Does ESOMEPRAZOLE Cause Device defective? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Device defective have been filed in association with ESOMEPRAZOLE (Esomeprazole Magnesium). This represents 0.0% of all adverse event reports for ESOMEPRAZOLE.
16
Reports of Device defective with ESOMEPRAZOLE
0.0%
of all ESOMEPRAZOLE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Device defective From ESOMEPRAZOLE?
Of the 16 reports, 11 (68.8%) required hospitalization, and 10 (62.5%) were considered life-threatening.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE. However, 16 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which ESOMEPRAZOLE Alternatives Have Lower Device defective Risk?
ESOMEPRAZOLE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESOMEPRAZOLE vs ESOMEPRAZOLE\NAPROXEN
ESOMEPRAZOLE vs ESTAZOLAM
ESOMEPRAZOLE vs ESTRADIOL
ESOMEPRAZOLE vs ESTRADIOL CYPIONATE