Does FUSIDATE Cause Hyperbilirubinaemia? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Hyperbilirubinaemia have been filed in association with FUSIDATE. This represents 7.2% of all adverse event reports for FUSIDATE.
14
Reports of Hyperbilirubinaemia with FUSIDATE
7.2%
of all FUSIDATE reports
5
Deaths
11
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From FUSIDATE?
Of the 14 reports, 5 (35.7%) resulted in death, 11 (78.6%) required hospitalization.
Is Hyperbilirubinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FUSIDATE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does FUSIDATE Cause?
Dysphagia (51)
Dyspepsia (49)
Cataract (48)
Dermatitis atopic (48)
Gastroenteritis (48)
Dyspnoea (20)
Pneumonia (19)
Lung disorder (18)
Therapeutic product effect incomplete (18)
Tachycardia (17)
What Other Drugs Cause Hyperbilirubinaemia?
METHOTREXATE (603)
RIBAVIRIN (560)
VINCRISTINE (479)
CYTARABINE (397)
PEGASPARGASE (349)
ACETAMINOPHEN (330)
CYCLOPHOSPHAMIDE (330)
DEXAMETHASONE (315)
CAPECITABINE (279)
SOFOSBUVIR (260)
Which FUSIDATE Alternatives Have Lower Hyperbilirubinaemia Risk?
FUSIDATE vs FUSIDIC ACID
FUSIDATE vs FUTIBATINIB
FUSIDATE vs GABAPENTIN
FUSIDATE vs GABAPENTIN ENACARBIL
FUSIDATE vs GADAVIST