Dexlansoprazole

Common brands: Dexilant, Nexium, Prevacid, Protonix Delayed-Release, Protonix I.V.

Top reporter: Takeda Pharmaceuticals America, Inc.

Proton Pump Inhibitor [EPC]Nonsteroidal Anti-inflammatory Drug [EPC]Corticosteroid [EPC]Benzodiazepine [EPC]Histamine-2 Receptor Antagonist [EPC]
41,146
Total Reports
11,230
Serious Reports
3,664
Death Reports
30
Reported Reactions
Death Report Ratio: High (8.90%)

Patient Demographics

Male
8,992
Female
19,389

Reported Adverse Reactions (30)

Side effects reported in FDA adverse event reports for Dexlansoprazole.

# Reaction Reports % of Total
1 CHRONIC KIDNEY DISEASE 16,100
20.9%
2 ACUTE KIDNEY INJURY 7,798
10.1%
3 RENAL FAILURE 6,721
8.7%
4 END STAGE RENAL DISEASE 4,859
6.3%
5 RENAL INJURY 4,339
5.6%
6 DRUG INEFFECTIVE 2,556
3.3%
7 FATIGUE 2,385
3.1%
8 OFF LABEL USE 2,274
3.0%
9 TUBULOINTERSTITIAL NEPHRITIS 2,190
2.8%
10 NAUSEA 2,161
2.8%
11 DIARRHOEA 1,971
2.6%
12 HEADACHE 1,933
2.5%
13 PAIN 1,927
2.5%
14 DEATH 1,856
2.4%
15 DYSPNOEA 1,581
2.1%
16 GASTROOESOPHAGEAL REFLUX DISEASE 1,440
1.9%
17 ARTHRALGIA 1,410
1.8%
18 DIZZINESS 1,193
1.5%
19 REBOUND ACID HYPERSECRETION 1,167
1.5%
20 COUGH 1,156
1.5%
21 VOMITING 1,126
1.5%
22 ABDOMINAL PAIN 1,120
1.5%
23 PNEUMONIA 1,097
1.4%
24 MALAISE 1,094
1.4%
25 CONDITION AGGRAVATED 1,082
1.4%
26 ASTHENIA 1,059
1.4%
27 WEIGHT DECREASED 879
1.1%
28 PAIN IN EXTREMITY 875
1.1%
29 ABDOMINAL PAIN UPPER 872
1.1%
30 NEPHROGENIC ANAEMIA 840
1.1%

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.