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

HEART RATE INCREASED ( 9 FDA reports)
MULTIPLE DRUG OVERDOSE ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
COMA ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
AGITATION ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
PCO2 INCREASED ( 5 FDA reports)
PO2 DECREASED ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BLOOD PH DECREASED ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CORNEAL REFLEX DECREASED ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PUPILS UNEQUAL ( 4 FDA reports)
REFLEXES ABNORMAL ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD PH INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD BICARBONATE DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG SCREEN POSITIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INTENTIONAL MISUSE ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMMONIA DECREASED ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
APNOEA ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM PR PROLONGATION ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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