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

DYSPNOEA ( 15 FDA reports)
ARTHRALGIA ( 11 FDA reports)
DEPRESSION ( 11 FDA reports)
RASH ( 11 FDA reports)
MYALGIA ( 10 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
SLEEP APNOEA SYNDROME ( 9 FDA reports)
ACNE ( 8 FDA reports)
ANAL STENOSIS ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
COLITIS ( 8 FDA reports)
COLITIS ULCERATIVE ( 8 FDA reports)
CROHN'S DISEASE ( 8 FDA reports)
FALL ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 8 FDA reports)
IRON DEFICIENCY ANAEMIA ( 8 FDA reports)
POUCHITIS ( 8 FDA reports)
ABDOMINAL DISTENSION ( 7 FDA reports)
EAR PAIN ( 7 FDA reports)
GASTROINTESTINAL DISORDER ( 7 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
PAIN IN JAW ( 7 FDA reports)
PARATHYROID DISORDER ( 7 FDA reports)
HYPERTENSION ( 6 FDA reports)
MALAISE ( 6 FDA reports)
OEDEMA PERIPHERAL ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PROCTITIS ( 6 FDA reports)
STOMACH DISCOMFORT ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
BACK PAIN ( 5 FDA reports)
DEATH ( 5 FDA reports)
DIABETES MELLITUS ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
HYPERHIDROSIS ( 5 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PAIN ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
LOWER EXTREMITY MASS ( 4 FDA reports)
ANAL FISSURE ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
FLUSHING ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEPATITIS INFECTIOUS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
INJECTION SITE ULCER ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
NOSOCOMIAL INFECTION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
SKIN WRINKLING ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
VEIN DISORDER ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
DEFORMITY ( 2 FDA reports)
DIABETIC COMA ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
SCAR ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC VALVE CALCIFICATION ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNS THIRD DEGREE ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHARLES BONNET SYNDROME ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COUGH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
LICHEN PLANUS ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOSS OF CONTROL OF LEGS ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARATHYROID GLAND ENLARGEMENT ( 1 FDA reports)
PATHOLOGICAL GAMBLING ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL SENSORIMOTOR NEUROPATHY ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL PNEUMONIA ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONDYLOLYSIS ( 1 FDA reports)
STENT OCCLUSION ( 1 FDA reports)
TENSION ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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