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

ANAEMIA ( 12 FDA reports)
DEHYDRATION ( 11 FDA reports)
FATIGUE ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
VOMITING ( 8 FDA reports)
OFF LABEL USE ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
HEADACHE ( 6 FDA reports)
ORAL MUCOSA ATROPHY ( 6 FDA reports)
MENORRHAGIA ( 5 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 4 FDA reports)
STOMATITIS ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
RASH ( 3 FDA reports)
DEATH ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
DYSPHAGIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
HAEMOPHILUS INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
TRICUSPID VALVE SCLEROSIS ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 1 FDA reports)
MITRAL VALVE SCLEROSIS ( 1 FDA reports)

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