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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 THALIDOMIDE Cause Device related sepsis? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Device related sepsis have been filed in association with THALIDOMIDE (Thalomid). This represents 0.1% of all adverse event reports for THALIDOMIDE.

23
Reports of Device related sepsis with THALIDOMIDE
0.1%
of all THALIDOMIDE reports
22
Deaths
23
Hospitalizations

How Dangerous Is Device related sepsis From THALIDOMIDE?

Of the 23 reports, 22 (95.7%) resulted in death, 23 (100.0%) required hospitalization, and 16 (69.6%) were considered life-threatening.

Is Device related sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for THALIDOMIDE. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does THALIDOMIDE Cause?

Plasma cell myeloma (1,652) Off label use (1,356) Death (1,161) Neuropathy peripheral (1,068) Drug ineffective (789) Pneumonia (694) Fatigue (643) Constipation (461) Thrombocytopenia (429) Neutropenia (420)

What Other Drugs Cause Device related sepsis?

TEDUGLUTIDE (226) TREPROSTINIL (225) CYCLOPHOSPHAMIDE (130) RITUXIMAB (113) EPOPROSTENOL (89) CYCLOSPORINE (82) METHYLPREDNISOLONE (82) BORTEZOMIB (79) MACITENTAN (55) DEXAMETHASONE (53)

Which THALIDOMIDE Alternatives Have Lower Device related sepsis Risk?

THALIDOMIDE vs THALOMID THALIDOMIDE vs THEOPHYLLINE THALIDOMIDE vs THEOPHYLLINE ANHYDROUS THALIDOMIDE vs THIAMINE THALIDOMIDE vs THIOCOLCHICOSIDE

Related Pages

THALIDOMIDE Full Profile All Device related sepsis Reports All Drugs Causing Device related sepsis THALIDOMIDE Demographics