Naproxen Sodium Tablet side effects: what 52,720 FDA adverse event reports show
Drug class
Nonsteroidal Anti-inflammatory Drug
Who reports
52,720 reports · 32% serious · 1,132 with death outcome · 68% female
Used for
Naproxen tablets and naproxen sodium tablets are indicated for: the relief of the signs and symptoms of: • rheumatoid arthritis • osteoarthritis • ankylosing spondylitis • Polyarticular Juvenile Idiopathic Arthritis Naproxen tablets and naproxen sodium.
What it is
Naproxen Tablets, USP and Naproxen Sodium Tablets, USP are nonsteroidal anti-inflammatory drugs available as follows: Naproxen Tablets, USP are available as follows for oral administration: 25.
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 (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- 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). 1,134 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 |
|---|---|---|---|---|---|---|
| Joint laxity | 36 | 53.6 37.8–75.9ROR 53.6 · calibrated p 2e-5 ✓ | 46.2 EB05 34.8 · IC025 +4.3 3/3 methods agree vs other NSAIDs: PRR 10.1 (7.0–14.4) | Not in label — unassessed | serious n=35 · ♀ 100% (drug 68%) | not reported in cached trials |
| Therapeutic product effective for unapproved indication | 26 | 30.5 20.4–45.4ROR 30.5 · calibrated p 4e-4 ✓ | 27.8 EB05 20.0 · IC025 +3.6 3/3 methods agree vs other NSAIDs: only this drug | Labeled (related wording) related wording | 100% consumer | not reported in cached trials |
| Inappropriate prescribing | 41 | 27.9 20.3–38.3ROR 27.9 · calibrated p 5e-4 ✓ | 25.8 EB05 19.9 · IC025 +3.8 3/3 methods agree vs other NSAIDs: only this drug | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Foreign body trauma | 45 | 25.7 19.0–34.7ROR 25.7 · calibrated p 8e-4 ✓ | 23.9 EB05 18.6 · IC025 +3.8 3/3 methods agree vs other NSAIDs: only this drug | Not in label — unassessed | 100% consumer | not reported in cached trials |
| Incorrect dosage administered | 278 | 23.8 21.1–26.9ROR 23.9 · calibrated p 9e-4 ✓ | 22.5 EB05 20.4 · IC025 +4.2 3/3 methods agree vs other NSAIDs: PRR 43.4 (36.9–51.1) | Reporting / coding artifact | serious n=22 · 90% consumer | not reported in cached trials |
| Failure of child resistant mechanism for pharmaceutical product | 20 | 18.7 12.0–29.3ROR 18.7 · calibrated p 0.004 ✓ | 17.5 EB05 11.7 · IC025 +2.9 3/3 methods agree vs other NSAIDs: only this drug | Labeled (related wording) related wording | – | not reported in cached trials |
| Incorrect drug administration duration | 1,272 | 18.5 17.5–19.6ROR 19.0 · calibrated p 0.003 ✓ | 17.7 EB05 16.9 · IC025 +4.0 3/3 methods agree vs other NSAIDs: PRR 13.8 (13.0–14.7) | Reporting / coding artifact | serious PRR 10.0 · 99% consumer | not reported in cached trials |
| Device ineffective | 47 | 18.2 13.6–24.4ROR 18.2 · calibrated p 0.004 ✓ | 17.3 EB05 13.5 · IC025 +3.4 3/3 methods agree vs other NSAIDs: only this drug | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Expired product administered | 1,190 | 14.8 13.9–15.6ROR 15.1 · calibrated p 0.007 ✓ | 14.3 EB05 13.6 · IC025 +3.7 3/3 methods agree vs other NSAIDs: PRR 10.4 (9.7–11.0) | Reporting / coding artifact | serious n=42 · 98% consumer | not reported in cached trials |
| Poor quality drug administered | 229 | 14.3 12.6–16.4ROR 14.4 · calibrated p 0.008 ✓ | 13.8 EB05 12.4 · IC025 +3.5 3/3 methods agree vs other NSAIDs: PRR 10.0 (8.7–11.5) | Not in label — unassessed | 100% consumer | not reported in cached trials |
| Foreign body in respiratory tract | 44 | 13.6 10.1–18.4ROR 13.6 · calibrated p 0.012 ✓ | 13.0 EB05 9.9 · IC025 +3.0 3/3 methods agree vs other NSAIDs: PRR 30.3 (20.8–44.2) | Not in label — unassessed | ♀ 48% (drug 68%) · 100% consumer | not reported in cached trials |
| Therapeutic response unexpected | 1,458 | 13.3 12.6–14.0ROR 13.6 · calibrated p 0.010 ✓ | 12.9 EB05 12.3 · IC025 +3.6 3/3 methods agree vs other NSAIDs: PRR 8.0 (7.5–8.4) | Reporting / coding artifact | serious PRR 5.8 · 97% consumer | not reported in cached trials |
| Gastrointestinal ulcer haemorrhage | 36 | 13.2 9.4–18.4ROR 13.2 · calibrated p 0.014 ✓ | 12.4 EB05 9.2 · IC025 +2.9 3/3 methods agree vs other NSAIDs: only this drug | Not in label — unassessed | serious n=36 · 100% consumer | not reported in cached trials |
| Oropharyngeal swelling | 28 | 11.5 7.9–16.7ROR 11.5 · calibrated p 0.024 ✓ | 10.5 EB05 7.4 · IC025 +2.6 3/3 methods agree vs other NSAIDs: only this drug | Not in label — unassessed | serious n=27 | not reported in cached trials |
| Gastric ulcer haemorrhage | 157 | 11.5 9.8–13.4ROR 11.5 · calibrated p 0.020 ✓ | 11.1 EB05 9.7 · IC025 +3.2 3/3 methods agree vs other NSAIDs: PRR 2.4 (2.0–2.8) | Not in label — unassessed | serious n=157 · 82% consumer | NCT00346216: 2/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Blood urine | 27 | 11.4 7.8–16.7ROR 11.4 · calibrated p 0.025 ✓ | 10.4 EB05 7.2 · IC025 +2.6 3/3 methods agree vs other NSAIDs: only this drug | Not in label — unassessed | serious n=24 | NCT00346216: 1/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Stomach discomfort | 144 | 11.2 9.5–13.2ROR 11.2 · calibrated p 0.022 ✓ | 10.8 EB05 9.4 · IC025 +3.1 3/3 methods agree vs other NSAIDs: PRR 20.7 (17.0–25.2) | Not in label — unassessed | serious n=40 · 93% consumer | not reported in cached trials |
| Red blood cell sedimentation rate abnormal | 61 | 10.7 8.3–13.8ROR 10.7 · calibrated p 0.028 ✓ | 10.1 EB05 8.1 · IC025 +2.9 3/3 methods agree vs other NSAIDs: PRR 2.0 (1.5–2.6) | Lab value / disease marker | serious n=60 · ♀ 100% (drug 68%) | not reported in cached trials |
| Ulcer haemorrhage | 174 | 10.5 9.0–12.2ROR 10.5 · calibrated p 0.028 ✓ | 10.1 EB05 8.9 · IC025 +3.1 3/3 methods agree vs other NSAIDs: PRR 1.7 (1.4–1.9) | Not in label — unassessed | serious n=170 · 86% consumer | NCT00346216: 1/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Oesophageal spasm | 47 | 10.4 7.8–13.9ROR 10.4 · calibrated p 0.031 ✓ | 9.7 EB05 7.5 · IC025 +2.7 3/3 methods agree vs other NSAIDs: PRR 5.9 (4.3–8.0) | Not in label — unassessed | serious n=47 · ♀ 100% (drug 68%) | NCT00346216: 1/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Accidental exposure to product by child | 173 | 10.3 8.9–12.0ROR 10.4 · calibrated p 0.029 ✓ | 10.0 EB05 8.8 · IC025 +3.0 3/3 methods agree vs other NSAIDs: PRR 6.4 (5.4–7.4) | Reporting / coding artifact | 78% consumer | not reported in cached trials |
| Product commingling | 26 | 10.1 6.8–14.9ROR 10.1 · calibrated p 0.038 ✓ | 9.1 EB05 6.3 · IC025 +2.4 3/3 methods agree vs other NSAIDs: PRR 41.2 (24.3–69.6) | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Foreign body | 94 | 9.4 7.7–11.6ROR 9.5 · calibrated p 0.041 ✓ | 9.0 EB05 7.5 · IC025 +2.8 3/3 methods agree vs other NSAIDs: PRR 7.9 (6.4–9.8) | Not in label — unassessed | serious n=19 · 100% consumer | NCT00346216: 1/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Extra dose administered | 924 | 9.4 8.8–10.0ROR 9.6 · calibrated p 0.038 ✓ | 9.2 EB05 8.7 · IC025 +3.1 3/3 methods agree vs other NSAIDs: PRR 10.4 (9.7–11.1) | Not in label — unassessed | serious n=58 · 94% consumer | not reported in cached trials |
| Product closure removal difficult | 21 | 8.5 5.5–13.1ROR 8.5 · calibrated p 0.066 | 7.4 EB05 5.0 · IC025 +2.1 3/3 methods agree vs other NSAIDs: only this drug | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Pre-existing condition improved | 132 | 8.5 7.1–10.1ROR 8.5 · calibrated p 0.057 | 8.2 EB05 7.0 · IC025 +2.7 3/3 methods agree vs other NSAIDs: PRR 2.4 (2.0–2.8) | Not in label — unassessed | serious n=63 | not reported in cached trials |
| Obstructive sleep apnoea syndrome | 28 | 8.1 5.6–11.8ROR 8.1 · calibrated p 0.073 | 7.3 EB05 5.2 · IC025 +2.2 3/3 methods agree vs other NSAIDs: PRR 2.0 (1.3–2.9) | Not in label — unassessed | serious n=28 · ♀ 100% (drug 68%) | not reported in cached trials |
| Product use issue | 3,735 | 8.1 7.8–8.3ROR 8.6 · calibrated p 0.053 | 7.9 EB05 7.7 · IC025 +2.9 3/3 methods agree vs other NSAIDs: PRR 4.4 (4.2–4.5) | Reporting / coding artifact | serious PRR 3.4 · 97% consumer | not reported in cached trials |
| Product coating issue | 20 | 7.9 5.1–12.4ROR 8.0 · calibrated p 0.081 | 6.9 EB05 4.6 · IC025 +2.0 3/3 methods agree vs other NSAIDs: PRR 11.4 (7.0–18.6) | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Product physical consistency issue | 104 | 7.7 6.3–9.3ROR 7.7 · calibrated p 0.077 | 7.4 EB05 6.2 · IC025 +2.5 3/3 methods agree vs other NSAIDs: PRR 42.6 (32.7–55.5) | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Gastric haemorrhage | 209 | 7.3 6.4–8.4ROR 7.3 · calibrated p 0.088 | 7.1 EB05 6.3 · IC025 +2.6 3/3 methods agree vs other NSAIDs: PRR 2.0 (1.7–2.3) | Not in label — unassessed | serious PRR 13.3 · 92% consumer | NCT00346216: 2/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Product package associated injury | 39 | 7.1 5.2–9.8ROR 7.1 · calibrated p 0.102 | 6.5 EB05 5.0 · IC025 +2.2 3/3 methods agree vs other NSAIDs: only this drug | Reporting / coding artifact | ♀ 100% (drug 68%) · 100% consumer | not reported in cached trials |
| Incorrect product administration duration | 355 | 7.1 6.4–7.8ROR 7.1 · calibrated p 0.095 | 6.9 EB05 6.3 · IC025 +2.6 3/3 methods agree vs other NSAIDs: PRR 5.7 (5.1–6.3) | Reporting / coding artifact | serious n=55 · 100% consumer | not reported in cached trials |
| Drug effect delayed | 80 | 7.0 5.6–8.8ROR 7.0 · calibrated p 0.101 | 6.7 EB05 5.5 · IC025 +2.4 3/3 methods agree vs other NSAIDs: PRR 8.6 (6.8–10.9) | Reporting / coding artifact | 100% consumer | not reported in cached trials |
| Oesophageal pain | 67 | 6.9 5.4–8.7ROR 6.9 · calibrated p 0.109 | 6.5 EB05 5.3 · IC025 +2.3 3/3 methods agree vs other NSAIDs: PRR 6.9 (5.3–8.9) | Not in label — unassessed | serious n=45 · ♀ 100% (drug 68%) · 70% consumer | not reported in cached trials |
| Gastric ulcer perforation | 21 | 6.7 4.3–10.3ROR 6.7 · calibrated p 0.129 | 5.8 EB05 4.0 · IC025 +1.8 3/3 methods agree vs other NSAIDs: PRR 1.0 (0.6–1.5) | Labeled — boxed warning synonym match | serious n=21 | not reported in cached trials |
| Drug effect incomplete | 599 | 6.6 6.1–7.1ROR 6.6 · calibrated p 0.116 | 6.4 EB05 6.0 · IC025 +2.6 3/3 methods agree vs other NSAIDs: PRR 4.9 (4.5–5.3) | Reporting / coding artifact | serious PRR 3.0 · 93% consumer | not reported in cached trials |
| Gastrointestinal ulcer | 36 | 6.5 4.7–9.1ROR 6.5 · calibrated p 0.129 | 6.0 EB05 4.5 · IC025 +2.0 3/3 methods agree vs other NSAIDs: PRR 17.6 (12.0–25.8) | Labeled (related wording) related wording | serious n=31 · 77% consumer | NCT00346216: 1/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Gastric ulcer | 298 | 6.3 5.6–7.1ROR 6.3 · calibrated p 0.131 | 6.2 EB05 5.6 · IC025 +2.4 3/3 methods agree vs other NSAIDs: PRR 1.3 (1.2–1.5) | Labeled — boxed warning synonym match | serious PRR 11.5 · 79% consumer | NCT00346216: 5/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE) |
| Drug effective for unapproved indication | 454 | 6.3 5.7–6.9ROR 6.3 · calibrated p 0.132 | 6.1 EB05 5.7 · IC025 +2.5 3/3 methods agree vs other NSAIDs: PRR 4.8 (4.3–5.3) | Labeled (related wording) related wording | 100% consumer | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Naproxen Sodium Tablet 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 (8 of 40 signal terms matched).
- NCT00346216 — Prospective Randomized Evaluation Of Celecoxib Integrated Safety Vs Ibuprofen Or Naproxen (N=24081, PHASE4; 1238 AE terms posted; arms: Celecoxib; Ibuprofen; Naproxen)
- NCT03161093 — A Study to Determine the Safety and the Efficacy of Fasinumab Compared to Placebo and Naproxen for Treatment o (N=3307, PHASE3; 221 AE terms posted; arms: Placebo; Naproxen; Fasinumab 1mg Q8W; Fasinumab 1mg Q4W)
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) | 8,095 | 2.5 2.4–2.5ROR 2.7 · calibrated p 0.725 | 2.4 EB05 2.4 · IC025 +1.3 3/3 methods agree vs other NSAIDs: PRR 2.0 (1.9–2.0) | Reporting / coding artifact | serious PRR 1.4 · 90% consumer | not reported in cached trials |
| Product use issue | 3,735 | 8.1 7.8–8.3ROR 8.6 · calibrated p 0.053 | 7.9 EB05 7.7 · IC025 +2.9 3/3 methods agree vs other NSAIDs: PRR 4.4 (4.2–4.5) | Reporting / coding artifact | serious PRR 3.4 · 97% consumer | not reported in cached trials |
| Fatigue (tiredness) | 2,397 | 1.2 1.2–1.3ROR 1.2 · calibrated p 0.466 | 1.2 EB05 1.2 · IC025 +0.2 vs other NSAIDs: PRR 0.7 (0.6–0.7) | Labeled adverse reaction exact term | serious PRR 2.2 | NCT00346216: 2/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Nausea | 2,279 | 1.1 1.1–1.2ROR 1.2 · calibrated p 0.410 | 1.1 EB05 1.1 · IC025 +0.1 vs other NSAIDs: PRR 0.7 (0.7–0.7) | Labeled adverse reaction exact term | serious PRR 1.8 | NCT00346216: 6/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE) |
| Pain | 2,169 | 1.4 1.3–1.5ROR 1.4 · calibrated p 0.589 | 1.4 EB05 1.4 · IC025 +0.4 vs other NSAIDs: PRR 0.6 (0.6–0.7) | Likely indication confounding term in indications; also in warnings | serious PRR 2.2 | NCT00346216: 13/7,933 (0.2%) on Naproxen Sodium Tablet (serious AE) |
| Headache | 2,075 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.530 | 1.3 EB05 1.3 · IC025 +0.3 vs other NSAIDs: PRR 0.7 (0.7–0.8) | Labeled adverse reaction exact term | serious PRR 2.1 · 70% consumer | NCT00346216: 4/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Dizziness | 1,876 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.654 | 1.5 EB05 1.4 · IC025 +0.5 vs other NSAIDs: PRR 0.9 (0.8–0.9) | Labeled adverse reaction exact term | serious PRR 2.3 · 73% consumer | NCT00346216: 6/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE) |
| Arthralgia (joint pain) | 1,784 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.794 | 1.7 EB05 1.6 · IC025 +0.7 vs other NSAIDs: PRR 0.7 (0.6–0.7) | Not in label — unassessed | serious PRR 2.6 | NCT00346216: 39/7,933 (0.5%) on Naproxen Sodium Tablet (serious AE) |
| Diarrhoea (diarrhea) | 1,668 | 1.0 1.0–1.1ROR 1.0 · calibrated p 0.328 | 1.0 EB05 1.0 · IC025 -0.0 PRR-only: not supported by EBGM or IC vs other NSAIDs: PRR 0.6 (0.6–0.7) | Labeled adverse reaction exact term | serious PRR 1.6 | NCT00346216: 5/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE) |
| Therapeutic response unexpected | 1,458 | 13.3 12.6–14.0ROR 13.6 · calibrated p 0.010 ✓ | 12.9 EB05 12.3 · IC025 +3.6 3/3 methods agree vs other NSAIDs: PRR 8.0 (7.5–8.4) | Reporting / coding artifact | serious PRR 5.8 · 97% consumer | not reported in cached trials |
| Drug hypersensitivity | 1,445 | 3.0 2.8–3.1ROR 3.0 · calibrated p 0.617 | 3.0 EB05 2.8 · IC025 +1.5 3/3 methods agree vs other NSAIDs: PRR 1.0 (0.9–1.0) | Labeled (related wording) related wording | serious PRR 3.6 · 72% consumer | NCT00346216: 3/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Off label use (used outside approved label) | 1,393 | 0.6 0.6–0.7ROR 0.6 · calibrated p 0.097 | 0.6 EB05 0.6 · IC025 -0.7 PRR-only: not supported by EBGM or IC vs other NSAIDs: PRR 0.6 (0.5–0.6) | Reporting / coding artifact | serious PRR 0.7 · 78% consumer | not reported in cached trials |
| Dyspnoea (shortness of breath) | 1,380 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.287 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC vs other NSAIDs: PRR 0.5 (0.5–0.6) | Labeled adverse reaction exact term | serious PRR 1.7 | NCT00346216: 24/7,933 (0.3%) on Naproxen Sodium Tablet (serious AE) |
| Pruritus (itching) | 1,310 | 1.4 1.3–1.5ROR 1.4 · calibrated p 0.568 | 1.4 EB05 1.3 · IC025 +0.4 vs other NSAIDs: PRR 0.7 (0.7–0.8) | Labeled adverse reaction exact term | serious PRR 2.4 · 74% consumer | NCT00346216: 1/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE) |
| Abdominal pain upper | 1,290 | 2.5 2.4–2.6ROR 2.5 · calibrated p 0.794 | 2.5 EB05 2.4 · IC025 +1.2 3/3 methods agree vs other NSAIDs: PRR 1.0 (0.9–1.0) | Labeled (related wording) related wording | serious PRR 3.2 · 83% consumer | NCT00346216: 13/7,933 (0.2%) on Naproxen Sodium Tablet (serious AE) |
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.
- Joint laxity — n=36, PRR 53.6
- Foreign body trauma — n=45, PRR 25.7
- Poor quality drug administered — n=229, PRR 14.3
- Foreign body in respiratory tract — n=44, PRR 13.6
- Gastrointestinal ulcer haemorrhage — n=36, PRR 13.2
- Oropharyngeal swelling — n=28, PRR 11.5
- Gastric ulcer haemorrhage — n=157, PRR 11.5 (also seen in trial arm)
- Blood urine — n=27, PRR 11.4 (also seen in trial arm)
- Stomach discomfort — n=144, PRR 11.2
- Ulcer haemorrhage — n=174, PRR 10.5 (also seen in trial arm)
✓ A hand-written Bradford Hill causality assessment exists for this drug: Methotrexate Sodium ↔ Rheumatoid Arthritis.
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 Naproxen Sodium Tablet?
In FDA FAERS, the most frequently co-reported reaction terms for Naproxen Sodium Tablet are fatigue, nausea, pain, headache, dizziness, arthralgia. 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 Naproxen Sodium Tablet 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 Naproxen Sodium Tablet 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 000155a8-709c-44e5-a75f-cd890f3a7caf, effective 20260129; matched on
openfda.generic_name.exact:"NAPROXEN") - 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, 1,174 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
NAPROXEN, 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.