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Index of reports
> Cases resulting in death (7)
Below is the selection of adverse event reports related to Zyrtec (Cetirizine) that includes cases resulting in death.
Adverse event in male receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-05-25
Patient: male
Adverse reactions / side effects: Abnormal Behaviour
Adverse event resulted in: death
Suspect drug(s):
Zyrtec (Cetirizine)
Other drugs received by patient: Clemastine Fumarate
Adverse event in male receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-05-08
Patient: male
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Zyrtec (Cetirizine)
Other drugs received by patient: Clemastine Fumarate
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-03-23
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Hepatic Cyst, Coma Hepatic, Hepatic Failure, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-03-16
Patient: female
Adverse reactions / side effects: Foetal Distress Syndrome, Oligohydramnios, Drug Exposure During Pregnancy, Intra-Uterine Death, Foetal Growth Retardation
Adverse event resulted in: death
Suspect drug(s):
Temesta
Dosage: df; unk; tran-p
Start date: 2005-01-25
End date: 2005-07-07
Fluctine
Dosage: df; unk; tran-p
Start date: 2005-01-25
End date: 2005-07-07
Zyrtec
Dosage: df;;tran-p
Start date: 2005-01-25
End date: 2005-07-07
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-03-15
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Coma Hepatic, Hepatic Failure, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-03-02
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Coma Hepatic, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-02-26
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Coma Hepatic, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
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