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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 TIAPRIDE Cause Wrong patient received product? 19 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Wrong patient received product have been filed in association with TIAPRIDE. This represents 1.8% of all adverse event reports for TIAPRIDE.

19
Reports of Wrong patient received product with TIAPRIDE
1.8%
of all TIAPRIDE reports
0
Deaths
18
Hospitalizations

How Dangerous Is Wrong patient received product From TIAPRIDE?

Of the 19 reports, 18 (94.7%) 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 TIAPRIDE. However, 19 reports have been filed with the FAERS database.

What Other Side Effects Does TIAPRIDE Cause?

Fall (102) Somnolence (93) Drug ineffective (81) Confusional state (78) Off label use (76) Hypotension (70) Extrapyramidal disorder (59) Neuroleptic malignant syndrome (56) Vertigo (47) Hyponatraemia (43)

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 TIAPRIDE Alternatives Have Lower Wrong patient received product Risk?

TIAPRIDE vs TIAPROFENIC ACID TIAPRIDE vs TICAGRELOR TIAPRIDE vs TICLOPIDINE TIAPRIDE vs TIGECYCLINE TIAPRIDE vs TIKOSYN

Related Pages

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