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

THROMBOCYTOPENIA ( 3 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 3 FDA reports)
THROMBOSIS ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
DYSPNOEA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
DELAYED EFFECTS OF RADIATION ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
INFECTION PROPHYLAXIS ( 1 FDA reports)
INJURY ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOFASCITIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
COUGH ( 1 FDA reports)
POLYMYOSITIS ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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