Does ACALABRUTINIB Cause Condition aggravated? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Condition aggravated have been filed in association with ACALABRUTINIB (CALQUENCE). This represents 0.3% of all adverse event reports for ACALABRUTINIB.
30
Reports of Condition aggravated with ACALABRUTINIB
0.3%
of all ACALABRUTINIB reports
6
Deaths
10
Hospitalizations
How Dangerous Is Condition aggravated From ACALABRUTINIB?
Of the 30 reports, 6 (20.0%) resulted in death, 10 (33.3%) required hospitalization, and 2 (6.7%) 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 ACALABRUTINIB. However, 30 reports have been filed with the FAERS database.
What Other Side Effects Does ACALABRUTINIB Cause?
Death (1,857)
Fatigue (536)
Headache (534)
Product dose omission issue (349)
Diarrhoea (320)
Fall (289)
Malignant neoplasm progression (285)
Contusion (270)
Dyspnoea (259)
Pneumonia (244)
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 ACALABRUTINIB Alternatives Have Lower Condition aggravated Risk?
ACALABRUTINIB vs ACAMPROSATE
ACALABRUTINIB vs ACARBOSE
ACALABRUTINIB vs ACCUTANE
ACALABRUTINIB vs ACEBUTOLOL
ACALABRUTINIB vs ACECLOFENAC