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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

DEXLANSOPRAZOLE for Gastrooesophageal reflux disease: Side Effects & Safety Data

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There are 5,185 adverse event reports in the FDA FAERS database where DEXLANSOPRAZOLE was used for Gastrooesophageal reflux disease.

Most Reported Side Effects for DEXLANSOPRAZOLE

Side Effect Reports % Deaths Hosp.
Chronic kidney disease 15,973 66.5% 1,581 895
Acute kidney injury 7,599 31.7% 1,018 756
Renal failure 6,618 27.6% 1,319 677
End stage renal disease 4,800 20.0% 965 448
Renal injury 4,320 18.0% 319 409
Tubulointerstitial nephritis 2,177 9.1% 347 178
Death 1,417 5.9% 1,415 105
Rebound acid hypersecretion 1,160 4.8% 139 108
Gastrooesophageal reflux disease 1,013 4.2% 40 201
Drug ineffective 859 3.6% 60 294
Nephrogenic anaemia 825 3.4% 134 207
Renal haemangioma 786 3.3% 43 2
Hyperchlorhydria 751 3.1% 60 1
Off label use 706 2.9% 123 218
Renal impairment 666 2.8% 71 56

Other Indications for DEXLANSOPRAZOLE

Product used for unknown indication (7,779) Dyspepsia (450) Gastrointestinal disorder (280) Barrett's oesophagus (162) Gastritis (134) Oesophagitis (82) Hiatus hernia (80) Ulcer (59) Gastric disorder (54) Hyperchlorhydria (53)

Other Drugs Used for Gastrooesophageal reflux disease

RANITIDINE (141,291) OMEPRAZOLE (28,339) ESOMEPRAZOLE (27,743) PANTOPRAZOLE (18,706) LANSOPRAZOLE (17,671) RABEPRAZOLE (1,689) NEXIUM (1,209) FAMOTIDINE (1,099) VONOPRAZAN (766) OMEPRAZOLE\SODIUM BICARBONATE (762)

Related Pages

DEXLANSOPRAZOLE Full Profile All Gastrooesophageal reflux disease Drugs DEXLANSOPRAZOLE Demographics DEXLANSOPRAZOLE Timeline