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Index of reports
> Cases resulting in other serious reactions (34)
> Cases with Hypersensitivity (8)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in other serious reactions 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 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 2007-02-09
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 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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