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

SYNCOPE ( 16 FDA reports)
DIZZINESS ( 12 FDA reports)
CIRCULATORY COLLAPSE ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
DEHYDRATION ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
CHEST PAIN ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 6 FDA reports)
FALL ( 6 FDA reports)
BACK PAIN ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
CONDITION AGGRAVATED ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PAIN ( 5 FDA reports)
RENAL FAILURE ACUTE ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ACCIDENT ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
CONTUSION ( 4 FDA reports)
COUGH ( 4 FDA reports)
EXOSTOSIS ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
INTERVERTEBRAL DISC COMPRESSION ( 4 FDA reports)
LIGAMENT SPRAIN ( 4 FDA reports)
LUMBAR SPINE FLATTENING ( 4 FDA reports)
MUSCLE DISORDER ( 4 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
RIB FRACTURE ( 4 FDA reports)
SPINAL CORD INJURY LUMBAR ( 4 FDA reports)
SPINAL CORD INJURY THORACIC ( 4 FDA reports)
SPINAL DEFORMITY ( 4 FDA reports)
SPINAL DEFORMITY CORRECTION ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 4 FDA reports)
TRANSPLANT REJECTION ( 4 FDA reports)
VERTEBROPLASTY ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ANAL HAEMORRHAGE ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTERIOSCLEROSIS ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
DIVERTICULUM ( 3 FDA reports)
FACIAL PARESIS ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
PYELONEPHRITIS CHRONIC ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
SURGERY ( 3 FDA reports)
VENTRICULAR FAILURE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
AMYOTROPHIC LATERAL SCLEROSIS ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
APHONIA ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RETINAL VEIN THROMBOSIS ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
TONGUE ATROPHY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD OSMOLARITY DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHEYNE-STOKES RESPIRATION ( 1 FDA reports)
CHOLESTEATOMA ( 1 FDA reports)
CLONIC CONVULSION ( 1 FDA reports)
CORNEAL DEPOSITS ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLARE ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MICROSCOPIC POLYANGIITIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PERIODONTITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL HYPERTENSION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL STRICTURE POSTOPERATIVE ( 1 FDA reports)
URINE OSMOLARITY INCREASED ( 1 FDA reports)
URINE POTASSIUM INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use