Does TRABECTEDIN Cause Intentional product use issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional product use issue have been filed in association with TRABECTEDIN (YONDELIS). This represents 0.3% of all adverse event reports for TRABECTEDIN.
6
Reports of Intentional product use issue with TRABECTEDIN
0.3%
of all TRABECTEDIN reports
1
Deaths
3
Hospitalizations
How Dangerous Is Intentional product use issue From TRABECTEDIN?
Of the 6 reports, 1 (16.7%) resulted in death, 3 (50.0%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRABECTEDIN. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does TRABECTEDIN Cause?
Neutropenia (207)
Anaemia (189)
Thrombocytopenia (172)
Nausea (160)
Febrile neutropenia (142)
Pancytopenia (124)
Vomiting (121)
Rhabdomyolysis (117)
Off label use (105)
Alanine aminotransferase increased (104)
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 TRABECTEDIN Alternatives Have Lower Intentional product use issue Risk?
TRABECTEDIN vs TRACLEER
TRABECTEDIN vs TRADJENTA
TRABECTEDIN vs TRALOKINUMAB-LDRM
TRABECTEDIN vs TRAMADOL
TRABECTEDIN vs TRAMADOL\TRAMADOL