|
Index of reports
> All cases (100)
> Cases with Hypersensitivity (11)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes all cases 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 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
|
