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COMA ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 9 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 8 FDA reports)
HEART RATE INCREASED ( 8 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 6 FDA reports)
BODY TEMPERATURE INCREASED ( 6 FDA reports)
MULTIPLE DRUG OVERDOSE ( 6 FDA reports)
PCO2 INCREASED ( 6 FDA reports)
PO2 DECREASED ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
BLOOD PH DECREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
BODY TEMPERATURE DECREASED ( 4 FDA reports)
CORNEAL ABRASION ( 4 FDA reports)
CORNEAL REFLEX DECREASED ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EMOTIONAL DISTRESS ( 4 FDA reports)
LETHARGY ( 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)
ASPIRATION ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG SCREEN POSITIVE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
POLYSUBSTANCE ABUSE ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANOXIC ENCEPHALOPATHY ( 1 FDA reports)
APNOEA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ACCIDENTAL ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
PATIENT RESTRAINT ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PO2 ABNORMAL ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
STUPOR ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)

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