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Index of reports
> Cases resulting in hospitalization (124)
> Cases with Abdominal Pain (10)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in hospitalization where reactions include abdominal pain.
Adverse event in 65 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-15
Patient: 65 year old male
Adverse reactions / side effects: Abdominal Pain, Mechanical Ileus, Diarrhoea, Anorexia, Gastrointestinal Sounds Abnormal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Vasotec; Warfarin Potassium; Probucol
Adverse event in 58 year old male receiving Zetia (Ezetimibe)
Reported by a individual with unspecified qualification from United States on 2007-07-12
Patient: 58 year old male, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Angina Pectoris, Intestinal Obstruction, Constipation, Haemoglobin Decreased, Haematocrit Decreased, Enterovesical Fistula, Sleep Disorder, Colorectal Cancer Metastatic, Blood Cholesterol, Bladder Disorder, Blood Sodium Decreased, Arteriosclerosis, Hypertension
Adverse event resulted in: hospitalization
Suspect drug(s):
Ciprofloxacin HCL
Dosage: total daily dose: 250 mg unit dose: 250 mg
Administration route: Oral
Indication: Prophylaxis
Aspirin
Dosage: total daily dose: 81 mg unit dose: 81 mg
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Irinotecan HCL
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Irinotecan HCL
Start date: 2003-08-18
End date: 2003-08-18
Fluorouracil
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Fluorouracil
Start date: 2003-08-18
End date: 2003-08-18
Xanax
Dosage: total daily dose: 0.5 mg
Administration route: Oral
Indication: Sleep Disorder
Leucovorin Calcium
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Toprol-XL
Dosage: total daily dose: 50 mg
Administration route: Oral
Indication: Hypertension
Zetia
Dosage: total daily dose: 10 mg
Administration route: Oral
Indication: Hypercholesterolaemia
Protonix
Dosage: total daily dose: 40 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Amiodarone HCL
Dosage: total daily dose: 400 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 82 year old female receiving Zetia (Ezetimibe)
Reported by a pharmacist from United States on 2007-05-01
Patient: 82 year old female
Adverse reactions / side effects: Abdominal Pain, Alanine Aminotransferase Increased, Adverse Drug Reaction, Aspartate Aminotransferase Increased, Constipation
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 57 year old male receiving Zetia (Ezetimibe)
Reported by a individual with unspecified qualification from United States on 2007-04-26
Patient: 57 year old male
Adverse reactions / side effects: Haemoglobin Decreased, Abdominal Pain, Haematocrit Decreased, Angina Pectoris, Intestinal Obstruction, Constipation, Blood Sodium Decreased, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia
Dosage: 10 mg/daily/po
Administration route: Oral
Indication: Blood Cholesterol
Cipro
Dosage: 250 mg/daily
Indication: Prophylaxis
Aspirin
Dosage: 81 mg/daily
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Xanax
Dosage: 0.5 mg/daily/po
Administration route: Oral
Indication: Sleep Disorder
Toprol-XL
Dosage: 50 mg/daily/po
Administration route: Oral
Indication: Hypertension
Protonix
Dosage: 40 mg/daily/po
Administration route: Oral
Indication: Hypertension
Amiodarone HCL
Dosage: 200mg/bid/po
Administration route: Oral
Other drugs received by patient: Fluorouracil; Irinotecan HCL; Leucovorin Calcium
Adverse event in 58 year old male receiving Zetia (Ezetimibe)
Reported by a individual with unspecified qualification from United States on 2007-04-17
Patient: 58 year old male, weighing 69.0 kg (151.8 pounds)
Adverse reactions / side effects: Abdominal Pain, Angina Pectoris, Intestinal Obstruction, Constipation
Adverse event resulted in: hospitalization
Suspect drug(s):
Ciprofloxacin HCL
Dosage: total daily dose: 250 mg unit dose: 250 mg
Administration route: Oral
Indication: Prophylaxis
Acetylsalicylic Acid SRT
Dosage: total daily dose: 81 mg unit dose: 81 mg
Administration route: Oral
Indication: Prophylaxis
Start date: 1986-01-01
End date: 2003-08-10
Irinotecan HCL
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Irinotecan HCL
Start date: 2003-08-18
End date: 2003-08-18
Fluorouracil
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-11
Fluorouracil
Start date: 2003-08-18
End date: 2003-08-18
Xanax
Dosage: total daily dose: 0.5 mg
Administration route: Oral
Indication: Sleep Disorder
Leucovorin Calcium
Indication: Colorectal Cancer Metastatic
Start date: 2003-08-11
End date: 2003-08-18
Toprol-XL
Dosage: total daily dose: 50 mg
Administration route: Oral
Indication: Hypertension
Zetia
Dosage: total daily dose: 10 mg
Administration route: Oral
Indication: Hypercholesterolaemia
Protonix
Dosage: total daily dose: 40 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Amiodarone HCL
Dosage: total daily dose: 400 mg
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in 66 year old male receiving Zetia (Ezetimibe)
Reported by a pharmacist from United States on 2007-03-20
Patient: 66 year old male
Adverse reactions / side effects: Abdominal Pain, Thrombocytopenia, Lymphoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-03-05
Patient: 50 year old male
Adverse reactions / side effects: Abdominal Pain, Syncope, Oesophageal Pain, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor
Adverse event in 70 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Canada on 2007-01-24
Patient: 70 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Dyspnoea, Rhabdomyolysis, Hyperkalaemia, Hyperphosphataemia, Urinary Tract Infection, General Physical Health Deterioration, Haemoglobin Decreased, Malaise, Renal Tubular Necrosis, Muscle Spasms, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Start date: 2006-02-01
End date: 2006-04-01
Zetia
Administration route: Oral
Start date: 2006-04-01
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-07-01
End date: 2006-04-01
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-03-20
End date: 2005-07-01
Other drugs received by patient: Valsartan; Aspirin; Hydrochlorothiazide; Atenolol; Atenolol; Dimenhydrinate; Aspirin and Caffeine, Citrated and Codeine Phosphate; Aspirin and Caffeine, Citrated and Codeine Phosphate
Adverse event in 70 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Canada on 2007-01-19
Patient: 70 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Dyspnoea, Rhabdomyolysis, Hyperkalaemia, Hyperphosphataemia, Urinary Tract Infection, General Physical Health Deterioration, Haemoglobin Decreased, Malaise, Renal Tubular Necrosis, Muscle Spasms, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Start date: 2006-02-01
End date: 2006-04-01
Zetia
Administration route: Oral
Start date: 2006-04-01
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-07-01
End date: 2006-04-01
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-03-20
End date: 2005-07-01
Other drugs received by patient: Valsartan; Aspirin; Hydrochlorothiazide; Atenolol; Atenolol; Dimenhydrinate; Aspirin and Caffeine, Citrated and Codeine Phosphate; Aspirin and Caffeine, Citrated and Codeine Phosphate
Adverse event in 84 year old male receiving Zetia (Ezetimibe)
Reported by a pharmacist from Australia on 2007-01-19
Patient: 84 year old male
Adverse reactions / side effects: Abdominal Pain, Vomiting, Dyspnoea, Swelling Face, Pain in Extremity, Nausea
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Amlodipine Besylate; Atenolol; Aspirin
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