Does BORTEZOMIB Cause Condition aggravated? 436 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 436 reports of Condition aggravated have been filed in association with BORTEZOMIB (bortezomib). This represents 0.9% of all adverse event reports for BORTEZOMIB.
436
Reports of Condition aggravated with BORTEZOMIB
0.9%
of all BORTEZOMIB reports
99
Deaths
152
Hospitalizations
How Dangerous Is Condition aggravated From BORTEZOMIB?
Of the 436 reports, 99 (22.7%) resulted in death, 152 (34.9%) required hospitalization, and 50 (11.5%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BORTEZOMIB. However, 436 reports have been filed with the FAERS database.
What Other Side Effects Does BORTEZOMIB Cause?
Plasma cell myeloma (6,683)
Off label use (4,754)
Neuropathy peripheral (4,067)
Drug ineffective (2,730)
Diarrhoea (2,244)
Thrombocytopenia (2,082)
Death (2,025)
Pneumonia (2,020)
Fatigue (1,757)
Neutropenia (1,530)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which BORTEZOMIB Alternatives Have Lower Condition aggravated Risk?
BORTEZOMIB vs BOSENTAN
BORTEZOMIB vs BOSENTAN\BOSENTAN
BORTEZOMIB vs BOSULIF
BORTEZOMIB vs BOSUTINIB
BORTEZOMIB vs BOTOX