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

AGITATION ( 8 FDA reports)
COMA ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
INTENTIONAL OVERDOSE ( 5 FDA reports)
MIOSIS ( 5 FDA reports)
MULTIPLE DRUG OVERDOSE ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
POLYSUBSTANCE ABUSE ( 5 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BOWEL SOUNDS ABNORMAL ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ALANINE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD AMYLASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD UREA ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DEPERSONALISATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIASTOLIC HYPERTENSION ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
FEAR ( 1 FDA reports)
FOCAL NODULAR HYPERPLASIA ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
URINE KETONE BODY PRESENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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