DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Zyrtec (Cetirizine) - Adverse Event Reports - Death - Coma Hepatic

 



Index of reports > Cases resulting in death (7) > Cases with Coma Hepatic (4)

Below is the selection of adverse event reports related to Zyrtec (Cetirizine) that includes cases resulting in death where reactions include coma hepatic.

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 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

-- advertisement -- The American Red Cross
We comply with
HONcode standard.
Verify here.
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2009