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

DEHYDRATION ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
VOMITING ( 6 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
FALL ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
YAWNING ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ARTHROSCOPY ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
NEUTROPHIL COUNT DECREASED ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
PANCOAST'S TUMOUR ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
SYNOVIORTHESIS ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ARTHRODESIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 2 FDA reports)
BILE DUCT CANCER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPONDYLOSIS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYNOVECTOMY ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TUBERCULOSIS TEST POSITIVE ( 2 FDA reports)
ULCERATIVE KERATITIS ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
AGGRESSION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTROENTERITIS BACTERIAL ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATE CANCER STAGE II ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use