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Index of reports
> All cases (23)
Below is the selection of adverse event reports related to Tagamet (Cimetidine) that includes all cases.
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 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 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 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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