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Amaryl (Glimepiride) - Adverse Event Reports - All Cases - Weight Decreased

 



Index of reports > All cases (147) > Cases with Weight Decreased (12)

Below is the selection of adverse event reports related to Amaryl (Glimepiride) that includes all cases where reactions include weight decreased.

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 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 55 year old female receiving Amaryl (Glimepiride)

Reported by a consumer/non-health professional from United States on 2007-05-30

Patient: 55 year old female

Adverse reactions / side effects: Weight Decreased, Injection Site Haemorrhage, Somnolence, Tremor, Blood Glucose Decreased, Diarrhoea, Dizziness, Asthenia, Feeling Abnormal, Blood Glucose Increased

Suspect drug(s):
Amaryl
    Dosage: see image
    Administration route: Oral
    End date: 2007-01-01

Amaryl
    Dosage: see image
    Administration route: Oral
    Start date: 2003-01-01

Amaryl
    Dosage: see image
    Administration route: Oral
    Start date: 2007-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2007-02-03
    End date: 2007-03-04

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2007-03-05



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

Reported by a consumer/non-health professional from United States on 2007-05-30

Patient: 60 year old female, weighing 85.3 kg (187.6 pounds)

Adverse reactions / side effects: Weight Decreased, Blood Glucose Decreased, Injection Site Erythema, Injection Site Pain, Injection Site Bruising, Tremor

Suspect drug(s):
Amaryl
    Dosage: 3 mg; qd; po
    Administration route: Oral
    Indication: Diabetes Mellitus non-Insulin-Dependent
    End date: 2006-11-24

Byetta
    Dosage: 10 mcg; bid; sc, 5 mcg; bid; sc
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-11-20
    End date: 2006-12-19

Byetta
    Dosage: 10 mcg; bid; sc, 5 mcg; bid; sc
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-12-20

Other drugs received by patient: Aspirin



Adverse event in 59 year old female receiving Amaryl (Glimepiride)

Reported by a consumer/non-health professional from United States on 2007-05-30

Patient: 59 year old female, weighing 99.8 kg (219.5 pounds)

Adverse reactions / side effects: Weight Decreased, Nausea, Injection Site Bruising, Constipation, Tremor, Blood Glucose Decreased, Feeling Jittery, Energy Increased, Blood Glucose Increased, Decreased Appetite

Suspect drug(s):
Amaryl
    Indication: Diabetes Mellitus non-Insulin-Dependent

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-01-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-06-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-07-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-09-01
    End date: 2006-01-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-06-01
    End date: 2006-08-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-08-19
    End date: 2006-09-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-09-01

Byetta
    Dosage: see image
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2007-01-01

Byetta

Byetta

Byetta

Pred Forte
    Indication: Drug USE FOR Unknown Indication
    Start date: 2006-12-20
    End date: 2007-01-18

Other drugs received by patient: Amaryl



Adverse event in 77 year old female receiving Amaryl (Glimepiride)

Reported by a consumer/non-health professional from United States on 2007-05-30

Patient: 77 year old female

Adverse reactions / side effects: Blood Glucose Decreased, Weight Decreased, Drug Effect Decreased, Injection Site Extravasation, Injection Site Haemorrhage, Decreased Appetite

Suspect drug(s):
Amaryl
    Dosage: 4 mg
    Indication: Diabetes Mellitus non-Insulin-Dependent

Byetta
    Dosage: 5 mcg;bid;sc
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2007-01-01

Other drugs received by patient: Glucophage XR; Actos



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 receiving Amaryl (Glimepiride)

Reported by a consumer/non-health professional from France on 2007-05-04

Patient:

Adverse reactions / side effects: Weight Decreased, Pruritus

Adverse event resulted in: hospitalization

Suspect drug(s):
Altace
    Dosage: 10 mg, qd
    Administration route: Oral

Amaryl
    Dosage: 2 mg, qd
    Administration route: Oral

Cardensiel
    Dosage: 10 mg, qd
    Administration route: Oral

Lasilix / 00032601 /
    Dosage: 60 mg, qd
    Administration route: Oral

Previscan / 00789001 /
    Dosage: unk, unk
    Administration route: Oral

Tahor
    Dosage: 10 mg, qd
    Administration route: Oral



Adverse event in 73 year old female receiving Amaryl (Glimepiride)

Reported by a health professional (non-physician/pharmacist) from France on 2007-04-30

Patient: 73 year old female

Adverse reactions / side effects: Weight Decreased, Pruritus, Cardiac Pacemaker Insertion, Anorexia

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Administration route: Oral

Cardensiel
    Administration route: Oral

Lasix
    Dosage: daily dose:60mg
    Administration route: Oral

Previscan
    Administration route: Oral

Tahor
    Administration route: Oral

Triatec
    Administration route: Oral



Adverse event in 73 year old female receiving Amaryl (Glimepiride)

Reported by a individual with unspecified qualification from France on 2007-04-27

Patient: 73 year old female

Adverse reactions / side effects: Weight Decreased, Pruritus

Adverse event resulted in: hospitalization

Suspect drug(s):
Amaryl
    Dosage: 2 mg (2 mg, 1 d); oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Atorvastatin Calcium
    Dosage: 10 mg (10 mg, 1 d); oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Bisoprolol Fumarate
    Dosage: 10 mg (10 mg, 1 d); oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Lasix
    Dosage: 1.5 dosage forms (1,5 dosage forms, 1 d); oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Previscan (20 MG, Tablet) (Fluindione)
    Dosage: oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ramipril
    Dosage: 10 mg (5 mg, 2 in 1 d); oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 73 year old female receiving Amaryl (Glimepiride)

Reported by a individual with unspecified qualification on 2007-04-26

Patient: 73 year old female

Adverse reactions / side effects: Weight Decreased, Pruritus

Adverse event resulted in: hospitalization

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

Cardensiel
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Lasilix / 00032601 /
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Previscan / 00789001 /
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Tahor
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Triatec / 00885601 /
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication



Adverse event in 73 year old female receiving Amaryl (Glimepiride)

Reported by a individual with unspecified qualification on 2007-04-26

Patient: 73 year old female

Adverse reactions / side effects: Weight Decreased, Pruritus

Adverse event resulted in: hospitalization

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

Cardensiel
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Lasilix / 00032601 /
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Previscan / 00789001 /
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Tahor
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Triatec / 00885601 /
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

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