Does RABEPRAZOLE Cause Wrong technique in product usage process? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Wrong technique in product usage process have been filed in association with RABEPRAZOLE (Rabeprazole Sodium). This represents 0.1% of all adverse event reports for RABEPRAZOLE.
11
Reports of Wrong technique in product usage process with RABEPRAZOLE
0.1%
of all RABEPRAZOLE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Wrong technique in product usage process From RABEPRAZOLE?
Of the 11 reports, 2 (18.2%) required hospitalization, and 1 (9.1%) 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 RABEPRAZOLE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does RABEPRAZOLE Cause?
Chronic kidney disease (4,773)
Renal failure (3,135)
Acute kidney injury (2,545)
End stage renal disease (1,295)
Tubulointerstitial nephritis (1,125)
Death (857)
Drug ineffective (732)
Dyspnoea (423)
Gastrooesophageal reflux disease (416)
Headache (387)
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 RABEPRAZOLE Alternatives Have Lower Wrong technique in product usage process Risk?
RABEPRAZOLE vs RACECADOTRIL
RABEPRAZOLE vs RADIATION THERAPY
RABEPRAZOLE vs RADIUM RA-223 DICHLORIDE
RABEPRAZOLE vs RALOXIFENE
RABEPRAZOLE vs RALTEGRAVIR