Does BRENTUXIMAB VEDOTIN Cause C-reactive protein abnormal? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of C-reactive protein abnormal have been filed in association with BRENTUXIMAB VEDOTIN (ADCETRIS). This represents 0.3% of all adverse event reports for BRENTUXIMAB VEDOTIN.
27
Reports of C-reactive protein abnormal with BRENTUXIMAB VEDOTIN
0.3%
of all BRENTUXIMAB VEDOTIN reports
0
Deaths
16
Hospitalizations
How Dangerous Is C-reactive protein abnormal From BRENTUXIMAB VEDOTIN?
Of the 27 reports, 16 (59.3%) required hospitalization.
Is C-reactive protein abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BRENTUXIMAB VEDOTIN. However, 27 reports have been filed with the FAERS database.
What Other Side Effects Does BRENTUXIMAB VEDOTIN Cause?
Off label use (1,370)
Neuropathy peripheral (695)
Pyrexia (693)
Febrile neutropenia (684)
Death (602)
Neutropenia (561)
Hodgkin's disease (512)
Nausea (392)
Diarrhoea (385)
Anaemia (374)
What Other Drugs Cause C-reactive protein abnormal?
METHOTREXATE (3,734)
ADALIMUMAB (3,629)
ETANERCEPT (3,592)
ABATACEPT (3,402)
LEFLUNOMIDE (3,279)
TOCILIZUMAB (3,259)
HYDROXYCHLOROQUINE (3,245)
SULFASALAZINE (2,823)
INFLIXIMAB (2,676)
RITUXIMAB (2,608)
Which BRENTUXIMAB VEDOTIN Alternatives Have Lower C-reactive protein abnormal Risk?
BRENTUXIMAB VEDOTIN vs BREO ELLIPTA
BRENTUXIMAB VEDOTIN vs BREXANOLONE
BRENTUXIMAB VEDOTIN vs BREXPIPRAZOLE
BRENTUXIMAB VEDOTIN vs BREXUCABTAGENE AUTOLEUCEL
BRENTUXIMAB VEDOTIN vs BRIGATINIB