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Index of reports
> Cases resulting in life threatening events (25)
Below is the selection of adverse event reports related to Zantac (Ranitidine) that includes cases resulting in life threatening events.
Reports 1 - 25 of 25 Next >>
Adverse event in male receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-10-19
Patient: male
Adverse reactions / side effects: Interstitial Lung Disease, Lung Abscess
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Finibax
Finibax
Indication: Lung Abscess
Norvasc
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Itraconazole
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Zantac
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Ferromia
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Erythrocin Lactobionate
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Biofermin R
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Sucralfate
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Slow-K
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Mucosta
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Juzen-Taiho-TO
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Levofloxacin
Adverse event in 65 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-10-05
Patient: 65 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Vomiting, Cyanosis, Angiopathy, Pallor, Cough, Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Fallopian Tube Cancer
Start date: 2006-12-07
End date: 2007-04-05
Kytril
Dosage: 3mg per day
Indication: Fallopian Tube Cancer
Start date: 2006-12-07
End date: 2007-04-05
Other drugs received by patient: Decadron; Vena; Sodium Chloride 0.9%; Veen-D; Bosmin
Adverse event in 77 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-06-26
Patient: 77 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Hypoaesthesia, Long QT Syndrome, Dysstasia, Convulsions Local, C-Reactive Protein Increased, Aspartate Aminotransferase Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Cyanocobalamin; Vitamedin; Mucosta
Adverse event in 58 year old male receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from France on 2007-06-20
Patient: 58 year old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Bone Marrow Failure
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac
Start date: 2006-09-15
End date: 2006-09-15
Trandate
Start date: 2006-09-07
End date: 2006-09-17
Ciflox
Dosage: 750mg per day
Indication: Prostatitis
Start date: 2006-08-25
End date: 2006-09-14
Omeprazole
Start date: 2006-07-05
End date: 2006-09-12
Vfend
Start date: 2006-07-27
End date: 2006-09-11
Valganciclovir HCL
Start date: 2006-08-16
End date: 2006-09-11
Adverse event in 58 year old male receiving Zantac (Ranitidine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-20
Patient: 58 year old male
Adverse reactions / side effects: Bone Marrow Failure
Adverse event resulted in: life threatening event
Suspect drug(s):
Vfend
Start date: 2006-07-27
End date: 2006-09-11
Ciprofloxacin
Dosage: daily dose:750mg
Indication: Prostatitis
Start date: 2006-08-25
End date: 2006-09-14
Zantac
Start date: 2006-09-15
End date: 2006-09-15
Trandate
Start date: 2006-09-07
End date: 2006-09-17
Omeprazole
Start date: 2006-07-05
End date: 2006-09-12
Valganciclovir HCL
Start date: 2006-08-16
End date: 2006-09-11
Adverse event in 68 year old male receiving Zantac (Ranitidine)
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-05-23
Patient: 68 year old male
Adverse reactions / side effects: Dyspnoea, Suffocation Feeling
Adverse event resulted in: life threatening event
Suspect drug(s):
Toradol
Dosage: dose rptd as 1xod
Indication: Postoperative Analgesia
Start date: 2007-04-19
End date: 2007-04-19
Zantac
Dosage: dose rptd as 1xod
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-19
End date: 2007-04-19
Adverse event in 65 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-05-22
Patient: 65 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Vomiting, Cyanosis, Pallor, Cough, Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac
Dosage: 50mg per day
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-07
End date: 2007-04-05
Kytril
Dosage: 3mg per day
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-07
End date: 2007-04-05
Other drugs received by patient: Decadron; Vena; Sodium Chloride 0.9%; Veen-D; Bosmin
Adverse event in 72 year old male receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from Italy on 2007-05-21
Patient: 72 year old male
Adverse reactions / side effects: Dyspnoea, Suffocation Feeling
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-19
End date: 2007-04-19
Toradol
Start date: 2007-04-19
End date: 2007-04-19
Adverse event in 77 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-05-02
Patient: 77 year old female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Dysstasia, Convulsions Local, Hypoaesthesia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Cyanocobalamin; Vitamedin; Mucosta
Adverse event in 48 year old female receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from France on 2007-04-26
Patient: 48 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Nausea, Anaphylactic Shock, Skin Test Positive, Sense of Oppression, Loss of Consciousness, Generalised Erythema, Face Oedema, Cyanosis, Respiratory Arrest, Blood Pressure Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac
Start date: 2006-08-16
End date: 2006-08-16
Zantac
Dosage: 1unit single dose
Start date: 2006-09-13
End date: 2006-09-13
Polaramine
Start date: 2006-08-16
End date: 2006-08-16
Polaramine
Dosage: 1unit single dose
Start date: 2006-09-13
End date: 2006-09-13
Adverse event in 73 year old male receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-04-25
Patient: 73 year old male
Adverse reactions / side effects: Cholecystitis Acute, Duodenal Ulcer Haemorrhage, Cholestasis, Lymphocyte Stimulation Test Positive, Arrhythmia, Liver Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid RPD
Administration route: Oral
Indication: Duodenal Ulcer
Start date: 2006-12-17
End date: 2007-02-12
Promac
Administration route: Oral
Indication: Duodenal Ulcer
Start date: 2006-10-22
End date: 2007-02-15
Zantac
Indication: Cholecystitis
Start date: 2007-02-15
End date: 2007-02-21
Other drugs received by patient: Cefoperazone Sodium and Sulbactam Sodium; Allopurinol; Norvasc; Flivas
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 73 year old male receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-04-19
Patient: 73 year old male
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Pepcid RPD
Administration route: Oral
Indication: Duodenal Ulcer
Start date: 2006-12-17
End date: 2007-02-12
Promac
Administration route: Oral
Indication: Duodenal Ulcer
Zantac
Indication: Cholecystitis
Start date: 2007-02-15
End date: 2007-02-21
Other drugs received by patient: Cefoperazone Sodium and Sulbactam Sodium; Allopurinol; Norvasc; Flivas
Adverse event in 65 year old male receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-04-19
Patient: 65 year old male
Adverse reactions / side effects: Cardio-Respiratory Arrest, Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: Kytril; Decadron
Adverse event in 57 year old female receiving Zantac (Ranitidine)
Reported by a individual with unspecified qualification from Germany on 2007-04-10
Patient: 57 year old female
Adverse reactions / side effects: Myoclonus, Overdose, Bradypnoea, Miosis, Drug Interaction, Respiratory Depression, Hyperhidrosis, Somnolence
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Zantac
Dosage: unk / unknown / injection
Morphine
Dosage: unk / unknown / intravenous
Other drugs received by patient: Paclitaxel; ME-Prednisolone NA Succ.; Dexchlorpheniram.maleate; Alprazolam; Amitriptyline HCL; Gabapentin; Esomeprazole Magnesium; Ondansetron HCL; Metoclopramide HCL
Adverse event in 77 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-04-02
Patient: 77 year old female, weighing 55.0 kg (121.0 pounds)
Adverse reactions / side effects: Urinary Incontinence, Hypotension, Cyanosis, Palpitations, Depressed Level of Consciousness, Cold Sweat, Shock, Oxygen Saturation Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac
Dosage: 8ml per day
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Decadron
Dosage: 8ml per day
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Restamin
Dosage: 5tab per day
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-27
Other drugs received by patient: Solita-T No.3
Adverse event in 87 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-03-29
Patient: 87 year old female, weighing 38.0 kg (83.6 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Delirium, Anorexia, Depressed Level of Consciousness, Renal Failure Acute, Shock, White Blood Cell Count Increased
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Allopurinol
Dosage: 100mg per day
Administration route: Oral
Start date: 2007-02-08
Zantac
Dosage: 150mg per day
Administration route: Oral
Start date: 2007-02-08
Other drugs received by patient: Renivace; Artist; Amlodin; Unknown Medication
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 87 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-03-16
Patient: 87 year old female, weighing 38.0 kg (83.6 pounds)
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Allopurinol
Dosage: 100mg per day
Administration route: Oral
Start date: 2007-02-08
Zantac
Dosage: 150mg per day
Administration route: Oral
Start date: 2007-02-08
Other drugs received by patient: Renivace; Artist; Amlodin; Unknown Medication
Adverse event in 30 year old female receiving Zantac (Ranitidine)
Reported by a pharmacist from United Kingdom on 2007-02-20
Patient: 30 year old female
Adverse reactions / side effects: Anaphylactic Reaction
Adverse event resulted in: life threatening event
Suspect drug(s):
Maxolon
Dosage: 10 mg, intravenous
Start date: 2006-05-01
Zantac
Dosage: 50 mg, qd, intravenous
Start date: 2006-05-01
Zantac
Dosage: 50 mg, qdm, intravenous
Indication: Premedication
Start date: 2006-05-15
End date: 2006-05-15
Other drugs received by patient: Metoclopramide
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 79 year old female receiving Zantac (Ranitidine)
Reported by a physician from Japan on 2007-01-19
Patient: 79 year old female, weighing 42.0 kg (92.4 pounds)
Adverse reactions / side effects: Haemoglobin Decreased, Dyspnoea, Malaise, RED Blood Cell Count Decreased, Platelet Count Decreased, Neutropenia, Lymphocyte Stimulation Test Positive
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Indication: Rhinitis
Start date: 2006-11-02
End date: 2006-11-03
Ebastel
Administration route: Oral
Indication: Eczema
Start date: 2006-11-02
End date: 2006-11-05
Zantac
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-19
End date: 2006-11-10
Other drugs received by patient: Prednisolone; Calonal
Adverse event in 58 year old male receiving Zantac (Ranitidine)
Reported by a consumer/non-health professional from France on 2007-01-05
Patient: 58 year old male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Bone Marrow Failure, Bone Marrow Toxicity
Adverse event resulted in: life threatening event
Suspect drug(s):
Zantac
Start date: 2006-09-15
End date: 2006-09-15
Trandate
Start date: 2006-09-07
End date: 2006-09-17
Ciprofloxacin
Dosage: 750mg per day
Indication: Prostatitis
Start date: 2006-08-25
End date: 2006-09-14
Omeprazole
Start date: 2006-07-05
End date: 2006-09-12
Vfend
Start date: 2006-07-27
End date: 2006-09-11
Valganciclovir HCL
Start date: 2006-08-16
End date: 2006-09-11
Adverse event in 28 year old female receiving Zantac (Ranitidine)
Reported by a physician from Viet NAM on 2007-01-05
Patient: 28 year old female, weighing 65.0 kg (143.0 pounds)
Adverse reactions / side effects: Dyspnoea, Face Oedema, Drug Exposure During Pregnancy, Hypotension, Rash, Laryngeal Oedema
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zantac (Ranitidine)
Other drugs received by patient: General Endotracheal Anesthesia
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