Does ATAZANAVIR Cause Hyperbilirubinaemia? 140 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 140 reports of Hyperbilirubinaemia have been filed in association with ATAZANAVIR (Atazanavir Sulfate). This represents 2.6% of all adverse event reports for ATAZANAVIR.
140
Reports of Hyperbilirubinaemia with ATAZANAVIR
2.6%
of all ATAZANAVIR reports
1
Deaths
27
Hospitalizations
How Dangerous Is Hyperbilirubinaemia From ATAZANAVIR?
Of the 140 reports, 1 (0.7%) resulted in death, 27 (19.3%) required hospitalization, and 3 (2.1%) were considered life-threatening.
Is Hyperbilirubinaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATAZANAVIR. However, 140 reports have been filed with the FAERS database.
What Other Side Effects Does ATAZANAVIR Cause?
Foetal exposure during pregnancy (903)
Drug interaction (730)
Maternal exposure during pregnancy (653)
Depression (590)
Exposure during pregnancy (295)
Abortion spontaneous (275)
Premature baby (256)
Virologic failure (201)
Loss of personal independence in daily activities (167)
Premature delivery (159)
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 ATAZANAVIR Alternatives Have Lower Hyperbilirubinaemia Risk?
ATAZANAVIR vs ATAZANAVIR\COBICISTAT
ATAZANAVIR vs ATAZANAVIR\RITONAVIR
ATAZANAVIR vs ATENOLOL
ATAZANAVIR vs ATENOLOL\CHLORTHALIDONE
ATAZANAVIR vs ATEZOLIZUMAB