Intervention not reported
Adverse effects Events · Adult participants receiving propofol for induction of anaesthesia
1 finding from 1 review
Adverse events · adults with CF
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 · people with hypertrophic scars
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Other serious adverse events · patients with posterior cruciate retaining total knee arthroplasty for postoperative functional status in patients with osteoarthritis and…
Mobile bearing may leads to higher other serious adverse events compared with fixed bearing prosthesis (low certainty).
1 finding from 1 review
Adverse events · Patients requiring local anaesthesia
1 finding from 1 review
Shivering · patients with rapid emergence from anaesthesia after undergoing brain tumour surgery
Propofol showed no clear difference in adverse event ‐ shivering, number of events compared with sevoflurane (low certainty).
1 finding from 1 review
Nausea and vomiting · patients with rapid emergence from anaesthesia after undergoing brain tumour surgery
Propofol may leads to lower adverse event ‐ nausea and vomiting, number of events compared with sevoflurane (low certainty).
1 finding from 1 review
Adverse event ‐ haemodynamic changes, number of events · patients with rapid emergence from anaesthesia after undergoing brain tumour surgery
Propofol may leads to higher adverse event ‐ haemodynamic changes, number of events compared with sevoflurane (low certainty).
1 finding from 1 review
Adverse events · participants with depressive or anxiety disorders
It is very uncertain whether discontinuation by "tapering" changes adverse events compared with continuation (or usual care) (very low certainty).
1 finding from 1 review
Adverse events · participants with long‐term antidepressants for depressive disorders
1 finding from 1 review
Adverse events · participants with long‐term antidepressants for depressive or anxiety disorders
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 · participants with depressive or anxiety disorders
It is very uncertain whether abrupt discontinuation changes adverse events compared with continuation of long‐term antidepressants (very low certainty).
1 finding from 1 review
Adverse events · women having gynaecological surgery
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 · women during gynaecological surgery
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 · women after gynaecological surgery
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 · women having gynaecological surgery
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 · women with persistent or prolonged retention of placenta
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 · Individuals of any age with no reported disability that might affect toothbrushing (including people wearing orthodontic appliances)
1 finding from 1 review
Adverse events · Individuals of any age with no reported disability that might affect toothbrushing (including people wearing orthodontic appliances)
1 finding from 1 review
Adverse events · Individuals of any age with no reported disability that might affect toothbrushing (including people wearing orthodontic appliances)
1 finding from 1 review