Intervention not reported
Adverse events · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
Withdrawals · people with cancer pain
1 finding from 1 review
no estimate extracted
Studies not reported
Very low
Intervention not reported
Death · people with cancer pain
1 finding from 1 review
Participant‐reported pain relief of 50% or greater · adults with moderate or severe acute postoperative pain
1 finding from 1 review
Median (mean) time to use of rescue medication · adults with moderate or severe acute postoperative pain
1 finding from 1 review
Number of women requiring rescue medication · adults with moderate or severe acute postoperative pain
1 finding from 1 review
Participants with ≥ 1 adverse event following a single dose, and after 3 to 5 days · adults with moderate or severe acute postoperative pain
1 finding from 1 review
Participants with a serious adverse event following a single dose, and after 3 to 5 days · adults with moderate or severe acute postoperative pain
1 finding from 1 review
Intervention not reported
At least 50% of maximum pain relief over 4 to 6 hours · Adults with acute pain
The intervention leads to higher at least 50% of maximum pain relief over 4 to 6 hours (high certainty).
1 finding from 1 review
Intervention not reported
Participants remedicating within 8 hours · Adults with acute pain
The intervention leads to lower participants remedicating within 8 hours (high certainty).
1 finding from 1 review
Intervention not reported
Participants with at least 1 adverse event (all diclofenac potassium doses, 25 mg to 100 mg) · Adults with acute pain
The intervention showed no clear difference in participants with at least 1 adverse event (all diclofenac potassium… (moderate certainty).
1 finding from 1 review
Intervention not reported
Participants with a serious adverse event (whole data set) · Adults with acute pain
1 finding from 1 review
Intervention not reported
At least 50% of maximum pain relief over 4 to 6 h · adults with moderate or severe acute postoperative pain
The intervention leads to higher at least 50% of maximum pain relief over 4 to 6 h (high certainty).
1 finding from 1 review
RR 4.1 [2.8, 5.9]
Studies not reported
High
Intervention not reported
Participants with at least 1 adverse event · adults with moderate or severe acute postoperative pain
The intervention showed no clear difference in participants with at least 1 adverse event (moderate certainty).
1 finding from 1 review
RR 1.2 [0.84, 1.7]
Studies not reported
Moderate
Intervention not reported
Participants with a serious adverse event · adults with moderate or severe acute postoperative pain
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Deaths · adults with moderate or severe acute postoperative pain
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
At least 50% of maximum pain relief over 4 to 6 h · Adults with acute pain
The intervention probably leads to higher at least 50% of maximum pain relief over 4 to 6 h (moderate certainty).
1 finding from 1 review
Intervention not reported
Participants remedicating within 8 hours · Adults with acute pain
The intervention probably leads to lower participants remedicating within 8 hours (moderate certainty).
1 finding from 1 review
Intervention not reported
Participants with at least 1 adverse event · Adults with acute pain
The intervention showed no clear difference in participants with at least 1 adverse event (low certainty).
1 finding from 1 review
Intervention not reported
Participants with a serious adverse event · Adults with acute pain
1 finding from 1 review