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

ANAEMIA ( 8 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 8 FDA reports)
ORTHOSTATIC HYPOTENSION ( 7 FDA reports)
PLATELET COUNT DECREASED ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
PYREXIA ( 6 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
COAGULATION TIME PROLONGED ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOPROTEINAEMIA ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY INFARCTION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD ALUMINIUM INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COAGULATION TEST ABNORMAL ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECHINOCOCCIASIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
ILEUS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MILIARY PNEUMONIA ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
URINARY SEDIMENT PRESENT ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VULVAL ULCERATION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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