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Amaryl (Glimepiride) - Adverse Event Reports - Other Serious Reactions - Blood Creatine Phosphokinase Increased

 



Index of reports > Cases resulting in other serious reactions (57) > Cases with Blood Creatine Phosphokinase Increased (7)

Below is the selection of adverse event reports related to Amaryl (Glimepiride) that includes cases resulting in other serious reactions where reactions include blood creatine phosphokinase increased.

Adverse event in 74 year old male receiving Amaryl (Glimepiride)

Reported by a pharmacist from Japan on 2007-10-23

Patient: 74 year old male

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased

Suspect drug(s):
Amaryl (Glimepiride)

Other drugs received by patient: Lipitor



Adverse event in 74 year old male receiving Amaryl (Glimepiride)

Reported by a pharmacist from Japan on 2007-10-11

Patient: 74 year old male

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased

Suspect drug(s):
Amaryl (Glimepiride)

Other drugs received by patient: Lipitor



Adverse event in 69 year old female receiving Amaryl (Glimepiride)

Reported by a physician from Japan on 2007-07-03

Patient: 69 year old female, weighing 59.0 kg (129.8 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Weight Decreased, White Blood Cell Count Decreased, Blood Creatine Phosphokinase Increased, Alanine Aminotransferase Increased, Monocyte Count Increased, Hypokalaemia, Blood Potassium Decreased, Aspartate Aminotransferase Increased, Blood Sodium Increased, Oedema, Platelet Count Decreased, Muscle Spasms

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Dosage: 1 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Diovan
    Dosage: 80 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Fluitran
    Dosage: 2 mg/day
    Administration route: Oral
    Indication: Oedema
    End date: 2007-03-19

Glycyron
    Dosage: 3 df/day
    Administration route: Oral
    Indication: Hepatic Cirrhosis
    End date: 2007-03-19

Norvasc
    Dosage: 5 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Norvasc
    Start date: 2007-04-04

Other drugs received by patient: Aldactone



Adverse event in 61 year old male receiving Amaryl (Glimepiride)

Reported by a physician from Japan on 2007-06-25

Patient: 61 year old male

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased

Suspect drug(s):
Amaryl (Glimepiride)

Other drugs received by patient: Glimicron; Glimicron



Adverse event in 69 year old female receiving Amaryl (Glimepiride)

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

Patient: 69 year old female, weighing 59.0 kg (129.8 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Weight Decreased, White Blood Cell Count Decreased, Blood Creatine Phosphokinase Increased, Alanine Aminotransferase Increased, Monocyte Count Increased, Hypokalaemia, Blood Potassium Decreased, Aspartate Aminotransferase Increased, Blood Sodium Increased, Oedema, Platelet Count Decreased, Muscle Spasms

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Dosage: 1 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Diovan
    Dosage: 80 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Fluitran
    Dosage: 2 mg/day
    Administration route: Oral
    Indication: Oedema
    End date: 2007-03-19

Glycyron
    Dosage: 3 df/day
    Administration route: Oral
    Indication: Hepatic Cirrhosis
    End date: 2007-03-19

Norvasc
    Dosage: 5 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Norvasc
    Start date: 2007-04-04

Other drugs received by patient: Aldactone



Adverse event in 69 year old female receiving Amaryl (Glimepiride)

Reported by a physician from Japan on 2007-05-23

Patient: 69 year old female, weighing 59.0 kg (129.8 pounds)

Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Weight Decreased, White Blood Cell Count Decreased, Blood Creatine Phosphokinase Increased, Alanine Aminotransferase Increased, Monocyte Count Increased, Muscle Twitching, Hypokalaemia, Blood Potassium Decreased, Aspartate Aminotransferase Increased, Oedema, Blood Sodium Increased, Platelet Count Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Dosage: 1 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Diovan
    Dosage: 80 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Fluitran
    Dosage: 2 mg/day
    Administration route: Oral
    Indication: Oedema
    End date: 2007-03-19

Glycyron
    Dosage: 3 df/day
    Administration route: Oral
    Indication: Hepatic Cirrhosis
    End date: 2007-03-19

Norvasc
    Dosage: 5 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Norvasc
    Start date: 2007-04-04

Other drugs received by patient: Aldactone



Adverse event in 69 year old female receiving Amaryl (Glimepiride)

Reported by a physician from Japan on 2007-04-30

Patient: 69 year old female

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased

Suspect drug(s):
Amaryl
    Dosage: 1 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Diovan
    Dosage: 80 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Fluitran
    Dosage: 2 mg/day
    Administration route: Oral
    End date: 2007-03-19

Glycyron
    Dosage: 3 df/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

Norvasc
    Dosage: 5 mg/day
    Administration route: Oral
    Indication: Hypertension
    End date: 2007-03-19

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