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Index of reports
> Cases resulting in life threatening events (12)
Below is the selection of adverse event reports related to Tenormin (Atenolol) that includes cases resulting in life threatening events.
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-10-30
Patient: male, weighing 47.0 kg (103.4 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal, Rhabdomyolysis, Disseminated Intravascular Coagulation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2006-01-01
End date: 2007-09-26
Alpiny
Indication: Pyrexia
Start date: 2007-09-24
End date: 2007-09-24
Other drugs received by patient: Warfarin Sodium; Pletal; Rythmodan; Norvasc; Unasyn; Unasyn
Adverse event in 71 year old female receiving Tenormin (Atenolol)
Reported by a physician from France on 2007-10-05
Patient: 71 year old female
Adverse reactions / side effects: Haematoma
Adverse event resulted in: life threatening event
Suspect drug(s):
Dafalgan
Indication: Pain in Extremity
Pravadual Tabs
Administration route: Oral
Indication: Cardiac Disorder
End date: 2007-04-16
Pravadual Tabs
Administration route: Oral
Indication: Hypertension
End date: 2007-04-16
Previscan
Administration route: Oral
Indication: Cardiac Disorder
End date: 2007-04-16
Previscan
Administration route: Oral
Indication: Hypertension
End date: 2007-04-16
Tenormin
Administration route: Oral
End date: 2007-04-16
Augmentin '125'
Administration route: Oral
Indication: Varicose Ulceration
Start date: 2007-04-12
End date: 2007-04-16
Nureflex
Administration route: Oral
Indication: Pain in Extremity
Other drugs received by patient: Lamaline
Adverse event in 57 year old male receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-10-02
Patient: 57 year old male, weighing 59.0 kg (129.8 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Dyspnoea, Pericardial Effusion, Haemoglobin Decreased, Haematocrit Decreased, Thrombocytopenic Purpura, Platelet Count Decreased, Haemorrhagic Diathesis, Rash Maculo-Papular
Adverse event resulted in: life threatening event
Suspect drug(s):
Lasix
Dosage: 20 mg/day
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2007-06-12
End date: 2007-07-13
Aldactone
Dosage: 25 mg/day
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2007-06-27
End date: 2007-07-20
Tenormin
Dosage: 25 mg/day
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2004-04-01
End date: 2007-07-20
Micardis
Dosage: 20 mg/day
Administration route: Oral
Indication: Cardiac Failure Congestive
Start date: 2004-04-01
End date: 2007-07-20
Warfarin Sodium
Dosage: 3 mg/day
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2007-06-07
End date: 2007-07-09
Propylthiouracil
Dosage: 300 mg/day
Administration route: Oral
Start date: 1987-01-01
End date: 2007-07-12
Propylthiouracil
Dosage: 200 mg/day
Administration route: Oral
Start date: 2007-07-13
End date: 2007-07-20
Propylthiouracil
Dosage: 300 mg/day
Administration route: Oral
Start date: 2007-08-03
Mucosta
Dosage: 300 mg/day
Administration route: Oral
Indication: Gastric Mucosal Lesion
Start date: 2007-05-18
End date: 2007-07-13
Sigmart
Dosage: 15 mg/day
Administration route: Oral
Indication: Angina Pectoris
Start date: 2004-04-01
End date: 2007-07-13
Bepricor
Dosage: 150 mg/day
Administration route: Oral
Indication: Atrial Fibrillation
Start date: 2007-07-02
End date: 2007-07-20
Nitroderm
Dosage: 1 patch/day
Indication: Angina Pectoris
Start date: 2007-07-13
Amlodipine Besylate
Indication: Angina Pectoris
Start date: 2004-04-01
Aspirin
Dosage: 100mg
Administration route: Oral
End date: 2007-07-12
Other drugs received by patient: Unasyn; Gentacin
Adverse event in 56 year old male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-07-19
Patient: 56 year old male
Adverse reactions / side effects: Electrocardiogram QT Prolonged, Intentional Overdose, Shock Haemorrhagic, Bradycardia, Blood Pressure Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Candesartan Cilexetil
Administration route: Oral
Indication: Hypertension
Start date: 2006-07-29
End date: 2006-07-29
Tenormin
Administration route: Oral
Start date: 2006-07-29
End date: 2006-07-29
Other drugs received by patient: Gasport; Aspirin
Adverse event in 46 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-06-18
Patient: 46 year old female
Adverse reactions / side effects: Encephalopathy, Hepatitis, Prothrombin Level Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Micardis HCT
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Amlodipino
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Adverse event in 71 year old female receiving Tenormin (Atenolol)
Reported by a physician from France on 2007-06-08
Patient: 71 year old female
Adverse reactions / side effects: Haematoma
Adverse event resulted in: life threatening event
Suspect drug(s):
Dafalgan
Indication: Pain in Extremity
Pravadual Tabs
Administration route: Oral
Indication: Cardiac Disorder
End date: 2007-04-16
Pravadual Tabs
Administration route: Oral
Indication: Hypertension
End date: 2007-04-16
Acetylsalicylic Acid SRT
Previscan
Administration route: Oral
Indication: Cardiac Disorder
End date: 2007-04-16
Previscan
Administration route: Oral
Indication: Hypertension
End date: 2007-04-16
Tenormin
Administration route: Oral
End date: 2007-04-16
Augmentin '125'
Administration route: Oral
Indication: Varicose Ulceration
Start date: 2007-04-12
End date: 2007-04-16
Nureflex
Administration route: Oral
Indication: Pain in Extremity
Other drugs received by patient: Lamaline
Adverse event in 46 year old female receiving Tenormin (Atenolol)
Reported by a physician on 2007-06-07
Patient: 46 year old female
Adverse reactions / side effects: Hepatic Encephalopathy, Prothrombin Level Decreased, Hepatitis Fulminant
Adverse event resulted in: life threatening event
Suspect drug(s):
Micardis HCT
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Tenormin
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Amlodipino
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Other drugs received by patient: Enalapril Maleate
Adverse event in 71 year old female receiving Tenormin (Atenolol)
Reported by a consumer/non-health professional from France on 2007-06-07
Patient: 71 year old female
Adverse reactions / side effects: Mydriasis, International Normalised Ratio Abnormal, Pupils Unequal, Loss of Consciousness, Renal Failure, Brain Oedema, Nervous System Disorder, Haematoma
Adverse event resulted in: life threatening event
Suspect drug(s):
Augmentin '125'
Administration route: Oral
Indication: Erysipelas
Start date: 2007-04-12
End date: 2007-04-16
Previscan
Administration route: Oral
Indication: Hypertensive Heart Disease
End date: 2007-04-16
Tenormin
Administration route: Oral
Indication: Essential Hypertension
End date: 2007-04-16
Pravastatin
Administration route: Oral
Indication: Hypertensive Heart Disease
End date: 2007-04-16
Acetylsalicylic Acid SRT
Administration route: Oral
Indication: Hypertensive Heart Disease
End date: 2007-04-16
Nureflex
Dosage: 300mg per day
Administration route: Oral
Other drugs received by patient: Dafalgan; Atacand; Desloratadine; Lamaline; NON Steroidal Antiinflammatory
Adverse event in 71 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-05
Patient: 71 year old female
Adverse reactions / side effects: Drug Interaction, Cerebral Haematoma
Adverse event resulted in: life threatening event
Suspect drug(s):
Tenormin (Atenolol)
Other drugs received by patient possibly interacting with the suspect drug:
Previscan
Dosage: 0.5 df every three days
Administration route: Oral
Indication: Hypertensive Cardiomyopathy
Previscan
Dosage: 0.75 df daily two days out of three
Administration route: Oral
End date: 2007-04-16
Augmentin '125'
Administration route: Oral
Indication: Erysipelas
Start date: 2007-04-12
End date: 2007-04-16
Pravadual
Administration route: Oral
Indication: Hypertensive Cardiomyopathy
End date: 2007-04-16
Nureflex
Administration route: Oral
Indication: Pain in Extremity
Other drugs received by patient: Atacand; Dafalgan; Desloratadine; Lamaline
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-05-31
Patient: male
Adverse reactions / side effects: Myocardial Infarction
Adverse event resulted in: life threatening event
Suspect drug(s):
Tenormin (Atenolol)
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-05-30
Patient: male
Adverse reactions / side effects: Myocardial Infarction
Adverse event resulted in: life threatening event
Suspect drug(s):
Tenormin (Atenolol)
Adverse event in 50 year old female receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-03-05
Patient: 50 year old female
Adverse reactions / side effects: Drug Toxicity, Intentional Overdose, Hypotension, Suicide Attempt
Adverse event resulted in: life threatening event
Suspect drug(s):
Tenormin
Dosage: 30 * 50 mg tablets
Administration route: Oral
Start date: 2006-11-11
End date: 2006-11-11
Adalat
Dosage: 30 * 20 mg tablets
Administration route: Oral
Start date: 2006-11-11
End date: 2006-11-11
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