Pantoprazole

Common brands: Pantoprazole Sodium, Protonix Delayed-Release, Protonix I.V., Pantoprazole Sodium I.V., Pain Relief

Top reporter: Amneal Pharmaceuticals Llc

Nonsteroidal Anti-inflammatory Drug [EPC]Corticosteroid [EPC]Loop Diuretic [EPC]Benzodiazepine [EPC]Platelet Aggregation Inhibitor [EPC]
245,972
Total Reports
119,741
Serious Reports
27,811
Death Reports
30
Reported Reactions
Death Report Ratio: High (11.31%)

Patient Demographics

Male
94,131
Female
129,101

Reported Adverse Reactions (30)

Side effects reported in FDA adverse event reports for Pantoprazole.

# Reaction Reports % of Total
1 FATIGUE 20,312
6.0%
2 OFF LABEL USE 18,109
5.3%
3 NAUSEA 17,380
5.1%
4 DIARRHOEA 17,059
5.0%
5 DYSPNOEA 16,902
5.0%
6 DRUG INEFFECTIVE 16,837
5.0%
7 PAIN 15,247
4.5%
8 HEADACHE 12,998
3.8%
9 VOMITING 12,455
3.7%
10 ARTHRALGIA 11,973
3.5%
11 PYREXIA 11,366
3.3%
12 ACUTE KIDNEY INJURY 11,363
3.3%
13 ASTHENIA 11,194
3.3%
14 DIZZINESS 10,610
3.1%
15 CHRONIC KIDNEY DISEASE 10,569
3.1%
16 PNEUMONIA 10,388
3.1%
17 RASH 10,335
3.0%
18 CONDITION AGGRAVATED 8,956
2.6%
19 MALAISE 8,826
2.6%
20 PRURITUS 8,787
2.6%
21 FALL 8,661
2.6%
22 DEATH 8,547
2.5%
23 WEIGHT DECREASED 8,096
2.4%
24 ABDOMINAL PAIN 7,985
2.4%
25 GENERAL PHYSICAL HEALTH DETERIORATION 7,671
2.3%
26 WEIGHT INCREASED 7,489
2.2%
27 PERIPHERAL SWELLING 7,478
2.2%
28 ANAEMIA 7,327
2.2%
29 HYPERTENSION 7,293
2.1%
30 COUGH 7,228
2.1%

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.