Does ESOMEPRAZOLE Cause Incorrect dose administered by device? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect dose administered by device have been filed in association with ESOMEPRAZOLE (Esomeprazole Magnesium). This represents 0.0% of all adverse event reports for ESOMEPRAZOLE.
14
Reports of Incorrect dose administered by device with ESOMEPRAZOLE
0.0%
of all ESOMEPRAZOLE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect dose administered by device From ESOMEPRAZOLE?
Of the 14 reports, 2 (14.3%) required hospitalization.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE. However, 14 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which ESOMEPRAZOLE Alternatives Have Lower Incorrect dose administered by device Risk?
ESOMEPRAZOLE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESOMEPRAZOLE vs ESOMEPRAZOLE\NAPROXEN
ESOMEPRAZOLE vs ESTAZOLAM
ESOMEPRAZOLE vs ESTRADIOL
ESOMEPRAZOLE vs ESTRADIOL CYPIONATE