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

NAUSEA ( 8 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
VOMITING ( 4 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
BLISTER ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SCRATCH ( 2 FDA reports)
DEATH ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
ABASIA ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
LACRIMAL DISORDER ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
CORNEAL TRANSPLANT ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORNEAL NEOVASCULARISATION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

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