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Index of reports
> Cases resulting in a serious event (95)
> Cases with Hypersensitivity (11)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in a serious event where reactions include hypersensitivity.
Adverse event in 55 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-04-23
Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Vomiting, Hypersensitivity, Dyspnoea, Feeling Cold, Loss of Consciousness, Malaise, Depressed Level of Consciousness, Blood Pressure Decreased, Cold Sweat, Shock
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Decadron
Dosage: 20mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Kytril
Dosage: 3mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Other drugs received by patient: Unknown Medication; Pursennid; Magnesium Oxide; Flomox; Solantal; Slow-FE; Seishoku; Restamin; Paclitaxel; Pirarubicin Hydrochloride; Carboplatin
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from United Kingdom on 2007-04-23
Patient: 35 year old female
Adverse reactions / side effects: Hypersensitivity, Mydriasis, Pharyngeal Oedema, Miosis, Aphasia, Vision Blurred, Oxygen Saturation Decreased, Laryngospasm
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Cefuroxime; Cyclizine; Metronidazole; Ondansetron; Paracetamol; Tinzaparin; Paracetamol
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-03-20
Patient: 35 year old female
Adverse reactions / side effects: Mydriasis, Hypersensitivity, Aphasia, Pharyngeal Oedema, Miosis, Vision Blurred, Pharmaceutical Product Complaint, Laryngospasm, Oxygen Saturation Decreased
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 74 year old female receiving Zantac (Ranitidine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-03-16
Patient: 74 year old female, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Vomiting, Pruritus, Hypersensitivity, Formication, Erythema, Sense of Oppression
Adverse event resulted in: hospitalization
Suspect drug(s):
Solu-Medrol
Dosage: daily dose:120mg-freq:every day
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Carboplatin
Dosage: daily dose:340mg-freq:every day
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Paclitaxel
Dosage: daily dose:220mg
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Polaramine
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Zantac
Dosage: daily dose:50mg-freq:every day
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Other drugs received by patient: Ondansetron HCL
Adverse event in 74 year old female receiving Zantac (Ranitidine)
Reported by a individual with unspecified qualification from France on 2007-03-13
Patient: 74 year old female, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Vomiting, Pruritus, Hypersensitivity, Formication, Erythema, Sense of Oppression
Adverse event resulted in: hospitalization
Suspect drug(s):
Solu-Medrol
Dosage: daily dose:120mg
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Carboplatin
Dosage: daily dose:340mg
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Paclitaxel
Dosage: daily dose:220mg
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Polaramine
Indication: Ovarian Cancer
Start date: 2007-01-23
End date: 2007-01-23
Zantac
Dosage: daily dose:50mg
Indication: Ovarian Cancer
Other drugs received by patient: Ondansetron HCL
Adverse event in 74 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from France on 2007-02-26
Patient: 74 year old female, weighing 49.0 kg (107.8 pounds)
Adverse reactions / side effects: Vomiting, Pruritus, Hypersensitivity, Formication, Erythema, Sense of Oppression
Adverse event resulted in: hospitalization
Suspect drug(s):
Zantac
Dosage: 50mg per day
Start date: 2007-01-23
End date: 2007-01-23
Taxol
Dosage: 220mg per day
Start date: 2007-01-23
End date: 2007-01-23
Carboplatin
Dosage: 340mg per day
Start date: 2007-01-23
End date: 2007-01-23
Solu-Medrol
Dosage: 120mg per day
Start date: 2007-01-23
End date: 2007-01-23
Polaramine
Dosage: 5mg per day
Start date: 2007-01-23
End date: 2007-01-23
Other drugs received by patient: Zofran
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-02-09
Patient: 35 year old female
Adverse reactions / side effects: Mydriasis, Hypersensitivity, Aphasia, Pharyngeal Oedema, Miosis, Vision Blurred, Pharmaceutical Product Complaint, Laryngospasm, Oxygen Saturation Decreased
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 55 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-02-09
Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Vomiting, Hypersensitivity, Dyspnoea, Feeling Cold, Loss of Consciousness, Malaise, Depressed Level of Consciousness, Blood Pressure Decreased, Cold Sweat, Shock
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Decadron
Dosage: 20mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Kytril
Dosage: 3mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Other drugs received by patient: Unknown Medication; Pursennid; Magnesium Oxide; Flomox; Solantal; Slow-FE; Seishoku; Restamin; Paclitaxel; Pirarubicin Hydrochloride; Carboplatin
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-02-08
Patient: 35 year old female
Adverse reactions / side effects: Mydriasis, Hypersensitivity, Aphasia, Pharyngeal Oedema, Miosis, Vision Blurred, Pharmaceutical Product Complaint, Laryngospasm, Oxygen Saturation Decreased
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 35 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-01-25
Patient: 35 year old female
Adverse reactions / side effects: Mydriasis, Hypersensitivity, Aphasia, Pharyngeal Oedema, Miosis, Vision Blurred, Pharmaceutical Product Complaint, Laryngospasm, Oxygen Saturation Decreased
Suspect drug(s):
Zantac (Ranitidine)
Adverse event in 55 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from Japan on 2007-01-18
Patient: 55 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Vomiting, Dyspnoea, Hypersensitivity, Loss of Consciousness, Feeling Cold, Malaise, Depressed Level of Consciousness, Blood Pressure Decreased, Cold Sweat
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Decadron
Dosage: 20mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Kytril
Dosage: 3mg per day
Indication: Premedication
Start date: 2006-12-11
End date: 2006-12-11
Other drugs received by patient: Unknown Medication; Pursennid; Magnesium Oxide; Flomox; Solantal; Slow-FE; Seishoku; Restamin; Paclitaxel; Pirarubicin Hydrochloride; Carboplatin
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