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

COLON CANCER ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
RASH ( 4 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
STAPHYLOCOCCAL INFECTION ( 3 FDA reports)
AGEUSIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BURNS SECOND DEGREE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
SELF-INJURIOUS IDEATION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
ANAEMIA ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
FALL ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GAMMOPATHY ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPLANT SITE ERYTHEMA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL PAIN ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use