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

DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
ATRIAL SEPTAL DEFECT ( 7 FDA reports)
MITRAL VALVE INCOMPETENCE ( 7 FDA reports)
FALLOT'S TETRALOGY ( 7 FDA reports)
TACHYPNOEA ( 6 FDA reports)
AORTIC VALVE INCOMPETENCE ( 6 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 6 FDA reports)
RIGHT ATRIAL HYPERTROPHY ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
PULMONARY ARTERY STENOSIS CONGENITAL ( 6 FDA reports)
PERIPHERAL COLDNESS ( 6 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 6 FDA reports)
NODAL ARRHYTHMIA ( 6 FDA reports)
HEART DISEASE CONGENITAL ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
ABDOMINAL PAIN ( 4 FDA reports)
BILIARY DYSKINESIA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
RENAL VEIN THROMBOSIS ( 3 FDA reports)
BRAIN INJURY ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
VOMITING ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
SURGERY ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BILIARY COLIC ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
PLACENTAL INSUFFICIENCY ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
PLACENTA PRAEVIA ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
MITRAL VALVE PROLAPSE ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
LIMB MALFORMATION ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
EXOMPHALOS ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)

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