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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 PROGESTERONE Cause Hyperbilirubinaemia? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hyperbilirubinaemia have been filed in association with PROGESTERONE (Progesterone). This represents 0.2% of all adverse event reports for PROGESTERONE.

12
Reports of Hyperbilirubinaemia with PROGESTERONE
0.2%
of all PROGESTERONE reports
2
Deaths
12
Hospitalizations

How Dangerous Is Hyperbilirubinaemia From PROGESTERONE?

Of the 12 reports, 2 (16.7%) resulted in death, 12 (100.0%) required hospitalization, and 3 (25.0%) 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 PROGESTERONE. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does PROGESTERONE Cause?

Off label use (736) Headache (701) Exposure during pregnancy (684) Pain (591) Hypersensitivity (579) Product use issue (542) Fatigue (535) Hyperhidrosis (534) Drug hypersensitivity (512) Hepatic enzyme increased (509)

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 PROGESTERONE Alternatives Have Lower Hyperbilirubinaemia Risk?

PROGESTERONE vs PROGRAF PROGESTERONE vs PROHANCE PROGESTERONE vs PROLIA PROGESTERONE vs PROMACTA PROGESTERONE vs PROMAZINE

Related Pages

PROGESTERONE Full Profile All Hyperbilirubinaemia Reports All Drugs Causing Hyperbilirubinaemia PROGESTERONE Demographics