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Lanoxin (Digoxin) - Adverse Event Reports - Death - Glycosylated Haemoglobin Increased

 



Index of reports > Cases resulting in death (6) > Cases with Glycosylated Haemoglobin Increased (1)

Below is the selection of adverse event reports related to Lanoxin (Digoxin) that includes cases resulting in death where reactions include glycosylated haemoglobin increased.

Adverse event in 65 year old male receiving Lanoxin (Digoxin)

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;

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