Does ESOMEPRAZOLE Cause Wrong technique in product usage process? 138 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 138 reports of Wrong technique in product usage process have been filed in association with ESOMEPRAZOLE (Esomeprazole Magnesium). This represents 0.2% of all adverse event reports for ESOMEPRAZOLE.
138
Reports of Wrong technique in product usage process with ESOMEPRAZOLE
0.2%
of all ESOMEPRAZOLE reports
22
Deaths
44
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ESOMEPRAZOLE?
Of the 138 reports, 22 (15.9%) resulted in death, 44 (31.9%) required hospitalization, and 1 (0.7%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ESOMEPRAZOLE. However, 138 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ESOMEPRAZOLE Alternatives Have Lower Wrong technique in product usage process Risk?
ESOMEPRAZOLE vs ESOMEPRAZOLE\ESOMEPRAZOLE\ESOMEPRAZOLE
ESOMEPRAZOLE vs ESOMEPRAZOLE\NAPROXEN
ESOMEPRAZOLE vs ESTAZOLAM
ESOMEPRAZOLE vs ESTRADIOL
ESOMEPRAZOLE vs ESTRADIOL CYPIONATE