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

MULTIPLE DRUG OVERDOSE ( 4 FDA reports)
LETHARGY ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
COMA ( 2 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
MECHANICAL VENTILATION ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANTICHOLINERGIC SYNDROME ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POISONING DELIBERATE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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