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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 THIOTEPA Cause Hemiparesis? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hemiparesis have been filed in association with THIOTEPA (Thiotepa). This represents 0.1% of all adverse event reports for THIOTEPA.

8
Reports of Hemiparesis with THIOTEPA
0.1%
of all THIOTEPA reports
4
Deaths
2
Hospitalizations

How Dangerous Is Hemiparesis From THIOTEPA?

Of the 8 reports, 4 (50.0%) resulted in death, 2 (25.0%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Hemiparesis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for THIOTEPA. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does THIOTEPA Cause?

Off label use (762) Febrile neutropenia (645) Mucosal inflammation (616) Cytomegalovirus infection (446) Product use in unapproved indication (425) Pyrexia (359) Drug ineffective (358) Acute graft versus host disease in skin (355) Acute graft versus host disease (331) Cytomegalovirus infection reactivation (325)

What Other Drugs Cause Hemiparesis?

ASPIRIN (538) FINGOLIMOD (534) METHOTREXATE (534) RIVAROXABAN (363) PREDNISONE (359) METFORMIN (353) DIMETHYL (345) RITUXIMAB (331) CLOPIDOGREL BISULFATE (327) ATORVASTATIN (317)

Which THIOTEPA Alternatives Have Lower Hemiparesis Risk?

THIOTEPA vs THIOTHIXENE THIOTEPA vs THROMBIN THIOTEPA vs THROMBIN HUMAN THIOTEPA vs THYMOCYTE IMMUNE GLOBULIN NOS THIOTEPA vs THYMOGLOBULINE

Related Pages

THIOTEPA Full Profile All Hemiparesis Reports All Drugs Causing Hemiparesis THIOTEPA Demographics