Does THALIDOMIDE Cause Intentional product use issue? 243 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 243 reports of Intentional product use issue have been filed in association with THALIDOMIDE (Thalomid). This represents 1.4% of all adverse event reports for THALIDOMIDE.
243
Reports of Intentional product use issue with THALIDOMIDE
1.4%
of all THALIDOMIDE reports
26
Deaths
30
Hospitalizations
How Dangerous Is Intentional product use issue From THALIDOMIDE?
Of the 243 reports, 26 (10.7%) resulted in death, 30 (12.3%) required hospitalization, and 9 (3.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for THALIDOMIDE. However, 243 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which THALIDOMIDE Alternatives Have Lower Intentional product use issue Risk?
THALIDOMIDE vs THALOMID
THALIDOMIDE vs THEOPHYLLINE
THALIDOMIDE vs THEOPHYLLINE ANHYDROUS
THALIDOMIDE vs THIAMINE
THALIDOMIDE vs THIOCOLCHICOSIDE