Question · asked by 1 review

Oral diclofenac sodium (NSAID) vs placebo: Adverse events (reported; mild, no withdrawals)

Population
Adult patients aged >=18 years, clinically or radiographically diagnosed with TMD (McNeill 1997 criteria); moderate to severe pain of minimum 3 months' duration
Intervention
Oral diclofenac sodium (NSAID)
Comparison
placebo
Outcome
Adverse events (reported; mild, no withdrawals)

What each review found

Current versions only
FindingEffectStudiesGRADE certainty
Oral diclofenac sodium (NSAID) vs Placebo
Adverse events (reported; mild, no withdrawals) · Adult patients aged >=18 years, clinically or radiographically diagnosed with TMD (McNeill 1997 criteria); moderate to… · 2 weeks
Pharmacological interventions for pain in patients with temporomandibular disorders (2010) · Cochrane All outcomes
Ekberg et al 1996 (diclofenac) reported adverse effects. Per the review's Adverse effects of interventions section: 'All but one study (Lobo et al 2004) reported adverse effects. Most of the reported adverse effects…1 study · 32 participantsGRADE not reported

Findings are shown side by side, never pooled across reviews.

The reviews

ReviewSearched up toIncluded studiesAMSTAR 2
Pharmacological interventions for pain in patients with temporomandibular disorders
2010 · Cochrane All outcomes
2010-08Not listedNot assessed
How reviews are matched to this question

Reviews word the same question differently. Four decision models (TypeSafe's Jev, Liquid AI's d1-ultra, SubQ Snap and Baseten's Elephant) judged each wording of the population, intervention, comparator and outcome against the others; two wordings count as the same when at least three of them agree and none clearly disagrees, and findings count as this question only when all four elements match. Timing, setting and subgroup never split a question: they are shown on each finding.