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FATIGUE ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
SPEECH DISORDER ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 6 FDA reports)
BLINDNESS ( 5 FDA reports)
BLOOD GLUCOSE INCREASED ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
APPLICATION SITE SCAR ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
DEATH ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
HEMIPARESIS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
IIIRD NERVE PARALYSIS ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
PEMPHIGUS ( 4 FDA reports)
PRODUCT ADHESION ISSUE ( 4 FDA reports)
TOOTH EXTRACTION ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
BONE DISORDER ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
GALLBLADDER OPERATION ( 3 FDA reports)
GINGIVAL INFECTION ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 3 FDA reports)
MANIA ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
REFLEXES ABNORMAL ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
TIC ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ALVEOLAR OSTEITIS ( 2 FDA reports)
ASEPTIC NECROSIS BONE ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CARBON DIOXIDE INCREASED ( 2 FDA reports)
CARDIAC ANEURYSM ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
COMMINUTED FRACTURE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DENTAL TREATMENT ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
EDENTULOUS ( 2 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INTERMEDIATE DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 2 FDA reports)
LOOSE TOOTH ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MASTICATION DISORDER ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
POOR PERSONAL HYGIENE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SPINAL COLUMN STENOSIS ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
ULTRASOUND DOPPLER ABNORMAL ( 2 FDA reports)
VERY LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACID FAST BACILLI INFECTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTERIOR CHAMBER INFLAMMATION ( 1 FDA reports)
APALLIC SYNDROME ( 1 FDA reports)
APATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENTEROSTOMY ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT AND COLD ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HUMORAL IMMUNE DEFECT ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOPYON ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INSULIN-REQUIRING TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IRITIS ( 1 FDA reports)
LARYNGEAL STENOSIS ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYCOBACTERIAL INFECTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC ABSCESS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBCUTANEOUS NODULE ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TRACHEOSTOMY ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITRECTOMY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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