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Index of reports
> Cases resulting in life threatening events (13)
Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in life threatening events.
Adverse event in 56 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-10-30
Patient: 56 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Anaphylactic Reaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ranitidine
Adverse event in 56 year old female receiving Ranitidine
Reported by a pharmacist from Japan on 2007-10-05
Patient: 56 year old female
Adverse reactions / side effects: Anaphylactic Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Betamethasone Sodium Phosphate
Dosage: 24 mg; qd; iv
Indication: Allergy Prophylaxis
Start date: 2007-07-18
End date: 2007-07-18
Ranitidine
Dosage: 50 m;qd; iv
Start date: 2007-07-18
End date: 2007-07-18
Other drugs received by patient: Taxol; Solita-T; Veen-F
Adverse event in 17 year old male receiving Ranitidine
Reported by a physician from United States on 2007-06-29
Patient: 17 year old male
Adverse reactions / side effects: Mucosal Inflammation, Bacterial Sepsis, Diverticular Perforation, Gastritis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Decadron
Administration route: Oral
Pegaspargase
Indication: Acute Lymphocytic Leukaemia
Vincristine Sulfate
Indication: Acute Lymphocytic Leukaemia
Doxorubicin
Indication: Acute Lymphocytic Leukaemia
Ranitidine
Indication: Prophylaxis
Adverse event in 52 year old female receiving Ranitidine
Reported by a physician from Argentina on 2007-05-25
Patient: 52 year old female
Adverse reactions / side effects: Renal Failure, Skin Exfoliation, Intentional Self-Injury, Rash Pruritic
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Eskalith
Dosage: 900mg per day
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2007-04-27
End date: 2007-05-10
Lamotrigine
Dosage: 150mg per day
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-07-01
End date: 2007-04-27
Ranitidine
Indication: Drug USE FOR Unknown Indication
Levothyroxine Sodium
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: NO Concurrent Medication
Adverse event in 63 year old female receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-05-14
Patient: 63 year old female
Adverse reactions / side effects: Anaphylactic Reaction, Respiratory Arrest, Rash, Radial Pulse Abnormal, Discomfort, Loss of Consciousness
Adverse event resulted in: life threatening event
Suspect drug(s):
Ranitidine
Indication: Premedication
Ranitidine
Indication: Chemotherapy
Dexchlorpheniramine
Indication: Premedication
Dexchlorpheniramine
Indication: Chemotherapy
Other drugs received by patient: Methylprednisolone 16mg TAB; Methylprednisolone 16mg TAB; Granisetron; Paclitaxel; Carboplatin
Adverse event in 32 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-23
Patient: 32 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Rash Generalised, Drug Exposure During Pregnancy, Urticaria, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Ranitidine
Adverse event in 32 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-04-17
Patient: 32 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Rash Generalised, Urticaria, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Ranitidine
Adverse event in male receiving Ranitidine
Reported by a consumer/non-health professional from Spain on 2007-04-16
Patient: male
Adverse reactions / side effects: Urticaria, Bronchospasm, Laryngeal Oedema
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Augmentin '125'
Indication: Drug USE FOR Unknown Indication
Start date: 2007-03-05
End date: 2007-03-05
Ranitidine
Dosage: 50mg per day
Indication: Prophylaxis
Start date: 2007-03-05
End date: 2007-03-05
Perfalgan
Indication: Prophylaxis
Start date: 2007-03-05
End date: 2007-03-05
Adverse event in 32 year old female receiving Ranitidine
Reported by a individual with unspecified qualification from United States on 2007-04-13
Patient: 32 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Rash Generalised, Drug Exposure During Pregnancy, Urticaria, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Ranitidine
Adverse event in 54 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-02
Patient: 54 year old male
Adverse reactions / side effects: Incorrect Dose Administered, Multiple Drug Overdose, Blood Pressure Decreased, Haemodynamic Instability
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Simvastatin
Dosage: 600 mg, oral
Administration route: Oral
Ramipril
Dosage: 300 mg, oral
Administration route: Oral
Ranitidine
Dosage: 4500 mg, oral
Administration route: Oral
Adverse event in female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-03-02
Patient: female
Adverse reactions / side effects: Apgar Score LOW, Caesarean Section, Drug Exposure During Pregnancy, Foetal Heart Rate Decreased, Convulsion Neonatal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ranitidine
Adverse event in 80 year old female receiving Ranitidine
Reported by a individual with unspecified qualification from United Kingdom on 2007-01-30
Patient: 80 year old female
Adverse reactions / side effects: Respiratory Arrest, Cardiac Arrest, Hypoxic Encephalopathy, Electromechanical Dissociation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Chlorpheniramine Maleate
Dosage: 10 mg, intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Ranitidine
Dosage: 50 mg, intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Adverse event in 80 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-01-29
Patient: 80 year old female
Adverse reactions / side effects: Respiratory Arrest, Cardiac Arrest, Hypoxic Encephalopathy, Electromechanical Dissociation
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Chlorpheniramine Maleate
Dosage: 10mg unknown
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
Ranitidine
Dosage: 50mg unknown
Indication: Drug USE FOR Unknown Indication
Start date: 2006-01-02
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