatment‐limiting adverse events · Children with TB1
It is very uncertain whether intermittent short‐course anti‐TB regimens changes treatment‐limiting adverse events compared with daily anti‐TB regimens (very low certainty).
1 finding from 1 review
Withdrawals due to adverse events · lateral elbow pain
It is very uncertain whether autologous blood or PRP changes withdrawal due to adverse events  compared with placebo at 3 months' follow‐up (very low certainty).
1 finding from 1 review
Adverse events mild adverse events · children aged over eight and adults with cystic fibrosis and chronic pulmonary infection with P aeruginosa
1 finding from 1 review
Intervention not reported
Severe adverse events: neutropenia · antiretroviral‐naïve individuals
The intervention leads to lower severe adverse events: neutropenia (high certainty).
1 finding from 1 review
Intervention not reported
Adverse events: arthralgia/myalgia · People with AML in first complete remission
It is very uncertain whether the intervention changes adverse events: arthralgia/myalgia (very low certainty).
1 finding from 1 review
Intervention not reported
Discontinuation for adverse events · HIV‐infected adult patients treated with a PI‐containing regimen with undetectable viral load
The intervention showed no clear difference in discontinuation for adverse events (moderate certainty).
1 finding from 1 review
Adverse events (fistulae formation) · adults with an open abdomen after surgery who have not experienced trauma
It is very uncertain whether NPWT changes adverse events (fistulae formation) compared with the Bogota bag (very low certainty).
1 finding from 1 review
Adverse events (fistulae formation) · adults with an open abdomen after surgery who have not experienced trauma
It is very uncertain whether suprasorb CNP system changes adverse events (fistulae formation) compared with the ABThera system (very low certainty).
1 finding from 1 review
Intervention not reported
MST vs ECT ‐ serious adverse events · patients with schizophrenia
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Other adverse events ‐ not reported · patients with Shigella dysentery
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Other adverse events ‐ not reported · patients with Shigella dysentery
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found