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Index of reports
> Cases resulting in hospitalization (66)
> Cases with Bradycardia (12)
Below is the selection of adverse event reports related to Tenormin (Atenolol) that includes cases resulting in hospitalization where reactions include bradycardia.
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):
Tenormin
Administration route: Oral
Indication: Hypertension
End date: 2007-08-24
Digoxin
Administration route: Oral
Indication: Arrhythmia
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):
Tenormin
Administration route: Oral
Indication: Hypertension
End date: 2007-08-24
Digoxin
Administration route: Oral
Indication: Arrhythmia
End date: 2007-08-24
Other drugs received by patient: Atacand; Esidrix
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 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):
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
End date: 2007-05-09
Norvasc
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
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):
Tenormin
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
Norvasc
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 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 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 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):
Tenormin
Administration route: Oral
Start date: 2007-06-02
End date: 2007-06-02
Doliprane
Indication: Pharyngolaryngeal Pain
Adverse event in 86 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-13
Patient: 86 year old female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Drug Interaction, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tenormin (Atenolol)
Other drugs received by patient possibly interacting with the suspect drug:
Aricept
Administration route: Oral
Adverse event in 86 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from France on 2007-02-02
Patient: 86 year old female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Drug Interaction, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Aricept
Dosage: 10 mg, 1 in 1 d, oral
Administration route: Oral
Indication: Dementia Alzheimer's Type
Tenormin
Dosage: 50 mg, oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 94 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from Sweden on 2007-01-11
Patient: 94 year old female
Adverse reactions / side effects: Renal Failure, Poisoning, Bradycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Hypertension
End date: 2005-11-08
Lanacrist
Administration route: Oral
End date: 2005-11-08
Diclofenac Sodium
Administration route: Oral
End date: 2005-11-08
Other drugs received by patient: Acetaminophen; Allopurinol Sodium; Furosemide; Aspirin
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