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

DYSPNOEA ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
VIRAL PHARYNGITIS ( 5 FDA reports)
LETHARGY ( 5 FDA reports)
LUPUS-LIKE SYNDROME ( 5 FDA reports)
CARPAL TUNNEL SYNDROME ( 5 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PERICARDITIS ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
PAIN ( 5 FDA reports)
JOINT SWELLING ( 4 FDA reports)
ARTHRALGIA ( 4 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 4 FDA reports)
INJURY ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
PARAESTHESIA ( 3 FDA reports)
BONE INFECTION ( 3 FDA reports)
RENAL MASS ( 3 FDA reports)
ARTHRITIS INFECTIVE ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
DYSPEPSIA ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
COLITIS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
BLOODY DISCHARGE ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
MALAISE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
LEPROSY ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
FALL ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)

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