Duloxetine

Common brands: Duloxetine Delayed-Release, Duloxetine Hydrochloride, Drizalma Sprinkle, Cymbalta, Neurontin

Top reporter: Aurobindo Pharma Limited

Nonsteroidal Anti-inflammatory Drug [EPC]Benzodiazepine [EPC]Proton Pump Inhibitor [EPC]Corticosteroid [EPC]Provitamin D2 Compound [EPC]
67,134
Total Reports
35,655
Serious Reports
6,960
Death Reports
30
Reported Reactions
Death Report Ratio: High (10.37%)

Patient Demographics

Male
18,104
Female
42,847

Reported Adverse Reactions (30)

Side effects reported in FDA adverse event reports for Duloxetine.

# Reaction Reports % of Total
1 DRUG INEFFECTIVE 5,251
6.8%
2 NAUSEA 4,956
6.5%
3 FATIGUE 4,917
6.4%
4 OFF LABEL USE 4,206
5.5%
5 PAIN 3,784
4.9%
6 HEADACHE 3,765
4.9%
7 DIARRHOEA 3,376
4.4%
8 DIZZINESS 3,118
4.1%
9 FALL 2,860
3.7%
10 VOMITING 2,543
3.3%
11 ARTHRALGIA 2,439
3.2%
12 DYSPNOEA 2,375
3.1%
13 TOXICITY TO VARIOUS AGENTS 2,293
3.0%
14 DEPRESSION 2,201
2.9%
15 COMPLETED SUICIDE 2,178
2.8%
16 DRUG INTERACTION 2,097
2.7%
17 ANXIETY 2,027
2.6%
18 ASTHENIA 1,993
2.6%
19 SOMNOLENCE 1,961
2.6%
20 MALAISE 1,847
2.4%
21 INSOMNIA 1,751
2.3%
22 CONDITION AGGRAVATED 1,747
2.3%
23 PAIN IN EXTREMITY 1,747
2.3%
24 DEATH 1,720
2.2%
25 HYPERHIDROSIS 1,720
2.2%
26 PRODUCT DOSE OMISSION ISSUE 1,658
2.2%
27 PNEUMONIA 1,618
2.1%
28 BACK PAIN 1,590
2.1%
29 CONSTIPATION 1,547
2.0%
30 PRURITUS 1,491
1.9%

Important Disclaimer

FDA adverse event reports are submitted voluntarily and do not prove causation. A reported reaction does not mean the drug caused it. Drugs with more users naturally have more reports. Always consult your doctor or pharmacist before making medication decisions.