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COMPLETED SUICIDE ( 41 FDA reports)
CARDIAC ARREST ( 19 FDA reports)
RESPIRATORY ARREST ( 18 FDA reports)
INTENTIONAL MISUSE ( 12 FDA reports)
MULTIPLE DRUG OVERDOSE ( 11 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 9 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 7 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
INTENTIONAL DRUG MISUSE ( 6 FDA reports)
OVERDOSE ( 5 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
COMA ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
VOMITING ( 3 FDA reports)
AGGRESSION ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BRAIN DAMAGE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DEATH ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CANNABINOIDS ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
FALL ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS C POSITIVE ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFUSION SITE BURNING ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL TUBULAR ACIDOSIS ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
VICTIM OF HOMICIDE ( 1 FDA reports)

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