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Index of reports
> Cases resulting in a serious event (23)
Below is the selection of adverse event reports related to Tagamet (Cimetidine) that includes cases resulting in a serious event.
Adverse event in 66 year old female receiving Tagamet (Cimetidine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-17
Patient: 66 year old female
Adverse reactions / side effects: Jaundice, Pyrexia, Liver Disorder, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Tagamet
Dosage: 600mg per day
Administration route: Oral
Indication: Abdominal Discomfort
Start date: 2007-09-25
End date: 2007-09-30
Oxatomide
Administration route: Oral
Indication: Eczema
Start date: 2007-09-03
End date: 2007-09-29
Other drugs received by patient: Maglax
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 79 year old female receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from Canada on 2007-10-04
Patient: 79 year old female
Adverse reactions / side effects: Dystonia, Tachycardia, Delirium
Suspect drug(s):
Tagamet
Dosage: 300mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Diphenhydramine HCL
Dosage: 25mg three times per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Maalox; Mercurochrome; Multi-Vitamin; Folic Acid; Zinc Sulfate; Isopto Tears
Adverse event in 90 year old male receiving Tagamet (Cimetidine)
Reported by a individual with unspecified qualification from Japan on 2007-10-01
Patient: 90 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, RED Blood Cell Count Decreased, Drug Ineffective, Gamma-Glutamyltransferase Increased, Platelet Count Decreased, Idiopathic Thrombocytopenic Purpura, Blood Immunoglobulin E Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Rifampicin
Administration route: Oral
Indication: Tuberculosis
Start date: 2007-04-26
End date: 2007-08-03
Iscotin / 00030201 /
Administration route: Oral
Indication: Tuberculosis
Start date: 2007-04-26
End date: 2007-08-03
Ebutol / 00022301 /
Administration route: Oral
Indication: Pulmonary Tuberculosis
Start date: 2007-04-26
End date: 2007-08-03
Ebutol / 00022301 /
Administration route: Oral
Indication: Tuberculous Pleurisy
Start date: 2007-04-26
End date: 2007-08-03
Tagamet
Administration route: Oral
Indication: Gastrooesophageal Reflux Prophylaxis
Start date: 2007-04-15
End date: 2007-08-03
Other drugs received by patient: Mucodyne; Mucosolvan; Codiene; Magmitt; Halfdigoxin
Adverse event in 77 year old male receiving Tagamet (Cimetidine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-31
Patient: 77 year old male
Adverse reactions / side effects: Drug Eruption, Dyspnoea, Interstitial Lung Disease, Rash Erythematous, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tagamet (Cimetidine)
Other drugs received by patient: Aspirin; Ferromia
Adverse event in 64 year old female receiving Tagamet (Cimetidine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-07-31
Patient: 64 year old female
Adverse reactions / side effects: C-Reactive Protein Increased, Pancytopenia, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tagamet
Start date: 2007-06-13
End date: 2007-06-22
Omeprazole
Start date: 2007-05-22
End date: 2007-06-12
Ciprofloxacin
Start date: 2007-06-12
End date: 2007-06-15
Prodif
Start date: 2007-06-13
End date: 2007-06-18
Vancomycin Hydrochloride
Start date: 2007-06-13
End date: 2007-06-14
Maxipime
Start date: 2007-06-15
End date: 2007-06-18
Other drugs received by patient: Gran; Predonine
Adverse event in 78 year old female receiving Tagamet (Cimetidine)
Reported by a pharmacist from Japan on 2007-07-30
Patient: 78 year old female, weighing 42.0 kg (92.4 pounds)
Adverse reactions / side effects: Drug Eruption, Oral Intake Reduced, Stomatitis, Rash Generalised, Mouth Ulceration, Rash, Oral Neoplasm, Eating Disorder, Oedema Mouth, Blood Glucose Increased, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Allopurinol
Dosage: 100mg per day
Administration route: Oral
Indication: Hyperuricaemia
Start date: 2007-05-11
End date: 2007-06-01
Towamin
Dosage: 50mg per day
Administration route: Oral
Indication: Hypertension
End date: 2007-06-04
Diovan
Dosage: 80mg twice per day
Administration route: Oral
Indication: Hypertension
End date: 2007-06-04
Coniel
Dosage: 4mg twice per day
Administration route: Oral
Indication: Hypertension
End date: 2007-06-04
Natrix
Dosage: 2mg per day
Administration route: Oral
Indication: Hypertension
End date: 2007-06-04
Furosemide
Dosage: 40mg per day
Administration route: Oral
Indication: Hypertension
End date: 2007-06-04
Glyburide
Dosage: 1.25mg per day
Administration route: Oral
Indication: Diabetes Mellitus
End date: 2007-06-19
Tagamet
Dosage: 200mg twice per day
Administration route: Oral
Indication: Gastritis
End date: 2007-06-04
Mecobalamin
Dosage: 500mcg twice per day
Administration route: Oral
Indication: Neuropathy Peripheral
End date: 2007-06-04
Other drugs received by patient: Japanese Medication; Halcion
Adverse event in male receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from United States on 2007-06-22
Patient: male
Adverse reactions / side effects: Haemorrhage, Drug Detoxification, Adverse Drug Reaction, Liver Disorder, Anxiety, Incoherent, Hyperplasia, T-Lymphocyte Count Decreased, Adverse Event, Leukopenia
Suspect drug(s):
Geodon
Paxil
Administration route: Oral
Indication: Dizziness
Start date: 2004-01-01
Tagamet
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 49 year old male receiving Tagamet (Cimetidine)
Reported by a physician from Japan on 2007-06-06
Patient: 49 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased
Suspect drug(s):
Mevalotin
Dosage: 10 mg/day
Administration route: Oral
Indication: Hyperlipidaemia
Tagamet
Dosage: 400 mg/day
Administration route: Oral
Aspirin
Dosage: 100 mg/day
Administration route: Oral
Indication: Cerebral Infarction
Sermion
Dosage: 15 mg/day
Administration route: Oral
Lamisil
Dosage: 125 mg/day
Administration route: Oral
Indication: Nail Tinea
Start date: 2006-12-28
End date: 2007-05-18
Adverse event in male receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from United States on 2007-05-29
Patient: male
Adverse reactions / side effects: Haemorrhage, Drug Detoxification, Adverse Drug Reaction, Liver Disorder, Anxiety, Incoherent, Hyperplasia, T-Lymphocyte Count Decreased, Adverse Event, Leukopenia
Suspect drug(s):
Paxil
Administration route: Oral
Indication: Dizziness
Start date: 2004-01-01
Geodon
Tagamet
Other drugs received by patient: NO Concurrent Medication
Adverse event in 46 year old female receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from Japan on 2007-05-25
Patient: 46 year old female
Adverse reactions / side effects: Hepatitis Acute
Suspect drug(s):
Tagamet (Cimetidine)
Other drugs received by patient: Omeprazole; Sofalcone; Tiquizium Bromide; Azulene Sulfonate Sodium L-Glutamine; Glucose; Blood Extract; Methylmethionine Sulfonium Chloride
Adverse event in 74 year old female receiving Tagamet (Cimetidine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-30
Patient: 74 year old female
Adverse reactions / side effects: Angle Closure Glaucoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Atarax
Dosage: daily dose:50mg-freq:frequency: once
Start date: 2007-03-19
End date: 2007-03-19
Ephedrine Hydrochloride
Dosage: daily dose:15mg-freq:frequency: once
Start date: 2007-03-19
End date: 2007-03-19
Nefopam Hydrochloride
Dosage: daily dose:40mg
Start date: 2007-03-19
End date: 2007-03-20
Tagamet
Dosage: daily dose:400mg
Administration route: Oral
Start date: 2007-03-19
End date: 2007-03-19
Cefuroxime Sodium
Dosage: daily dose:750mg
Start date: 2007-03-19
End date: 2007-03-20
Heparin-Fraction
Dosage: daily dose:40mg
Sodium
Other drugs received by patient: Bupivacaine; Morphine; Sufentanil Citrate; Paracetamol; Ketoprofen; Celiprolol; Ergotamine Tartrate and Caffeine; Saccharated Iron Oxide; Pantoprazole
Adverse event in 46 year old female receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from Japan on 2007-04-27
Patient: 46 year old female
Adverse reactions / side effects: Hepatitis Acute
Suspect drug(s):
Tagamet (Cimetidine)
Other drugs received by patient: Omeprazole; Sofalcone; Tiquizium Bromide; Azulene Sulfonate Sodium L-Glutamine; Glucose; Blood Extract; Methylmethionine Sulfonium Chloride
Adverse event in receiving Tagamet (Cimetidine)
Reported by a physician from Japan on 2007-04-23
Patient:
Adverse reactions / side effects: Dermatitis Bullous
Suspect drug(s):
Tagamet (Cimetidine)
Adverse event in 45 year old female receiving Tagamet (Cimetidine)
Reported by a pharmacist from Japan on 2007-04-23
Patient: 45 year old female
Adverse reactions / side effects: Asthma, Dyspnoea, Palpitations, Cough
Suspect drug(s):
Tagamet (Cimetidine)
Other drugs received by patient: Fero-Gradumet
Adverse event in 48 year old male receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from United States on 2007-03-01
Patient: 48 year old male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Nausea, Cerebral Atrophy, Drug Interaction, Amnesia, Haematemesis, Convulsion, Pancreatic Disorder, Overdose, Malaise, Hiccups, Multiple Sclerosis
Suspect drug(s):
Betaseron
Dosage: 8 miu, every 2d
Indication: Relapsing-Remitting Multiple Sclerosis
Start date: 2005-03-04
Prednisone
Dosage: 1 g, x 4 days
Start date: 2005-11-07
End date: 2005-11-10
Tagamet
Other drugs received by patient: Neurontin; Neurontin; Elavil; Elavil; Cimetidine HCL; Corticosteroids; Clonazepam
Adverse event in 60 year old male receiving Tagamet (Cimetidine)
Reported by a consumer/non-health professional from Japan on 2007-02-15
Patient: 60 year old male
Adverse reactions / side effects: Hallucination, Delusion
Suspect drug(s):
Tagamet (Cimetidine)
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
Adverse event in receiving Tagamet (Cimetidine)
Reported by a individual with unspecified qualification from Denmark on 2007-01-26
Patient:
Adverse reactions / side effects: Drug Exposure During Pregnancy, Congenital Musculoskeletal Anomaly
Suspect drug(s):
Azathioprine
Dosage: transplacentary
Tagamet
Dosage: transplacentary
Metoclopramide HCL
Dosage: transplacentary
Phenoxymethylpenicillin
Dosage: transplacentary
Prednisone TAB
Dosage: transplacentary
Acetaminophen and Codeine Phospahte
Dosage: transplacentary
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