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Naproxen Sodium Tablet side effects: what 52,720 FDA adverse event reports show

Naproxen Sodium Tablet · 1,174 reaction terms · 153,354 drug–reaction co-reports · data 2026-09-14
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Drug class

Nonsteroidal Anti-inflammatory Drug

FDA label (Established Pharmacologic Class) · compare the class

Who reports

52,720 reports · 32% serious · 1,132 with death outcome · 68% female

openFDA FAERS counts, all years, deduplication not applied

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.

FDA label, Indications and Usage

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.

FDA label, Description section

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.

FDA label
How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled — boxed warning 2Labeled (related wording) 4Reporting / coding artifact 16Lab value / disease marker 1Not in label — unassessed 17
What the badges mean

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.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Joint laxity3653.6
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 — unassessedserious n=35 · ♀ 100% (drug 68%)not reported in cached trials
Inappropriate prescribing4127.9
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 artifact100% consumernot reported in cached trials
Foreign body trauma4525.7
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 — unassessed100% consumernot reported in cached trials
Incorrect dosage administered27823.8
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 artifactserious n=22 · 90% consumernot reported in cached trials
Incorrect drug administration duration1,27218.5
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 artifactserious PRR 10.0 · 99% consumernot reported in cached trials
Device ineffective4718.2
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 artifact100% consumernot reported in cached trials
Expired product administered1,19014.8
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 artifactserious n=42 · 98% consumernot reported in cached trials
Poor quality drug administered22914.3
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 — unassessed100% consumernot reported in cached trials
Foreign body in respiratory tract4413.6
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% consumernot reported in cached trials
Therapeutic response unexpected1,45813.3
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 artifactserious PRR 5.8 · 97% consumernot reported in cached trials
Gastrointestinal ulcer haemorrhage3613.2
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 — unassessedserious n=36 · 100% consumernot reported in cached trials
Oropharyngeal swelling2811.5
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 — unassessedserious n=27not reported in cached trials
Gastric ulcer haemorrhage15711.5
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 — unassessedserious n=157 · 82% consumerNCT00346216: 2/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE)
Blood urine2711.4
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 — unassessedserious n=24NCT00346216: 1/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE)
Stomach discomfort14411.2
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 — unassessedserious n=40 · 93% consumernot reported in cached trials
Red blood cell sedimentation rate abnormal6110.7
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 markerserious n=60 · ♀ 100% (drug 68%)not reported in cached trials
Ulcer haemorrhage17410.5
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 — unassessedserious n=170 · 86% consumerNCT00346216: 1/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE)
Oesophageal spasm4710.4
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 — unassessedserious n=47 · ♀ 100% (drug 68%)NCT00346216: 1/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE)
Accidental exposure to product by child17310.3
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 artifact78% consumernot reported in cached trials
Product commingling2610.1
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 artifact100% consumernot reported in cached trials
Foreign body949.4
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 — unassessedserious n=19 · 100% consumerNCT00346216: 1/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE)
Extra dose administered9249.4
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 — unassessedserious n=58 · 94% consumernot reported in cached trials
Product closure removal difficult218.5
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 artifact100% consumernot reported in cached trials
Pre-existing condition improved1328.5
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 — unassessedserious n=63not reported in cached trials
Obstructive sleep apnoea syndrome288.1
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 — unassessedserious n=28 · ♀ 100% (drug 68%)not reported in cached trials
Product use issue3,7358.1
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 artifactserious PRR 3.4 · 97% consumernot reported in cached trials
Product coating issue207.9
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 artifact100% consumernot reported in cached trials
Product physical consistency issue1047.7
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 artifact100% consumernot reported in cached trials
Gastric haemorrhage2097.3
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 — unassessedserious PRR 13.3 · 92% consumerNCT00346216: 2/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE)
Product package associated injury397.1
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% consumernot reported in cached trials
Incorrect product administration duration3557.1
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 artifactserious n=55 · 100% consumernot reported in cached trials
Drug effect delayed807.0
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 artifact100% consumernot reported in cached trials
Oesophageal pain676.9
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 — unassessedserious n=45 · ♀ 100% (drug 68%) · 70% consumernot reported in cached trials
Gastric ulcer perforation216.7
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=21not reported in cached trials
Drug effect incomplete5996.6
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 artifactserious PRR 3.0 · 93% consumernot reported in cached trials
Gastric ulcer2986.3
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% consumerNCT00346216: 5/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE)

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).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Drug ineffective (drug did not work)8,0952.5
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 artifactserious PRR 1.4 · 90% consumernot reported in cached trials
Product use issue3,7358.1
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 artifactserious PRR 3.4 · 97% consumernot reported in cached trials
Fatigue (tiredness)2,3971.2
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 2.2NCT00346216: 2/7,933 (0.0%) on Naproxen Sodium Tablet (serious AE)
Nausea2,2791.1
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 1.8NCT00346216: 6/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE)
Pain2,1691.4
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 2.2NCT00346216: 13/7,933 (0.2%) on Naproxen Sodium Tablet (serious AE)
Headache2,0751.3
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% consumerNCT00346216: 4/8,030 (0.0%) on Naproxen Sodium Tablet (serious AE)
Dizziness1,8761.5
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% consumerNCT00346216: 6/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE)
Arthralgia (joint pain)1,7841.7
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 — unassessedserious PRR 2.6NCT00346216: 39/7,933 (0.5%) on Naproxen Sodium Tablet (serious AE)
Diarrhoea (diarrhea)1,6681.0
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 1.6NCT00346216: 5/7,933 (0.1%) on Naproxen Sodium Tablet (serious AE)
Therapeutic response unexpected1,45813.3
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 artifactserious PRR 5.8 · 97% consumernot reported in cached trials
Off label use (used outside approved label)1,3930.6
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 artifactserious PRR 0.7 · 78% consumernot reported in cached trials
Dyspnoea (shortness of breath)1,3801.0
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 1.7NCT00346216: 24/7,933 (0.3%) on Naproxen Sodium Tablet (serious AE)
Pruritus (itching)1,3101.4
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% consumerNCT00346216: 1/7,933 (0.0%) 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.

✓ 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

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.