Buspirone

Common brands: Buspirone Hcl, Neurontin, Vitamin D, Bucapsol, Acid Reducer

Top reporter: Advagen Pharma Ltd

Nonsteroidal Anti-inflammatory Drug [EPC]Benzodiazepine [EPC]Provitamin D2 Compound [EPC]Corticosteroid [EPC]Proton Pump Inhibitor [EPC]
10,587
Total Reports
5,329
Serious Reports
710
Death Reports
30
Reported Reactions
Death Report Ratio: High (6.71%)

Patient Demographics

Male
2,511
Female
7,402

Reported Adverse Reactions (30)

Side effects reported in FDA adverse event reports for Buspirone.

# Reaction Reports % of Total
1 FATIGUE 780
6.3%
2 NAUSEA 769
6.2%
3 HEADACHE 695
5.6%
4 ANXIETY 657
5.3%
5 DRUG INEFFECTIVE 646
5.2%
6 PAIN 556
4.5%
7 DYSPNOEA 545
4.4%
8 DEPRESSION 493
4.0%
9 DIZZINESS 485
3.9%
10 DIARRHOEA 483
3.9%
11 PRODUCT DOSE OMISSION ISSUE 461
3.7%
12 FALL 402
3.3%
13 OFF LABEL USE 351
2.8%
14 VOMITING 345
2.8%
15 MALAISE 331
2.7%
16 INSOMNIA 326
2.6%
17 COUGH 325
2.6%
18 ARTHRALGIA 320
2.6%
19 FEELING ABNORMAL 314
2.5%
20 PRURITUS 311
2.5%
21 WEIGHT DECREASED 300
2.4%
22 PNEUMONIA 296
2.4%
23 WEIGHT INCREASED 286
2.3%
24 CONDITION AGGRAVATED 285
2.3%
25 TREMOR 280
2.3%
26 BACK PAIN 272
2.2%
27 RASH 272
2.2%
28 SOMNOLENCE 266
2.2%
29 SINUSITIS 251
2.0%
30 ASTHENIA 248
2.0%

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.