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DRUG EXPOSURE DURING PREGNANCY ( 13 FDA reports)
EBSTEIN'S ANOMALY ( 10 FDA reports)
ASTHMA ( 9 FDA reports)
PNEUMONIA ( 9 FDA reports)
RESPIRATORY DISTRESS ( 7 FDA reports)
ATRIAL SEPTAL DEFECT ( 6 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 6 FDA reports)
CARDIAC MURMUR ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
MULTIPLE CONGENITAL ABNORMALITIES ( 6 FDA reports)
TRANSIENT TACHYPNOEA OF THE NEWBORN ( 6 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 3 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEBORRHOEIC KERATOSIS ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
ANHEDONIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FALL ( 2 FDA reports)
FEMORAL PULSE ABNORMAL ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MALOCCLUSION ( 2 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
PAIN ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RADIAL PULSE ABNORMAL ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TIC ( 2 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
COLLATERAL CIRCULATION ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
DISSOCIATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL SHORTENED ( 1 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
IMPLANT SITE HAEMORRHAGE ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PEDAL PULSE ABNORMAL ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
URINE AMPHETAMINE POSITIVE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)

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