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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 TRIMEBUTINE Cause Product administration error? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration error have been filed in association with TRIMEBUTINE. This represents 0.8% of all adverse event reports for TRIMEBUTINE.

5
Reports of Product administration error with TRIMEBUTINE
0.8%
of all TRIMEBUTINE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product administration error From TRIMEBUTINE?

Of the 5 reports, 5 (100.0%) 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 TRIMEBUTINE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does TRIMEBUTINE Cause?

Vomiting (46) Cardio-respiratory arrest (38) Fall (38) Acute kidney injury (37) Coma (36) Intentional overdose (33) Rash maculo-papular (33) Interstitial lung disease (32) Somnolence (31) Toxicity to various agents (30)

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 TRIMEBUTINE Alternatives Have Lower Product administration error Risk?

TRIMEBUTINE vs TRIMEPRAZINE TRIMEBUTINE vs TRIMETAZIDINE TRIMEBUTINE vs TRIMETHOBENZAMIDE TRIMEBUTINE vs TRIMETHOPRIM TRIMEBUTINE vs TRIMIPRAMINE

Related Pages

TRIMEBUTINE Full Profile All Product administration error Reports All Drugs Causing Product administration error TRIMEBUTINE Demographics