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

PAIN IN EXTREMITY ( 7 FDA reports)
SKIN EXFOLIATION ( 7 FDA reports)
DEATH ( 6 FDA reports)
JAUNDICE ( 5 FDA reports)
RASH ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
SKIN NECROSIS ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
SKIN INDURATION ( 5 FDA reports)
SKIN HYPERPIGMENTATION ( 5 FDA reports)
SKIN FIBROSIS ( 5 FDA reports)
PAIN OF SKIN ( 5 FDA reports)
PEAU D'ORANGE ( 5 FDA reports)
PURPURA ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
OEDEMA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
ANTI-ERYTHROPOIETIN ANTIBODY POSITIVE ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
DIARRHOEA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER RELATED COMPLICATION ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)

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