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

ARTHRALGIA ( 12 FDA reports)
OSTEOARTHRITIS ( 12 FDA reports)
FALL ( 11 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
MOBILITY DECREASED ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
AORTIC ANEURYSM ( 6 FDA reports)
BLOOD URINE PRESENT ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
FOOT DEFORMITY ( 6 FDA reports)
GASTROINTESTINAL INFECTION ( 6 FDA reports)
GROIN PAIN ( 6 FDA reports)
INJECTION SITE NODULE ( 6 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 6 FDA reports)
JOINT SWELLING ( 6 FDA reports)
MUSCULOSKELETAL PAIN ( 6 FDA reports)
NEPHROLITHIASIS ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
CATARACT ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
ASTHMATIC CRISIS ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
THYROID NEOPLASM ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
INJECTION SITE WARMTH ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MITRAL VALVE DISEASE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
PAIN ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
URINE ANALYSIS ABNORMAL ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ANXIETY ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DEVICE BREAKAGE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCLE HERNIA ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ONYCHOCLASIS ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL INFLAMMATION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)

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