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

DYSPNOEA ( 6 FDA reports)
PAIN ( 6 FDA reports)
FATIGUE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
AFFECTIVE DISORDER ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
CLUMSINESS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPRAXIA ( 3 FDA reports)
GAIT SPASTIC ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
PERIARTHRITIS ( 3 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
TUMOUR NECROSIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ALTERED VISUAL DEPTH PERCEPTION ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
COLON CANCER METASTATIC ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FALL ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO LUNG ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NIGHT BLINDNESS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PHOTOPSIA ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
THIRST ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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