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

ABDOMINAL PAIN ( 20 FDA reports)
AGRANULOCYTOSIS ( 20 FDA reports)
ANAEMIA ( 20 FDA reports)
BONE DENSITY DECREASED ( 20 FDA reports)
BONE DISORDER ( 20 FDA reports)
DIARRHOEA ( 20 FDA reports)
FISTULA ( 20 FDA reports)
IMPAIRED HEALING ( 20 FDA reports)
NAUSEA ( 20 FDA reports)
OVARIAN CANCER ( 20 FDA reports)
PAIN IN JAW ( 20 FDA reports)
PURULENT DISCHARGE ( 20 FDA reports)
SWELLING ( 20 FDA reports)
TOOTH DISORDER ( 20 FDA reports)
VOMITING ( 20 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 20 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 19 FDA reports)
BLOOD GLUCOSE INCREASED ( 19 FDA reports)
COLITIS ( 19 FDA reports)
DEEP VEIN THROMBOSIS ( 19 FDA reports)
HYPOAESTHESIA ( 19 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 19 FDA reports)
LUNG NEOPLASM MALIGNANT ( 19 FDA reports)
NEOPLASM ( 19 FDA reports)
OEDEMA PERIPHERAL ( 19 FDA reports)
PLATELET COUNT DECREASED ( 19 FDA reports)
SALPINGO-OOPHORECTOMY UNILATERAL ( 19 FDA reports)
SOFT TISSUE DISORDER ( 19 FDA reports)
TENDERNESS ( 19 FDA reports)
TOOTH EXTRACTION ( 19 FDA reports)
WOUND TREATMENT ( 19 FDA reports)
JAW OPERATION ( 18 FDA reports)
OSTEOSCLEROSIS ( 18 FDA reports)
BACTERIAL INFECTION ( 17 FDA reports)
ENDODONTIC PROCEDURE ( 17 FDA reports)
HAEMATOCHEZIA ( 17 FDA reports)
INJURY ( 17 FDA reports)
PRIMARY SEQUESTRUM ( 17 FDA reports)
RIB FRACTURE ( 17 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 16 FDA reports)
GINGIVAL BLEEDING ( 16 FDA reports)
STOMATOCYTES PRESENT ( 16 FDA reports)
ULCER ( 16 FDA reports)
HEART VALVE INCOMPETENCE ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
PERIODONTAL DISEASE ( 15 FDA reports)
SURGERY ( 15 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
CERVICAL SPINAL STENOSIS ( 14 FDA reports)
DEBRIDEMENT ( 14 FDA reports)
DIVERTICULUM INTESTINAL ( 14 FDA reports)
EXOSTOSIS ( 14 FDA reports)
HEPATIC CYST ( 14 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 14 FDA reports)
OEDEMA MUCOSAL ( 14 FDA reports)
ORAL PAIN ( 14 FDA reports)
OSTEOLYSIS ( 14 FDA reports)
PARAESTHESIA ORAL ( 14 FDA reports)
RADICULAR PAIN ( 14 FDA reports)
RHINITIS ( 14 FDA reports)
CALCIFIC DEPOSITS REMOVAL ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
ONYCHOMYCOSIS ( 13 FDA reports)
STOMATITIS ( 13 FDA reports)
ACCIDENT AT WORK ( 12 FDA reports)
ASTHENIA ( 12 FDA reports)
BURSITIS ( 12 FDA reports)
EAR PAIN ( 12 FDA reports)
EPICONDYLITIS ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
PAIN IN EXTREMITY ( 12 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 12 FDA reports)
SYNOVIAL CYST ( 12 FDA reports)
SYNOVITIS ( 12 FDA reports)
TENDONITIS ( 12 FDA reports)
CARPAL TUNNEL SYNDROME ( 11 FDA reports)
FOREIGN BODY ( 11 FDA reports)
MASS EXCISION ( 11 FDA reports)
NECK PAIN ( 11 FDA reports)
ONYCHALGIA ( 10 FDA reports)
OSTEONECROSIS OF JAW ( 10 FDA reports)
ARTHROSCOPY ( 9 FDA reports)
LIGAMENT RUPTURE ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
OSTEONECROSIS ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
STRESS FRACTURE ( 9 FDA reports)
MENISCUS REMOVAL ( 8 FDA reports)
MIGRAINE ( 8 FDA reports)
TENOSYNOVITIS ( 8 FDA reports)
ATROPHY ( 7 FDA reports)
DISTURBANCE IN ATTENTION ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
RADICULOPATHY ( 7 FDA reports)
SLEEP DISORDER ( 7 FDA reports)
SPINAL OSTEOARTHRITIS ( 7 FDA reports)
TENDON SHEATH INCISION ( 7 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
GALLBLADDER POLYP ( 5 FDA reports)
WOUND DEBRIDEMENT ( 5 FDA reports)
FATIGUE ( 4 FDA reports)
ARTHROPATHY ( 3 FDA reports)
HYPOAESTHESIA ORAL ( 3 FDA reports)
DISCOMFORT ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
HEART VALVE INSUFFICIENCY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
TENDON OPERATION ( 2 FDA reports)
ADNEXA UTERI MASS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PAIN ( 1 FDA reports)
PELVIC MASS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)

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