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Duloxetine side effects: what 69,236 FDA adverse event reports show

Duloxetine · Duloxetine Hydrochloride · 1,185 reaction terms · 284,386 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Brand names

Duloxetine Hydrochloride

openFDA label

Who reports

69,236 reports · 71% serious · 7,118 with death outcome · 70% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Duloxetine delayed-release capsules are indicated for the treatment of: Major depressive disorder in adults Generalized anxiety disorder in adults and pediatric patients 7 years of age and older Diabetic peripheral neuropathic pain in adults Fibromyalg.

FDA label, Indications and Usage

What it is

Duloxetine hydrochloride is a selective serotonin and norepinephrine reuptake inhibitor (SNRI) for oral administration.

FDA label, Description section

Boxed warning

SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These studies did not show an increase in the ris.

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 1Labeled adverse reaction 5Labeled (related wording) 3Likely indication confounding 1Reporting / coding artifact 2Lab value / disease marker 6Not in label — unassessed 22
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). 1,145 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
Bronchial neoplasm46153.9
107.8–219.6ROR 154.0 · calibrated p 1e-8 ✓
97.7 EB05 76.3 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=46 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Nasal turbinate hypertrophy7676.7
59.6–98.7ROR 76.8 · calibrated p 1e-6 ✓
60.3 EB05 49.8 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=76 · ♀ 100% (drug 70%)no trial arm names this drug
Pulmonary malformation6162.8
47.7–82.8ROR 62.9 · calibrated p 5e-6 ✓
51.3 EB05 41.4 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=61 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Post cholecystectomy syndrome4760.6
44.3–82.9ROR 60.6 · calibrated p 6e-6 ✓
49.5 EB05 38.8 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=48 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Delusion of grandeur7056.0
43.4–72.3ROR 56.1 · calibrated p 9e-6 ✓
46.7 EB05 38.3 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=69 · ♀ 0% (drug 70%) · 100% clinicianno trial arm names this drug
Bronchial haemorrhage4651.7
37.8–70.7ROR 51.7 · calibrated p 2e-5 ✓
43.4 EB05 33.9 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=46 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Endometrial ablation4645.0
33.0–61.4ROR 45.1 · calibrated p 4e-5 ✓
38.7 EB05 30.2 · IC025 +4.3
3/3 methods agree
Not in label — unassessedserious n=46 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Granulocyte count increased4840.6
30.0–54.9ROR 40.6 · calibrated p 7e-5 ✓
35.4 EB05 27.8 · IC025 +4.2
3/3 methods agree
Lab value / disease markerserious n=48 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Reversible airways obstruction5334.7
26.1–46.1ROR 34.7 · calibrated p 2e-4 ✓
30.9 EB05 24.5 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=53 · ♀ 0% (drug 70%) · 100% clinicianno trial arm names this drug
Blood immunoglobulin a increased4930.4
22.7–40.8ROR 30.4 · calibrated p 3e-4 ✓
27.4 EB05 21.5 · IC025 +4.0
3/3 methods agree
Lab value / disease markerserious n=48 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Electric shock6625.5
19.8–32.8ROR 25.5 · calibrated p 7e-4 ✓
23.4 EB05 19.0 · IC025 +3.9
3/3 methods agree
Labeled adverse reaction
exact term
serious n=63 · ♀ 100% (drug 70%)no trial arm names this drug
Myofascial pain syndrome5223.7
17.9–31.4ROR 23.7 · calibrated p 0.001 ✓
21.9 EB05 17.3 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=50 · ♀ 100% (drug 70%)no trial arm names this drug
Vitamin b12 increased5623.0
17.5–30.2ROR 23.0 · calibrated p 0.001 ✓
21.3 EB05 17.0 · IC025 +3.7
3/3 methods agree
Lab value / disease markerserious n=51 · ♀ 100% (drug 70%)no trial arm names this drug
Dactylitis6421.1
16.3–27.1ROR 21.1 · calibrated p 0.002 ✓
19.6 EB05 15.9 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=63 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Somatic symptom disorder6619.6
15.3–25.2ROR 19.6 · calibrated p 0.002 ✓
18.4 EB05 14.9 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=66 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Glomerular filtration rate increased4919.4
14.5–25.9ROR 19.4 · calibrated p 0.003 ✓
18.1 EB05 14.2 · IC025 +3.5
3/3 methods agree
Lab value / disease markerserious n=49 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Serotonin syndrome1,12418.8
17.8–20.0ROR 19.1 · calibrated p 0.002 ✓
17.8 EB05 16.9 · IC025 +4.0
3/3 methods agree
Labeled — boxed warning
exact term
age-adj. PRR 16.3 · serious PRR 14.4no trial arm names this drug
Electric shock sensation15818.8
16.0–22.1ROR 18.9 · calibrated p 0.003 ✓
17.7 EB05 15.5 · IC025 +3.8
3/3 methods agree
Labeled adverse reaction
exact term
serious n=121 · 81% consumerno trial arm names this drug
Rheumatoid factor increased6117.4
13.4–22.5ROR 17.4 · calibrated p 0.004 ✓
16.4 EB05 13.2 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=61 · ♀ 100% (drug 70%)no trial arm names this drug
Reversible cerebral vasoconstriction syndrome10216.5
13.6–20.2ROR 16.6 · calibrated p 0.005 ✓
15.7 EB05 13.3 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=102 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Lymphocyte count abnormal5615.7
12.0–20.6ROR 15.8 · calibrated p 0.007 ✓
14.9 EB05 11.8 · IC025 +3.3
3/3 methods agree
Lab value / disease markerserious n=56 · ♀ 0% (drug 70%) · 100% clinicianno trial arm names this drug
Bezoar6214.2
11.0–18.3ROR 14.2 · calibrated p 0.010 ✓
13.5 EB05 10.8 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=62 · 100% clinicianno trial arm names this drug
Joint noise8614.0
11.3–17.4ROR 14.0 · calibrated p 0.010 ✓
13.3 EB05 11.1 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=82no trial arm names this drug
Product used for unknown indication5313.4
10.2–17.6ROR 13.4 · calibrated p 0.012 ✓
12.6 EB05 9.9 · IC025 +3.1
3/3 methods agree
Reporting / coding artifactserious n=52 · ♀ 0% (drug 70%) · 100% clinicianno trial arm names this drug
Clonus10211.7
9.6–14.2ROR 11.7 · calibrated p 0.020 ✓
11.1 EB05 9.4 · IC025 +3.1
3/3 methods agree
Labeled adverse reaction
exact term
serious n=99 · 100% clinicianno trial arm names this drug
Intervertebral discitis7011.6
9.1–14.7ROR 11.6 · calibrated p 0.021 ✓
11.0 EB05 8.9 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=70 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Rhonchi4911.1
8.3–14.7ROR 11.1 · calibrated p 0.025 ✓
10.3 EB05 8.0 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious n=50 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Product monitoring error5010.9
8.2–14.4ROR 10.9 · calibrated p 0.027 ✓
10.2 EB05 7.9 · IC025 +2.8
3/3 methods agree
Reporting / coding artifactserious n=50 · 100% clinicianno trial arm names this drug
Hyperreflexia12010.7
8.9–12.9ROR 10.7 · calibrated p 0.026 ✓
10.2 EB05 8.7 · IC025 +3.0
3/3 methods agree
Labeled adverse reaction
exact term
serious n=117 · 100% clinicianno trial arm names this drug
Anxiety disorder10810.0
8.3–12.1ROR 10.0 · calibrated p 0.033 ✓
9.5 EB05 8.1 · IC025 +2.9
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=104no trial arm names this drug
Hyperparathyroidism secondary779.5
7.5–11.9ROR 9.5 · calibrated p 0.041 ✓
8.9 EB05 7.3 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=77no trial arm names this drug
Inappropriate antidiuretic hormone secretion3089.4
8.4–10.5ROR 9.5 · calibrated p 0.040 ✓
9.1 EB05 8.3 · IC025 +3.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 7.4 · 91% clinicianno trial arm names this drug
Respiratory disorder neonatal489.4
7.0–12.5ROR 9.4 · calibrated p 0.044 ✓
8.7 EB05 6.7 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious n=48 · ♀ 0% (drug 70%) · 100% clinicianno trial arm names this drug
Bronchial disorder469.2
6.8–12.3ROR 9.2 · calibrated p 0.047 ✓
8.5 EB05 6.5 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=46 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug
Affective disorder2258.9
7.8–10.2ROR 8.9 · calibrated p 0.048 ✓
8.6 EB05 7.7 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=208no trial arm names this drug
Cleft palate538.5
6.5–11.2ROR 8.5 · calibrated p 0.059
7.9 EB05 6.2 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious n=53 · 100% clinicianno trial arm names this drug
White blood cells urine positive508.3
6.3–11.0ROR 8.3 · calibrated p 0.064
7.7 EB05 6.0 · IC025 +2.4
3/3 methods agree
Lab value / disease markerserious n=50 · ♀ 100% (drug 70%) · 100% clinicianno trial arm names this drug

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.

ConceptReportsPRR 95% CIReading
Suicidality4,2265.35.1–5.4signal
Hyponatraemia8453.23.0–3.4signal
Depression2,7973.02.9–3.1signal
Extrapyramidal1,0313.02.8–3.2signal
Fall / fracture3,1052.52.4–2.6signal
Rhabdomyolysis / myopathy4491.71.5–1.8raised
Tendon disorder2101.71.5–1.9raised
Serious infection4,0591.61.5–1.6raised
Dependence / withdrawal1,5441.61.5–1.7raised
Arrhythmia / qt9841.51.4–1.6raised
Kidney injury2,3131.51.5–1.6raised
Opportunistic infection6401.41.3–1.5raised
Anaphylaxis / angioedema5651.41.3–1.5raised
Seizure8421.31.2–1.4raised
Liver injury1,2791.31.2–1.4raised
Hypoglycaemia3611.11.0–1.3raised

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Duloxetine only as a background or rescue medication (NCT01360866, NCT01838681); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

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)5,4341.3
1.2–1.3ROR 1.3 · calibrated p 0.489
1.2 EB05 1.2 · IC025 +0.3Reporting / coding artifactage-adj. PRR 1.4 · serious PRR 1.8no trial arm names this drug
Nausea5,1372.0
1.9–2.0ROR 2.1 · calibrated p 0.974
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.2no trial arm names this drug
Fatigue (tiredness)5,0592.0
1.9–2.0ROR 2.1 · calibrated p 0.974
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.0no trial arm names this drug
Off label use (used outside approved label)4,3901.5
1.5–1.6ROR 1.6 · calibrated p 0.687
1.5 EB05 1.5 · IC025 +0.6Reporting / coding artifactage-adj. PRR 1.5 · serious PRR 1.8no trial arm names this drug
Pain3,9151.9
1.9–2.0ROR 2.0 · calibrated p 0.937
1.9 EB05 1.9 · IC025 +0.9Likely indication confounding
term in indications; also in warnings
age-adj. PRR 1.9 · serious PRR 1.8no trial arm names this drug
Headache3,9121.9
1.8–2.0ROR 2.0 · calibrated p 0.917
1.9 EB05 1.8 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.2no trial arm names this drug
Diarrhoea (diarrhea)3,5071.7
1.6–1.7ROR 1.7 · calibrated p 0.762
1.7 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.6no trial arm names this drug
Dizziness3,2182.0
1.9–2.0ROR 2.0 · calibrated p 0.949
2.0 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.0no trial arm names this drug
Fall2,9482.7
2.6–2.8ROR 2.8 · calibrated p 0.704
2.7 EB05 2.6 · IC025 +1.4
3/3 methods agree
Labeled — boxed warning
exact term
age-adj. PRR 2.3 · serious PRR 2.2no trial arm names this drug
Vomiting2,6241.7
1.6–1.8ROR 1.7 · calibrated p 0.785
1.7 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.6no trial arm names this drug
Arthralgia (joint pain)2,5001.8
1.8–1.9ROR 1.9 · calibrated p 0.866
1.8 EB05 1.8 · IC025 +0.8Not in label — unassessedage-adj. PRR 1.5 · serious PRR 2.0no trial arm names this drug
Dyspnoea (shortness of breath)2,4701.3
1.3–1.4ROR 1.3 · calibrated p 0.532
1.3 EB05 1.3 · IC025 +0.3Not in label — unassessedage-adj. PRR 1.2 · serious PRR 1.2no trial arm names this drug
Depression2,2513.0
2.9–3.1ROR 3.1 · calibrated p 0.604
3.0 EB05 2.9 · IC025 +1.5
3/3 methods agree
Labeled — boxed warning
synonym match
age-adj. PRR 2.6 · serious PRR 2.5no trial arm names this drug
Completed suicide (death by suicide)2,2048.1
7.8–8.5ROR 8.4 · calibrated p 0.058
7.9 EB05 7.6 · IC025 +2.9
3/3 methods agree
Outcome field, not a reaction
boxed warning mentions mortality
age-adj. PRR 6.6 · serious PRR 6.4 · 96% clinicianno trial arm names this drug

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: Duloxetine ↔ Completed suicide.

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 Duloxetine?

In FDA FAERS, the most frequently co-reported reaction terms for Duloxetine are nausea, fatigue, pain, headache, diarrhoea, dizziness. 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 Duloxetine have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: SUICIDAL THOUGHTS AND BEHAVIORS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These studies did not show an increase in the ris.

Do FAERS signals prove that Duloxetine 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.