Adverse events grade 3 to 5 Range of
Early taxane‐based chemotherapy and androgen deprivation therapy (ADT) may leads to higher grade III to V adverse events compared with ADT only (low certainty).
1 finding from 1 review
Adverse events (control ‐ placebo) · young people
3 findings from 1 review
no estimate extracted
1 study · 207 participants
Very low
no estimate extracted
1 study · 211 participants
Very low
no estimate extracted
2 studies · 385 participants
Very low
Adverse events (not reported) · people with ALS
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: complete case · preventing C. difficile associated diarrhea
It is very uncertain whether probiotics changes adverse Events: complete case compared with control (very low certainty).
1 finding from 1 review
Adverse events: CMV infection · kidney transplant recipients
Low dose calcineurin inhibitors (CNI) showed no clear difference in adverse events: CMV infection compared with to standard dose CNI (moderate certainty).
1 finding from 1 review
Adverse events: CMV infection · kidney transplant recipients
Calcineurin inhibitor (CNI) withdrawal + mammalian target of… probably leads to lower adverse events: CMV Infection compared with standard dose CNI (moderate certainty).
1 finding from 1 review
Adverse events: CMV infection · kidney transplant recipients
Low dose CNI calcineurin inhibitor (CNI) + mammalian target of… showed no clear difference in adverse events: CMV infection compared with standard dose CNI (low certainty).
1 finding from 1 review
Adverse events: CMV infection · kidney transplant recipients
Calcineurin inhibitor (CNI) withdrawal showed no clear difference in adverse events: CMV infection compared with standard dose CNI (low certainty).
1 finding from 1 review
Frequency of adverse events ( · children with haematological malignancy at risk of tumour lysis syndrome
Summary of findings: high‐dose urate oxidase showed no clear difference in frequency of adverse events ( compared with low‐dose urate oxidase (low certainty).
1 finding from 1 review
Frequency of adverse events ( · children with haematological malignancy at risk of tumour lysis syndrome
Summary of findings: urate oxidase may leads to higher frequency of adverse events ( compared with allopurinol (low certainty).
1 finding from 1 review
Intervention not reported
Adverse events (grade 3 or 4) · HIV‐positive adults
The intervention probably leads to higher adverse events (grade 3 or 4) (moderate certainty).
1 finding from 1 review
Adverse events ‐ not measured · patients with patellofemoral pain syndrome (symptoms > 4 weeks (1 study); symptoms > 6 weeks (1 study); symptoms > 8 weeks (1 study); not…
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Cardiovascular adverse events
Silodosin showed no clear difference in cardiovascular adverse events compared with naftopidil (low certainty).
1 finding from 1 review
Cardiovascular adverse events
Silodosin showed no clear difference in cardiovascular adverse events compared with alfuzosin (low certainty).
1 finding from 1 review
Cardiovascular adverse events
It is very uncertain whether silodosin changes cardiovascular adverse events compared with placebo (very low certainty).
1 finding from 1 review
Cardiovascular adverse events
Silodosin showed no clear difference in cardiovascular adverse events compared with tamsulosin (low certainty).
1 finding from 1 review
Adverse events: hypertension · patients with Guillain‐Barré syndrome
Corticosteroid leads to lower adverse events ‐ hypertension compared with control (high certainty).
1 finding from 1 review
Intervention not reported
Periprocedural adverse events · people with chronic ischaemic heart disease and congestive heart failure
1 finding from 1 review
Adverse events ‐ not reported · people with venous leg ulcers
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 · people with venous leg ulcers
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found