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COMPLETED SUICIDE ( 14 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
BLOOD COUNT ABNORMAL ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVERSION ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COMA ( 1 FDA reports)
COMA SCALE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPIATES ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
VENTRICULAR FIBRILLATION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISCERAL CONGESTION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)

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