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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 MOSUNETUZUMAB-AXGB Cause Disease progression? 25 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 25 reports of Disease progression have been filed in association with MOSUNETUZUMAB-AXGB. This represents 12.6% of all adverse event reports for MOSUNETUZUMAB-AXGB.

25
Reports of Disease progression with MOSUNETUZUMAB-AXGB
12.6%
of all MOSUNETUZUMAB-AXGB reports
2
Deaths
9
Hospitalizations

How Dangerous Is Disease progression From MOSUNETUZUMAB-AXGB?

Of the 25 reports, 2 (8.0%) resulted in death, 9 (36.0%) required hospitalization, and 1 (4.0%) were considered life-threatening.

Is Disease progression Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MOSUNETUZUMAB-AXGB. However, 25 reports have been filed with the FAERS database.

What Other Side Effects Does MOSUNETUZUMAB-AXGB Cause?

Cytokine release syndrome (52) Pyrexia (27) Off label use (20) Rash (18) No adverse event (16) Neutropenia (13) Thrombocytopenia (9) Chills (8) Fatigue (8) Death (7)

What Other Drugs Cause Disease progression?

RITUXIMAB (7,282) CYCLOPHOSPHAMIDE (7,100) DOXORUBICIN (6,165) VINCRISTINE (5,252) PREDNISONE (5,096) BEVACIZUMAB (4,653) DEXAMETHASONE (4,545) CARBOPLATIN (4,538) CAPECITABINE (3,808) ETOPOSIDE (3,776)

Which MOSUNETUZUMAB-AXGB Alternatives Have Lower Disease progression Risk?

MOSUNETUZUMAB-AXGB vs MOXIFLOXACIN MOSUNETUZUMAB-AXGB vs MOXIFLOXACIN\MOXIFLOXACIN MOSUNETUZUMAB-AXGB vs MOXONIDINE MOSUNETUZUMAB-AXGB vs MS CONTIN MOSUNETUZUMAB-AXGB vs MULTAQ

Related Pages

MOSUNETUZUMAB-AXGB Full Profile All Disease progression Reports All Drugs Causing Disease progression MOSUNETUZUMAB-AXGB Demographics