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

FALL ( 11 FDA reports)
FEMUR FRACTURE ( 11 FDA reports)
GAIT DISTURBANCE ( 11 FDA reports)
PAIN ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
FRACTURE DISPLACEMENT ( 7 FDA reports)
INFECTION ( 7 FDA reports)
MUSCLE ATROPHY ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
STRESS FRACTURE ( 7 FDA reports)
TENDERNESS ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
ANAEMIA POSTOPERATIVE ( 6 FDA reports)
BURSITIS ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
GROIN PAIN ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
BONE FORMATION INCREASED ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
NEOPLASM ( 4 FDA reports)
NO THERAPEUTIC RESPONSE ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BLINDNESS ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
GLAUCOMA ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOW TURNOVER OSTEOPATHY ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
PUBIS FRACTURE ( 3 FDA reports)
TRANSAMINASES INCREASED ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
APATHY ( 2 FDA reports)
APPENDICEAL ABSCESS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BENIGN NEOPLASM OF ADRENAL GLAND ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COAGULATION FACTOR DEFICIENCY ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
FOOT OPERATION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEMIANOPIA HETERONYMOUS ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LESION EXCISION ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MALIGNANT MELANOMA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NASAL INFLAMMATION ( 2 FDA reports)
NECROTISING FASCIITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OCULAR VASCULAR DISORDER ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN FISSURES ( 2 FDA reports)
SKULL FRACTURE ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VAGINAL LESION ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL WOUND DEHISCENCE ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY INCREASED ( 1 FDA reports)
ARACHNOID CYST ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE CANCER METASTATIC ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
CYSTOCELE REPAIR ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMYELINATING POLYNEUROPATHY ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAILURE OF IMPLANT ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HYPERACUSIS ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INJURY ASSOCIATED WITH DEVICE ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LATEX ALLERGY ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MASS ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTATIC SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL INJURY ( 1 FDA reports)
OESOPHAGEAL PERFORATION ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORBITAL PSEUDOTUMOUR ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PERIPHERAL ARTERY ANEURYSM ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THYROID CANCER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH ANKYLOSIS ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
UTERINE LEIOMYOMA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VITAMIN D INCREASED ( 1 FDA reports)

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