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COMPLETED SUICIDE ( 27 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 9 FDA reports)
ASPIRATION ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
CONVULSION ( 6 FDA reports)
OVERDOSE ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
AGITATION ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
APNOEA ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
DEATH ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
SERUM SEROTONIN DECREASED ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
COMA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
FOREIGN BODY ASPIRATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POISONING ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
UNINTENDED PREGNANCY ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FEEDING TUBE COMPLICATION ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HYPERDYNAMIC LEFT VENTRICLE ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
OSTEOSARCOMA RECURRENT ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY FATIGUE ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)

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