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

CARDIAC FAILURE ( 8 FDA reports)
INFECTION ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
CD4 LYMPHOCYTES INCREASED ( 4 FDA reports)
CHOKING ( 4 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 4 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
SKIN ULCER ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
COLITIS ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PERICARDITIS ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
5-HYDROXYINDOLACETIC ACID INCREASED ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BLAST CELLS PRESENT ( 1 FDA reports)
BLOOD CHROMOGRANIN A INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE NEOPLASM MALIGNANT ( 1 FDA reports)
CARCINOID SYNDROME ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL ANAESTHESIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
NASAL SEPTUM PERFORATION ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
REFRACTORY CYTOPENIA WITH MULTILINEAGE DYSPLASIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SODIUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
X-RAY DENTAL ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use