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

STAPHYLOCOCCAL INFECTION ( 16 FDA reports)
ANHEDONIA ( 15 FDA reports)
ANXIETY ( 15 FDA reports)
ARTHRITIS ( 15 FDA reports)
BACK PAIN ( 15 FDA reports)
BLADDER NEOPLASM ( 15 FDA reports)
BONE LESION ( 15 FDA reports)
BONE PAIN ( 15 FDA reports)
DEVICE RELATED INFECTION ( 15 FDA reports)
DISABILITY ( 15 FDA reports)
GAIT DISTURBANCE ( 15 FDA reports)
HIATUS HERNIA ( 15 FDA reports)
HOT FLUSH ( 15 FDA reports)
HYDRONEPHROSIS ( 15 FDA reports)
INJURY ( 15 FDA reports)
KYPHOSIS ( 15 FDA reports)
METASTASES TO BONE ( 15 FDA reports)
OSTEOARTHRITIS ( 15 FDA reports)
OSTEONECROSIS OF JAW ( 15 FDA reports)
PAIN ( 15 FDA reports)
PELVI-URETERIC OBSTRUCTION ( 15 FDA reports)
RENAL CYST ( 15 FDA reports)
RIB FRACTURE ( 15 FDA reports)
SCOLIOSIS ( 15 FDA reports)
SPINAL FRACTURE ( 15 FDA reports)
WHEELCHAIR USER ( 15 FDA reports)
BONE DISORDER ( 14 FDA reports)
BREATHING-RELATED SLEEP DISORDER ( 14 FDA reports)
BRUXISM ( 14 FDA reports)
DENTAL CARIES ( 14 FDA reports)
DENTAL PLAQUE ( 14 FDA reports)
DYSGEUSIA ( 14 FDA reports)
GINGIVAL EROSION ( 14 FDA reports)
GINGIVAL OEDEMA ( 14 FDA reports)
ORAL PAIN ( 14 FDA reports)
OSTEONECROSIS ( 14 FDA reports)
PERIODONTAL DISEASE ( 14 FDA reports)
TOOTH ABSCESS ( 14 FDA reports)
TOOTH DEPOSIT ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
BREAST CANCER RECURRENT ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
EMPHYSEMA ( 13 FDA reports)
ROAD TRAFFIC ACCIDENT ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
BRONCHITIS ( 12 FDA reports)
DIPLOPIA ( 12 FDA reports)
DIVERTICULUM ( 12 FDA reports)
HAEMATURIA ( 12 FDA reports)
INFECTION ( 12 FDA reports)
IRON DEFICIENCY ANAEMIA ( 12 FDA reports)
LIPOMA ( 12 FDA reports)
LUNG NEOPLASM ( 12 FDA reports)
FALL ( 11 FDA reports)
ILEUS ( 11 FDA reports)
MENISCUS LESION ( 11 FDA reports)
BARRETT'S OESOPHAGUS ( 10 FDA reports)
BURSITIS ( 10 FDA reports)
CONTUSION ( 10 FDA reports)
MUSCLE STRAIN ( 10 FDA reports)
HYPERCALCAEMIA ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PYELOCALIECTASIS ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
JOINT EFFUSION ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
METASTASES TO SPINE ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
OSTEOPOROSIS ( 8 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
PROTHROMBIN TIME PROLONGED ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
CHILLS ( 6 FDA reports)
DEEP VEIN THROMBOSIS ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
FLANK PAIN ( 6 FDA reports)
MUSCLE INJURY ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
SKIN LESION ( 6 FDA reports)
VOMITING ( 6 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 5 FDA reports)
VERTEBRAL WEDGING ( 5 FDA reports)
DEPRESSION ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 4 FDA reports)
KNEE ARTHROPLASTY ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
MAJOR DEPRESSION ( 4 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 4 FDA reports)
PATHOLOGICAL GAMBLING ( 4 FDA reports)
RADIOTHERAPY ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
COLONIC POLYP ( 2 FDA reports)
DERMAL CYST ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
ABASIA ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
LACERATION ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
URETERAL STENT INSERTION ( 1 FDA reports)
VULVOVAGINAL BURNING SENSATION ( 1 FDA reports)
VULVOVAGINAL PRURITUS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use