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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 BIPERIDEN Cause Wrong patient received product? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Wrong patient received product have been filed in association with BIPERIDEN. This represents 0.9% of all adverse event reports for BIPERIDEN.

16
Reports of Wrong patient received product with BIPERIDEN
0.9%
of all BIPERIDEN reports
0
Deaths
6
Hospitalizations

How Dangerous Is Wrong patient received product From BIPERIDEN?

Of the 16 reports, 6 (37.5%) required hospitalization.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BIPERIDEN. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does BIPERIDEN Cause?

Intentional overdose (164) Neuroleptic malignant syndrome (151) Suicide attempt (133) Intentional self-injury (127) Drug ineffective (124) Somnolence (123) Toxicity to various agents (99) Confusional state (93) Pyrexia (87) Intentional product misuse (86)

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 BIPERIDEN Alternatives Have Lower Wrong patient received product Risk?

BIPERIDEN vs BIRCH TRITERPENES BIPERIDEN vs BISACODYL BIPERIDEN vs BISACODYL OR DOCUSATE BIPERIDEN vs BISMUTH BIPERIDEN vs BISMUTH SUBCITRATE

Related Pages

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