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Index of reports
> Cases resulting in life threatening events (4)
Below is the selection of adverse event reports related to Allegra (Fexofenadine) that includes cases resulting in life threatening events.
Adverse event in male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-04-30
Patient: male, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Pruritus, Anaemia, Antineutrophil Cytoplasmic Antibody Positive, Vasculitis, Glomerulonephritis Rapidly Progressive, Leukopenia
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Hyzaar
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-25
End date: 2007-02-21
Urinorm
Administration route: Oral
Indication: Hyperuricaemia
Start date: 2006-12-25
End date: 2007-02-21
Olmetec
Administration route: Oral
Indication: Hypertension
Start date: 2007-02-22
End date: 2007-03-07
Salobel
Administration route: Oral
Indication: Hyperuricaemia
Start date: 2007-02-22
End date: 2007-03-07
Allegra
Administration route: Oral
Indication: Pruritus
Start date: 2007-02-22
End date: 2007-03-07
Depas
Administration route: Oral
Indication: Pruritus
Start date: 2007-02-22
End date: 2007-03-07
Adverse event in male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-04-12
Patient: male, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Anaemia, Glomerulonephritis Rapidly Progressive
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Hyzaar
Administration route: Oral
Indication: Hypertension
Start date: 2006-12-25
End date: 2007-02-21
Urinorm
Administration route: Oral
Indication: Hyperuricaemia
Start date: 2006-12-25
End date: 2007-02-21
Olmetec
Administration route: Oral
Indication: Hypertension
Start date: 2007-02-22
End date: 2007-03-07
Salobel
Administration route: Oral
Indication: Hyperuricaemia
Start date: 2007-02-22
End date: 2007-03-07
Allegra
Administration route: Oral
Indication: Pruritus
Start date: 2007-02-22
End date: 2007-03-07
Depas
Administration route: Oral
Indication: Pruritus
Start date: 2007-02-22
End date: 2007-03-07
Adverse event in 62 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-02-21
Patient: 62 year old male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: life threatening event
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Cerekinon; Colonel; BUP-4; Blopress; Simaron
Adverse event in 79 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-01-19
Patient: 79 year old female, weighing 42.0 kg (92.4 pounds)
Adverse reactions / side effects: Haemoglobin Decreased, Dyspnoea, Malaise, RED Blood Cell Count Decreased, Platelet Count Decreased, Neutropenia, Lymphocyte Stimulation Test Positive
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Indication: Rhinitis
Start date: 2006-11-02
End date: 2006-11-03
Ebastel
Administration route: Oral
Indication: Eczema
Start date: 2006-11-02
End date: 2006-11-05
Zantac
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-19
End date: 2006-11-10
Other drugs received by patient: Prednisolone; Calonal
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