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
Pelvic pain · 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
Live birth rate · 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
Incidence of adhesions at second‐look laparoscopy · women having gynaecological surgery
Gel agents leads to lower incidence of adhesions at second‐look laparoscopy compared with no gel agents (or placebo) (high certainty).
1 finding from 1 review
50% responder rate · people with focal epilepsy
Zonisamide probably leads to higher 50% responder rate (whole treatment period; any dose) compared with placebo (moderate certainty).
1 finding from 1 review
Withdrawal rates ‐ Any dose · people with focal epilepsy
Zonisamide probably leads to higher withdrawal rates (whole treatment period; any dose) compared with placebo (moderate certainty).
1 finding from 1 review
Ataxia · people with focal epilepsy
Zonisamide may leads to higher adverse effects: ataxia (whole treatment period; any dose) compared with placebo (low certainty).
1 finding from 1 review
Frequency of adverse effects ‐ dizziness ( · people with focal epilepsy
Zonisamide probably leads to higher adverse effects: dizziness (whole treatment period; any dose) compared with placebo (moderate certainty).
1 finding from 1 review
Adverse effect: fatigue · people with focal epilepsy
Zonisamide probably leads to higher adverse effects: fatigue (whole treatment period; any dose) compared with placebo (moderate certainty).
1 finding from 1 review
Nausea · people with focal epilepsy
Zonisamide probably leads to higher adverse effects: nausea (whole treatment period; any dose) compared with placebo (moderate certainty).
1 finding from 1 review
Somnolence · people with focal epilepsy
Zonisamide probably leads to higher adverse effects: somnolence (whole treatment period; any dose) compared with placebo (moderate certainty).
1 finding from 1 review
50% or greater reduction in focal seizure frequency (responders) intention to treat– all doses · people with drug‐resistant focal epilepsy
Levetiracetam probably leads to higher 50% or greater reduction in focal seizure frequency (responders)… compared with placebo (moderate certainty).
1 finding from 1 review
Withdrawal rates ‐ Any dose · people with drug‐resistant focal epilepsy
Levetiracetam showed no clear difference in treatment withdrawal– all doses compared with placebo (high certainty).
1 finding from 1 review
Somnolence · people with drug‐resistant focal epilepsy
Levetiracetam probably leads to higher adverse effects: 5 most common adverse effects (any age) – somnolence compared with placebo (moderate certainty).
1 finding from 1 review
Adverse effects: headache · people with drug‐resistant focal epilepsy
Levetiracetam showed no clear difference in adverse effects: 5 most common adverse effects (any age) – headache compared with placebo (low certainty).
1 finding from 1 review
Adverse effects: 5 most common adverse effects (any age) – dizziness · people with drug‐resistant focal epilepsy
Levetiracetam showed no clear difference in adverse effects: 5 most common adverse effects (any age) – dizziness compared with placebo (moderate certainty).
1 finding from 1 review
Response to treatment at 8 weeks · participants of any age with a primary diagnosis of major depressive disorder
Brexpiprazole leads to higher response to treatment at 8 weeks compared with antidepressive agents (high certainty).
1 finding from 1 review
Acceptability ‐ total dropouts · participants of any age with a primary diagnosis of major depressive disorder
Brexpiprazole leads to higher number of dropouts due to any cause at 8 weeks compared with antidepressive agents (high certainty).
1 finding from 1 review
Adverse effects (dropouts) · participants of any age with a primary diagnosis of major depressive disorder
Brexpiprazole leads to higher number of dropouts due to adverse effects at 8 weeks compared with antidepressive agents (high certainty).
1 finding from 1 review
Remission · participants of any age with a primary diagnosis of major depressive disorder
Brexpiprazole leads to higher remission rates at 8 weeks compared with antidepressive agents (high certainty).
1 finding from 1 review