1. Contact details
Name of organisation
1) Department/Research groupSicilian Pharmacovigilance Regional Centre
2) Organisation/affiliationUniversity of Messina
Short Name in the inventoryUniversity of Messina
Administrative Contact
Title Dr
Last name Trifirò
First name Gianluca
Address line 1Department of Clinical and Experimental Medicine
Address line 2Policlinico Universitario "G. Martino"
Address line 3
CityMessina
Postcode98125
CountryItaly
Phone number (incl. country code)39-090-2213264
Alternative phone number39-090-2213650
Fax number (incl. country code)39-090-2212711
Scientific Contact
Title Professor
Last name Caputi
First name Achille Patrizio
Address line 1Department of Clinical and Experimental Medicine
Address line 2Policlinico Universitario "G. Martino"
Address line 3
CityMessina
Postcode98125
CountryItaly
Phone number (incl. country code)39-090-2213878
Alternative phone number39-090-2213650
Fax number (incl. country code)39-090-2212711
Alternative Scientific Contact
Title Dr
Last name Trifirò
First name Gianluca
Address line 1Department of Clinical and Experimental Medicine
Address line 2Policlinico Universitario "G. Martino"
Address line 3
CityMessina
Postcode98125
CountryItaly
Phone number (incl. country code)39-090-2213264
Alternative phone number39-090-2213878
Fax number (incl. country code)
2. Description
The Centre is responsible for collecting and analyzing spontaneous reports of ADR from all over Sicily since 2003. The database include data from 1996. We collaborate with the National Authority (Agenzia Italiana del Farmaco - AIFA) for signal detection and other national/international initiatives concerning drug safety. The Centre has also expertises in the field of pharmacoepidemiology, drug information and drug utilization; several studies are conducted using prescription data from GPs Electronic Health Records. Overall, about 10 people are actively involved in these topics at different levels.
3. Category
University based
Hospital based
Government based
4. Available resources
In houseVia Contacts/Network
Epidemiologist/Pharmacoepidemiologist
Yes
Yes
Statistician
No
Yes
Clinician
Yes
No
Clinical Pharmacologist
Yes
No
Pharmacist
Yes
No
Geneticist/Pharmacogeneticist
No
Yes
IT specialist
Yes
No
Ethics expertise
Yes
No
Legal expertise
No
Yes
Regulatory expertise
No
Yes
5. Therapeutic/disease areas of research in drug safety/risk-benefit performed in the past 5 years
Cardiovascular diseases
Disorders of the central nervous system
Endocrine disorders
Geriatrics
Immunological products and vaccines
Infectious diseases
Liver disease
Malignant disease
Musculoskeletal and joint diseases
Psychiatry
Skin disorders
6. Design of drug safety/risk-benefit studies published in the past 5 years
Cohort Study
Case Control Study
Drug Utilisation
Meta-Analysis
Spontaneous reporting data mining
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 150 and 1499
8. Access to data collection resources
Capacity to conduct face-to-face interviews
Yes
In a clinic
Yes
In the community
Yes
Electronic data capture systems
Yes
System used:
SPSS, SOS, SQL
Interactive voice response systems
No
Call centre
No