Diclofenac side effects: what 85,620 FDA adverse event reports show
Drug class
Nonsteroidal anti-inflammatory drug
Brand names
Diclofenac Sodium
Who reports
85,620 reports · 80% serious · 11,042 with death outcome · 68% female
Used for
Diclofenac sodium topical solution is indicated for the treatment of the pain of osteoarthritis of the knee(s). Diclofenac sodium topical solution is a nonsteroidal anti-inflammatory drug indicated for the treatment of the pain of osteoarthritis of the knee(s). ( 1 )
What it is
Diclofenac is a monocarboxylic acid consisting of phenylacetic acid having a (2,6-dichlorophenyl)amino group at the 2-position. It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic, an antipyretic, an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor, a xenobiotic, an...
Boxed warning
RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS Cardiovascular Thrombotic Events Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction, and stroke, which can be fatal.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
Strongest disproportionality signals
Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,163 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Lupus vulgaris | 947 | 999.4 865.0–1,154.7ROR 1,010.6 · calibrated p 3e-17 ✓ | 194.0 EB05 183.8 · IC025 +7.4 3/3 methods agree | Not in label — unassessed | serious n=947 · ♀ 100% (drug 68%) · 96% clinician | not reported in cached trials |
| Anti-cyclic citrullinated peptide antibody positive | 5,519 | 887.7 838.8–939.5ROR 948.8 · calibrated p 5e-17 ✓ | 190.0 EB05 185.8 · IC025 +7.5 3/3 methods agree | Lab value / disease marker | serious PRR 136.9 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Anti-cyclic citrullinated peptide antibody | 513 | 845.5 703.6–1,016.0ROR 850.6 · calibrated p 3e-16 ✓ | 186.8 EB05 173.6 · IC025 +7.2 3/3 methods agree | Lab value / disease marker | serious n=513 · ♀ 100% (drug 68%) · 96% clinician | not reported in cached trials |
| Swollen joint count increased | 2,379 | 817.8 751.9–889.5ROR 841.1 · calibrated p 2e-16 ✓ | 186.4 EB05 180.2 · IC025 +7.4 3/3 methods agree | Lab value / disease marker | serious n=2,377 · ♀ 100% (drug 68%) · 95% clinician | not reported in cached trials |
| Rheumatic fever | 3,282 | 766.7 715.1–822.1ROR 797.3 · calibrated p 4e-16 ✓ | 183.7 EB05 178.5 · IC025 +7.4 3/3 methods agree | Not in label — unassessed | serious n=3,281 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Deep vein thrombosis postoperative | 1,428 | 676.4 611.4–748.3ROR 687.9 · calibrated p 2e-15 ✓ | 177.8 EB05 170.2 · IC025 +7.3 3/3 methods agree | Not in label — unassessed | serious n=1,428 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Duodenal ulcer perforation | 5,174 | 600.9 571.3–632.0ROR 639.4 · calibrated p 4e-15 ✓ | 172.4 EB05 168.5 · IC025 +7.4 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 123.7 · ♀ 99% (drug 68%) · 93% clinician | not reported in cached trials |
| Hepatic enzyme | 96 | 550.0 382.8–790.3ROR 550.6 · calibrated p 1e-13 ✓ | 162.7 EB05 137.2 · IC025 +6.2 3/3 methods agree | Labeled (related wording) related wording | serious n=96 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| C-reactive protein | 592 | 468.6 408.1–538.0ROR 471.8 · calibrated p 1e-13 ✓ | 158.8 EB05 148.4 · IC025 +7.0 3/3 methods agree | Lab value / disease marker | serious n=592 · ♀ 100% (drug 68%) · 95% clinician | not reported in cached trials |
| Grip strength | 148 | 439.7 335.4–576.4ROR 440.4 · calibrated p 5e-13 ✓ | 153.1 EB05 133.5 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=148 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| Pemphigus | 7,898 | 434.7 419.2–450.8ROR 478.8 · calibrated p 9e-14 ✓ | 155.5 EB05 152.6 · IC025 +7.2 3/3 methods agree | Not in label — unassessed | serious PRR 112.0 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Facet joint syndrome | 1,966 | 412.8 383.9–443.9ROR 422.5 · calibrated p 3e-13 ✓ | 152.4 EB05 146.9 · IC025 +7.1 3/3 methods agree | Not in label — unassessed | serious n=1,965 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Rheumatoid factor positive | 3,470 | 375.3 356.0–395.6ROR 391.1 · calibrated p 7e-13 ✓ | 147.1 EB05 143.0 · IC025 +7.1 3/3 methods agree | Lab value / disease marker | serious n=3,468 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Adjustment disorder with depressed mood | 1,104 | 299.8 274.5–327.5ROR 303.7 · calibrated p 9e-12 ✓ | 133.7 EB05 127.3 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious n=1,104 · ♀ 100% (drug 68%) · 96% clinician | not reported in cached trials |
| Swollen joint count | 134 | 295.8 229.8–380.9ROR 296.3 · calibrated p 2e-11 ✓ | 130.8 EB05 113.2 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=134 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| Hand deformity | 7,093 | 293.3 283.5–303.4ROR 319.7 · calibrated p 5e-12 ✓ | 132.7 EB05 130.1 · IC025 +7.0 3/3 methods agree | Not in label — unassessed | serious PRR 103.6 · ♀ 100% (drug 68%) · 92% clinician | not reported in cached trials |
| Fractional exhaled nitric oxide increased | 90 | 267.4 198.0–360.9ROR 267.6 · calibrated p 7e-11 ✓ | 123.9 EB05 103.9 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=90 · ♀ 0% (drug 68%) | not reported in cached trials |
| Dislocation of vertebra | 1,131 | 255.5 235.1–277.8ROR 258.9 · calibrated p 4e-11 ✓ | 124.2 EB05 118.2 · IC025 +6.8 3/3 methods agree | Not in label — unassessed | serious n=1,131 · ♀ 100% (drug 68%) · 95% clinician | not reported in cached trials |
| Helicobacter infection | 5,092 | 246.5 237.2–256.2ROR 262.1 · calibrated p 3e-11 ✓ | 122.2 EB05 119.4 · IC025 +6.9 3/3 methods agree | Not in label — unassessed | serious PRR 92.7 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Hypocholesterolaemia | 150 | 234.4 187.2–293.4ROR 234.8 · calibrated p 2e-10 ✓ | 117.5 EB05 102.5 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=150 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| Retinitis | 811 | 233.2 211.7–256.7ROR 235.4 · calibrated p 1e-10 ✓ | 118.6 EB05 111.9 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious n=811 · ♀ 100% (drug 68%) · 96% clinician | not reported in cached trials |
| Subcutaneous drug absorption impaired | 255 | 216.8 183.1–256.8ROR 217.5 · calibrated p 2e-10 ✓ | 113.6 EB05 102.3 · IC025 +6.3 3/3 methods agree | Labeled (related wording) related wording | serious n=255 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| X-ray abnormal | 834 | 216.3 197.0–237.4ROR 218.4 · calibrated p 2e-10 ✓ | 114.1 EB05 107.7 · IC025 +6.6 3/3 methods agree | Lab value / disease marker | serious n=834 · ♀ 100% (drug 68%) · 97% clinician | not reported in cached trials |
| Muscle injury | 3,779 | 210.4 201.5–219.7ROR 220.1 · calibrated p 2e-10 ✓ | 112.7 EB05 109.7 · IC025 +6.7 3/3 methods agree | Not in label — unassessed | serious PRR 87.7 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Embolia cutis medicamentosa | 345 | 186.1 161.8–214.2ROR 186.9 · calibrated p 8e-10 ✓ | 104.8 EB05 95.8 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=345 · 93% clinician | not reported in cached trials |
| Folliculitis | 4,285 | 174.5 167.8–181.4ROR 183.6 · calibrated p 8e-10 ✓ | 101.5 EB05 99.0 · IC025 +6.6 3/3 methods agree | Not in label — unassessed | serious PRR 85.7 · ♀ 100% (drug 68%) · 95% clinician | not reported in cached trials |
| Sleep disorder due to general medical condition, insomnia type | 2,594 | 166.0 157.9–174.4ROR 171.1 · calibrated p 2e-9 ✓ | 98.6 EB05 95.4 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=2,591 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Peripheral venous disease | 1,532 | 153.0 143.5–163.0ROR 155.7 · calibrated p 3e-9 ✓ | 93.8 EB05 89.9 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=1,529 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Pericarditis | 6,268 | 148.2 143.7–152.8ROR 159.8 · calibrated p 3e-9 ✓ | 92.1 EB05 90.2 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious PRR 66.7 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Seronegative arthritis | 407 | 139.7 123.7–157.8ROR 140.4 · calibrated p 9e-9 ✓ | 88.4 EB05 81.4 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=407 · ♀ 91% (drug 68%) · 95% clinician | not reported in cached trials |
| Synovitis | 6,513 | 138.7 134.6–142.9ROR 150.0 · calibrated p 5e-9 ✓ | 88.3 EB05 86.5 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious PRR 66.4 · ♀ 98% (drug 68%) · 92% clinician | not reported in cached trials |
| Inspiratory capacity decreased | 95 | 129.2 100.7–165.7ROR 129.3 · calibrated p 2e-8 ✓ | 83.0 EB05 69.9 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=95 · ♀ 0% (drug 68%) · 100% clinician | not reported in cached trials |
| Glossodynia (burning tongue/mouth pain) | 7,700 | 129.0 125.6–132.5ROR 141.6 · calibrated p 7e-9 ✓ | 84.3 EB05 82.7 · IC025 +6.4 3/3 methods agree | Labeled (related wording) related wording | serious PRR 87.5 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Intestinal diaphragm disease | 88 | 114.5 88.8–147.5ROR 114.6 · calibrated p 6e-8 ✓ | 76.6 EB05 64.1 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=88 · 100% clinician | not reported in cached trials |
| C-reactive protein abnormal | 1,865 | 100.6 95.4–106.2ROR 102.9 · calibrated p 9e-8 ✓ | 71.2 EB05 68.5 · IC025 +6.1 3/3 methods agree | Lab value / disease marker | serious n=1,864 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Ductus arteriosus stenosis foetal | 108 | 83.3 66.9–103.7ROR 83.4 · calibrated p 6e-7 ✓ | 61.5 EB05 52.4 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious n=108 · 100% clinician | not reported in cached trials |
| Porphyria acute | 347 | 82.2 72.8–92.8ROR 82.5 · calibrated p 5e-7 ✓ | 61.3 EB05 56.1 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=347 · ♀ 100% (drug 68%) · 94% clinician | not reported in cached trials |
| Breast cancer stage iii | 1,604 | 81.3 76.9–86.0ROR 82.8 · calibrated p 5e-7 ✓ | 61.0 EB05 58.5 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | serious n=1,604 · ♀ 100% (drug 68%) · 95% clinician | not reported in cached trials |
| Wound | 6,860 | 80.2 78.1–82.4ROR 87.1 · calibrated p 3e-7 ✓ | 60.4 EB05 59.2 · IC025 +5.9 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 61.3 · serious PRR 51.5 · ♀ 99% (drug 68%) · 92% clinician | NCT00141102: 1/2,237 (0.0%) on Diclofenac (serious AE) |
| Bone erosion | 824 | 74.2 68.6–80.2ROR 74.9 · calibrated p 9e-7 ✓ | 56.9 EB05 53.7 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=823 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
Clinical concept groups
MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Liver injury | 10,014 | 8.48.2–8.5 | signal |
| Interstitial lung disease | 2,020 | 5.25.0–5.5 | signal |
| Anaphylaxis / angioedema | 2,000 | 4.03.8–4.1 | signal |
| Gi bleeding | 2,570 | 3.53.3–3.6 | signal |
| Hyperglycaemia / diabetes | 4,823 | 3.43.4–3.5 | signal |
| Severe cutaneous reaction | 945 | 3.12.9–3.3 | signal |
| Serious infection | 9,626 | 3.13.0–3.1 | signal |
| Depression | 3,230 | 2.82.7–2.9 | signal |
| Tendon disorder | 420 | 2.72.5–3.0 | signal |
| Kidney injury | 4,600 | 2.52.4–2.6 | signal |
| Rhabdomyolysis / myopathy | 791 | 2.42.2–2.6 | signal |
| Fall / fracture | 3,040 | 2.01.9–2.0 | raised |
| Pancreatitis | 619 | 1.91.7–2.0 | raised |
| Hyponatraemia | 574 | 1.81.6–1.9 | raised |
| Anaemia | 2,106 | 1.71.7–1.8 | raised |
| Thrombocytopenia | 1,255 | 1.41.3–1.5 | raised |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Diclofenac as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (1 of 40 signal terms matched).
- NCT00141102 — Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With (N=4484, PHASE4; 146 AE terms posted; arms: Celecoxib; Oral Diclofenac Plus Omeprazole)
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
Most frequently reported reactions
By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 14,178 | 2.7 2.6–2.7ROR 3.0 · calibrated p 0.632 | 2.6 EB05 2.6 · IC025 +1.4 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 2.7 · serious PRR 4.4 | not reported in cached trials |
| Pain | 12,732 | 5.2 5.1–5.2ROR 5.9 · calibrated p 0.158 | 5.1 EB05 5.0 · IC025 +2.3 3/3 methods agree | Likely indication confounding term in indications; also in warnings | age-adj. PRR 4.6 · serious PRR 5.4 | NCT00141102: 1/2,237 (0.0%) on Diclofenac (serious AE) |
| Fatigue (tiredness) | 11,765 | 3.8 3.7–3.8ROR 4.2 · calibrated p 0.344 | 3.7 EB05 3.7 · IC025 +1.9 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 3.1 · serious PRR 4.7 · ♀ 89% (drug 68%) | not reported in cached trials |
| Rheumatoid arthritis | 9,585 | 22.6 22.2–23.1ROR 25.3 · calibrated p 6e-4 ✓ | 20.8 EB05 20.4 · IC025 +4.3 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 16.9 · serious PRR 18.1 · ♀ 98% (drug 68%) | NCT00141102: 1/2,237 (0.0%) on Diclofenac (serious AE) |
| Off label use (used outside approved label) | 9,194 | 2.6 2.6–2.7ROR 2.8 · calibrated p 0.693 | 2.6 EB05 2.5 · IC025 +1.3 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 2.3 · serious PRR 3.0 | not reported in cached trials |
| Rash | 9,190 | 5.3 5.2–5.4ROR 5.8 · calibrated p 0.164 | 5.2 EB05 5.1 · IC025 +2.3 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 4.4 · serious PRR 7.8 · ♀ 93% (drug 68%) | not reported in cached trials |
| Arthralgia (joint pain) | 9,058 | 5.5 5.3–5.6ROR 6.0 · calibrated p 0.151 | 5.4 EB05 5.3 · IC025 +2.4 3/3 methods agree | Not in label — unassessed | age-adj. PRR 4.8 · serious PRR 6.6 | not reported in cached trials |
| Abdominal discomfort | 8,779 | 13.5 13.3–13.8ROR 15.0 · calibrated p 0.007 ✓ | 12.9 EB05 12.6 · IC025 +3.6 3/3 methods agree | Not in label — unassessed | age-adj. PRR 10.6 · serious PRR 20.1 · ♀ 97% (drug 68%) | not reported in cached trials |
| Alopecia (hair loss) | 8,323 | 10.8 10.6–11.0ROR 11.8 · calibrated p 0.018 ✓ | 10.4 EB05 10.2 · IC025 +3.3 3/3 methods agree | Not in label — unassessed | age-adj. PRR 8.4 · serious PRR 15.6 · ♀ 98% (drug 68%) | not reported in cached trials |
| Joint swelling | 8,084 | 17.6 17.2–17.9ROR 19.3 · calibrated p 0.002 ✓ | 16.4 EB05 16.1 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | age-adj. PRR 14.2 · serious PRR 19.9 · ♀ 93% (drug 68%) | not reported in cached trials |
| Systemic lupus erythematosus | 8,044 | 72.0 70.3–73.8ROR 79.4 · calibrated p 6e-7 ✓ | 55.7 EB05 54.7 · IC025 +5.8 3/3 methods agree | Not in label — unassessed | age-adj. PRR 62.5 · serious PRR 41.0 · ♀ 100% (drug 68%) · 92% clinician | not reported in cached trials |
| Pemphigus | 7,898 | 434.7 419.2–450.8ROR 478.8 · calibrated p 9e-14 ✓ | 155.5 EB05 152.6 · IC025 +7.2 3/3 methods agree | Not in label — unassessed | serious PRR 112.0 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Glossodynia (burning tongue/mouth pain) | 7,700 | 129.0 125.6–132.5ROR 141.6 · calibrated p 7e-9 ✓ | 84.3 EB05 82.7 · IC025 +6.4 3/3 methods agree | Labeled (related wording) related wording | serious PRR 87.5 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Swelling | 7,546 | 21.5 21.0–22.0ROR 23.4 · calibrated p 9e-4 ✓ | 19.8 EB05 19.4 · IC025 +4.3 3/3 methods agree | Labeled adverse reaction exact term | age-adj. PRR 17.0 · serious PRR 22.7 · ♀ 97% (drug 68%) | not reported in cached trials |
| Arthropathy | 7,321 | 36.9 36.0–37.8ROR 40.3 · calibrated p 5e-5 ✓ | 32.1 EB05 31.5 · IC025 +5.0 3/3 methods agree | Not in label — unassessed | age-adj. PRR 29.0 · serious PRR 28.0 · ♀ 98% (drug 68%) | not reported in cached trials |
Unlabeled candidate signals
These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.
- Lupus vulgaris — n=947, PRR 999.4
- Rheumatic fever — n=3,282, PRR 766.7
- Deep vein thrombosis postoperative — n=1,428, PRR 676.4
- Grip strength — n=148, PRR 439.7
- Pemphigus — n=7,898, PRR 434.7
- Facet joint syndrome — n=1,966, PRR 412.8
- Adjustment disorder with depressed mood — n=1,104, PRR 299.8
- Swollen joint count — n=134, PRR 295.8
- Hand deformity — n=7,093, PRR 293.3
- Fractional exhaled nitric oxide increased — n=90, PRR 267.4
Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.
Common questions
What are the most reported side effects of Diclofenac?
In FDA FAERS, the most frequently co-reported reaction terms for Diclofenac are pain, fatigue, rheumatoid arthritis, rash, arthralgia, abdominal discomfort. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.
Does Diclofenac have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS Cardiovascular Thrombotic Events Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction, and stroke, which can be fatal.
Do FAERS signals prove that Diclofenac causes these side effects?
No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.
Sources & methods
- FDA label via openFDA (set ID 45321aec-368d-4ca4-a0c5-2ce56fae74b2, effective 20250529; matched on
openfda.generic_name.exact:"DICLOFENAC" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 3033 description (ChEBI)
- Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,203 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
DICLOFENAC, results-bearing studies sorted by enrollment)
Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.