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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PANTOPRAZOLE Cause Wrong patient received product? 48 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Wrong patient received product have been filed in association with PANTOPRAZOLE (Pantoprazole Sodium). This represents 0.1% of all adverse event reports for PANTOPRAZOLE.

48
Reports of Wrong patient received product with PANTOPRAZOLE
0.1%
of all PANTOPRAZOLE reports
8
Deaths
17
Hospitalizations

How Dangerous Is Wrong patient received product From PANTOPRAZOLE?

Of the 48 reports, 8 (16.7%) resulted in death, 17 (35.4%) required hospitalization, and 6 (12.5%) were considered life-threatening.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PANTOPRAZOLE. However, 48 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 Wrong patient received product?

INSULIN LISPRO (334) CLOZAPINE (198) RISPERIDONE (176) OXAZEPAM (152) BISOPROLOL (150) LEVETIRACETAM (126) ACETAMINOPHEN (123) METFORMIN (116) INSULIN GLARGINE (114) CLONAZEPAM (112)

Which PANTOPRAZOLE Alternatives Have Lower Wrong patient received product Risk?

PANTOPRAZOLE vs PANTOPRAZOLE ANHYDROUS PANTOPRAZOLE vs PANTOTHENIC ACID PANTOPRAZOLE vs PAPAVERINE PANTOPRAZOLE vs PARACETAMOL PANTOPRAZOLE vs PARATHYROID HORMONE

Related Pages

PANTOPRAZOLE Full Profile All Wrong patient received product Reports All Drugs Causing Wrong patient received product PANTOPRAZOLE Demographics