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

FEMUR FRACTURE ( 16 FDA reports)
FALL ( 13 FDA reports)
OSTEOARTHRITIS ( 10 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
ACTINIC KERATOSIS ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
DEVICE FAILURE ( 5 FDA reports)
HAEMORRHOIDS ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
LIMB DISCOMFORT ( 5 FDA reports)
LOW TURNOVER OSTEOPATHY ( 5 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
MAJOR DEPRESSION ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
VENOUS INSUFFICIENCY ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACUTE SINUSITIS ( 4 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 4 FDA reports)
ANASTOMOTIC ULCER ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHEST INJURY ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG INEFFECTIVE ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
FIBROADENOMA OF BREAST ( 4 FDA reports)
FIBROCYSTIC BREAST DISEASE ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HAEMORRHAGIC DISORDER ( 4 FDA reports)
HAND FRACTURE ( 4 FDA reports)
HEAD INJURY ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
LICHEN SCLEROSUS ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MORTON'S NEUROMA ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
ROAD TRAFFIC ACCIDENT ( 4 FDA reports)
SEASONAL ALLERGY ( 4 FDA reports)
SHIGELLA INFECTION ( 4 FDA reports)
SPINAL COLUMN STENOSIS ( 4 FDA reports)
SPINAL FRACTURE ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CHANGE OF BOWEL HABIT ( 3 FDA reports)
CHONDROPATHY ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
OCCULT BLOOD POSITIVE ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN LACERATION ( 3 FDA reports)
SPLENOMEGALY ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
FEAR ( 2 FDA reports)
HAEMORRHAGIC ANAEMIA ( 2 FDA reports)
MUCOSAL ULCERATION ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
STRESS ( 2 FDA reports)
TRIGGER FINGER ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ADENOIDAL DISORDER ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
FACET JOINT SYNDROME ( 1 FDA reports)
FRACTURE NONUNION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
RASH ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
UMBILICAL HERNIA ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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