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Aldactone (Spironolactone) - Adverse Event Reports - Disability - Arterial Occlusive Disease

 



Index of reports > Cases resulting in disability (11) > Cases with Arterial Occlusive Disease (7)

Below is the selection of adverse event reports related to Aldactone (Spironolactone) that includes cases resulting in disability where reactions include arterial occlusive disease.

Adverse event in female receiving Aldactone (Spironolactone)

Reported by a individual with unspecified qualification from Brazil on 2007-10-30

Patient: female

Adverse reactions / side effects: Drug Ineffective, Impaired Work Ability, Ill-Defined Disorder, Palpitations, Diarrhoea, Pulmonary Oedema, Oedema, Arterial Occlusive Disease, Depression, Myocardial Infarction, Blood Glucose Increased, Haematoma

Adverse event resulted in: disablity

Suspect drug(s):
Aldactone
    Dosage: (qd), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Caduet
    Dosage: 10/5 mg (bid),per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Coristina D (Acetysalicylic Acid, Cafffeine, Phenylephrine Hydrochlori
    Indication: Drug USE FOR Unknown Indication

Diabinese
    Dosage: 500 mg (250 mg,bid),per oral
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 1996-01-01
    End date: 2004-11-30

Norvasc
    Dosage: 5 mg (5 mg,qd),per oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication
    Start date: 2004-01-01
    End date: 2006-01-01

Olmesartan Medoxomil
    Dosage: 20 mg (20 mg,qd),per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Other drugs received by patient: Insulin (Insulin) (-Injection) (Insulin)



Adverse event in female receiving Aldactone (Spironolactone)

Reported by a consumer/non-health professional from Brazil on 2007-10-26

Patient: female

Adverse reactions / side effects: Syncope, Dyspnoea, Injection Site Haematoma, Coagulopathy, Oedema, Arterial Occlusive Disease, Pulmonary Oedema, Depression, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Aldactone
    Administration route: Oral
    Indication: Hypertension

Caduet
    Dosage: text:10mg/5mg;20mg/10mg
    Administration route: Oral
    Indication: Hypertension

Coristina D
    Administration route: Oral
    Indication: Influenza

Diabinese
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 1996-01-01
    End date: 2004-11-30

Insulin
    Indication: Diabetes Mellitus
    Start date: 2004-11-01

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

Novonorm

Olmetec
    Administration route: Oral
    Indication: Hypertension



Adverse event in female receiving Aldactone (Spironolactone)

Reported by a consumer/non-health professional from Brazil on 2007-05-08

Patient: female

Adverse reactions / side effects: Syncope, Dyspnoea, Oedema, Arterial Occlusive Disease, Pulmonary Oedema, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Aldactone
    Administration route: Oral
    Indication: Hypertension

Caduet
    Dosage: text:10mg/5mg;20mg/10mg
    Administration route: Oral
    Indication: Hypertension

Coristina D
    Administration route: Oral
    Indication: Influenza

Diabinese
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 1996-01-01
    End date: 2004-11-30

Insulin
    Indication: Diabetes Mellitus
    Start date: 2004-11-01

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

Olmetec
    Administration route: Oral
    Indication: Hypertension



Adverse event in female receiving Aldactone (Spironolactone)

Reported by a individual with unspecified qualification on 2007-05-04

Patient: female

Adverse reactions / side effects: Dyspnoea, Drug Ineffective, Impaired Work Ability, Fatigue, Malaise, Palpitations, Pulmonary Oedema, Arterial Occlusive Disease, Oedema, Myocardial Infarction

Adverse event resulted in: disablity

Suspect drug(s):
Aldactone
    Dosage: (qd), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Aldactone
    Dosage: (qd), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Caduet
    Dosage: 20/10 mg (mg, bid), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Caduet (Tablet)
    Dosage: 20/10 mg (mg, bid), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Norvasc

Olmesartan Medoxomil
    Dosage: 20 mg (20 mg, qd), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Olmetec (Olmesartan Medoxomil) (20 Milligram, Tablet) (Olmesartan Medo
    Dosage: 20 mg (20 mg, qd), per oral
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-01-01

Other drugs received by patient: Diabinese (Chlorpropamide) (Chlorpropamide); Norvasc; Insulin (Insulin) (Insulin); Diabinese; Insulin



Adverse event in female receiving Aldactone (Spironolactone)

Reported by a consumer/non-health professional from Brazil on 2007-05-01

Patient: female

Adverse reactions / side effects: Dyspnoea, Drug Ineffective, Syncope, Fatigue, Malaise, Palpitations, Arterial Occlusive Disease, Oedema, Pulmonary Oedema, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Aldactone
    Administration route: Oral
    Indication: Hypertension

Caduet
    Dosage: text:10mg/5mg;20mg/10mg
    Administration route: Oral
    Indication: Hypertension

Coristina D
    Administration route: Oral
    Indication: Influenza

Diabinese
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 1996-01-01
    End date: 2004-11-30

Insulin
    Indication: Diabetes Mellitus

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

Olmetec
    Administration route: Oral
    Indication: Hypertension



Adverse event in female receiving Aldactone (Spironolactone)

Reported by a consumer/non-health professional from Brazil on 2007-04-02

Patient: female

Adverse reactions / side effects: Dyspnoea, Malaise, Pulmonary Oedema, Arterial Occlusive Disease, Oedema, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Aldactone
    Dosage: text:5/10 mg (milligram)
    Administration route: Oral

Caduet
    Administration route: Oral

Coristina D
    Administration route: Oral

Diabinese
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 1996-01-01
    End date: 2004-11-30

Insulin
    Indication: Diabetes Mellitus

Norvasc
    Administration route: Oral

Olmetec
    Dosage: daily dose:20mg
    Administration route: Oral



Adverse event in female receiving Aldactone (Spironolactone)

Reported by a consumer/non-health professional from Brazil on 2007-03-20

Patient: female

Adverse reactions / side effects: Dyspnoea, Malaise, Pulmonary Oedema, Arterial Occlusive Disease, Oedema, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Aldactone
    Administration route: Oral

Caduet
    Administration route: Oral

Coristina D
    Administration route: Oral

Diabinese
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 1996-01-01
    End date: 2004-11-30

Insulin

Norvasc
    Administration route: Oral

Olmetec
    Administration route: Oral

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