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

PAIN ( 6 FDA reports)
FLUSHING ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
COMMUNICATION DISORDER ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
EMOTIONAL DISORDER ( 4 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 4 FDA reports)
FALL ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TINNITUS ( 4 FDA reports)
ANHEDONIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
INJURY ( 3 FDA reports)
OSTEOPOROSIS ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
POLYMYALGIA RHEUMATICA ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
TEMPORAL ARTERITIS ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VITAMIN D DEFICIENCY ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ASCITES ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FIBROMYALGIA ( 2 FDA reports)
HYALOSIS ASTEROID ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOACUSIS ( 2 FDA reports)
INTRAOCULAR LENS IMPLANT ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SINUS CONGESTION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BREAST CALCIFICATIONS ( 1 FDA reports)
BREAST MASS ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RESPIRATORY FUME INHALATION DISORDER ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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