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Index of reports
> Cases resulting in hospitalization (66)
Below is the selection of adverse event reports related to Tenormin (Atenolol) that includes cases resulting in hospitalization.
Reports 1 - 25 of 66 Next >>
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):
Alpiny
Indication: Pyrexia
Start date: 2007-09-24
End date: 2007-09-24
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2006-01-01
End date: 2007-09-26
Other drugs received by patient: Warfarin Sodium; Pletal; Rythmodan; Norvasc; Unasyn; Unasyn
Adverse event in female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-29
Patient: female
Adverse reactions / side effects: Lung Disorder, Hypoxia
Adverse event resulted in: hospitalization
Suspect drug(s):
Laroxyl
Administration route: Oral
End date: 2007-09-09
Tenormin
Administration route: Oral
End date: 2007-09-09
Tercian
Administration route: Oral
End date: 2007-09-09
Tiapridal
Administration route: Oral
End date: 2007-09-09
Other drugs received by patient: Cellcept; Cellcept; Neoral; Pravastatin; Solupred; Bactrim
Adverse event in female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-23
Patient: female
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Gamma-Glutamyltransferase Increased, Peritoneal Effusion, Pleural Effusion, Transaminases Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Actiskenan
Dosage: 6 dose total daily
Administration route: Oral
Indication: Cancer Pain
Start date: 2007-06-04
Doliprane
Dosage: on demand, 3 dose total daily
Administration route: Oral
Indication: Cancer Pain
Start date: 2007-06-04
Effexor XR
Dosage: 4 dose total daily
Administration route: Oral
Indication: Depression
Lexomil
Administration route: Oral
Indication: Anxiety
Start date: 2007-06-05
Risperdal
Administration route: Oral
Indication: Psychotic Disorder
End date: 2007-06-04
Risperdal
Administration route: Oral
Start date: 2007-06-05
Tenormin
Dosage: 1 dose total daily
Administration route: Oral
Indication: Hypertension
Adverse event in receiving Tenormin (Atenolol)
Reported by a consumer/non-health professional from France on 2007-10-22
Patient:
Adverse reactions / side effects: Cryptogenic Organising Pneumonia, Dyspnoea, Eosinophilic Pneumonia, Bronchomalacia, Asthenia, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Altace
Dosage: 5 mg, qd
Administration route: Oral
Indication: Hypertension
Start date: 2006-11-15
End date: 2007-01-15
Kardegic / 00002703 /
Dosage: 160 mg, qd
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-11-15
Plavix
Dosage: 75 mg, qd
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-11-15
End date: 2007-01-15
Tahor
Dosage: 80 mg, qd
Administration route: Oral
Start date: 2006-11-15
Tenormin
Dosage: 1 u, qd
Administration route: Oral
Start date: 2006-11-15
End date: 2007-06-13
Adverse event in 78 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: 78 year old female
Adverse reactions / side effects: Eosinophilic Pneumonia
Adverse event resulted in: hospitalization
Suspect drug(s):
Kardegic
Administration route: Oral
Indication: Myocardial Infarction
Start date: 2006-11-15
Kardegic
Administration route: Oral
Indication: Coronary Arterial Stent Insertion
Start date: 2006-11-15
Plavix
Administration route: Oral
Indication: Myocardial Infarction
Start date: 2006-11-15
End date: 2007-01-15
Plavix
Administration route: Oral
Indication: Coronary Arterial Stent Insertion
Start date: 2006-11-15
End date: 2007-01-15
Tahor
Dosage: 80 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-11-15
Tenormin
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-11-15
End date: 2007-06-13
Triatec
Administration route: Oral
Start date: 2006-11-15
End date: 2007-01-15
Other drugs received by patient: Clamoxyl; Erythrocine; Targocid; Amiklin; Tienam; Tavanic
Adverse event in female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: female
Adverse reactions / side effects: Head Injury, Bradycardia, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Digoxin
Administration route: Oral
Indication: Arrhythmia
End date: 2007-08-24
Tenormin
Administration route: Oral
Indication: Hypertension
End date: 2007-08-24
Other drugs received by patient: Atacand; Esidrix
Adverse event in female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-09
Patient: female
Adverse reactions / side effects: Head Injury, Bradycardia, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Digoxin
Administration route: Oral
Indication: Arrhythmia
End date: 2007-08-24
Tenormin
Administration route: Oral
Indication: Hypertension
End date: 2007-08-24
Other drugs received by patient: Atacand; Esidrix
Adverse event in 77 year old male receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-10-05
Patient: 77 year old male
Adverse reactions / side effects: Agranulocytosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Aspirin
Dosage: total daily dose: 100 mg unit dose: 100 mg
Administration route: Oral
End date: 2007-06-11
Bepricor
Administration route: Oral
End date: 2007-06-11
Lendormin
Administration route: Oral
Indication: Insomnia
End date: 2007-06-11
Lipitor
Dosage: total daily dose: 10 mg unit dose: 10 mg
Administration route: Oral
End date: 2007-06-11
Pletal
Administration route: Oral
End date: 2007-06-11
Sigmart
Administration route: Oral
End date: 2007-06-11
Tenormin
Dosage: total daily dose: 50 mg unit dose: 50 mg
Administration route: Oral
End date: 2007-06-11
Warfarin Potassium
Administration route: Oral
End date: 2007-06-11
Zantac
Dosage: total daily dose: 150 mg unit dose: 150 mg
Administration route: Oral
End date: 2007-06-11
Other drugs received by patient: Lasix; Mucosolvan
Adverse event in 78 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-02
Patient: 78 year old female
Adverse reactions / side effects: Eosinophilic Pneumonia, Cough
Adverse event resulted in: hospitalization
Suspect drug(s):
Kardegic
Administration route: Oral
Start date: 2006-11-15
Plavix
Administration route: Oral
Start date: 2006-11-15
End date: 2007-01-15
Tahor
Administration route: Oral
Start date: 2006-11-15
Tenormin
Administration route: Oral
Start date: 2006-11-15
End date: 2007-06-13
Triatec
Administration route: Oral
Start date: 2006-11-15
End date: 2007-01-15
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-07-25
Patient: male
Adverse reactions / side effects: Agranulocytosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Aspirin
Dosage: daily dose:100mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Bepricor
Dosage: daily dose:100mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Lendorm
Dosage: daily dose:.25mg-freq:day
Administration route: Oral
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Mucosolvan
Administration route: Oral
Sigmart
Dosage: daily dose:15mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Tenormin
Dosage: daily dose:50mg-freq:day
Administration route: Oral
Warfarin Sodium
Dosage: daily dose:.5mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Zantac 150
Dosage: daily dose:150mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-07-25
Patient: male
Adverse reactions / side effects: Blood Pressure Increased, Drug Ineffective, Dehydration, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Conan
Dosage: daily dose:10mg-freq:daily
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-28
End date: 2007-06-08
Lasix
Dosage: daily dose:20mg-freq:daily
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-28
End date: 2007-06-08
Omeprazole
Dosage: daily dose:20mg-freq:daily
Administration route: Oral
Indication: Reflux Oesophagitis
Start date: 2007-04-26
End date: 2007-06-08
Tenormin
Dosage: daily dose:50mg-freq:daily
Administration route: Oral
Indication: Hypertension
Start date: 2007-04-27
End date: 2007-06-08
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 male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-07-10
Patient: male
Adverse reactions / side effects: Dehydration, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Conan
Dosage: daily dose:10mg-freq:daily
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-28
End date: 2007-06-08
Lasix
Dosage: daily dose:20mg-freq:daily
Administration route: Oral
Indication: Hypertension
Start date: 2007-05-28
End date: 2007-06-08
Omepral
Dosage: daily dose:20mg-freq:daily
Administration route: Oral
Indication: Reflux Oesophagitis
Start date: 2007-04-26
End date: 2007-06-08
Tenormin
Dosage: daily dose:50mg-freq:daily
Administration route: Oral
Indication: Hypertension
Start date: 2007-04-27
End date: 2007-06-08
Adverse event in 76 year old male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-07-06
Patient: 76 year old male
Adverse reactions / side effects: Neutrophil Count Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Aspirin
Dosage: daily dose:100mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Bepricor
Dosage: daily dose:100mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Lendormin
Dosage: daily dose:.25mg-freq:day
Administration route: Oral
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Pletal
Administration route: Oral
Sigmart
Dosage: daily dose:15mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Tenormin
Dosage: daily dose:50mg-freq:day
Administration route: Oral
Warfarin Sodium
Dosage: daily dose:.5mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Zantac
Dosage: daily dose:150mg-freq:day
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Adverse event in 77 year old female receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-07-05
Patient: 77 year old female
Adverse reactions / side effects: Bradycardia, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Norvasc
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
End date: 2007-05-09
Adverse event in 77 year old female receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-06-28
Patient: 77 year old female
Adverse reactions / side effects: Bradycardia, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Norvasc
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
Adverse event in male receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-27
Patient: male, weighing 91.0 kg (200.2 pounds)
Adverse reactions / side effects: Malaise, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2003-07-01
End date: 2007-05-01
Tenormin
Administration route: Oral
Start date: 2007-05-01
End date: 2007-05-01
Tenormin
Administration route: Oral
Start date: 2007-05-01
End date: 2007-05-21
Other drugs received by patient: Omeprazole; Triatec; Aspirin; Pravastatin; Xatral
Adverse event in 68 year old male receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-27
Patient: 68 year old male
Adverse reactions / side effects: Multi-Organ Failure, Drug Ineffective, Interstitial Lung Disease, Alveolitis Allergic
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Cordarone
Dosage: 300 mg
Indication: Atrial Fibrillation
Start date: 2007-04-09
End date: 2007-04-09
Cordarone
Dosage: 3 vials
Start date: 2007-04-14
End date: 2007-04-14
Cordarone
Dosage: 6 vials
Start date: 2007-04-15
End date: 2007-04-15
Cordarone
Dosage: 1 vial
Start date: 2007-04-16
End date: 2007-04-18
Cordarone
Dosage: not provided
Start date: 2007-04-10
End date: 2007-04-13
Tenormin
Dosage: 2 mg once
Indication: Atrial Fibrillation
Start date: 2007-04-09
End date: 2007-04-09
Other drugs received by patient: Tazocilline; Tazocilline; Amikacin
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-06-26
Patient: male, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Blood Potassium Increased, Duodenal Ulcer, Bradycardia, Blood Creatinine Increased, Blood Pressure Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2007-01-23
End date: 2007-05-14
Tenormin
Administration route: Oral
Start date: 2007-05-15
End date: 2007-05-28
Other drugs received by patient: Glimicron; Micardis; Micardis; Norvasc; Nitorol; Cardenalin; Loxonin; Mucosta; Magmitt; Takepron; Renivace
Adverse event in 77 year old male receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-06-21
Patient: 77 year old male
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Aspirin
Dosage: total daily dose: 100 mg unit dose: 100 mg
Administration route: Oral
End date: 2007-06-11
Bepricor
Administration route: Oral
End date: 2007-06-11
Lendormin
Administration route: Oral
Indication: Insomnia
End date: 2007-06-11
Lipitor
Dosage: total daily dose: 10 mg unit dose: 10 mg
Administration route: Oral
End date: 2007-06-11
Pletal
Administration route: Oral
End date: 2007-06-11
Sigmart
Administration route: Oral
End date: 2007-06-11
Tenormin
Dosage: total daily dose: 50 mg unit dose: 50 mg
Administration route: Oral
End date: 2007-06-11
Warfarin Potassium
Administration route: Oral
End date: 2007-06-11
Zantac
Dosage: total daily dose: 150 mg unit dose: 150 mg
Administration route: Oral
End date: 2007-06-11
Other drugs received by patient: Lasix; Mucosolvan
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-06-20
Patient: male, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Blood Potassium Increased, Bradycardia, Blood Creatinine Increased, Blood Pressure Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2007-01-23
End date: 2007-05-14
Tenormin
Administration route: Oral
Start date: 2007-05-15
End date: 2007-05-28
Other drugs received by patient: Glimicron; Micardis; Micardis; Norvasc; Nitorol; Cardenalin; Loxonin; Mucosta; Magmitt; Takepron; Renivace
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-06-20
Patient: male, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage, Pneumothorax
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Micardis
Administration route: Oral
Indication: Hypertension
Start date: 2004-01-01
End date: 2006-11-15
Norvasc
Administration route: Oral
Indication: Hypertension
Start date: 2004-01-01
End date: 2006-11-15
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2004-01-01
End date: 2006-11-15
Adverse event in 12 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-19
Patient: 12 year old female, weighing 44.0 kg (96.8 pounds)
Adverse reactions / side effects: Hypotension, Wrong Drug Administered, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Doliprane
Indication: Pharyngolaryngeal Pain
Tenormin
Administration route: Oral
Start date: 2007-06-02
End date: 2007-06-02
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):
Amlodipino
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
Tenormin
Administration route: Oral
Indication: Essential Hypertension
Start date: 2007-01-01
End date: 2007-03-28
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-06-18
Patient: male, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage, Pneumothorax
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Micardis
Administration route: Oral
Indication: Hypertension
Start date: 2004-01-01
End date: 2006-11-15
Norvasc
Administration route: Oral
Indication: Hypertension
Start date: 2004-01-01
End date: 2006-11-15
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2004-01-01
End date: 2006-11-15
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