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

RESPIRATORY FAILURE ( 9 FDA reports)
ANXIETY ( 8 FDA reports)
CARDIAC MURMUR ( 8 FDA reports)
DEVELOPMENTAL DELAY ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SPEECH DISORDER DEVELOPMENTAL ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
ASTHENIA ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
NAUSEA ( 6 FDA reports)
CEREBROVASCULAR ACCIDENT ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
FATIGUE ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
ANHEDONIA ( 3 FDA reports)
BACK INJURY ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CORONARY ARTERY DISEASE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DEPRESSION SUICIDAL ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ECONOMIC PROBLEM ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTRODUODENITIS ( 3 FDA reports)
HYPERCHOLESTEROLAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
PAIN ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANAEMIA POSTOPERATIVE ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CAROTID BRUIT ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
EMBOLIC STROKE ( 2 FDA reports)
FUNGAL RASH ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
VERTEBRAL ARTERY STENOSIS ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
ABDOMINAL HERNIA REPAIR ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ADDISON'S DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ARTERY ATHEROMA ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
COMPLICATION OF DELIVERY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
IRRITABLE BOWEL SYNDROME ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOANING ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NEONATAL DISORDER ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OLIGODIPSIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN CANDIDA ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
VERTEBRAL ARTERY OCCLUSION ( 1 FDA reports)
VERTEBROBASILAR INSUFFICIENCY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)

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