Age
Item
male or female patients at least 20 years of age and less than 65 years old
boolean
C0001779 (UMLS CUI [1])
inpatient
Item
patients must be inpatients during the study
boolean
C0021562 (UMLS CUI [1])
Schizophrenia
Item
patients must have a diagnosis of schizophrenia as per the dsm-iv, as determined by the investigator
boolean
C0036341 (UMLS CUI [1])
Agitated Clinical | Indication Pharmaceutical Preparations Intramuscular
Item
patients must be considered by the investigator to be clinically agitated and to be clinically appropriate candidates for the treatment with intramuscular (im) medication
boolean
C0085631 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C1556154 (UMLS CUI [2,3])
Positive and negative syndrome scale
Item
patients must have a minimum total score of greater than or equal to 14 on the 5 items of the panss-ec and at least one individual item score of greater than or equal to 4 using the 1-7 scoring system, prior to the first im injection of study drug
boolean
C0451383 (UMLS CUI [1])
Illness Unstable Serious | Cessation of life Anticipated | Disease Intensive care unit Anticipated | Liver diseases | Icterus Degree Any | Kidney Diseases | Gastroenterology Disease | Respiration Disorders | Cardiovascular Diseases | Myocardial Ischemia | Endocrine System Diseases | nervous system disorder | Immune System Diseases | Hematological Disease
Item
serious, unstable illnesses such that death is anticipated within 1 year or intensive care unit hospitalization for the disease is anticipated within 6 months. this includes hepatic (specifically any degree of jaundice), renal, gastroenterologic, respiratory, cardiovascular (including ischemic heart disease), endocrinologic, neurologic, immunologic, or hematologic diseases
boolean
C0221423 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,3])
C0011065 (UMLS CUI [2,1])
C3840775 (UMLS CUI [2,2])
C0012634 (UMLS CUI [3,1])
C0021708 (UMLS CUI [3,2])
C3840775 (UMLS CUI [3,3])
C0023895 (UMLS CUI [4])
C0022346 (UMLS CUI [5,1])
C0441889 (UMLS CUI [5,2])
C1552551 (UMLS CUI [5,3])
C0022658 (UMLS CUI [6])
C0017163 (UMLS CUI [7,1])
C0012634 (UMLS CUI [7,2])
C0035204 (UMLS CUI [8])
C0007222 (UMLS CUI [9])
C0151744 (UMLS CUI [10])
C0014130 (UMLS CUI [11])
C0027765 (UMLS CUI [12])
C0021053 (UMLS CUI [13])
C0018939 (UMLS CUI [14])
Seizures | Patient Etiology | Patient Resolved
Item
known history of seizures; however, a patient whose etiology is identifiable and has been resolved may be enrolled
boolean
C0036572 (UMLS CUI [1])
C0030705 (UMLS CUI [2,1])
C1314792 (UMLS CUI [2,2])
C0030705 (UMLS CUI [3,1])
C3714811 (UMLS CUI [3,2])
Diabetes Mellitus | Complications of Diabetes Mellitus | Diabetes Mellitus potential | Blood glucose measurement Single | Fasting blood glucose measurement
Item
known history of diabetes mellitus, complications of diabetes mellitus, or potential diabetes mellitus as defined by patients with single blood glucose measurement based on site tests; patients with values greater than or equal to 140 mg/dl (non-fasting) or greater than or equal to 110 mg/dl (fasting) must be excluded from the study
boolean
C0011849 (UMLS CUI [1])
C0342257 (UMLS CUI [2])
C0011849 (UMLS CUI [3,1])
C3245505 (UMLS CUI [3,2])
C0392201 (UMLS CUI [4,1])
C0205171 (UMLS CUI [4,2])
C0428568 (UMLS CUI [5])
Allergic Reaction olanzapine | intolerance to olanzapine
Item
history of allergic reaction or intolerance to olanzapine
boolean
C1527304 (UMLS CUI [1,1])
C0171023 (UMLS CUI [1,2])
C1744706 (UMLS CUI [2,1])
C0171023 (UMLS CUI [2,2])
Psychostimulant | Reserpine
Item
have received treatment with psychostimulants or reserpine within 1 week prior to study drug administration
boolean
C0304403 (UMLS CUI [1])
C0035179 (UMLS CUI [2])