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Index of reports
> Cases resulting in death (6)
Below is the selection of adverse event reports related to Tagamet (Cimetidine) that includes cases resulting in death.
Adverse event in 83 year old female receiving Tagamet (Cimetidine)
Reported by a physician from Japan on 2007-10-16
Patient: 83 year old female
Adverse reactions / side effects: Multi-Organ Failure, Dialysis, Disseminated Intravascular Coagulation, Rash Papular, Condition Aggravated, Toxic Epidermal Necrolysis, Altered State of Consciousness, Renal Failure Acute
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Rinderon-VG (Betamethasone Valerate / Gentamicin Sulfate) (Betamethasone
Dosage: 10 mg, qd
Indication: Dermatitis Contact
Start date: 2006-09-12
End date: 2006-09-14
Baktar (Sulfamethoxazole / Trimethoprim) (NO Pref. Name)
Dosage: 2 df, qd; po
Administration route: Oral
Indication: Pneumocystis Jiroveci Pneumonia
Start date: 2006-06-17
End date: 2006-09-14
Tagamet
Dosage: 400 mg;qd;po
Administration route: Oral
Indication: Gastritis
Start date: 2006-01-31
End date: 2006-09-14
Stromectol (Overmectin) (NO Pref. Name)
Dosage: 9 mg, qd; po
Administration route: Oral
Indication: Acarodermatitis
Start date: 2006-09-05
End date: 2006-09-05
Other drugs received by patient: Basen; Norvasc; Prednisolone; Eurax
Adverse event in 83 year old female receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from Japan on 2007-10-11
Patient: 83 year old female
Adverse reactions / side effects: Pruritus, Disseminated Intravascular Coagulation, Rash Papular, Tongue Ulceration, Toxic Epidermal Necrolysis, Blood Potassium Increased, Rash, Skin Erosion, Acarodermatitis
Adverse event resulted in: death
Suspect drug(s):
Tagamet (Cimetidine)
Other drugs received by patient: Prednisolone; Norvasc; Basen; Baktar
Adverse event in 83 year old female receiving Tagamet (Cimetidine)
Reported by a physician from Japan on 2007-10-11
Patient: 83 year old female
Adverse reactions / side effects: Multi-Organ Failure, Disseminated Intravascular Coagulation, Toxic Epidermal Necrolysis
Adverse event resulted in: death
Suspect drug(s):
Stromectol
Administration route: Oral
Indication: Acarodermatitis
Start date: 2006-09-05
End date: 2006-09-05
Tagamet
Administration route: Oral
Indication: Gastritis
Start date: 2006-01-31
End date: 2006-09-14
Baktar
Administration route: Oral
Indication: Pneumocystis Jiroveci Pneumonia
Start date: 2006-05-17
End date: 2006-09-14
Other drugs received by patient: Basen; Norvasc; Prednisolone
Adverse event in 83 year old female receiving Tagamet (Cimetidine)
Reported by a physician from Japan on 2007-10-08
Patient: 83 year old female
Adverse reactions / side effects: Multi-Organ Failure, Disseminated Intravascular Coagulation, Toxic Epidermal Necrolysis
Adverse event resulted in: death
Suspect drug(s):
Stromectol
Administration route: Oral
Indication: Acarodermatitis
Start date: 2006-09-05
End date: 2006-09-05
Tagamet
Administration route: Oral
Indication: Gastritis
Start date: 2006-01-31
End date: 2006-09-14
Other drugs received by patient: Basen; Norvasc; Prednisolone; Baktar
Adverse event in 65 year old female receiving Tagamet (Cimetidine)
Reported by a physician from Japan on 2007-06-14
Patient: 65 year old female, weighing 54.0 kg (118.8 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Gastrointestinal Haemorrhage, Pneumonia, Anaemia, General Physical Health Deterioration, Disease Progression, Glioblastoma, Pneumocystis Jiroveci Pneumonia, Cardiac Failure, Platelet Count Decreased
Adverse event resulted in: death, life threatening event, disablity
Suspect drug(s):
Temodal
Dosage: 75 mg/m2; qd; po
Administration route: Oral
Indication: Glioblastoma Multiforme
Start date: 2006-12-22
End date: 2007-01-29
Valproate Sodium
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-22
End date: 2007-02-05
Tagamet
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-22
End date: 2007-02-05
Betamethasone
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-12-22
Other drugs received by patient: Nasea-OD; Dogmatyl; Maalox Fast Blocker; Maglax; Pursennid; Levofloxacin; Aleviatin; Zantac; Takepron OD; Thyradin-S; Pariet
Adverse event in 77 year old female receiving Tagamet (Cimetidine)
Reported by a pharmacist from United Kingdom on 2007-02-13
Patient: 77 year old female
Adverse reactions / side effects: Death, Pulmonary Fibrosis
Adverse event resulted in: death
Suspect drug(s):
Tagamet (Cimetidine)
Other drugs received by patient: Solpadol; CO-Proxamol; Loperamide HCL; Lansoprazole
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