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Ursodiol (Ursodiol) - Life Threatening Events - Suspected Cause - Side Effect Reports


Index of reports > Life Threatening Events (1)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Ursodiol life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Ursodiol side effects in

Reported by a health professional (non-physician/pharmacist) from France on 2012-01-05


Reactions: Portal Hypertension, Gastrointestinal Haemorrhage, Shock Haemorrhagic, Hepatic Failure, Gastric Ulcer, Cerebral Haemorrhage, Haemodynamic Instability, Hepatitis Cholestatic, Oesophagitis, Truncus Coeliacus Thrombosis, Metabolic Acidosis, Cholecystitis Infective, Neurological Decompensation, Hepatic Fibrosis, Pancytopenia, Ascites, Renal Failure, Respiratory Failure, Sepsis, Oliguria, Cytomegalovirus Infection, Bone Marrow Toxicity, Infectious Peritonitis

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
    Dosage: oral
    Administration route: Oral
    Indication: Cholestasis
    Start date: 2011-07-01
    End date: 2011-08-23

    Dosage: 125 mg, qd, oral
    Administration route: Oral
    Indication: Autoimmune Hepatitis
    Start date: 2011-07-01
    End date: 2011-08-23

Other drugs received by patient: Prednisone

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