Does RIBOCICLIB Cause Condition aggravated? 223 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 223 reports of Condition aggravated have been filed in association with RIBOCICLIB (KISQALI). This represents 0.8% of all adverse event reports for RIBOCICLIB.
223
Reports of Condition aggravated with RIBOCICLIB
0.8%
of all RIBOCICLIB reports
35
Deaths
88
Hospitalizations
How Dangerous Is Condition aggravated From RIBOCICLIB?
Of the 223 reports, 35 (15.7%) resulted in death, 88 (39.5%) required hospitalization, and 11 (4.9%) 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 RIBOCICLIB. However, 223 reports have been filed with the FAERS database.
What Other Side Effects Does RIBOCICLIB Cause?
Neutropenia (3,585)
Nausea (3,404)
Fatigue (3,327)
Malignant neoplasm progression (2,468)
Death (2,452)
Vomiting (1,953)
Diarrhoea (1,830)
White blood cell count decreased (1,683)
Pain (1,637)
Metastases to bone (1,538)
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 RIBOCICLIB Alternatives Have Lower Condition aggravated Risk?
RIBOCICLIB vs RIBOFLAVIN
RIBOCICLIB vs RIBOFLAVIN 5'-PHOSPHATE
RIBOCICLIB vs RIBOFLAVIN 5^-PHOSPHATE
RIBOCICLIB vs RIFABUTIN
RIBOCICLIB vs RIFAMPICIN