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Actos (Pioglitazone) - Adverse Event Reports - Life Threatening Events - Oedema Peripheral

 



Index of reports > Cases resulting in life threatening events (34) > Cases with Oedema Peripheral (6)

Below is the selection of adverse event reports related to Actos (Pioglitazone) that includes cases resulting in life threatening events where reactions include oedema peripheral.

Adverse event in 57 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from United States on 2007-10-12

Patient: 57 year old male, weighing 113.4 kg (249.5 pounds)

Adverse reactions / side effects: Weight Increased, Fatigue, Oedema Peripheral, Swelling

Adverse event resulted in: life threatening event, disablity

Suspect drug(s):
Actos (Pioglitazone)



Adverse event in female receiving Actos (Pioglitazone)

Reported by a physician from Japan on 2007-07-09

Patient: female, weighing 77.0 kg (169.4 pounds)

Adverse reactions / side effects: Chest Discomfort, Dizziness Postural, Oedema Peripheral, Pulmonary Embolism, Deep Vein Thrombosis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lipitor
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2006-08-21
    End date: 2007-04-14

Lipitor
    Indication: Hyperlipidaemia

Actos
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2006-05-08
    End date: 2007-04-14

Soleton
    Administration route: Oral
    Indication: Analgesia



Adverse event in female receiving Actos (Pioglitazone)

Reported by a physician from Japan on 2007-06-22

Patient: female, weighing 77.0 kg (169.4 pounds)

Adverse reactions / side effects: Chest Discomfort, Dizziness Postural, Oedema Peripheral, Pulmonary Embolism, Deep Vein Thrombosis

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lipitor
    Administration route: Oral
    Indication: Hypercholesterolaemia

Lipitor
    Indication: Hyperlipidaemia

Actos
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2006-05-08
    End date: 2007-04-10

Soleton
    Dosage: freq:every day
    Administration route: Oral
    Indication: Analgesic Effect



Adverse event in 75 year old female receiving Actos (Pioglitazone)

Reported by a consumer/non-health professional from United States on 2007-05-29

Patient: 75 year old female, weighing 136.1 kg (299.4 pounds)

Adverse reactions / side effects: Coronary Artery Bypass, Cardiac Failure, Oedema Peripheral, Pulmonary Oedema

Adverse event resulted in: life threatening event

Suspect drug(s):
Actos (Pioglitazone)



Adverse event in 56 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Japan on 2007-02-22

Patient: 56 year old male

Adverse reactions / side effects: Cardiomegaly, Pericardial Effusion, Face Oedema, Dyspnoea Exertional, Cardiac Failure, Oedema Peripheral, NO Therapeutic Response, Pleural Effusion, Cough

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amlodipine Besylate



Adverse event in 56 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Japan on 2007-01-31

Patient: 56 year old male

Adverse reactions / side effects: Respiratory Disorder, Pericardial Effusion, Face Oedema, Dyspnoea Exertional, Cardiac Failure, Oedema Peripheral, NO Therapeutic Response, Pleural Effusion, Cough

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amlodipine Besylate

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