Does PANTOPRAZOLE Cause Product dose omission issue? 261 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 261 reports of Product dose omission issue have been filed in association with PANTOPRAZOLE (Pantoprazole Sodium). This represents 0.3% of all adverse event reports for PANTOPRAZOLE.
261
Reports of Product dose omission issue with PANTOPRAZOLE
0.3%
of all PANTOPRAZOLE reports
18
Deaths
165
Hospitalizations
How Dangerous Is Product dose omission issue From PANTOPRAZOLE?
Of the 261 reports, 18 (6.9%) resulted in death, 165 (63.2%) required hospitalization, and 26 (10.0%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PANTOPRAZOLE. However, 261 reports have been filed with the FAERS database.
What Other Side Effects Does PANTOPRAZOLE Cause?
Chronic kidney disease (28,127)
Acute kidney injury (15,961)
Renal failure (11,543)
End stage renal disease (8,523)
Renal injury (7,070)
Drug ineffective (5,487)
Off label use (4,279)
Pain (4,057)
Dyspnoea (4,052)
Fatigue (3,797)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which PANTOPRAZOLE Alternatives Have Lower Product dose omission issue Risk?
PANTOPRAZOLE vs PANTOPRAZOLE ANHYDROUS
PANTOPRAZOLE vs PANTOTHENIC ACID
PANTOPRAZOLE vs PAPAVERINE
PANTOPRAZOLE vs PARACETAMOL
PANTOPRAZOLE vs PARATHYROID HORMONE