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Index of reports
> Cases resulting in other serious reactions (152)
> Cases with Fatigue (14)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in other serious reactions where reactions include fatigue.
Adverse event in 72 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-12
Patient: 72 year old male, weighing 74.8 kg (164.7 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Musculoskeletal Pain, Cognitive Disorder, Myalgia, Fatigue, Gait Disturbance, Muscle Spasms, Pain in JAW
Suspect drug(s):
Zetia
Dosage: 10 mgm daily po
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-04-10
End date: 2006-09-02
Crestor
Dosage: 5mgm daily po
Administration route: Oral
Start date: 2007-10-02
End date: 2007-10-09
Adverse event in 80 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-30
Patient: 80 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Fatigue, Nausea, Subcutaneous Abscess, Pyrexia
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2006-09-06
End date: 2007-06-20
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-09-06
End date: 2007-06-20
Adverse event in 76 year old male receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-07-23
Patient: 76 year old male, weighing 72.6 kg (159.7 pounds)
Adverse reactions / side effects: Osteoporosis, Upper Limb Fracture, Amnesia, Fall, Walking AID User, HIP Fracture, Dysarthria, Fatigue, Balance Disorder, Dementia Alzheimer's Type, Blood Cholesterol Increased, Blood Testosterone Decreased, Gait Disturbance, Asthenia, Hallucination
Adverse event resulted in: hospitalization
Suspect drug(s):
Lupron Depot
Dosage: depo-lupron injections1x mo. -every 4 mos im
Indication: Prostate Cancer
Start date: 1995-11-10
End date: 2007-03-03
Zetia 10 MG Don't Remember
Dosage: zetia 1 a day po
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2002-12-14
End date: 2005-12-10
Lupron Depot
Dosage: depo-lupron injections1x mo. -every 4 mos im
Indication: Prostate Cancer
Start date: 1995-11-10
End date: 2007-03-03
Zetia
Dosage: 1 a day
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2002-12-14
End date: 2005-12-10
Adverse event in 80 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-20
Patient: 80 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Fatigue, Nausea, Subcutaneous Abscess, Pyrexia
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2006-09-06
End date: 2007-06-20
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-09-06
End date: 2007-06-20
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-11
Patient: female, weighing 53.5 kg (117.7 pounds)
Adverse reactions / side effects: Blood Thyroid Stimulating Hormone, Pain in Extremity, Muscular Weakness, Exercise Tolerance Decreased, Discomfort, Myalgia, Fatigue, Limb Discomfort, Muscle Fatigue, Emotional Disorder, Gait Disturbance, Spinal Operation
Suspect drug(s):
Lipitor
Indication: Blood Cholesterol Increased
Start date: 2004-01-01
End date: 2006-07-01
Drug, Unspecified
Indication: Blood Cholesterol Increased
Start date: 2006-11-01
End date: 2006-12-01
Vytorin
Indication: Blood Cholesterol Increased
Zocor
Indication: Blood Cholesterol Increased
Zetia
Indication: Blood Cholesterol Increased
Start date: 2007-02-01
End date: 2007-03-01
Other drugs received by patient: Synthroid; Acyclovir; Premarin; Zoloft; Diovan; Hydrochlorothiazide
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-11
Patient: male, weighing 73.5 kg (161.7 pounds)
Adverse reactions / side effects: Diabetes Mellitus, Drug Interaction, Left Ventricular Failure, Hot Flush, Fatigue, Dizziness, Vision Blurred, Nervousness
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient possibly interacting with the suspect drug:
Tikosyn
Indication: Atrial Fibrillation
Sitagliptin
Indication: Type 2 Diabetes Mellitus
Other drugs received by patient: Coumadin; Aspirin; Omeprazole; Potassium Chloride; Isosorbide Mononitrate; Bumex; Atenolol
Adverse event in 64 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-06-29
Patient: 64 year old female
Adverse reactions / side effects: Fatigue, Urinary Incontinence, Dizziness, Headache, Nocturia, Micturition Urgency, Blood Glucose Increased
Suspect drug(s):
Detrol LA
Indication: Bladder Disorder
Detrol LA
Indication: Incontinence
Oxybutynin Chloride
Indication: Bladder Disorder
Start date: 2007-05-15
End date: 2007-05-29
Oxybutynin Chloride
Indication: Incontinence
Zetia
Indication: Blood Cholesterol
Other drugs received by patient: Actos
Adverse event in 65 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-06-26
Patient: 65 year old female
Adverse reactions / side effects: Urticaria Generalised, Fatigue, Blood Lactate Dehydrogenase Increased, Muscular Weakness, Dizziness, Platelet Count Decreased
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Norvasc; Micardis; Juvela N; Juvela N; Livalo
Adverse event in 76 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-30
Patient: 76 year old male
Adverse reactions / side effects: Fatigue, Blood Creatine Phosphokinase Abnormal, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2007-04-01
End date: 2007-04-01
Zocor
End date: 2007-04-01
Other drugs received by patient: Gemfibrozil; Amiodarone; Lasix; [therapy Unspecified]
Adverse event in 76 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-29
Patient: 76 year old male
Adverse reactions / side effects: Fatigue, Blood Creatine Phosphokinase Normal, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2007-04-01
End date: 2007-04-01
Zocor
End date: 2007-04-01
Other drugs received by patient: Gemfibrozil; Amiodarone; Lasix; [therapy Unspecified]
Adverse event in 77 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-04-30
Patient: 77 year old female
Adverse reactions / side effects: Abdominal Pain, Lymphadenopathy, Haemorrhage, Chills, Pain, Wheezing, Headache, Pyrexia, Abdominal Pain Upper, Hand Deformity, Myalgia, Fatigue, Lymph Node Pain, DRY Throat, Chest Pain, Oedema Peripheral, Abdominal Distension, Adverse Event, Pharyngolaryngeal Pain, Aneurysm, Muscle Spasms, Back Pain, Gingival Bleeding, Dyspnoea, Dysphagia, Blood Urine Present, Coronary Artery Disease, Muscular Weakness, Rash, Arthralgia, Asthenia
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2003-12-01
End date: 2006-06-28
Zetia
Administration route: Oral
Other drugs received by patient: Singulair; Tricor; Nystatin; Quinine; Prilosec; Asmanex Twisthaler; Albuterol; Levothyroxine Sodium; Plavix; Spiriva; Xalatan
Adverse event in 79 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-07
Patient: 79 year old male, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Fatigue, Anorexia, Macular Degeneration
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Inositol Niacinate
Adverse event in 68 year old receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-02
Patient: 68 year old , weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Dyspnoea, Fatigue, Oedema, Atrial Fibrillation, Dizziness, Shock, Paraesthesia
Suspect drug(s):
Zetia
Administration route: Oral
Acipimox
Amiodarone
Aspirin
Bisoprolol
Digoxin
Furosemide
Lansoprazole
Perindopril
Adverse event in 58 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-01-30
Patient: 58 year old female
Adverse reactions / side effects: Staphylococcal Skin Infection, Toxic Epidermal Necrolysis, Oral Mucosal Exfoliation, Eosinophilia, Fatigue, Malaise, Erythema Multiforme, Application Site Scab
Suspect drug(s):
Aldara
Dosage: (0.5 sachet, 5 in 1 week (s)), topical
Administration route: Topical
Indication: Actinic Keratosis
Start date: 2006-01-01
End date: 2006-01-01
Aldara
Dosage: (0.5 sachet, 5 in 1 week (s)), topical
Administration route: Topical
Indication: Basal Cell Carcinoma
Start date: 2006-01-01
End date: 2006-01-01
Aldara
Dosage: (0.5 sachet, 5 in 1 week (s)), topical
Administration route: Topical
Indication: Actinic Keratosis
Start date: 2006-12-25
End date: 2007-01-13
Aldara
Dosage: (0.5 sachet, 5 in 1 week (s)), topical
Administration route: Topical
Indication: Basal Cell Carcinoma
Start date: 2006-12-25
End date: 2007-01-13
Altace
Hydrochlorothiazide
Zetia
Folic Acid
Aspirin
Fish OIL
Keflex
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