Please choose an event type to view the corresponding MedsFacts report:

WHITE BLOOD CELL COUNT DECREASED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
BRONCHITIS CHRONIC ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SCAPULA FRACTURE ( 2 FDA reports)
CATHETER SITE INFECTION ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
FALL ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
ASTHENIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OLIGOMENORRHOEA ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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