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AHRI.ISISEKELOSEMPILO.CLINICAL.MANAGEMENT.DATASETS.V2.0
Isisekelo Sempilo:Clinical Management Datasets
South Africa
,
2020 - 2022
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Reference ID
AHRI.IsisekeloSempilo.Clinical.Management.Datasets.v2.0
Producer(s)
Dr Maryam, Shahmanesh, ,
Collections
Multilevel HIV Prevention
Metadata
Documentation in PDF
DDI/XML
JSON
Created on
Oct 24, 2022
Last modified
Oct 24, 2022
Page views
61493
Downloads
115
Study Description
Data Dictionary
Downloads
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Data files
AHRI.IsisekeloSempilo.AdverseEvents.2022.v2
AHRI.IsisekeloSempilo.Clinical.CombinedDataset.2022.v2
AHRI.IsisekeloSempilo.Clinical.CombinedDataset_Exclu_PInfo.2022.v2
AHRI.IsisekeloSempilo.ClinicVisits.2022.v2
AHRI.IsisekeloSempilo.ClinScreenHealthPro.2022.v2
AHRI.IsisekeloSempilo.Consents.2022.v2
AHRI.IsisekeloSempilo.EndOfStudy.2022.v2
AHRI.IsisekeloSempilo.PersonalInformation.2022.v2
AHRI.IsisekeloSempilo.PhoneCalls.2022.v2
AHRI.IsisekeloSempilo.PrEPEligibilityCheck.2022.v2
AHRI.IsisekeloSempilo.ReasonsStopPrEP.2022.v2
AHRI.IsisekeloSempilo.TestResults.2022.v2
AHRI.IsisekeloSempilo.VitalSigns.2022.v2
Data file: AHRI.IsisekeloSempilo.AdverseEvents.2022.v2
Cases:
191
Variables:
21
Variables
IIntId
Internal Individual ID
VisitId
Clinic Visit Identifier
Instance
Instance
AnyAEs
Did the participant reported any side effects or adverse events since the last v
SideEffect
Common side effects of PrEP - Code
SideEffectDesc
Common side effects of PrEP - Description
SideEffectOth
Details of other side effect or adverse event
StartDate
Start date of event
Ongoing
Is the event ongoing?
StopDate
Stop date of event
Severity
Severity of event - Code
SeverityDesc
Severity of event - Description
Relationship
Relationship to study - Code
RelationshipDesc
Relationship to study - Description
ActionTaken
Action Taken Regarding Drug adverse event - Code
ActionTakenDesc
Action Taken Regarding Drug adverse event - Description
ActionTakenOth
Please specify details on other action taken
Outcome
Outcome of event - Code
OutcomeDesc
Outcome of event - Description
Expected
Is this an expected event for this study?
Serious
Is this a Serious Adverse Event?
Total: 21
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