Does ESOMEPRAZOLE Cause Product dose omission issue? 213 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 213 reports of Product dose omission issue have been filed in association with ESOMEPRAZOLE (Esomeprazole Magnesium). This represents 0.3% of all adverse event reports for ESOMEPRAZOLE.
213
Reports of Product dose omission issue with ESOMEPRAZOLE
0.3%
of all ESOMEPRAZOLE reports
3
Deaths
109
Hospitalizations
How Dangerous Is Product dose omission issue From ESOMEPRAZOLE?
Of the 213 reports, 3 (1.4%) resulted in death, 109 (51.2%) required hospitalization, and 2 (0.9%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE. However, 213 reports have been filed with the FAERS database.
What Other Side Effects Does ESOMEPRAZOLE Cause?
Chronic kidney disease (35,281)
Acute kidney injury (18,678)
Renal failure (14,633)
End stage renal disease (10,231)
Renal injury (9,440)
Gastrooesophageal reflux disease (4,746)
Drug ineffective (4,420)
Tubulointerstitial nephritis (4,024)
Off label use (3,180)
Pain (2,898)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which ESOMEPRAZOLE Alternatives Have Lower Product dose omission issue Risk?
ESOMEPRAZOLE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESOMEPRAZOLE vs ESOMEPRAZOLE\NAPROXEN
ESOMEPRAZOLE vs ESTAZOLAM
ESOMEPRAZOLE vs ESTRADIOL
ESOMEPRAZOLE vs ESTRADIOL CYPIONATE