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Tenormin (Atenolol) - Adverse Event Reports - Serious Event - Bradycardia

 



Index of reports > Cases resulting in a serious event (100) > Cases with Bradycardia (12)

Below is the selection of adverse event reports related to Tenormin (Atenolol) that includes cases resulting in a serious event 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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