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

DRUG EXPOSURE DURING PREGNANCY ( 10 FDA reports)
AORTIC VALVE INCOMPETENCE ( 9 FDA reports)
COUGH ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
ACQUIRED OESOPHAGEAL WEB ( 8 FDA reports)
ATRIAL SEPTAL DEFECT ( 8 FDA reports)
BLOOD IRON DECREASED ( 8 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 8 FDA reports)
CARDIAC MURMUR ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CHYLOTHORAX ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DARK CIRCLES UNDER EYES ( 8 FDA reports)
DEVELOPMENTAL DELAY ( 8 FDA reports)
EPIGLOTTIC CYST ( 8 FDA reports)
FAILURE TO THRIVE ( 8 FDA reports)
FATIGUE ( 8 FDA reports)
LUNG ABSCESS ( 8 FDA reports)
MASS ( 8 FDA reports)
MITRAL VALVE INCOMPETENCE ( 8 FDA reports)
NIGHT SWEATS ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PULMONARY HYPERTENSION ( 8 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 8 FDA reports)
PULMONARY VALVE STENOSIS ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 8 FDA reports)
VOMITING ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
ANGIOPATHY ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
PAIN ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
MALAISE ( 3 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ANXIETY DISORDER ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD IRON INCREASED ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
GENE MUTATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
MIGRAINE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
OBESITY ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ACARIASIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTESTINAL POLYP ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LUMBAR RADICULOPATHY ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
POISONING ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VITAMIN B COMPLEX DEFICIENCY ( 1 FDA reports)

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