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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 TAFASITAMAB Cause Haemoglobin decreased? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Haemoglobin decreased have been filed in association with TAFASITAMAB (MONJUVI). This represents 0.4% of all adverse event reports for TAFASITAMAB.

6
Reports of Haemoglobin decreased with TAFASITAMAB
0.4%
of all TAFASITAMAB reports
4
Deaths
2
Hospitalizations

How Dangerous Is Haemoglobin decreased From TAFASITAMAB?

Of the 6 reports, 4 (66.7%) resulted in death, 2 (33.3%) required hospitalization, and 5 (83.3%) 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 TAFASITAMAB. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does TAFASITAMAB Cause?

Disease progression (470) Diffuse large b-cell lymphoma (346) Off label use (203) Death (146) Neutropenia (99) Covid-19 (96) General physical health deterioration (75) Pneumonia (66) Febrile neutropenia (64) Drug ineffective (62)

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 TAFASITAMAB Alternatives Have Lower Haemoglobin decreased Risk?

TAFASITAMAB vs TAFASITAMAB-CXIX TAFASITAMAB vs TAFINLAR TAFASITAMAB vs TAFLUPROST TAFASITAMAB vs TAGRAXOFUSP-ERZS TAFASITAMAB vs TAHOR

Related Pages

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