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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 TRABECTEDIN Cause Haemoglobin decreased? 32 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Haemoglobin decreased have been filed in association with TRABECTEDIN (YONDELIS). This represents 1.6% of all adverse event reports for TRABECTEDIN.

32
Reports of Haemoglobin decreased with TRABECTEDIN
1.6%
of all TRABECTEDIN reports
10
Deaths
19
Hospitalizations

How Dangerous Is Haemoglobin decreased From TRABECTEDIN?

Of the 32 reports, 10 (31.3%) resulted in death, 19 (59.4%) required hospitalization, and 12 (37.5%) were considered life-threatening.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for TRABECTEDIN. However, 32 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 Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which TRABECTEDIN Alternatives Have Lower Haemoglobin decreased Risk?

TRABECTEDIN vs TRACLEER TRABECTEDIN vs TRADJENTA TRABECTEDIN vs TRALOKINUMAB-LDRM TRABECTEDIN vs TRAMADOL TRABECTEDIN vs TRAMADOL\TRAMADOL

Related Pages

TRABECTEDIN Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased TRABECTEDIN Demographics