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

SHOCK HAEMORRHAGIC ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 6 FDA reports)
STEVENS-JOHNSON SYNDROME ( 6 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
HEART VALVE INCOMPETENCE ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
TRANSPLANT FAILURE ( 4 FDA reports)
ARTERIAL STENOSIS ( 4 FDA reports)
GRAFT DYSFUNCTION ( 4 FDA reports)
RETROPERITONEAL HAEMATOMA ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
ENDOCARDITIS ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
HEPATITIS ACUTE ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
VOCAL CORD PARALYSIS ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
ACNE ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
ORAL MUCOSA EROSION ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CAVERNOUS SINUS THROMBOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLENIC HAEMORRHAGE ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL BYPASS OPERATION ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)

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