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Actos (Pioglitazone) - Adverse Event Reports - Death - Blood Glucose Increased

 



Index of reports > Cases resulting in death (47) > Cases with Blood Glucose Increased (9)

Below is the selection of adverse event reports related to Actos (Pioglitazone) that includes cases resulting in death where reactions include blood glucose increased.

Adverse event in 49 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Korea, Republic of on 2007-06-26

Patient: 49 year old male

Adverse reactions / side effects: Alanine Aminotransferase Increased, Sudden Death, Blood Cholesterol Increased, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amaryl; Thioctacid (Thioctic Acid); Pentoxifylline; Saccharomyces Medicinalis; Otilonium Bromide



Adverse event in 74 year old female receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Korea, Republic of on 2007-06-19

Patient: 74 year old female

Adverse reactions / side effects: Cardiac Disorder, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amaryl



Adverse event in 66 year old female receiving Actos (Pioglitazone)

Reported by a physician from Korea, Republic of on 2007-06-19

Patient: 66 year old female

Adverse reactions / side effects: Glycosylated Haemoglobin Increased, Hepatic Neoplasm Malignant, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amaryl



Adverse event in 74 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Korea, Republic of on 2007-06-12

Patient: 74 year old male

Adverse reactions / side effects: Cardiac Disorder, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amaryl



Adverse event in 66 year old female receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Korea, Republic of on 2007-06-12

Patient: 66 year old female

Adverse reactions / side effects: Glycosylated Haemoglobin Increased, Hepatic Neoplasm Malignant, Blood Cholesterol Increased, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amaryl



Adverse event in 49 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from Korea, Republic of on 2007-06-12

Patient: 49 year old male

Adverse reactions / side effects: Sudden Death, Blood Cholesterol Increased, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Actos (Pioglitazone)

Other drugs received by patient: Amaryl; Thioctacid (Thioctic Acid); Pentoxifylline; Saccharomyces Medicinalis



Adverse event in 65 year old male receiving Actos (Pioglitazone)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-02-26

Patient: 65 year old male

Adverse reactions / side effects: Ultrasound Scan Abnormal, Alanine Aminotransferase Increased, Incorrect Dose Administered, Skin Disorder, High Density Lipoprotein Decreased, Flushing, Haemoglobin Decreased, Glycosylated Haemoglobin Increased, Cardio-Respiratory Arrest, Aspartate Aminotransferase Increased, Depressed Level of Consciousness, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Lorazepam
    Dosage: 2 mg q day; po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Niaspan
    Dosage: 1000 mg once;po
    Administration route: Oral
    Indication: High Density Lipoprotein Decreased
    Start date: 2006-06-11
    End date: 2006-06-11

Niaspan
    Dosage: 1000 mg once;po
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2006-06-11
    End date: 2006-06-11

Effexor XR
    Dosage: 150 mg q day; po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Actos
    Dosage: 45 mg q day;po
    Administration route: Oral
    Indication: Diabetes Mellitus
    End date: 2006-06-11

Glucophage
    Dosage: 1000 mg bid;po
    Administration route: Oral
    Indication: Diabetes Mellitus
    End date: 2006-06-11

Glucotrol XL
    Dosage: 10 mg q day;po
    Administration route: Oral
    Indication: Diabetes Mellitus
    End date: 2006-06-11

Lanoxin
    Dosage: 0.375 mg q day;po
    Administration route: Oral
    Indication: Tachyarrhythmia
    End date: 2006-06-11

Lantus
    Dosage: 70 u q day;sc
    Indication: Diabetes Mellitus
    Start date: 2006-06-09
    End date: 2006-06-11

Lantus
    Dosage: 65 u q day;sc
    Indication: Diabetes Mellitus
    End date: 2006-06-08

Lipitor
    Dosage: df;
    End date: 2006-06-11

Tenormin
    Dosage: 1000 mg q day;po
    Administration route: Oral
    Indication: Tachyarrhythmia
    End date: 2006-06-11

Trazodone HCL
    Dosage: 200 mg q day;po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Tricor
    Dosage: 160 mg q day;po
    Administration route: Oral
    Indication: Dyslipidaemia
    End date: 2006-06-11

Wellbutrin
    Dosage: 300 mg q day;po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Risperdal
    Dosage: 3 mg; po
    Administration route: Oral

Multi-Vitamins
    Dosage: df;



Adverse event in 65 year old male receiving Actos (Pioglitazone)

Reported by a physician from United States on 2007-02-16

Patient: 65 year old male, weighing 94.8 kg (208.6 pounds)

Adverse reactions / side effects: Flushing, Cardio-Respiratory Arrest, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Niaspan
    Dosage: 1000 mg qd po
    Administration route: Oral
    Indication: Blood Cholesterol Increased
    Start date: 2006-06-11
    End date: 2006-06-11

Niaspan
    Dosage: 1000 mg qd po
    Administration route: Oral
    Indication: High Density Lipoprotein Decreased
    Start date: 2006-06-11
    End date: 2006-06-11

Wellbutrin
    Dosage: 300 mg qd po
    Administration route: Oral
    Indication: Depression

Effexor
    Dosage: 150 mg daily po
    Administration route: Oral
    Indication: Depression

Lorazepam
    Dosage: 2 mg qd po
    Administration route: Oral
    Indication: Depression

Trazodone HCL
    Dosage: 200 mg qd po
    Administration route: Oral
    Indication: Depression

Tenormin
    Dosage: 100 mg qd po
    Administration route: Oral
    Indication: Tachyarrhythmia

Lanoxin
    Dosage: 0.375 mg qd po
    Administration route: Oral

Glucophage
    Dosage: 1000 mg bid po
    Administration route: Oral

Glucotrol XL
    Dosage: 10 mg qd po
    Administration route: Oral

Actos
    Dosage: 45 mg qd po
    Administration route: Oral

Tricor
    Dosage: 160 mg qd po
    Administration route: Oral

Lantus
    Dosage: 70 qd sc
    Start date: 2006-06-09

Lipitor

Vitamin CAP

Risperdal
    Dosage: 3 mg po
    Administration route: Oral



Adverse event in 65 year old male receiving Actos (Pioglitazone)

Reported by a individual with unspecified qualification from United States on 2007-02-07

Patient: 65 year old male

Adverse reactions / side effects: Alanine Aminotransferase Increased, Pallor, High Density Lipoprotein Decreased, Hepatic Steatosis, Flushing, Haemoglobin Decreased, Cardio-Respiratory Arrest, Aspartate Aminotransferase Increased, Myocardial Infarction, Blood Glucose Increased

Adverse event resulted in: death

Suspect drug(s):
Lorazepam
    Dosage: 2 mg q day po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Niaspan
    Dosage: 1000 mg once po
    Administration route: Oral
    Indication: High Density Lipoprotein Decreased
    Start date: 2006-06-11
    End date: 2006-06-11

Niaspan
    Dosage: 1000 mg once po
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2006-06-11
    End date: 2006-06-11

Niaspan
    Dosage: 500 mg q day po
    Administration route: Oral
    Indication: High Density Lipoprotein Decreased

Niaspan
    Dosage: 500 mg q day po
    Administration route: Oral
    Indication: Hypercholesterolaemia

Effexor XR
    Dosage: 150 mg q day po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Actos
    Dosage: 45 mg q day po
    Administration route: Oral
    Indication: Diabetes Mellitus
    End date: 2006-06-11

Glucophage
    Dosage: 1000 mg bid po
    Administration route: Oral
    Indication: Diabetes Mellitus
    End date: 2006-06-11

Glucotrol XL
    Dosage: 10 mg q day po
    Administration route: Oral
    Indication: Diabetes Mellitus
    End date: 2006-06-11

Lanoxin
    Dosage: 0.375 g q day po
    Administration route: Oral
    Indication: Tachyarrhythmia
    End date: 2006-06-11

Lantus
    Dosage: 70 u q day sc
    Indication: Diabetes Mellitus
    Start date: 2006-06-09
    End date: 2006-06-11

Lantus
    Dosage: 65 u q day sc
    Indication: Diabetes Mellitus
    End date: 2006-06-08

Lipitor
    Dosage: df
    End date: 2006-06-11

Tenormin
    Dosage: 100 mg q day po
    Administration route: Oral
    Indication: Tachyarrhythmia
    End date: 2006-06-11

Trazodone HCL
    Dosage: 200 mg q day po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Tricor
    Dosage: 160 mg q day po
    Administration route: Oral
    Indication: Dyslipidaemia
    End date: 2006-06-11

Wellbutrin
    Dosage: 300 mg q day po
    Administration route: Oral
    Indication: Depression
    End date: 2006-06-11

Risperdal
    Dosage: 3 mg po
    Administration route: Oral

Vitamin CAP
    Dosage: df

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