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Index of reports
> All cases (65)
> Cases with Hepatic Function Abnormal (6)
Below is the selection of adverse event reports related to Allegra (Fexofenadine) that includes all cases where reactions include hepatic function abnormal.
Adverse event in 67 year old female receiving Allegra (Fexofenadine)
Reported by a pharmacist from Japan on 2007-10-02
Patient: 67 year old female
Adverse reactions / side effects: Malaise, Chest Discomfort, Hepatic Function Abnormal
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Herbal Preparation
Adverse event in 20 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-31
Patient: 20 year old male
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Celtect
Adverse event in receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-23
Patient:
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Celtect
Adverse event in 51 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-06
Patient: 51 year old female, weighing 46.0 kg (101.2 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal, C-Reactive Protein Increased, Pyrexia, White Blood Cell Count Increased, Hepatocellular Damage
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Rinderon / 00008501 /; Hirudoid / 00723701 /
Adverse event in 51 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-06-25
Patient: 51 year old female, weighing 46.0 kg (101.2 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal, Pyrexia, Hepatocellular Damage
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Rinderon / 00008501 /; Hirudoid / 00723701 /
Adverse event in 34 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-01-26
Patient: 34 year old male, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Indication: Dermatitis Atopic
Start date: 2006-03-01
End date: 2006-06-01
Allegra
Administration route: Oral
Start date: 2006-08-01
End date: 2006-12-05
Ourengedokutou
Indication: Dermatitis Atopic
Start date: 2006-03-01
End date: 2006-06-01
Ourengedokutou
Administration route: Oral
Start date: 2006-08-01
End date: 2006-12-05
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