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

INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
MALAISE ( 5 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 5 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CEREBRAL INFARCTION ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FALL ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
MALIGNANT MELANOMA ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FELTY'S SYNDROME ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LEUKAEMIA ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
XERODERMA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FLOPPY IRIS SYNDROME ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERMAGNESAEMIA ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
METASTASES TO ADRENALS ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO EYE ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PELVIC ABSCESS ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)

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