Does OMEPRAZOLE Cause Wrong technique in product usage process? 346 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 346 reports of Wrong technique in product usage process have been filed in association with OMEPRAZOLE (omeprazole sodium bicarbonate). This represents 0.4% of all adverse event reports for OMEPRAZOLE.
346
Reports of Wrong technique in product usage process with OMEPRAZOLE
0.4%
of all OMEPRAZOLE reports
30
Deaths
53
Hospitalizations
How Dangerous Is Wrong technique in product usage process From OMEPRAZOLE?
Of the 346 reports, 30 (8.7%) resulted in death, 53 (15.3%) required hospitalization, and 2 (0.6%) 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 OMEPRAZOLE. However, 346 reports have been filed with the FAERS database.
What Other Side Effects Does OMEPRAZOLE Cause?
Chronic kidney disease (35,759)
Acute kidney injury (19,260)
Renal failure (14,721)
End stage renal disease (10,356)
Renal injury (9,482)
Tubulointerstitial nephritis (4,809)
Drug ineffective (4,355)
Gastrooesophageal reflux disease (3,929)
Pain (3,602)
Nephrogenic anaemia (2,873)
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 OMEPRAZOLE Alternatives Have Lower Wrong technique in product usage process Risk?
OMEPRAZOLE vs OMEPRAZOLE\SODIUM BICARBONATE
OMEPRAZOLE vs OMNIPAQUE
OMEPRAZOLE vs OMNISCAN
OMEPRAZOLE vs ONABOTULINUMTOXINA
OMEPRAZOLE vs ONASEMNOGENE ABEPARVOVEC