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.

  • last updated 20 Aug 2025
  • by GoMask
The brief that made it

Drug efficacy and safety analysis for regulatory submissions

Sample rows

preview · 8 of 200 rows · all 19 columns
patient_idstringtrial_completion_statusstringdosage_mgfloatserious_adverse_eventbooleancountrystringtrial_idstringdrug_namestringadministration_routestringenrollment_datedateageintegersexstringethnicitystringprimary_outcomestringoutcome_measure_valuefloatoutcome_measure_unitstringadverse_event_reportedbooleanadverse_event_descriptionstringwithdrawal_reasonstringfollowup_datedate
P001-TRX12completed35.5falseUSTRIAL-001Zyproxiloral2022-06-1422femaleHispanicremissionblankblankfalseblankblank2023-06-10
P002-JPX34completed50falseUKTRIAL-001Zyproxiloral2023-09-0548maleWhiteimprovementblankblankfalseblankblank2024-01-22
P003-VLT56completed10falseSGTRIAL-001Zyproxiloral2024-04-2039femaleAsianremissionblankblankfalseblankblank2024-06-20
P004-CY89Acompleted5falseUSTRIAL-001Zyproxiloral2022-12-1117maleNative Americanno changeblankblankfalseblankblank2023-11-18
P005-MEL22completed0.01falseCATRIAL-001Zyproxiloral2023-03-0167femaleBlackimprovementblankblanktrueMild rash and dizzinessblank2024-01-05
P006-TLX41completed120falseDETRIAL-002Cytostateintravenous2022-05-2255maleEuropeanbiomarker_change7.9mg/dLtrueSevere headache post-infusionblank2023-05-21
P007-PLK32completed60falseAUTRIAL-002Cytostateintravenous2023-01-3083maleWhitesymptom_score3.3pointsfalseblankblank2023-12-01
P008-CTJ87withdrawn200.5trueINTRIAL-002Cytostateintravenous2023-07-0847femaleSouth Asianbiomarker_change12.1mg/dLtrueTransient chest painSerious adverse reaction required withdrawal2023-07-15

What the 200 rows show

from the 200-row sample

Withdrawn (trial completion status) stands out: 20 of its 24 rows have serious_adverse_event = true, against 9 of 176 for the rest.

  • 14%serious_adverse_event = true
  • 35.0median dosage_mg
  • 2outcome measure units
  • 4sexes
  • 5trials
  • 5drug names
Serious adverse event rate by trial_completion_statusserious_adverse_event = true
0%50%100%1%completed2 of 15783%withdrawn20 of 240%ongoing0 of 1078%lost_to_…7 of 9
dosage_mg200 rows, in bands of 100k
01002001980000000020500k1Mdosage_mg →

Median 35.0, from 0.0 to 1,000,000.

country200 rows · top 10 of 18 values
  1. US37
  2. CA13
  3. DE13
  4. FJ13
  5. UK12
  6. IN12
  7. ZA12
  8. JP12
  9. SG10
  10. BR9
19 columns by typefrom the column list below
  • string 12
  • integer 1
  • float 2
  • date 2
  • boolean 2

Columns

19 columns in four groups
blueprint · 19 columns
columntypedescriptionexample
Text 12 columns
patient_idstringUnique identifier for each patient enrolled in the drug trialuniqueP001-TRX12
trial_idstringUnique identifier for the clinical drug trial5 trialsTRIAL-001
drug_namestringName of the drug being tested in the trial5 namesZyproxil
administration_routestringRoute of drug administration (e.g., oral, intravenous, subcutaneous)6 valuesoral
sexstringSex of the patientmale · female · other · unknownfemale
ethnicitystringEthnicity of the patientoptionalHispanic
countrystringCountry where the trial was conducted for this patientUS
primary_outcomestringPrimary clinical outcome measured for the patient (e.g., remission, improvement, no change)5 outcomesremission
outcome_measure_unitstringUnit of measurement for the outcome value (e.g., mg/dL, points)2 units · optionalmg/dL
adverse_event_descriptionstringDescription of the adverse event(s) experienced by the patient, if anyoptionalMild rash and dizziness
trial_completion_statusstringStatus of the patient's participation in the trial (e.g., completed, withdrawn, ongoing)completed · withdrawn · ongoing · lost_to_followupcompleted
withdrawal_reasonstringReason for withdrawal from the trial, if applicableoptionalSerious adverse reaction
Numbers 3 columns
dosage_mgfloatDosage of the drug administered to the patient in milligrams0 or more35.5
ageintegerAge of the patient at the time of enrollment0 to 12022
outcome_measure_valuefloatNumeric value of the primary outcome measure (e.g., change in biomarker, symptom score)optional7.9
Dates and times 2 columns
enrollment_datedateDate the patient was enrolled in the trial2022-06-14
followup_datedateDate of last follow-up with the patientoptional2023-06-10
True or false 2 columns
adverse_event_reportedbooleanIndicates if any adverse event was reported by the patient during the trialfalse
serious_adverse_eventbooleanIndicates if a serious adverse event occurred for the patientfalse

Use it for

  • serious advers…14%29 of 200 rowsmean dosage mg by tri…52.9comp…42.3kwith…90.5ongo…113klost…

    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.

  • A software demo

    Believable patients with trial_id, drug_name and dosage_mg to fill a screen in front of a buyer.

Not quite right?

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This dataset200 rows19 columns
Yours1,000 rows19 columnscountry: UK only

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.

Rules it was built with
  • Record patient baseline health
  • Track outcomes and side effects
  • Include trial phase information
  • Exclude incomplete participation
Rows
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Exports
CSV, JSON, JSONL, Parquet, SQL, Excel, TSV, XML
Licence
yours to use, including commercially
API slug
drug-trial-patient-outcomes

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