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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 Product administration error? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product administration error have been filed in association with BIPERIDEN. This represents 0.7% of all adverse event reports for BIPERIDEN.

12
Reports of Product administration error with BIPERIDEN
0.7%
of all BIPERIDEN reports
0
Deaths
9
Hospitalizations

How Dangerous Is Product administration error From BIPERIDEN?

Of the 12 reports, 9 (75.0%) required hospitalization.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for BIPERIDEN. However, 12 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 Product administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which BIPERIDEN Alternatives Have Lower Product administration error 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 Product administration error Reports All Drugs Causing Product administration error BIPERIDEN Demographics