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Index of reports
> Cases resulting in a serious event (55)
> Cases with Hepatic Function Abnormal (6)
Below is the selection of adverse event reports related to Allegra (Fexofenadine) that includes cases resulting in a serious event 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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