Does CEFOTAXIME Cause Hyperbilirubinaemia? 41 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 41 reports of Hyperbilirubinaemia have been filed in association with CEFOTAXIME (Cefotaxime). This represents 1.2% of all adverse event reports for CEFOTAXIME.
41
Reports of Hyperbilirubinaemia with CEFOTAXIME
1.2%
of all CEFOTAXIME reports
2
Deaths
10
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From CEFOTAXIME?
Of the 41 reports, 2 (4.9%) resulted in death, 10 (24.4%) required hospitalization.
Is Hyperbilirubinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CEFOTAXIME. However, 41 reports have been filed with the FAERS database.
What Other Side Effects Does CEFOTAXIME Cause?
Drug reaction with eosinophilia and systemic symptoms (276)
Drug ineffective (242)
Pyrexia (211)
Off label use (182)
Acute kidney injury (170)
Rash maculo-papular (151)
Toxic epidermal necrolysis (151)
Rash (125)
Hepatocellular injury (122)
Eosinophilia (121)
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 CEFOTAXIME Alternatives Have Lower Hyperbilirubinaemia Risk?
CEFOTAXIME vs CEFOXITIN
CEFOTAXIME vs CEFPODOXIME
CEFOTAXIME vs CEFPODOXIME PROXETIL
CEFOTAXIME vs CEFPROZIL
CEFOTAXIME vs CEFTAROLINE