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

THROMBOCYTOPENIA ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
RENAL FAILURE ACUTE ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
AORTIC CALCIFICATION ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBRAL HAEMATOMA ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
CORONARY ARTERY STENOSIS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CONGENITAL HYDROCEPHALUS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
DEAFNESS CONGENITAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
MICROGNATHIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECK DEFORMITY ( 1 FDA reports)
NEONATAL APNOEIC ATTACK ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
POST CHOLECYSTECTOMY SYNDROME ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREAURICULAR CYST ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETROGNATHIA ( 1 FDA reports)
RIB DEFORMITY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
VASODILATATION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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