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

DRUG EXPOSURE DURING PREGNANCY ( 7 FDA reports)
CAESAREAN SECTION ( 7 FDA reports)
FOETAL DISTRESS SYNDROME ( 6 FDA reports)
PREMATURE BABY ( 5 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ECLAMPSIA ( 1 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
APHASIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GLOBULINS DECREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MALAISE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MICROCEPHALY ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
POST PROCEDURAL NAUSEA ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
ALBUMIN GLOBULIN RATIO INCREASED ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRI-IODOTHYRONINE UPTAKE DECREASED ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)

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