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

ARTHRALGIA ( 5 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BREAST CANCER ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
STRESS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FALL ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMA ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL MYOCARDIAL INFARCTION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
TETANY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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