1 Establishing a Pharmacovigilance Centre Sten Olsson the Uppsala Monitoring Centre.
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Transcript of 1 Establishing a Pharmacovigilance Centre Sten Olsson the Uppsala Monitoring Centre.
![Page 1: 1 Establishing a Pharmacovigilance Centre Sten Olsson the Uppsala Monitoring Centre.](https://reader036.fdocuments.us/reader036/viewer/2022081512/56649e255503460f94b1448a/html5/thumbnails/1.jpg)
1
Establishing a Pharmacovigilance
CentreSten Olsson
the Uppsala Monitoring Centre
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2
Decide about a Plan
• location• organisation• funding• staffing• reporting form +
routines
• equipment • promotion• feed-back• use of data
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Affiliation
• drug regulatory authority
• university institution
• hospital department
• poison information or drug
information centre
• association of professionals
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Integrate systems needing similar
competence and resources
• drug information
• poison information
• pharmacovigilance
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Organisation
• Centralised
• Regional Centres
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Where to report?
Patient Health
Professional
Regional Centre
Manufacturer
HospitalDTC
National Centre
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Gains and losses in report chain
PatientHospital
DTC
FactsJudgement
SpeedReports
SpeedReports
FactsJudgement
Health Professional
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Where to report?
Patient Health
Professional
Regional Centre
Manufacturer
HospitalDTC
National Centre
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Countries with decentralised reporting system
ArgentinaBrazilCanada ChinaCubaFrance Italy India
the NetherlandsPolandPortugalRussiaSpainSwedenThailandUnited Kingdom
16 of 73 member countries
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Support
• political
• economical
stable and on a long-
term basis
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Staff
• pharmaceutical competence
• medical competence• secretarial assistance
•dedication•education
– formal training course– visit established centre
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Centre facilities
• computer with printer
•word processor
•report recording system
• literature sources
• telephone, fax , e-mail
• internet access
• photocopier
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Routines
• who should report?
• what should be reported?
• voluntary or mandatory reporting?
• coding system
• method of causality assessment
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Mandatory Reporting for Health Professionals
• Austria• Bulgaria• Croatia• Czech Republic• France • Greece• Hungary• Italy
• Mongolia• Morocco• Norway• Oman• Russia• Slovak Republic• Spain• Sweden
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Methods to stimulate reporting by professionals
• Facilitate access to reporting forms
• Facilitate reporting
• Acknowledge receipt of report
• Feedback
• Publication in medical journals
• Participation in scientific conferences
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Methods to stimulate reporting by professionals
• Include ADR monitoring in curricula
• Set up regional centres
• Engage drug/therapeutics committees
• Approach professional associations
• Support development of clinical pharmacology/pharmacy
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Methods to stimulate reporting by patients
• Approach patient associations
• Publication in lay press
• Include in patient drug information advice to report to doctor
• Telephone medicines information service
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Highest reporting rates
• More than 200 reports/ million inhabitants/year– Australia– Denmark– Cuba– Ireland– the Netherlands– New Zealand– Norway– Sweden– United Kingdom– USA
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Use of data
• method of signal identification• establishment of advisory
committee• feed-back routines
– individual response– adverse reactions newsletter– web site
• educational activities
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Use of data (2)
• National Centre
– follow-up cases– preliminary
case assessment
– recording– carry out
actions
• Advisory Committee
– final case assessment
– promote reporting
– analyse problems– propose actions
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Relationships to consider
• drug regulatory authority• public health programmes• pharmaceutical companies• journalists• academic institutions• professional associations• pharmacovigilance centres in other
countries• consumer and patient organisations