Healthcare
26 columns
200 rows
8 formats

Pharmaceutical Adverse Event Dataset

This dataset provides detailed, structured records of patient-reported and clinician-documented adverse drug events, including drug exposure, event characteristics, patient demographics, and clinical outcomes. It is designed to support pharmacovigilance, drug safety monitoring, and regulatory reporting, enabling robust analysis of drug risks and patient safety signals.

last updated 20 Aug 2025
by GoMask

The brief that made it

Drug safety signal detection and risk assessment

Sample rows

preview · 8 of 200 rows · all 26 columns

event_idstring	drug_routestring	ageinteger	hospitalization_requiredboolean	severitystring	patient_idstring	reporter_typestring	reporter_idstring	event_datedate	report_datedate	drug_namestring	drug_generic_namestring	drug_dosestring	drug_start_datedate	drug_end_datedate	adverse_event_termstring	outcomestring	action_takenstring	seriousboolean	concomitant_drugsstring	medical_historystring	sexstring	countrystring	citystring	source_systemstring	adverse_event_descriptionstring
EVT0001	oral	68	false	moderate	PAT001	clinician	CLN101	2023-05-11	2023-05-12	Lipitor	atorvastatin	20mg	2022-12-01	blank	muscle pain	recovering	dose reduced	false	aspirin	hypertension, diabetes	male	USA	Chicago	EMR12345	Patient reported persistent muscle pain in lower limbs after starting Lipitor.
EVT0002	oral	23	false	mild	PAT002	patient	blank	2023-04-03	2023-04-03	Amoxil	amoxicillin	500mg	2023-04-01	2023-04-05	rash	recovered	discontinued	false	blank	allergy	female	UK	London	PatientPortal202	Patient noticed red rash on hands and neck two days after starting Amoxil.
EVT0003	inhalation	16	false	mild	PAT003	pharmacist	PHM201	2023-02-14	2023-02-15	Advair Diskus	fluticasone/salmeterol	1 puff	2023-01-20	blank	throat irritation	recovering	no change	false	blank	asthma	female	Canada	Toronto	PharmacyChain01	Patient reported mild throat irritation after Advair Diskus use.
EVT0004	oral	77	true	severe	PAT004	clinician	CLN102	2023-06-10	2023-06-11	Coumadin	warfarin	5mg	2023-05-18	blank	nosebleed	recovering	dose reduced	true	aspirin, metformin	atrial fibrillation, diabetes	male	USA	Houston	SeniorCarePlatform	Patient experienced spontaneous nosebleed after 3 weeks of Coumadin.
EVT0005	oral	34	false	mild	PAT005	patient	blank	2023-03-01	2023-03-02	Zyrtec	cetirizine	10mg	2023-02-28	blank	drowsiness	recovered	no change	false	blank	blank	male	Brazil	Rio de Janeiro	MobileHealthLog21	Patient reported excessive drowsiness after taking Zyrtec.
EVT0006	oral	69	false	moderate	PAT006	clinician	CLN103	2023-07-13	2023-07-14	Plavix	clopidogrel	75mg	2023-06-30	blank	easy bruising	not recovered	no change	false	aspirin	hypertension	female	Germany	Berlin	CardioCareDB	Patient developed easy bruising on arms during Plavix therapy.
EVT0007	subcutaneous	44	false	moderate	PAT007	other	OTH301	2023-01-09	2023-01-10	Humira	adalimumab	40mg	2022-12-20	blank	injection site reaction	recovering	no change	false	blank	rheumatoid arthritis	female	France	Paris	ImmunologyRegister	Patient experienced pain and swelling at injection site after Humira administration.
EVT0008	intravenous	72	true	life-threatening	PAT008	clinician	CLN104	2023-08-20	2023-08-22	Morphine	morphine sulfate	5mg	2023-08-20	2023-08-21	respiratory depression	recovered	discontinued	true	paracetamol	COPD, hypertension	male	USA	Los Angeles	EmergencyDeptLA	Patient developed respiratory depression after IV morphine in emergency department.
EVT0009	oral	56	false	moderate	PAT009	patient	blank	2023-02-07	2023-02-09	Metformin	metformin	500mg	2022-11-15	blank	diarrhea	not recovered	no change	false	lisinopril	diabetes, hypertension	female	India	Mumbai	PatientSelfReportIND	Patient reported frequent loose stools after starting Metformin.
EVT0010	inhalation	17	false	moderate	PAT010	pharmacist	PHM202	2023-05-23	2023-05-24	Ventolin	albuterol	2 puffs	2023-05-22	blank	palpitations	recovering	dose reduced	false	blank	asthma	male	Australia	Sydney	PharmacyBranchSYD	Patient developed palpitations after increased Ventolin use.
EVT0011	oral	29	false	mild	PAT011	patient	blank	2023-09-13	2023-09-14	Ibuprofen	ibuprofen	400mg	2023-09-12	blank	stomach pain	recovered	no change	false	blank	blank	female	Spain	Madrid	MobileHealthLog22	Patient developed stomach pain after taking Ibuprofen for headache.
EVT0012	oral	81	true	severe	PAT012	clinician	CLN105	2023-06-21	2023-06-22	Xarelto	rivaroxaban	15mg	2023-06-01	2023-06-21	gastrointestinal bleeding	recovering	discontinued	true	aspirin	atrial fibrillation	male	USA	New York	HISNYC	Patient presented to hospital with GI bleeding after Xarelto therapy.
EVT0013	intravenous	36	true	life-threatening	PAT013	other	OTH302	2023-07-12	2023-07-14	Remicade	infliximab	100mg	2023-06-15	2023-07-12	anaphylaxis	recovering	discontinued	true	blank	Crohn's disease	female	Italy	Rome	ImmunologyRegister23	Patient experienced sudden anaphylaxis during Remicade infusion, requiring ICU admission.
EVT0014	subcutaneous	52	false	severe	PAT014	clinician	CLN106	2023-02-25	2023-02-27	Enbrel	etanercept	50mg	2023-02-01	blank	headache	not recovered	no change	true	naproxen	rheumatoid arthritis	male	UK	Manchester	EMR34567	Patient developed severe headache after Enbrel injection.
EVT0015	oral	19	false	mild	PAT015	patient	blank	2023-04-08	2023-04-09	Tamiflu	oseltamivir	75mg	2023-04-07	2023-04-08	nausea	recovered	discontinued	false	blank	blank	female	Japan	Tokyo	PatientPortalJP	Patient reported feeling nauseous after Tamiflu dosing.
EVT0016	oral	62	false	moderate	PAT016	clinician	CLN107	2023-05-10	2023-05-11	Januvia	sitagliptin	100mg	2023-04-20	blank	joint pain	recovering	dose reduced	false	metformin	diabetes	male	USA	Dallas	EMR67890	Patient developed moderate joint pain after starting Januvia.
EVT0017	subcutaneous	48	false	severe	PAT017	other	OTH303	2023-03-16	2023-03-17	Neulasta	pegfilgrastim	6mg	2023-03-01	2023-03-16	bone pain	recovering	discontinued	true	cyclophosphamide	breast cancer	female	Russia	Moscow	OncologySystemRU	Patient experienced severe bone pain after Neulasta injection during chemotherapy.
EVT0018	oral	15	false	mild	PAT018	patient	blank	2023-07-26	2023-07-27	Singulair	montelukast	10mg	2023-07-20	blank	nightmares	not recovered	no change	false	blank	asthma	male	South Africa	Cape Town	PatientSelfReportSA	Patient reported vivid nightmares while using Singulair for asthma.
EVT0019	oral	32	false	moderate	PAT019	pharmacist	PHM203	2023-09-02	2023-09-03	Synthroid	levothyroxine	75mcg	2023-08-28	blank	hair loss	recovering	dose reduced	false	blank	hypothyroidism	female	USA	San Francisco	PharmacyChainCA	Patient reported increased hair loss after adjusting Synthroid dose.
EVT0020	oral	63	false	moderate	PAT020	clinician	CLN108	2023-10-31	2023-11-01	Cymbalta	duloxetine	60mg	2023-10-01	blank	dizziness	not recovered	no change	false	lisinopril	hypertension, depression	female	USA	Seattle	EMRSeattl1	Patient complained of persistent dizziness after increasing Cymbalta dosage.

What the 200 rows show

from the 200-row sample

Intravenous (drug route) stands out: 32 of its 37 rows have hospitalization_required = true, against 8 of 163 for the rest.

20%hospitalization_required = true
52median age
2sexes
3action takens
4reporter types
4outcomes

Hospitalization required rate by drug_routehospitalization_required = true

age200 rows, in bands of 10

Median 52, from 13 to 83.

severity200 rows · 5 values

moderate72
mild70
severe40
life-threatening15
fatal3

26 columns by typefrom the column list below

string 19
integer 1
date 4
boolean 2

Columns

26 columns in four groups

blueprint · 26 columns
column	type	description	example
Text 19 columns
`event_id`	string	Unique identifier for each adverse event recordunique	EVT0001
`patient_id`	string	Unique identifier for the patient reporting or experiencing the adverse event	PAT001
`reporter_type`	string	Type of reporter (e.g., patient, clinician, pharmacist)patient · clinician · pharmacist · other	clinician
`reporter_id`	string	Unique identifier for the individual reporting the adverse eventoptional	CLN101
`drug_name`	string	Name of the drug suspected to be associated with the adverse event	Lipitor
`drug_generic_name`	string	Generic name of the drugoptional	atorvastatin
`drug_dose`	string	Dosage of the drug administered (e.g., 500mg, 1 tablet)optional	20mg
`drug_route`	string	Route of drug administration (e.g., oral, intravenous)6 values · optional	oral
`adverse_event_term`	string	Standardized term describing the adverse event (e.g., headache, rash)	muscle pain
`adverse_event_description`	string	Detailed description of the adverse event as reportedoptional	Patient reported persiste…
`severity`	string	Severity of the adverse event6 values · optional	moderate
`outcome`	string	Outcome of the adverse eventrecovered · recovering · not recovered · fatal · unknown · optional	recovering
`action_taken`	string	Action taken regarding the drug after the adverse event (e.g., discontinued, dose reduced, no change)discontinued · dose reduced · no change · unknown · optional	dose reduced
`concomitant_drugs`	string	Comma-separated list of other drugs taken concurrentlyoptional	aspirin
`medical_history`	string	Comma-separated list of relevant patient medical history termsoptional	hypertension, diabetes
`sex`	string	Sex of the patientmale · female · other · unknown · optional	male
`country`	string	Country where the adverse event occurredoptional	USA
`city`	string	City where the adverse event occurredoptional	Chicago
`source_system`	string	Source system or registry from which the record was obtainedoptional	EMR12345
Numbers 1 column
`age`	integer	Age of the patient at the time of the adverse event0 to 120 · optional	68
Dates and times 4 columns
`event_date`	date	Date when the adverse event occurred	2023-05-11
`report_date`	date	Date when the adverse event was reported	2023-05-12
`drug_start_date`	date	Date when the drug treatment startedoptional	2022-12-01
`drug_end_date`	date	Date when the drug treatment endedoptional	2023-04-05
True or false 2 columns
`serious`	boolean	Indicates if the adverse event is considered serious (per regulatory criteria)optional	false
`hospitalization_required`	boolean	Indicates if the adverse event required hospitalizationoptional	false

Pharmaceutical Adverse Event Dataset

Sample rows

What the 200 rows show

Columns

Use it for

A healthcare dashboard

A root-cause class exercise

A software demo

Make it yours.

Same schema. As many rows as you need.

What should your data show?

Sample rows

What the 200 rows show

Columns

Use it for

A healthcare dashboard

A root-cause class exercise

A software demo

Make it yours.

Same schema. As many rows as you need.

More in Healthcare

What should your data show?