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Index of reports
> Cases resulting in hospitalization (6)
Below is the selection of adverse event reports related to Tagamet (Cimetidine) that includes cases resulting in hospitalization.
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 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 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
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