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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 GLOFITAMAB-GXBM Cause Hyperpyrexia? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Hyperpyrexia have been filed in association with GLOFITAMAB-GXBM. This represents 1.8% of all adverse event reports for GLOFITAMAB-GXBM.

9
Reports of Hyperpyrexia with GLOFITAMAB-GXBM
1.8%
of all GLOFITAMAB-GXBM reports
1
Deaths
1
Hospitalizations

How Dangerous Is Hyperpyrexia From GLOFITAMAB-GXBM?

Of the 9 reports, 1 (11.1%) resulted in death, 1 (11.1%) required hospitalization.

Is Hyperpyrexia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for GLOFITAMAB-GXBM. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does GLOFITAMAB-GXBM Cause?

Cytokine release syndrome (107) Disease progression (68) Off label use (68) Death (67) Pyrexia (45) No adverse event (28) Immune effector cell-associated neurotoxicity syndrome (25) Infection (20) Pneumonia (14) Condition aggravated (12)

What Other Drugs Cause Hyperpyrexia?

TRASTUZUMAB (146) RITUXIMAB (139) CYCLOPHOSPHAMIDE (133) PACLITAXEL (100) ZOLEDRONIC ACID (96) OXALIPLATIN (94) CARBOPLATIN (73) GEMCITABINE (72) VINCRISTINE (69) DABRAFENIB (68)

Which GLOFITAMAB-GXBM Alternatives Have Lower Hyperpyrexia Risk?

GLOFITAMAB-GXBM vs GLUCAGON GLOFITAMAB-GXBM vs GLUCAGON\GLUCAGON\WATER GLOFITAMAB-GXBM vs GLUCARPIDASE GLOFITAMAB-GXBM vs GLUCOPHAGE GLOFITAMAB-GXBM vs GLUCOSAMINE

Related Pages

GLOFITAMAB-GXBM Full Profile All Hyperpyrexia Reports All Drugs Causing Hyperpyrexia GLOFITAMAB-GXBM Demographics