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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 RIBOCICLIB Cause Product use complaint? 42 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Product use complaint have been filed in association with RIBOCICLIB (KISQALI). This represents 0.2% of all adverse event reports for RIBOCICLIB.

42
Reports of Product use complaint with RIBOCICLIB
0.2%
of all RIBOCICLIB reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product use complaint From RIBOCICLIB?

Of the 42 reports, 5 (11.9%) required hospitalization.

Is Product use complaint Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RIBOCICLIB. However, 42 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 Product use complaint?

TROFINETIDE (472) ENZALUTAMIDE (336) LIFITEGRAST (326) VOXELOTOR (298) CLASCOTERONE (285) NIRMATRELVIR\RITONAVIR (248) ABALOPARATIDE (224) ESTRADIOL (208) MOLNUPIRAVIR (206) ACETAMINOPHEN (202)

Which RIBOCICLIB Alternatives Have Lower Product use complaint Risk?

RIBOCICLIB vs RIBOFLAVIN RIBOCICLIB vs RIBOFLAVIN 5'-PHOSPHATE RIBOCICLIB vs RIBOFLAVIN 5^-PHOSPHATE RIBOCICLIB vs RIFABUTIN RIBOCICLIB vs RIFAMPICIN

Related Pages

RIBOCICLIB Full Profile All Product use complaint Reports All Drugs Causing Product use complaint RIBOCICLIB Demographics