Name of organisation
1) Department/Research groupPorto Pharmacovigilance Centre
2) Organisation/affiliationFaculty of Medicine, University of Porto.
Short Name in the inventoryUFPorto
Administrative Contact
Title Dr
Last name Vaz
First name Inês
Address line 1Faculdade de Medicina da Universidade do Porto
Address line 2Rua Doutor Plácido da Costa
Address line 3
CityPorto
Postcode4200-450
CountryPortugal
Phone number (incl. country code)351-220426952
Alternative phone number351-220426943
Fax number (incl. country code)351-225513682
Scientific Contact
Title Professor
Last name Polónia
First name Jorge
Address line 1Faculdade de Medicina da Universidade do Porto
Address line 2Rua Doutor Plácido da Costa
Address line 3
CityPorto
Postcode4200-450
CountryPortugal
Phone number (incl. country code)351-220426952
Alternative phone number351-220426943
Fax number (incl. country code)351-225513682
Alternative Scientific Contact
Title Professor
Last name Costa Pereira
First name Altamiro
Address line 1Faculdade de Medicina da Universidade do Porto
Address line 2Rua Doutor Plácido da Costa
Address line 3
CityPorto
Postcode4200-450
CountryPortugal
Phone number (incl. country code)351-220426952
Alternative phone number351-220426943
Fax number (incl. country code)351-225513682
2. Description
The Porto Pharmacovigilance Centre (UFPorto) is a regional centre of the Portuguese Pharmacovigilance System.
This Centre is responsible for the collection, validation, processing and assessment of spontaneous reports of Adverse Drug Reaction in the Porto District, Portugal. UFPortoalso performs research on pharmacovigilance and drug safety.
3. Category
University based
Government based
4. Available resources
In houseVia Contacts/Network
5. Therapeutic/disease areas of research in drug safety/risk-benefit performed in the past 5 years
Cardiovascular diseases
Immunological products and vaccines
Allergic reactions
6. Design of drug safety/risk-benefit studies published in the past 5 years
Case Control Study
Meta-Analysis
Cluster-randomized controlled trial
7. Experience in collecting data directly from individual patients/respondents
Number of Studies
Less than 5
Number of patients/respondents involved in the study(ies)
Between 1500 and 14999
8. Access to data collection resources
Capacity to conduct face-to-face interviews
No
Electronic data capture systems
No
Interactive voice response systems
Yes
Call centre
No