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PULMONARY EMBOLISM ( 5 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
PULMONARY HAEMORRHAGE ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
VOMITING ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
FACTOR VIII INHIBITION ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
COUGH ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
VON WILLEBRAND'S FACTOR ACTIVITY INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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