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Amaryl (Glimepiride) - Adverse Event Reports - Other Serious Reactions - Aspartate Aminotransferase Increased

 



Index of reports > Cases resulting in other serious reactions (57) > Cases with Aspartate Aminotransferase Increased (8)

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

Adverse event in male receiving Amaryl (Glimepiride)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-31

Patient: male

Adverse reactions / side effects: Abdominal Pain, Vomiting, Alanine Aminotransferase Increased, Liver Disorder, Malaise, Diarrhoea, Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Anorexia, Cough

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2007-03-23
    End date: 2007-07-03

Miglitol Tablet
    Dosage: daily dose:150mg
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2007-01-27
    End date: 2007-06-23

Other drugs received by patient: Glucobay; Valsartan; Lansoprazole; Lendormin; Glyburide



Adverse event in male receiving Amaryl (Glimepiride)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-26

Patient: male

Adverse reactions / side effects: Abdominal Pain, Malaise, Diarrhoea, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Anorexia, Aspartate Aminotransferase Increased, Liver Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2007-03-23
    End date: 2007-07-03

Miglitol Tablet
    Dosage: daily dose:150mg
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2007-01-27
    End date: 2007-06-23

Other drugs received by patient: Glucobay; Valsartan; Lansoprazole; Lendormin; Glyburide



Adverse event in male receiving Amaryl (Glimepiride)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-10-06

Patient: male

Adverse reactions / side effects: Abdominal Pain, Malaise, Diarrhoea, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Anorexia, Aspartate Aminotransferase Increased, Liver Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2007-03-23
    End date: 2007-07-03

Miglitol Tablet
    Dosage: daily dose:150mg
    Administration route: Oral
    Indication: Diabetes Mellitus
    Start date: 2007-01-27
    End date: 2007-06-23

Other drugs received by patient: Glucobay; Valsartan; Lansoprazole; Lendormin; Daonil



Adverse event in 60 year old male receiving Amaryl (Glimepiride)

Reported by a consumer/non-health professional from Canada on 2007-10-01

Patient: 60 year old male

Adverse reactions / side effects: Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Drug Interaction

Suspect drug(s):
Altace
    Dosage: 10mg per day
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Amaryl
    Dosage: 4mg per day
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Atacand HCT
    Dosage: 1tab per day
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Avandamet
    Dosage: 2mg twice per day
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Imipramine
    Dosage: 10mg twice per day
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Lipitor
    Dosage: 10mg per day
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



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 58 year old female receiving Amaryl (Glimepiride)

Reported by a consumer/non-health professional from Canada on 2007-06-11

Patient: 58 year old female

Adverse reactions / side effects: Confusional State, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Abnormal, Dehydration, Hypoglycaemia, Blood Creatinine Increased

Suspect drug(s):
Amaryl
    Indication: Drug USE FOR Unknown Indication

Avandia
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Crestor



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

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