Pain intensity ‐ as reported by child, at 2 to 24 hours № of participants: 300 (3 RCTs) · children with acute postoperative pain
1 finding from 1 review
Nausea and vomiting · children with acute postoperative pain
It is very uncertain whether diclofenac changes nausea, vomiting, or both during study period № of participants: 348… compared with paracetamol (very low certainty).
1 finding from 1 review
Any bleeding during study period № of participants: 100(2 RCTs)d · children with acute postoperative pain
It is very uncertain whether diclofenac changes any bleeding during study period № of participants: 332 (5 RCTs) compared with paracetamol (very low certainty).
1 finding from 1 review
Serious adverse events during the study period · children with acute postoperative pain
It is very uncertain whether diclofenac changes serious adverse events during study period № of participants: 60 (1… compared with paracetamol (very low certainty).
1 finding from 1 review
At least 30% reduction in pain · people with cancer pain
1 finding from 1 review
At least 50% reduction in pain · people with cancer pain
1 finding from 1 review
Pain no worse than mild at one or two weeks (or equivalent) · people with cancer pain
1 finding from 1 review
Patient Global Impression of Change much or very much improved · people with cancer pain
1 finding from 1 review
Serious adverse events (death) · people with cancer pain
1 finding from 1 review
Other adverse events · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Treatment withdrawal · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
Participants with at least 30% or at least 50% reduction in pain · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
PGIC much or very much improved · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
Mean pain intensity at end of study · people with cancer pain
1 finding from 1 review
Intervention not reported
Pain no worse than mild at one or two weeks (or equivalent) · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
Mean quality of life or "well‐being" · people with cancer pain
1 finding from 1 review
Intervention not reported
Participant preference · people with cancer pain
1 finding from 1 review
Intervention not reported
Adverse events · people with cancer pain
1 finding from 1 review
Intervention not reported
Serious adverse events · people with cancer pain
1 finding from 1 review
Intervention not reported
Para/propacetamol vs placebo see footnote1 · patients with postoperative pain
The intervention leads to higher para/propacetamol vs placebo see footnote1 (high certainty).
1 finding from 1 review