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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 DARATUMUMAB Cause Hypersensitivity? 176 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 176 reports of Hypersensitivity have been filed in association with DARATUMUMAB (DARZALEX). This represents 0.6% of all adverse event reports for DARATUMUMAB.

176
Reports of Hypersensitivity with DARATUMUMAB
0.6%
of all DARATUMUMAB reports
8
Deaths
45
Hospitalizations

How Dangerous Is Hypersensitivity From DARATUMUMAB?

Of the 176 reports, 8 (4.5%) resulted in death, 45 (25.6%) required hospitalization, and 25 (14.2%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for DARATUMUMAB.

What Other Side Effects Does DARATUMUMAB Cause?

Plasma cell myeloma (2,980) Infusion related reaction (2,557) Off label use (2,494) Pneumonia (1,450) Neutropenia (1,351) Drug ineffective (1,110) Thrombocytopenia (1,089) Death (1,088) Pyrexia (1,032) Dyspnoea (996)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which DARATUMUMAB Alternatives Have Lower Hypersensitivity Risk?

DARATUMUMAB vs DARATUMUMAB\HYALURONIDASE-FIHJ DARATUMUMAB vs DARBEPOETIN ALFA DARATUMUMAB vs DARIDOREXANT DARATUMUMAB vs DARIFENACIN HYDROBROMIDE DARATUMUMAB vs DAROLUTAMIDE

Related Pages

DARATUMUMAB Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity DARATUMUMAB Demographics