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

PAIN ( 33 FDA reports)
PNEUMONIA ( 32 FDA reports)
ANXIETY ( 31 FDA reports)
OSTEOMYELITIS ( 30 FDA reports)
PLEURAL EFFUSION ( 28 FDA reports)
INJURY ( 27 FDA reports)
OSTEONECROSIS OF JAW ( 27 FDA reports)
DIARRHOEA ( 25 FDA reports)
DEPRESSION ( 24 FDA reports)
FALL ( 24 FDA reports)
SPINAL COMPRESSION FRACTURE ( 24 FDA reports)
BONE DISORDER ( 23 FDA reports)
ANAEMIA ( 22 FDA reports)
ATELECTASIS ( 22 FDA reports)
BRONCHITIS ( 21 FDA reports)
FACIAL PAIN ( 20 FDA reports)
MALNUTRITION ( 20 FDA reports)
CARDIOMEGALY ( 19 FDA reports)
FATIGUE ( 19 FDA reports)
ABSCESS DRAINAGE ( 18 FDA reports)
CHOLELITHIASIS ( 18 FDA reports)
CONTUSION ( 18 FDA reports)
HIATUS HERNIA ( 18 FDA reports)
OSTEOPOROSIS ( 18 FDA reports)
THROMBOCYTOSIS ( 18 FDA reports)
TOOTH EXTRACTION ( 18 FDA reports)
ABSCESS ORAL ( 17 FDA reports)
ANHEDONIA ( 17 FDA reports)
ARTHRALGIA ( 17 FDA reports)
EMPHYSEMA ( 17 FDA reports)
ERB'S PALSY ( 17 FDA reports)
FACIAL BONES FRACTURE ( 17 FDA reports)
GASTRINOMA ( 17 FDA reports)
MENTAL DISORDER ( 17 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 17 FDA reports)
NEPHROLITHIASIS ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
PERIODONTAL DISEASE ( 17 FDA reports)
RECTAL PROLAPSE ( 17 FDA reports)
ROTATOR CUFF SYNDROME ( 17 FDA reports)
ULCER HAEMORRHAGE ( 17 FDA reports)
WEIGHT DECREASED ( 17 FDA reports)
OESOPHAGEAL STENOSIS ( 16 FDA reports)
ADENOMA BENIGN ( 15 FDA reports)
COMPRESSION FRACTURE ( 15 FDA reports)
DEHYDRATION ( 15 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
HYPERTENSION ( 15 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 15 FDA reports)
ARTERIOSCLEROSIS ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLINDNESS TRANSIENT ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 14 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 14 FDA reports)
DYSPHAGIA ( 14 FDA reports)
EXTRASYSTOLES ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 14 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
OSTEOPENIA ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
RIB FRACTURE ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
BONE OPERATION ( 13 FDA reports)
CHOROIDAL DETACHMENT ( 13 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 13 FDA reports)
ENDODONTIC PROCEDURE ( 13 FDA reports)
EYE INJURY ( 13 FDA reports)
GINGIVAL SWELLING ( 13 FDA reports)
MASS ( 13 FDA reports)
OPEN REDUCTION OF FRACTURE ( 13 FDA reports)
RECTAL PROLAPSE REPAIR ( 13 FDA reports)
SWELLING FACE ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
DIPLOPIA ( 12 FDA reports)
ECTROPION ( 12 FDA reports)
GLAUCOMA ( 12 FDA reports)
HEAD INJURY ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 12 FDA reports)
MYOPIA ( 12 FDA reports)
VITREOUS DETACHMENT ( 12 FDA reports)
VITREOUS FLOATERS ( 12 FDA reports)
BASAL CELL CARCINOMA ( 11 FDA reports)
CAECUM OPERATION ( 11 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
GAIT DISTURBANCE ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
PERIARTHRITIS ( 10 FDA reports)
SCOLIOSIS ( 10 FDA reports)
SYNCOPE ( 10 FDA reports)
TENDERNESS ( 10 FDA reports)
TENDONITIS ( 10 FDA reports)
CONSTIPATION ( 9 FDA reports)
HYPOXIA ( 9 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
HAEMORRHOIDS ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
METASTASES TO BONE ( 8 FDA reports)
ORAL PAIN ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PURULENT DISCHARGE ( 8 FDA reports)
RECTAL HAEMORRHAGE ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
BALANCE DISORDER ( 7 FDA reports)
BONE LESION ( 7 FDA reports)
BREAST CANCER RECURRENT ( 7 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 7 FDA reports)
CYST ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
DYSPNOEA EXERTIONAL ( 7 FDA reports)
ENDOMETRIAL DISORDER ( 7 FDA reports)
HAEMANGIOMA OF LIVER ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
HYPOVENTILATION ( 7 FDA reports)
LUNG INFILTRATION ( 7 FDA reports)
MOUTH HAEMORRHAGE ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OPEN WOUND ( 7 FDA reports)
PAINFUL DEFAECATION ( 7 FDA reports)
PHARYNGITIS ( 7 FDA reports)
PNEUMOTHORAX ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
RASH ( 7 FDA reports)
RECTAL FISSURE ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKELETAL INJURY ( 7 FDA reports)
SKIN NEOPLASM EXCISION ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
TOOTH ABSCESS ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
UTERINE LEIOMYOMA ( 7 FDA reports)
WALKING AID USER ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ANIMAL BITE ( 6 FDA reports)
BENIGN NEOPLASM OF THYROID GLAND ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
COLON NEOPLASM ( 6 FDA reports)
DECREASED INTEREST ( 6 FDA reports)
DEFAECATION URGENCY ( 6 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 6 FDA reports)
EDENTULOUS ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
FISTULA ( 6 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GINGIVAL ERYTHEMA ( 6 FDA reports)
GRANULOMA ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LOCALISED INFECTION ( 6 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 6 FDA reports)
METASTASES TO LUNG ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PANCREATIC NEOPLASM ( 6 FDA reports)
PLANTAR FASCIITIS ( 6 FDA reports)
RASH PRURITIC ( 6 FDA reports)
RENAL ATROPHY ( 6 FDA reports)
SENSATION OF PRESSURE ( 6 FDA reports)
TRAUMATIC HAEMATOMA ( 6 FDA reports)
ANASTOMOTIC LEAK ( 5 FDA reports)
ASPIRATION PLEURAL CAVITY ( 5 FDA reports)
BRONCHIAL NEOPLASM ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
COLONIC OBSTRUCTION ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
FAECALOMA ( 5 FDA reports)
JAW LESION EXCISION ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 5 FDA reports)
METASTASES TO SPINE ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PERICARDIAL EFFUSION ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
SWELLING ( 5 FDA reports)
URETERIC OBSTRUCTION ( 5 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
OEDEMA MUCOSAL ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
SEROSITIS ( 4 FDA reports)
VOMITING ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
INFECTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE LOSS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
LIGAMENT SPRAIN ( 2 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 2 FDA reports)
METASTASES TO PERITONEUM ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
ORAL INFECTION ( 2 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 2 FDA reports)
ORAL NEOPLASM ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
PATHOLOGICAL FRACTURE ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SPLENIC GRANULOMA ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ADJUSTMENT DISORDER WITH MIXED DISTURBANCE OF EMOTION AND CONDUCT ( 1 FDA reports)
AORTIC VALVE SCLEROSIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISORDER ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BUNION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
LACTOSE INTOLERANCE ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOSS OF LIBIDO ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MACROGNATHIA ( 1 FDA reports)
MAMMOGRAM ABNORMAL ( 1 FDA reports)
MASTECTOMY ( 1 FDA reports)
MENIERE'S DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PHYSICAL BREAST EXAMINATION ABNORMAL ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMEAR CERVIX ABNORMAL ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ULTRASOUND PELVIS ABNORMAL ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VAGINAL DISCHARGE ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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