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| ID | Type | Description | Link |
|---|---|---|---|
| F1D-JE-HGMS | Other Identifier | Eli Lilly and Company |
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To assess the efficacy and safety of olanzapine in the long-term treatment for patients with bipolar I disorder, depressed.
This is an open-label, multi-center, long-term treatment study conducted only in Japanese sites. The subjects are patients who fulfill the diagnostic criteria for bipolar I disorder, most recent episode depressed, as defined in the Diagnostic and Statistical Manual of Mental Disorders Fourth Edition, Text Revision (DSM-IV-TR) (296.50=unspecified, 296.52=moderate severity, 296.53=severe without psychotic features, 296.54=severe with psychotic features), who have completed Study HGMP (NCT#00510146) and patients who did not participate in Study HGMP who have been recruited to participate in Study HGMS.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Pre-Olanzapine | Experimental | Participants who received olanzapine 5-20 mg/day in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
|
| Pre-Placebo | Experimental | Participants who received placebo in acute phase of Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
|
| New Olanzapine | Experimental | Participants who did not participate in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 48 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Olanzapine | Drug | 5-20 mg/day, oral, daily |
|
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of Participants With Adverse Events Leading to Discontinuation | An adverse event (AE) is an untoward medical event associated with the use of the study drug or study procedure, whether or not it is considered related to the study drug or study procedure. Results presented are the percentage of participants who experienced an adverse event that resulted in the discontinuation of the study. | Baseline through 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Measure | Description | Time Frame |
|---|---|---|
| Change From Baseline in Glucose and Lipid Panel at Week 24 or Week 48 Endpoint | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) | |
| Change From Baseline in Weight at Week 24 or Week 48 Endpoint | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Call 1-877-CTLILLY (1-877-285-4599) or 1-317-615-4559 Mon-Fri 9 AM-5 PM Eastern time (UTC/GMT - 5 hours, EST) | Eli Lilly and Company | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Aichi | 470-1168 |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 24417745 | Derived | Katagiri H, Tohen M, McDonnell DP, Fujikoshi S, Case M, Kanba S, Takahashi M, Gomez JC. Safety and efficacy of olanzapine in the long-term treatment of Japanese patients with bipolar I disorder, depression: an integrated analysis. Psychiatry Clin Neurosci. 2014 Jul;68(7):498-505. doi: 10.1111/pcn.12156. Epub 2014 Mar 4. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Pre-Olanzapine | Participants who received olanzapine in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
| FG001 | Pre-Placebo | Participants who received placebo in acute phase of Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
| FG002 | New Olanzapine | Participants who did not participate in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 48 weeks. |
| Title | Milestones | Reasons Not Completed | |||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Pre-Olanzapine | Participants who received olanzapine in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
| BG001 | Pre-Placebo | Participants who received placebo in acute phase of Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Percentage of Participants With Adverse Events Leading to Discontinuation | An adverse event (AE) is an untoward medical event associated with the use of the study drug or study procedure, whether or not it is considered related to the study drug or study procedure. Results presented are the percentage of participants who experienced an adverse event that resulted in the discontinuation of the study. | All randomized Participants. | Posted | Number | percentage of participants | Baseline through 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
Not provided
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Pre-Olanzapine | Participants who received olanzapine in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Pancreatitis acute | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Iron deficiency anaemia | Blood and lymphatic system disorders | MedDRA (13.0) | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Chief Medical Officer | Eli Lilly and Company | 800-545-5979 |
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| ID | Term |
|---|---|
| D000077152 | Olanzapine |
| ID | Term |
|---|---|
| D001569 | Benzodiazepines |
| D001552 | Benzazepines |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |
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| Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score at Week 24 or Week 48 Endpoint | The MADRS is a rating scale for severity of depressive mood symptoms. The MADRS has a 10-item checklist. Items are rated on a scale of 0-6, for a total score range of 0 (low severity of depressive symptoms) to 60 (high severity of depressive symptoms). | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Change From Baseline in Young Mania Rating Scale (YMRS) Total Score at Week 24 or Week 48 Endpoint | The YMRS is an 11-item scale that measures the severity of manic episodes. Four items are rated on a scale from 0 (symptom not present) to 8 (symptom extremely severe). The remaining items are rated on a scale from 0 (symptom not present) to 4 (symptom extremely severe). The YMRS total score ranges from 0 to 60. | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Change From Baseline in Clinical Global Improvement- Bipolar (CGI-BP) at Week 24 or Week 48 Endpoint | CGI-BP is a measure of illness severity especially adapted for bipolar illness. It allows rating of mania, depression, and overall illness. The scores for mania, depression, and overall illness each range from 1 (normal, not ill) to 7 (very seriously ill). | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Percentage of Participants With Emergence of Mania at Week 24 or Week 48 | Emergence of mania is defined as first occurrence of score of >=15 in the YMRS total score in the post-baseline period of Acute Phase. The YMRS is an 11-item scale that measures the severity of manic episodes. Four items are rated on a scale from 0 (symptom not present) to 8 (symptom extremely severe). The remaining items are rated on a scale from 0 (symptom not present) to 4 (symptom extremely severe). The YMRS total score ranges from 0 to 60. | 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Percentage of Participants With High Suicidality at Week 24 or Week 48 | The MINI module C (MINI-C) is a rating scale for severity of suicidal thoughts and behaviors. The MINI-C is composed of 12 Yes/No questions with variable scores assigned to each question. The scale ranges from 0 to 52 with higher scores indicating a greater presence of suicidal thoughts and/or behaviors. Based upon scores, suicidality is defined as Low (1-8), Medium (9-16), and High (>=17). | 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Percentage of Participants With Extra-Pyramidal Symptoms (EPS) at Week 24 or Week 48 | EPS symptoms measured by DIEPSS are grouped into 4 categories: Parkinsonism, akathisia, dystonia, and dyskinesia. Severity ranges from level 0 (none, normal) to 4 (severe). A participant is deemed to have EPS at endpoint if they have an abnormal endpoint. Normal baseline Parkinsonism is defined as a score not ≥3 on 1 item or ≥2 on 2 items; abnormal endpoint is a score ≥3 on 1 item or ≥2 on 2 items, or an increase of 3 on Parkinsonism total. Normal baseline akathisia, dystonia and dyskinesia is defined as a score <2; abnormal endpoint is a score ≥2 or an increase ≥2 from that baseline score. | 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Change From Baseline in Hemoglobin (HbA1c) at Week 24 or Week 48 Endpoint | HbA1c is a test that measures the amount of glycated hemoglobin in the blood over prolonged periods of time. | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Change From Baseline in Prolactin at Week 24 or Week 48 Endpoint | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Change From Baseline to in QTcF at Week 24 or Week 48 Endpoint | Time from electrocardiogram Q wave to the end of the T wave corresponding to electrical systole, fixed correction factor (QTcF interval) | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
| Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Chiba | 270-1694 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Hiroshima | 731-0501 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Kanagawa | 231-0027 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Kyoto | 616-8421 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Numakunai | 023-0801 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Saitama | 332-0012 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Shiga | 525-0037 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Tokyo | 170-0002 | Japan |
| For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. | Yamaguchi | 755-8505 | Japan |
| Withdrawal by Subject |
|
| BG002 | New Olanzapine | Participants who did not participate in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 48 weeks. |
| BG003 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Race/Ethnicity, Customized | Number | participants |
|
| Region of Enrollment | Number | participants |
|
| Montgomery- Asberg Depression Rating Scale (MADRS) Total Score | The MADRS is a rating scale for severity of depressive mood symptoms. The MADRS has a 10-item checklist. Items are rated on a scale of 0-6, for a total score range of 0 (low severity of depressive symptoms) to 60 (high severity of depressive symptoms). | Mean | Standard Deviation | units on a scale |
|
| Young Mania Rating Scale (YMRS) Total Score | The YMRS is an 11-item scale that measures the severity of manic episodes. Four items are rated on a scale from 0 (symptom not present) to 8 (symptom extremely severe). The remaining items are rated on a scale from 0 (symptom not present) to 4 (symptom extremely severe). The YMRS total score ranges from 0 to 60. | Mean | Standard Deviation | units on a scale |
|
| Clinical Global Improvement- Bipolar (CGI-BP) - Mania | CGI-BP is a measure of illness severity especially adapted for bipolar illness. It allows rating of mania, depression, and overall illness. The Mania score ranges from 1 (normal, not ill) to 7 (very seriously ill). | Mean | Standard Deviation | units on a scale |
|
| CGI-BP - Depression | CGI-BP is a measure of illness severity especially adapted for bipolar illness. It allows rating of mania, depression, and overall illness. The Depression score ranges from 1 (normal, not ill) to 7 (very seriously ill). | Mean | Standard Deviation | units on a scale |
|
| CGI-BP - Overall | CGI-BP is a measure of illness severity especially adapted for bipolar illness. It allows rating of mania, depression, and overall illness. The Overall Illness score ranges from 1 (normal, not ill) to 7 (very seriously ill). | Mean | Standard Deviation | units on a scale |
|
Participants who received placebo in acute phase of Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. |
| OG002 | New Olanzapine | Participants who did not participate in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 48 weeks. |
|
|
| Secondary | Change From Baseline in Glucose and Lipid Panel at Week 24 or Week 48 Endpoint | Participants with non-missing baseline value and the specified visit result. | Posted | Mean | Standard Deviation | millimole/Liter | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline in Weight at Week 24 or Week 48 Endpoint | Participants with non-missing baseline value and the specified visit result. | Posted | Mean | Standard Deviation | kilograms | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score at Week 24 or Week 48 Endpoint | The MADRS is a rating scale for severity of depressive mood symptoms. The MADRS has a 10-item checklist. Items are rated on a scale of 0-6, for a total score range of 0 (low severity of depressive symptoms) to 60 (high severity of depressive symptoms). | Participants with non-missing baseline value and at least one non-missing post baseline value, last observation carried forward (LOCF). | Posted | Mean | Standard Deviation | units on a scale | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline in Young Mania Rating Scale (YMRS) Total Score at Week 24 or Week 48 Endpoint | The YMRS is an 11-item scale that measures the severity of manic episodes. Four items are rated on a scale from 0 (symptom not present) to 8 (symptom extremely severe). The remaining items are rated on a scale from 0 (symptom not present) to 4 (symptom extremely severe). The YMRS total score ranges from 0 to 60. | Participants with non-missing baseline value and at least one non-missing post baseline value, last observation carried forward (LOCF). | Posted | Mean | Standard Deviation | units on a scale | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline in Clinical Global Improvement- Bipolar (CGI-BP) at Week 24 or Week 48 Endpoint | CGI-BP is a measure of illness severity especially adapted for bipolar illness. It allows rating of mania, depression, and overall illness. The scores for mania, depression, and overall illness each range from 1 (normal, not ill) to 7 (very seriously ill). | Participants with non-missing baseline value and at least one non-missing post baseline value, last observation carried forward (LOCF). | Posted | Mean | Standard Deviation | units on a scale | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Percentage of Participants With Emergence of Mania at Week 24 or Week 48 | Emergence of mania is defined as first occurrence of score of >=15 in the YMRS total score in the post-baseline period of Acute Phase. The YMRS is an 11-item scale that measures the severity of manic episodes. Four items are rated on a scale from 0 (symptom not present) to 8 (symptom extremely severe). The remaining items are rated on a scale from 0 (symptom not present) to 4 (symptom extremely severe). The YMRS total score ranges from 0 to 60. | All Randomized participants. | Posted | Number | percentage of participants | 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Percentage of Participants With High Suicidality at Week 24 or Week 48 | The MINI module C (MINI-C) is a rating scale for severity of suicidal thoughts and behaviors. The MINI-C is composed of 12 Yes/No questions with variable scores assigned to each question. The scale ranges from 0 to 52 with higher scores indicating a greater presence of suicidal thoughts and/or behaviors. Based upon scores, suicidality is defined as Low (1-8), Medium (9-16), and High (>=17). | Participants with non-missing baseline value and the specified visit value. | Posted | Number | percentage of participants | 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Percentage of Participants With Extra-Pyramidal Symptoms (EPS) at Week 24 or Week 48 | EPS symptoms measured by DIEPSS are grouped into 4 categories: Parkinsonism, akathisia, dystonia, and dyskinesia. Severity ranges from level 0 (none, normal) to 4 (severe). A participant is deemed to have EPS at endpoint if they have an abnormal endpoint. Normal baseline Parkinsonism is defined as a score not ≥3 on 1 item or ≥2 on 2 items; abnormal endpoint is a score ≥3 on 1 item or ≥2 on 2 items, or an increase of 3 on Parkinsonism total. Normal baseline akathisia, dystonia and dyskinesia is defined as a score <2; abnormal endpoint is a score ≥2 or an increase ≥2 from that baseline score. | Participants with a normal baseline and an endpoint result. For Parkinsonism, normal baseline is defined as a score not ≥3 on 1 item or ≥2 on 2 items. Normal baseline akathisia, dystonia and dyskinesia is defined as a score <2. | Posted | Number | percentage of participants | 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline in Hemoglobin (HbA1c) at Week 24 or Week 48 Endpoint | HbA1c is a test that measures the amount of glycated hemoglobin in the blood over prolonged periods of time. | Participants with non-missing baseline value and the specified visit result. | Posted | Mean | Standard Deviation | percentage of glycated hemoglobin | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline in Prolactin at Week 24 or Week 48 Endpoint | Participants with non-missing baseline value and the specified visit result. | Posted | Mean | Standard Deviation | microgram/Liter | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| Secondary | Change From Baseline to in QTcF at Week 24 or Week 48 Endpoint | Time from electrocardiogram Q wave to the end of the T wave corresponding to electrical systole, fixed correction factor (QTcF interval) | Participants with non-missing baseline value and the specified visit result. | Posted | Mean | Standard Deviation | millisecond (msec) | baseline, 24 weeks (pre-olanzapine and pre-placebo) or 48 weeks (new olanzapine) |
|
|
|
| 1 |
| 56 |
| 34 |
| 56 |
| EG001 | Pre-Placebo | Participants who received placebo in acute phase of Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 24 weeks. | 0 | 25 | 13 | 25 |
| EG002 | New Olanzapine | Participants who did not participate in Study HGMP (NCT#00510146), received olanzapine 5-20 mg/day, orally for 48 weeks. | 1 | 20 | 20 | 20 |
| Cholecystitis acute | Hepatobiliary disorders | MedDRA (13.0) | Systematic Assessment |
|
| Depressive symptom | Psychiatric disorders | MedDRA (13.0) | Systematic Assessment |
|
| Inner ear disorder | Ear and labyrinth disorders | MedDRA (13.0) | Systematic Assessment |
|
| Hyperprolactinaemia | Endocrine disorders | MedDRA (13.0) | Systematic Assessment |
|
| Abdominal pain | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Abdominal pain upper | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Constipation | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Diarrhoea | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Dry mouth | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Nausea | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Vomiting | Gastrointestinal disorders | MedDRA (13.0) | Systematic Assessment |
|
| Fatigue | General disorders | MedDRA (13.0) | Systematic Assessment |
|
| Irritability | General disorders | MedDRA (13.0) | Systematic Assessment |
|
| Oedema peripheral | General disorders | MedDRA (13.0) | Systematic Assessment |
|
| Thirst | General disorders | MedDRA (13.0) | Systematic Assessment |
|
| Hepatic function abnormal | Hepatobiliary disorders | MedDRA (13.0) | Systematic Assessment |
|
| Empyema | Infections and infestations | MedDRA (13.0) | Systematic Assessment |
|
| Influenza | Infections and infestations | MedDRA (13.0) | Systematic Assessment |
|
| Nasopharyngitis | Infections and infestations | MedDRA (13.0) | Systematic Assessment |
|
| Arthropod sting | Injury, poisoning and procedural complications | MedDRA (13.0) | Systematic Assessment |
|
| Alanine aminotransferase increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Aspartate aminotransferase increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood cholesterol increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood creatine phosphokinase increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood creatinine increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood glucose increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood lactate dehydrogenase increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood pressure increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood prolactin increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood triglycerides decreased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Blood triglycerides increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Electrocardiogram QT prolonged | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Glucose urine present | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Glycosylated haemoglobin increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| High density lipoprotein increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Liver function test abnormal | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Neutrophil count decreased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Neutrophil count increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Protein urine present | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Urine ketone body present | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Weight increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| White blood cell count decreased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| White blood cell count increased | Investigations | MedDRA (13.0) | Systematic Assessment |
|
| Decreased appetite | Metabolism and nutrition disorders | MedDRA (13.0) | Systematic Assessment |
|
| Glucose tolerance impaired | Metabolism and nutrition disorders | MedDRA (13.0) | Systematic Assessment |
|
| Hyperlipidaemia | Metabolism and nutrition disorders | MedDRA (13.0) | Systematic Assessment |
|
| Increased appetite | Metabolism and nutrition disorders | MedDRA (13.0) | Systematic Assessment |
|
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA (13.0) | Systematic Assessment |
|
| Back pain | Musculoskeletal and connective tissue disorders | MedDRA (13.0) | Systematic Assessment |
|
| Akathisia | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Dizziness | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Dysarthria | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Dystonia | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Headache | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Hypersomnia | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Parkinsonism | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Somnolence | Nervous system disorders | MedDRA (13.0) | Systematic Assessment |
|
| Pregnancy | Pregnancy, puerperium and perinatal conditions | MedDRA (13.0) | Systematic Assessment |
|
| Apathy | Psychiatric disorders | MedDRA (13.0) | Systematic Assessment |
|
| Depression | Psychiatric disorders | MedDRA (13.0) | Systematic Assessment |
|
| Insomnia | Psychiatric disorders | MedDRA (13.0) | Systematic Assessment |
|
| Dysmenorrhoea | Reproductive system and breast disorders | MedDRA (13.0) | Systematic Assessment |
|
| Menstruation irregular | Reproductive system and breast disorders | MedDRA (13.0) | Systematic Assessment |
|
| Eczema | Skin and subcutaneous tissue disorders | MedDRA (13.0) | Systematic Assessment |
|
| Urticaria | Skin and subcutaneous tissue disorders | MedDRA (13.0) | Systematic Assessment |
|
| Orthostatic hypotension | Vascular disorders | MedDRA (13.0) | Systematic Assessment |
|
Not provided
| D006571 | Heterocyclic Compounds |
|
| Low-density lipoprotein ( LDL) Cholesterol |
|
| High-density lipoprotein ( HDL) Cholesterol |
|
| Triglycerides |
|
|
| CGI-BP Overall Bipolar Illness |
|
| Title | Measurements |
|---|---|
|
| Dystonia |
|
| Parkinsonism |
|