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Index of reports
> Cases resulting in other serious reactions (30)
Below is the selection of adverse event reports related to Tenormin (Atenolol) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 30 Next >>
Adverse event in 30 year old male receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-10-31
Patient: 30 year old male
Adverse reactions / side effects: Overdose, Suicide Attempt
Suspect drug(s):
Tenormin
Dosage: 60 tablets
Administration route: Oral
Start date: 2007-10-17
Unknowndrug
Dosage: dose unknown
Administration route: Oral
Start date: 2007-10-17
Adverse event in 42 year old female receiving Tenormin (Atenolol)
Reported by a individual with unspecified qualification from United States on 2007-10-30
Patient: 42 year old female
Adverse reactions / side effects: Drug Ineffective, Hypertension
Suspect drug(s):
Tenormin
Administration route: Oral
Lisinopril
Administration route: Oral
Verapamil
Clonidine
Adverse event in 30 year old male receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-10-25
Patient: 30 year old male
Adverse reactions / side effects: Overdose, Suicide Attempt
Suspect drug(s):
Tenormin
Dosage: 60 tablets
Administration route: Oral
Start date: 2007-10-17
Unknowndrug
Dosage: dose unknown
Administration route: Oral
Start date: 2007-10-17
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
Tenormin
Dosage: 1 u, qd
Administration route: Oral
Start date: 2006-11-15
End date: 2007-06-13
Kardegic / 00002703 /
Dosage: 160 mg, qd
Administration route: Oral
Indication: Prophylaxis
Start date: 2006-11-15
Tahor
Dosage: 80 mg, qd
Administration route: Oral
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
Adverse event in 42 year old female receiving Tenormin (Atenolol)
Reported by a consumer/non-health professional from United States on 2007-10-09
Patient: 42 year old female
Adverse reactions / side effects: Hypertension
Suspect drug(s):
Tenormin
Administration route: Oral
Lisinopril
Administration route: Oral
Verapamil
Clonidine
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 female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-25
Patient: female, weighing 69.4 kg (152.7 pounds)
Adverse reactions / side effects: Dyspnoea, Disease Recurrence, Drug Ineffective, Arrhythmia
Suspect drug(s):
Tenormin (Atenolol)
Adverse event in female receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-07-20
Patient: female
Adverse reactions / side effects: Pharyngeal Oedema, Wheezing
Suspect drug(s):
Norvasc
Dosage: text:unknown
Administration route: Oral
Indication: Ill-Defined Disorder
Amlodipine
Dosage: text:unknown
Indication: Ill-Defined Disorder
Calblock
Dosage: text:unknown
Indication: Ill-Defined Disorder
Tenormin
Dosage: text:unknown
Indication: Ill-Defined Disorder
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-06-28
Patient: male
Adverse reactions / side effects: Dyspnoea, Pulmonary Oedema, Myelodysplastic Syndrome, Pleural Effusion, Neutrophil Count Decreased
Suspect drug(s):
Tenormin
Administration route: Oral
Indication: Cardiac Failure
End date: 2007-06-10
Aspirin
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Bepricor
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Lendormin
Administration route: Oral
End date: 2007-06-10
Lipitor
Administration route: Oral
End date: 2007-06-10
Pletal
Administration route: Oral
Sigmart
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Warfarin Potassium
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Zantac
Administration route: Oral
Start date: 2007-04-27
End date: 2007-06-10
Other drugs received by patient: Furosemide; Ambroxol Hydrochloride
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
Tenormin
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
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
Tenormin
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
Adverse event in 77 year old female receiving Tenormin (Atenolol)
Reported by a pharmacist from Japan on 2007-05-30
Patient: 77 year old female
Adverse reactions / side effects: Heart Rate Decreased, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Norvasc
Dosage: daily dose:2.5mg-text:2.5 mg daily
Administration route: Oral
Indication: Hypertension
Tenormin
Dosage: daily dose:25mg-text:25 mg daily
Administration route: Oral
Indication: Hypertension
Start date: 2003-11-01
Adverse event in male receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-05-23
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
Tenormin
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: 2006-01-15
Other drugs received by patient: Flomox; Kirpres; Mucosolvan; Medicon
Adverse event in receiving Tenormin (Atenolol)
Reported by a pharmacist from United States on 2007-05-22
Patient:
Adverse reactions / side effects: Anaphylactic Shock
Suspect drug(s):
Tenormin (Atenolol)
Adverse event in male receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-05-18
Patient: male
Adverse reactions / side effects: Rhabdomyolysis
Suspect drug(s):
Cardenalin
Dosage: daily dose:2mg-freq:daily
Administration route: Oral
Indication: Ill-Defined Disorder
Start date: 2002-10-05
End date: 2002-12-07
Cardenalin
Dosage: daily dose:2mg-freq:daily
Administration route: Oral
Start date: 2003-01-18
End date: 2003-04-07
Amlodipine
Dosage: daily dose:10mg-freq:daily
Administration route: Oral
Indication: Ill-Defined Disorder
Start date: 2002-08-10
End date: 2002-11-23
Amlodipine
Dosage: daily dose:5mg-freq:daily
Administration route: Oral
Start date: 2002-11-24
End date: 2002-12-06
Amlodipine
Dosage: daily dose:10mg
Administration route: Oral
Tenormin
Dosage: daily dose:25mg-freq:daily
Administration route: Oral
Indication: Ill-Defined Disorder
Other drugs received by patient: Fluitran
Adverse event in 84 year old male receiving Tenormin (Atenolol)
Reported by a physician from Germany on 2007-05-14
Patient: 84 year old male, weighing 76.0 kg (167.2 pounds)
Adverse reactions / side effects: Atrioventricular Block First Degree
Suspect drug(s):
Quilonum Retard
Dosage: 450mg per day
Administration route: Oral
Indication: Depression
Start date: 2007-03-20
Tenormin
Dosage: 50mg per day
Administration route: Oral
Other drugs received by patient: Hydrochlorothiazide; Zopiclon; Lorazepam
Adverse event in 78 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-05-10
Patient: 78 year old female
Adverse reactions / side effects: Insomnia
Suspect drug(s):
Tenormin (Atenolol)
Other drugs received by patient: Omeprazole; Penicillin V; Sintrom
Adverse event in 73 year old female receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-05-03
Patient: 73 year old female
Adverse reactions / side effects: Blood Cholesterol Increased, LOW Density Lipoprotein Increased
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Tenormin
Adverse event in 79 year old female receiving Tenormin (Atenolol)
Reported by a individual with unspecified qualification from France on 2007-04-13
Patient: 79 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Abdominal Pain, Haemoglobin Decreased, Cytolytic Hepatitis, Acute Coronary Syndrome, Hypertension, Haemolysis
Adverse event resulted in: hospitalization
Suspect drug(s):
Renagel
Dosage: 3.2 g daily po
Administration route: Oral
Indication: Hyperphosphataemia
Kayexalate
Dosage: 15 g daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Previscan
Dosage: 10 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Tenormin
Dosage: 50 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Kenzen
Dosage: 2 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Cordarone
Dosage: 200 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Vasten; Temesta; Zantac; Corvasal
Adverse event in 76 year old female receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-04-04
Patient: 76 year old female, weighing 52.0 kg (114.4 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Alanine Aminotransferase Increased, Blood Lactate Dehydrogenase Increased, Condition Aggravated, Lymphocyte Stimulation Test Positive, Liver Disorder, Gamma-Glutamyltransferase Increased, Heart Rate Increased, Aspartate Aminotransferase Increased, NO Therapeutic Response
Adverse event resulted in: hospitalization
Suspect drug(s):
Ternelin
Dosage: 1 mg tid po
Administration route: Oral
Indication: Back Pain
Start date: 2006-10-06
End date: 2006-12-13
Coniel
Dosage: df
Indication: Hypertension
End date: 2006-11-09
Tenormin
Dosage: 25 mg qday po
Administration route: Oral
Indication: Hypertension
Start date: 2006-11-09
End date: 2006-12-08
Other drugs received by patient: Opalmon; Loxonin; Kelnac; Bonalon; Mevalotin; Halcion; Elcitonin; Nsaid's
Adverse event in 65 year old male receiving Tenormin (Atenolol)
Reported by a individual with unspecified qualification from United States on 2007-03-09
Patient: 65 year old male, weighing 95.0 kg (209.0 pounds)
Adverse reactions / side effects: Flushing, Medication Error, Drug Interaction, Myocardial Infarction
Adverse event resulted in: death
Suspect drug(s):
Tenormin (Atenolol)
Other drugs received by patient possibly interacting with the suspect drug:
Niaspan
Administration route: Oral
Indication: High Density Lipoprotein Decreased
Start date: 2006-06-11
End date: 2006-06-11
Niaspan
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-06-11
End date: 2006-06-11
Wellbutrin
Administration route: Oral
Indication: Depression
Effexor
Administration route: Oral
Indication: Depression
Lorazepam
Administration route: Oral
Indication: Depression
Trazodone HCL
Administration route: Oral
Indication: Depression
Lanoxin
Administration route: Oral
Indication: Tachyarrhythmia
Glucophage
Administration route: Oral
Indication: Diabetes Mellitus
Glucotrol XL
Administration route: Oral
Indication: Diabetes Mellitus
Actos
Administration route: Oral
Indication: Diabetes Mellitus
Tricor
Administration route: Oral
Indication: Dyslipidaemia
Lantus
Indication: Diabetes Mellitus
Start date: 2006-06-09
Lantus
End date: 2006-06-01
Lipitor
Vitamin CAP
Risperdal
Administration route: Oral
Adverse event in 79 year old female receiving Tenormin (Atenolol)
Reported by a individual with unspecified qualification from France on 2007-03-09
Patient: 79 year old female, weighing 57.0 kg (125.4 pounds)
Adverse reactions / side effects: Abdominal Pain, Cytolytic Hepatitis, Acute Coronary Syndrome, Blood Sodium Decreased, Hypertension, Haemolysis
Adverse event resulted in: hospitalization
Suspect drug(s):
Renagel
Dosage: 3.2 g daily po
Administration route: Oral
Indication: Hyperphosphataemia
Kayexalate
Dosage: 15 g daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Previscan
Dosage: 10 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Tenormin
Dosage: 50 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Kenzen
Dosage: 2 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Cordarone
Dosage: 200 mg daily po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Vasten; Lorazepam; Zantac; Corvasal
Adverse event in 90 year old female receiving Tenormin (Atenolol)
Reported by a physician from Japan on 2007-03-07
Patient: 90 year old female
Adverse reactions / side effects: Hypoglycaemia, Anorexia, Drug Interaction, Arrhythmia
Suspect drug(s):
Tenormin (Atenolol)
Other drugs received by patient possibly interacting with the suspect drug:
Tenormin
Administration route: Oral
End date: 2007-02-24
Glucobay
Administration route: Oral
Indication: Diabetes Mellitus
Other drugs received by patient: Valsartan
Adverse event in male receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-02-28
Patient: male
Adverse reactions / side effects: Overdose, Suicide Attempt, Drug Withdrawal Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Tenormin
Seroxat
Start date: 2001-07-31
Anafranil
Simvastatin
Citalopram Hydrobromide
Alcohol
Adverse event in 56 year old female receiving Tenormin (Atenolol)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-02-22
Patient: 56 year old female
Adverse reactions / side effects: Overdose
Suspect drug(s):
Tenormin
Dosage: 20 tablets
Administration route: Oral
Unspecified Drugs
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