Drug Trial Patient Outcomes
This dataset provides detailed, patient-level outcome data from clinical drug trials, including demographics, drug administration, efficacy measures, and adverse event reporting. It enables comprehensive analysis of drug effectiveness and safety across diverse populations, supporting regulatory submissions, pharmacovigilance, and clinical research. The dataset is structured for interoperability and advanced analytics.
Sample rows
preview · 8 of 200 rows · all 19 columns| patient_idstring | trial_completion_statusstring | dosage_mgfloat | serious_adverse_eventboolean | countrystring | trial_idstring | drug_namestring | administration_routestring | enrollment_datedate | ageinteger | sexstring | ethnicitystring | primary_outcomestring | outcome_measure_valuefloat | outcome_measure_unitstring | adverse_event_reportedboolean | adverse_event_descriptionstring | withdrawal_reasonstring | followup_datedate |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| P001-TRX12 | completed | 35.5 | false | US | TRIAL-001 | Zyproxil | oral | 2022-06-14 | 22 | female | Hispanic | remission | blank | blank | false | blank | blank | 2023-06-10 |
| P002-JPX34 | completed | 50 | false | UK | TRIAL-001 | Zyproxil | oral | 2023-09-05 | 48 | male | White | improvement | blank | blank | false | blank | blank | 2024-01-22 |
| P003-VLT56 | completed | 10 | false | SG | TRIAL-001 | Zyproxil | oral | 2024-04-20 | 39 | female | Asian | remission | blank | blank | false | blank | blank | 2024-06-20 |
| P004-CY89A | completed | 5 | false | US | TRIAL-001 | Zyproxil | oral | 2022-12-11 | 17 | male | Native American | no change | blank | blank | false | blank | blank | 2023-11-18 |
| P005-MEL22 | completed | 0.01 | false | CA | TRIAL-001 | Zyproxil | oral | 2023-03-01 | 67 | female | Black | improvement | blank | blank | true | Mild rash and dizziness | blank | 2024-01-05 |
| P006-TLX41 | completed | 120 | false | DE | TRIAL-002 | Cytostate | intravenous | 2022-05-22 | 55 | male | European | biomarker_change | 7.9 | mg/dL | true | Severe headache post-infusion | blank | 2023-05-21 |
| P007-PLK32 | completed | 60 | false | AU | TRIAL-002 | Cytostate | intravenous | 2023-01-30 | 83 | male | White | symptom_score | 3.3 | points | false | blank | blank | 2023-12-01 |
| P008-CTJ87 | withdrawn | 200.5 | true | IN | TRIAL-002 | Cytostate | intravenous | 2023-07-08 | 47 | female | South Asian | biomarker_change | 12.1 | mg/dL | true | Transient chest pain | Serious adverse reaction required withdrawal | 2023-07-15 |
| P009-CTK88 | completed | 1000 | true | ZA | TRIAL-002 | Cytostate | intravenous | 2022-10-02 | 85 | male | Black or African American | symptom_score | 1.2 | points | true | Severe drop in blood pressure | blank | 2023-09-28 |
| P010-VIL23 | completed | 80 | false | BR | TRIAL-002 | Cytostate | subcutaneous | 2022-08-19 | 21 | female | Latino | improvement | blank | blank | false | blank | blank | 2023-01-03 |
| P011-MTR45 | completed | 2 | false | FJ | TRIAL-003 | Melatrin | topical | 2024-02-10 | 8 | unknown | Mixed | no change | blank | blank | false | blank | blank | 2024-06-18 |
| P012-TLX73 | completed | 75 | false | JP | TRIAL-003 | Melatrin | topical | 2023-05-28 | 32 | female | East Asian | remission | blank | blank | false | blank | blank | 2024-05-28 |
| P013-MEL99 | completed | 25 | false | SA | TRIAL-003 | Melatrin | topical | 2022-11-03 | 62 | female | Middle Eastern | improvement | blank | blank | false | blank | blank | 2023-06-01 |
| P014-VLT77 | withdrawn | 0 | false | FJ | TRIAL-003 | Melatrin | topical | 2023-08-12 | 0 | other | Pacific Islander | biomarker_change | -100 | mg/dL | true | Skin irritation observed | Parental withdrawal due to adverse effect | 2023-08-15 |
| P015-CYT52 | completed | 15.5 | false | PK | TRIAL-003 | Melatrin | topical | 2022-07-19 | 44 | male | South Asian | symptom_score | 5.7 | points | false | blank | blank | 2023-07-19 |
| P016-TLX15 | completed | 35 | false | US | TRIAL-004 | Viltera | subcutaneous | 2022-10-17 | 36 | female | Latino | improvement | blank | blank | false | blank | blank | 2023-09-18 |
| P017-ZPX67 | completed | 15 | false | NG | TRIAL-004 | Viltera | subcutaneous | 2023-04-14 | 52 | male | Black | remission | blank | blank | false | blank | blank | 2024-04-11 |
| P018-TLX27 | ongoing | 100 | false | SA | TRIAL-004 | Viltera | subcutaneous | 2022-12-04 | 38 | male | Middle Eastern | symptom_score | 9.8 | points | true | Injection site swelling | blank | 2024-06-09 |
| P019-VLT99 | withdrawn | 5000 | true | RU | TRIAL-004 | Viltera | subcutaneous | 2023-06-27 | 100 | other | Unknown | biomarker_change | 999999.99 | mg/dL | true | Extreme allergic reaction | Required hospitalization, withdrawn | 2023-07-10 |
| P020-TLX99 | completed | 60 | false | NZ | TRIAL-004 | Viltera | subcutaneous | 2022-09-23 | 29 | female | White | improvement | blank | blank | false | blank | blank | 2023-09-20 |
What the 200 rows show
from the 200-row sampleWithdrawn (trial completion status) stands out: 20 of its 24 rows have serious_
- 14%serious_
adverse_ event = true - 35.0median dosage_
mg - 2outcome measure units
- 4sexes
- 5trials
- 5drug names
Median 35.0, from 0.0 to 1,000,000.
- string 12
- integer 1
- float 2
- date 2
- boolean 2
Columns
19 columns in four groups| column | type | description | example |
|---|---|---|---|
| Text 12 columns | |||
patient_id | string | Unique identifier for each patient enrolled in the drug trialunique | P001-TRX12 |
trial_id | string | Unique identifier for the clinical drug trial5 trials | TRIAL-001 |
drug_name | string | Name of the drug being tested in the trial5 names | Zyproxil |
administration_route | string | Route of drug administration (e.g., oral, intravenous, subcutaneous)6 values | oral |
sex | string | Sex of the patientmale · female · other · unknown | female |
ethnicity | string | Ethnicity of the patientoptional | Hispanic |
country | string | Country where the trial was conducted for this patient | US |
primary_outcome | string | Primary clinical outcome measured for the patient (e.g., remission, improvement, no change)5 outcomes | remission |
outcome_measure_unit | string | Unit of measurement for the outcome value (e.g., mg/dL, points)2 units · optional | mg/dL |
adverse_event_description | string | Description of the adverse event(s) experienced by the patient, if anyoptional | Mild rash and dizziness |
trial_completion_status | string | Status of the patient's participation in the trial (e.g., completed, withdrawn, ongoing)completed · withdrawn · ongoing · lost_to_followup | completed |
withdrawal_reason | string | Reason for withdrawal from the trial, if applicableoptional | Serious adverse reaction |
| Numbers 3 columns | |||
dosage_mg | float | Dosage of the drug administered to the patient in milligrams0 or more | 35.5 |
age | integer | Age of the patient at the time of enrollment0 to 120 | 22 |
outcome_measure_value | float | Numeric value of the primary outcome measure (e.g., change in biomarker, symptom score)optional | 7.9 |
| Dates and times 2 columns | |||
enrollment_date | date | Date the patient was enrolled in the trial | 2022-06-14 |
followup_date | date | Date of last follow-up with the patientoptional | 2023-06-10 |
| True or false 2 columns | |||
adverse_event_reported | boolean | Indicates if any adverse event was reported by the patient during the trial | false |
serious_adverse_event | boolean | Indicates if a serious adverse event occurred for the patient | false |
Use it for
A healthcare dashboard
The serious_
adverse_ event rate, dosage_ mg by trial_ completion_ status and a breakdown of country. Excel, Power BI or Tableau. Why do 29 of 200 rows have serious_
adverse_ event = true? A root-cause class exercise
Hand out the rows and one question. The answer is in the data, not in the brief.
- Patients200P001-TRX1235.5completedP008-CTJ87200.5withdrawnP009-CTK881000completed
A software demo
Believable patients with trial_
id, drug_ name and dosage_ mg to fill a screen in front of a buyer.
blueprint · drug-trial-patient-outcomes
Behind this dataset
Same schema. As many rows as you need.
These 200 rows came out of a blueprint — 19 columns with generation rules behind each one. Open it in Data Factory to retune a column, add your own, wire in foreign keys, and run it at the size you actually need.
- Record patient baseline health
- Track outcomes and side effects
- Include trial phase information
- Exclude incomplete participation
1 credit per row. Preview 20 rows free. Buy rows for the full run.
- Exports
- CSV, JSON, JSONL, Parquet, SQL, Excel, TSV, XML
- Licence
- yours to use, including commercially
- API slug
- drug-trial-patient-outcomes