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Index of reports
> Cases resulting in life threatening events (34)
> Cases with Fatigue (5)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in life threatening events where reactions include fatigue.
Adverse event in 37 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10
Patient: 37 year old female
Adverse reactions / side effects: Pruritus, Pain, Muscular Weakness, Hypoaesthesia, Tremor, Menstruation Irregular, Myalgia, Fatigue, Poor Peripheral Circulation, Musculoskeletal Stiffness, Feeling Abnormal, Asthenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 56 year old female receiving Zetia (Ezetimibe)
Reported by a pharmacist from United Kingdom on 2007-05-31
Patient: 56 year old female
Adverse reactions / side effects: Fatigue, Suicidal Behaviour, Depression, Aggression
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Diclofenac; Lisinopril; Atorvastatin Calcium; Hormones (Unspecified)
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 56 year old female receiving Zetia (Ezetimibe)
Reported by a pharmacist from United Kingdom on 2007-04-09
Patient: 56 year old female
Adverse reactions / side effects: Fatigue, Suicidal Behaviour, Depression, Aggression
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Diclofenac; Lisinopril; Primaxin; Atorvastatin Calcium
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