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Index of reports
> Cases resulting in life threatening events (11)
Below is the selection of adverse event reports related to Atarax (Hydroxyzine) that includes cases resulting in life threatening events.
Adverse event in female receiving Atarax (Hydroxyzine)
Reported by a physician from Japan on 2007-06-18
Patient: female
Adverse reactions / side effects: Anaphylactoid Reaction
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax (Hydroxyzine)
Other drugs received by patient: Atropine Sulfate; Horizon
Adverse event in female receiving Atarax (Hydroxyzine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-02
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypotonia, Bradycardia, Respiratory Distress
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Largactil
Prozac
Dosage: daily dose:20mg-freq:once daily
Trandate
Indication: Complication of Pregnancy
Loxen
Indication: Complication of Pregnancy
Adverse event in female receiving Atarax (Hydroxyzine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-13
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Abortion Spontaneous
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Dosage: daily dose:25mg
Administration route: Oral
Start date: 2006-08-14
End date: 2006-11-21
Seropram
Dosage: daily dose:40mg
Administration route: Oral
Start date: 2006-07-04
End date: 2006-11-21
Zyprexa
Dosage: daily dose:7.5mg
Administration route: Oral
Zyprexa
Start date: 2006-08-14
End date: 2006-11-21
Lexomil
Administration route: Oral
Deroxat
Dosage: daily dose:40mg
Administration route: Oral
Other drugs received by patient: Largactil
Adverse event in 28 year old female receiving Atarax (Hydroxyzine)
Reported by a individual with unspecified qualification from Japan on 2007-02-21
Patient: 28 year old female
Adverse reactions / side effects: Overdose, Suicide Attempt, Coma
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax (Hydroxyzine)
Adverse event in female receiving Atarax (Hydroxyzine)
Reported by a physician from Japan on 2007-02-20
Patient: female
Adverse reactions / side effects: Respiratory Arrest, Bradycardia, Blood Pressure Decreased, Loss of Consciousness, Convulsion, Oxygen Saturation Decreased
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Xylocaine
Indication: Bronchoscopy
Start date: 2001-07-12
End date: 2001-07-12
Atropine Sulfate
Indication: Bronchoscopy
Start date: 2001-07-12
End date: 2001-07-12
Horizon
Indication: Epilepsy
Start date: 2001-07-12
End date: 2001-07-12
Atarax
Indication: Restlessness
Start date: 2001-07-12
End date: 2001-07-12
Pentazocine Lactate
Indication: Bronchoscopy
Start date: 2001-07-12
End date: 2001-07-12
Other drugs received by patient: Lanirapid; Bisoprolol Fumarate; Pilsicainide Hydrochloride; Warfarin Sodium
Adverse event in female receiving Atarax (Hydroxyzine)
Reported by a individual with unspecified qualification from France on 2007-02-16
Patient: female
Adverse reactions / side effects: Drug Exposure During Pregnancy, Hypotonia, Bradycardia, Respiratory Distress
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Largactil
Prozac
Dosage: daily dose:20mg-freq:once daily
Trandate
Indication: Complication of Pregnancy
Loxen
Indication: Complication of Pregnancy
Adverse event in 61 year old female receiving Atarax (Hydroxyzine)
Reported by a individual with unspecified qualification from France on 2007-02-13
Patient: 61 year old female
Adverse reactions / side effects: Renal Failure Acute, Haemodialysis
Adverse event resulted in: life threatening event
Suspect drug(s):
Lansoprazole
Dosage: 30 mg (1 d); per oral
Administration route: Oral
End date: 2006-12-17
Solupred (Prednisolone Sodium Sulfobenzoate) (Tablets)
Dosage: 20 mg (1 d); per oral
Administration route: Oral
Atarax
Dosage: per oral
Administration route: Oral
Glucophage
Dosage: 3000 mg (1 d) per oral
Administration route: Oral
End date: 2006-12-17
Solian (Amisulpride) (Tablets)
Dosage: 200 mg (1 d); per oral, per oral
Administration route: Oral
End date: 2006-12-17
Solian (Amisulpride) (Tablets)
Dosage: 200 mg (1 d); per oral, per oral
Administration route: Oral
Start date: 2006-12-27
Tegeline (Immunoglobulin Human Normal) (Injection)
Dosage: 80 mg (1 d); intravenous
Indication: Idiopathic Thrombocytopenic Purpura
Start date: 2006-12-13
End date: 2006-12-15
Other drugs received by patient: Potassium Acetate
Adverse event in receiving Atarax (Hydroxyzine)
Reported by a physician from Japan on 2007-02-12
Patient:
Adverse reactions / side effects: Ventricular Fibrillation
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax (Hydroxyzine)
Adverse event in 61 year old male receiving Atarax (Hydroxyzine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-06
Patient: 61 year old male
Adverse reactions / side effects: Renal Failure
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Administration route: Oral
Glucophage
Administration route: Oral
Solupred
Dosage: daily dose:20mg
Administration route: Oral
Solian
Dosage: daily dose:200mg
Administration route: Oral
Tegeline
Indication: Idiopathic Thrombocytopenic Purpura
Start date: 2006-12-13
End date: 2006-12-15
Lanzor
Dosage: daily dose:30mg
Administration route: Oral
Adverse event in 61 year old male receiving Atarax (Hydroxyzine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-05
Patient: 61 year old male
Adverse reactions / side effects: Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Glucophage
Administration route: Oral
End date: 2006-12-17
Tegeline
Indication: Idiopathic Thrombocytopenic Purpura
Start date: 2006-12-13
End date: 2006-12-15
Atarax
Administration route: Oral
Solupred
Solian
Administration route: Oral
Start date: 2006-12-17
Lanzor
Administration route: Oral
Start date: 2006-12-17
Other drugs received by patient: Potassium Acetate
Adverse event in 84 year old female receiving Atarax (Hydroxyzine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-19
Patient: 84 year old female
Adverse reactions / side effects: Agranulocytosis
Adverse event resulted in: life threatening event
Suspect drug(s):
Atarax
Dosage: daily dose:25mg
Administration route: Oral
Atenolol
Dosage: daily dose:12.5mg
Administration route: Oral
Hyperium
Dosage: daily dose:1mg
Administration route: Oral
Plavix
Dosage: text:1 df
Administration route: Oral
Indication: Ischaemic Stroke
Start date: 2006-07-17
End date: 2006-09-08
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