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Tenormin (Atenolol) - Adverse Event Reports - Serious Event - Pulmonary Alveolar Haemorrhage

 



Index of reports > Cases resulting in a serious event (100) > Cases with Pulmonary Alveolar Haemorrhage (9)

Below is the selection of adverse event reports related to Tenormin (Atenolol) that includes cases resulting in a serious event where reactions include pulmonary alveolar haemorrhage.

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 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



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

Norvasc
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-01-15

Tenormin
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-15

Other drugs received by patient: Flomox; Kirpres; Mucosolvan; Medicon



Adverse event in male receiving Tenormin (Atenolol)

Reported by a physician from Japan on 2007-04-26

Patient: male, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage

Adverse event resulted in: hospitalization

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: 2006-01-15

Tenormin
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-15

Other drugs received by patient: Flomox; Kirpres; Mucosolvan; Medicon



Adverse event in male receiving Tenormin (Atenolol)

Reported by a pharmacist from Japan on 2007-03-27

Patient: male, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Micardis
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Tenormin
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Other drugs received by patient: Norvasc



Adverse event in male receiving Tenormin (Atenolol)

Reported by a pharmacist from Japan on 2007-02-22

Patient: male, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Micardis
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Tenormin
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Other drugs received by patient: Norvasc



Adverse event in male receiving Tenormin (Atenolol)

Reported by a pharmacist from Japan on 2007-02-22

Patient: male, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Micardis
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Tenormin
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Other drugs received by patient: Norvasc



Adverse event in male receiving Tenormin (Atenolol)

Reported by a pharmacist from Japan on 2007-02-08

Patient: male, weighing 64.0 kg (140.8 pounds)

Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Micardis
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Tenormin
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01
    End date: 2006-11-03

Other drugs received by patient: Norvasc



Adverse event in male receiving Tenormin (Atenolol)

Reported by a pharmacist from Japan on 2007-01-19

Patient: male

Adverse reactions / side effects: Interstitial Lung Disease, Pulmonary Alveolar Haemorrhage

Suspect drug(s):
Micardis
    Administration route: Oral

Norvasc
    Administration route: Oral

Tenormin
    Administration route: Oral

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