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

ARTHRALGIA ( 38 FDA reports)
BONE DISORDER ( 37 FDA reports)
OSTEOMYELITIS ( 37 FDA reports)
CHOLELITHIASIS ( 36 FDA reports)
PAIN ( 35 FDA reports)
DYSPHAGIA ( 34 FDA reports)
DEPRESSION ( 32 FDA reports)
VISION BLURRED ( 32 FDA reports)
BASAL CELL CARCINOMA ( 31 FDA reports)
GLAUCOMA ( 31 FDA reports)
VITREOUS DETACHMENT ( 31 FDA reports)
OSTEONECROSIS OF JAW ( 29 FDA reports)
ROTATOR CUFF SYNDROME ( 29 FDA reports)
TENDERNESS ( 29 FDA reports)
VITREOUS FLOATERS ( 29 FDA reports)
OSTEOARTHRITIS ( 28 FDA reports)
RIB FRACTURE ( 26 FDA reports)
DYSGEUSIA ( 25 FDA reports)
OEDEMA PERIPHERAL ( 25 FDA reports)
TOOTH EXTRACTION ( 24 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 23 FDA reports)
CONTUSION ( 23 FDA reports)
ABDOMINAL PAIN UPPER ( 21 FDA reports)
ANXIETY ( 21 FDA reports)
PERIODONTAL DISEASE ( 21 FDA reports)
SWELLING FACE ( 21 FDA reports)
FATIGUE ( 20 FDA reports)
GINGIVAL ULCERATION ( 20 FDA reports)
IMPAIRED HEALING ( 20 FDA reports)
INFLAMMATION ( 20 FDA reports)
NECROSIS ( 20 FDA reports)
TOOTH INFECTION ( 20 FDA reports)
ABDOMINAL PAIN ( 19 FDA reports)
ABSCESS ( 19 FDA reports)
BACK PAIN ( 19 FDA reports)
BURSITIS ( 19 FDA reports)
CAROTID ARTERY STENOSIS ( 19 FDA reports)
CATARACT ( 19 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 19 FDA reports)
DIARRHOEA ( 19 FDA reports)
DILATATION VENTRICULAR ( 19 FDA reports)
FISTULA ( 19 FDA reports)
GINGIVAL BLEEDING ( 19 FDA reports)
HEPATIC CYST ( 19 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 19 FDA reports)
MITRAL VALVE INCOMPETENCE ( 19 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 19 FDA reports)
NASAL CONGESTION ( 19 FDA reports)
ORAL DISORDER ( 19 FDA reports)
ORAL PAIN ( 19 FDA reports)
OSTEOPOROSIS ( 19 FDA reports)
PRESYNCOPE ( 19 FDA reports)
PRIMARY SEQUESTRUM ( 19 FDA reports)
PURULENCE ( 19 FDA reports)
RENAL CYST ( 19 FDA reports)
SENSITIVITY OF TEETH ( 19 FDA reports)
SINUS DISORDER ( 19 FDA reports)
SINUS POLYP DEGENERATION ( 19 FDA reports)
SINUSITIS ( 19 FDA reports)
TOOTH DISORDER ( 19 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 19 FDA reports)
UPPER LIMB FRACTURE ( 19 FDA reports)
ABSCESS ORAL ( 18 FDA reports)
ANAEMIA ( 18 FDA reports)
ANHEDONIA ( 18 FDA reports)
ARTHRITIS ( 18 FDA reports)
CHEST PAIN ( 18 FDA reports)
EMPHYSEMA ( 18 FDA reports)
GASTRINOMA ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
HYDRONEPHROSIS ( 18 FDA reports)
INJURY ( 18 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 18 FDA reports)
MYELOPROLIFERATIVE DISORDER ( 18 FDA reports)
SPINAL COMPRESSION FRACTURE ( 18 FDA reports)
ULCER HAEMORRHAGE ( 18 FDA reports)
WEIGHT DECREASED ( 18 FDA reports)
COUGH ( 17 FDA reports)
ERB'S PALSY ( 17 FDA reports)
FACIAL BONES FRACTURE ( 17 FDA reports)
FALL ( 17 FDA reports)
HIATUS HERNIA ( 17 FDA reports)
MASTITIS ( 17 FDA reports)
MENTAL DISORDER ( 17 FDA reports)
NEPHROLITHIASIS ( 17 FDA reports)
RECTAL PROLAPSE ( 17 FDA reports)
THROMBOCYTOSIS ( 17 FDA reports)
DEHYDRATION ( 16 FDA reports)
FEELING ABNORMAL ( 16 FDA reports)
HYPERCHOLESTEROLAEMIA ( 16 FDA reports)
LYMPHOEDEMA ( 16 FDA reports)
MALIGNANT MELANOMA IN SITU ( 16 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 16 FDA reports)
OESOPHAGEAL STENOSIS ( 16 FDA reports)
PNEUMONIA ( 16 FDA reports)
ADENOMA BENIGN ( 15 FDA reports)
COMPRESSION FRACTURE ( 15 FDA reports)
FACIAL PAIN ( 15 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 15 FDA reports)
ABSCESS DRAINAGE ( 14 FDA reports)
ARTERIOSCLEROSIS ( 14 FDA reports)
ATELECTASIS ( 14 FDA reports)
BILIARY DILATATION ( 14 FDA reports)
BLINDNESS TRANSIENT ( 14 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 14 FDA reports)
BONE OPERATION ( 14 FDA reports)
BRONCHITIS ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
CHOLECYSTITIS ( 14 FDA reports)
CLAVICLE FRACTURE ( 14 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 14 FDA reports)
DIVERTICULUM OESOPHAGEAL ( 14 FDA reports)
ENDODONTIC PROCEDURE ( 14 FDA reports)
EXTRASYSTOLES ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
HYPERTENSION ( 14 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 14 FDA reports)
MALNUTRITION ( 14 FDA reports)
OESOPHAGEAL FOOD IMPACTION ( 14 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 14 FDA reports)
ORAL MUCOSAL HYPERTROPHY ( 14 FDA reports)
OSTEOPENIA ( 14 FDA reports)
PAIN IN EXTREMITY ( 14 FDA reports)
PANCREATITIS ACUTE ( 14 FDA reports)
PLEURAL EFFUSION ( 14 FDA reports)
PULMONARY MASS ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
VENTRICULAR TACHYCARDIA ( 14 FDA reports)
BONE SCAN ABNORMAL ( 13 FDA reports)
CHOROIDAL DETACHMENT ( 13 FDA reports)
COLONIC POLYP ( 13 FDA reports)
DIVERTICULUM ( 13 FDA reports)
EYE INJURY ( 13 FDA reports)
LUNG INFILTRATION ( 13 FDA reports)
MUSCULOSKELETAL PAIN ( 13 FDA reports)
OPEN REDUCTION OF FRACTURE ( 13 FDA reports)
RECTAL PROLAPSE REPAIR ( 13 FDA reports)
VITREOUS HAEMORRHAGE ( 13 FDA reports)
BREAST CANCER RECURRENT ( 12 FDA reports)
DIPLOPIA ( 12 FDA reports)
ECTROPION ( 12 FDA reports)
HEAD INJURY ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
HYPOTONY OF EYE ( 12 FDA reports)
KERATITIS ( 12 FDA reports)
KERATOCONJUNCTIVITIS SICCA ( 12 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 12 FDA reports)
MONOCYTE COUNT INCREASED ( 12 FDA reports)
MOOD SWINGS ( 12 FDA reports)
MYOPIA ( 12 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
SKIN NEOPLASM EXCISION ( 12 FDA reports)
SPINAL DISORDER ( 12 FDA reports)
CAECUM OPERATION ( 11 FDA reports)
METASTASES TO BONE ( 11 FDA reports)
MUSCULAR WEAKNESS ( 11 FDA reports)
RASH PRURITIC ( 11 FDA reports)
TOOTH ABSCESS ( 11 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 11 FDA reports)
BONE TRIMMING ( 10 FDA reports)
BRONCHIOLITIS ( 10 FDA reports)
CHOLECYSTECTOMY ( 10 FDA reports)
DEBRIDEMENT ( 10 FDA reports)
EYELID OPERATION ( 10 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 10 FDA reports)
PERIARTHRITIS ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
SCOLIOSIS ( 10 FDA reports)
SEQUESTRECTOMY ( 10 FDA reports)
SINUS ANTROSTOMY ( 10 FDA reports)
SINUS OPERATION ( 10 FDA reports)
TENDONITIS ( 10 FDA reports)
APPENDICECTOMY ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
TREMOR ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
FEELING COLD ( 8 FDA reports)
GINGIVAL DISORDER ( 8 FDA reports)
INTRAOCULAR LENS IMPLANT ( 8 FDA reports)
MAXILLOFACIAL OPERATION ( 8 FDA reports)
ORAL INFECTION ( 8 FDA reports)
OSTEONECROSIS ( 8 FDA reports)
POSTNASAL DRIP ( 8 FDA reports)
RENAL MASS ( 8 FDA reports)
RHINORRHOEA ( 8 FDA reports)
SWELLING ( 8 FDA reports)
BONE DENSITY DECREASED ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
INFLUENZA LIKE ILLNESS ( 7 FDA reports)
MEMORY IMPAIRMENT ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
RASH ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
TOOTH FRACTURE ( 7 FDA reports)
ADRENOMEGALY ( 6 FDA reports)
ARTHROPATHY ( 6 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 6 FDA reports)
CONGENITAL FOOT MALFORMATION ( 6 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
EXOSTOSIS ( 6 FDA reports)
HYPERMETABOLISM ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
TINNITUS ( 6 FDA reports)
ADRENAL MASS ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
THYROID DISORDER ( 5 FDA reports)
AZOTAEMIA ( 4 FDA reports)
BONE NEOPLASM MALIGNANT ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
EYE SWELLING ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERTENSIVE HEART DISEASE ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 4 FDA reports)
LUPUS-LIKE SYNDROME ( 4 FDA reports)
MALAISE ( 4 FDA reports)
NEUROPATHY PERIPHERAL ( 4 FDA reports)
OCULAR HYPERAEMIA ( 4 FDA reports)
RENAL CANCER ( 4 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 4 FDA reports)
VERTIGO POSITIONAL ( 4 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AUTOIMMUNE DISORDER ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
DEAFNESS UNILATERAL ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GINGIVAL DISCOLOURATION ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LABYRINTHITIS ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SPINAL OSTEOARTHRITIS ( 3 FDA reports)
SUNBURN ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ADENOCARCINOMA ( 2 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
AORTIC DILATATION ( 2 FDA reports)
APPARENT LIFE THREATENING EVENT ( 2 FDA reports)
BASEDOW'S DISEASE ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 2 FDA reports)
ETHMOID SINUS SURGERY ( 2 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 2 FDA reports)
FOOT DEFORMITY ( 2 FDA reports)
GINGIVAL EROSION ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LUNG CANCER METASTATIC ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
SALIVARY GLAND CANCER ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TYPE 1 DIABETES MELLITUS ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BONE FRAGMENTATION ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC ABLATION ( 1 FDA reports)
CARDIAC FIBRILLATION ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
LARYNGEAL ULCERATION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ORAL BACTERIAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PERIODONTAL DESTRUCTION ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH EROSION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRACHEAL OEDEMA ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use