Does URSODIOL Cause Condition aggravated? 97 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 97 reports of Condition aggravated have been filed in association with URSODIOL (Ursodiol). This represents 2.7% of all adverse event reports for URSODIOL.
97
Reports of Condition aggravated with URSODIOL
2.7%
of all URSODIOL reports
14
Deaths
60
Hospitalizations
How Dangerous Is Condition aggravated From URSODIOL?
Of the 97 reports, 14 (14.4%) resulted in death, 60 (61.9%) required hospitalization, and 2 (2.1%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for URSODIOL. However, 97 reports have been filed with the FAERS database.
What Other Side Effects Does URSODIOL Cause?
Off label use (444)
Drug ineffective (383)
Foetal exposure during pregnancy (262)
Maternal exposure during pregnancy (210)
Pruritus (197)
Premature baby (176)
Exposure during pregnancy (162)
Nausea (149)
Product use in unapproved indication (135)
Death (124)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which URSODIOL Alternatives Have Lower Condition aggravated Risk?
URSODIOL vs USTEKINUMAB
URSODIOL vs USTEKINUMAB-STBA
URSODIOL vs VADADUSTAT
URSODIOL vs VALACYCLOVIR
URSODIOL vs VALBENAZINE