Patients and HCP understanding on additonal monitoring

Study type

• Study topic:
  Other
• Study topic, other:
  To assess attitudes towards adverse drug reactions (ADR) reporting and reasons for not reporting an ADR and awareness of additional monitoring (AM) among HCPs, patients or their careers
• Study type:
  Non-interventional study
• Scope of the study:
  Other
• If ‘other’, further details on the scope of the study:
  Assessment of awareness of additional monitoring
• Data collection methods:
  Primary data collection

Non-interventional study

• Non-interventional study design:
  Other
• Non-interventional study design, other:
  Survey questionnaire

Population studied

• Short description of the study population:
  Health care professionals (HCPs), patients or their careers in EU countries.
• Age groups:
  • Adults (18 to < 46 years)
  • Adults (46 to < 65 years)
  • Adults (65 to < 75 years)
  • Adults (75 to < 85 years)
  • Adults (85 years and over)
• Estimated number of subjects:
  2918

Study design details

• Main study objective:
  To assess (a) attitudes towards ADR reporting and reasons for not reporting an ADR and (b) awareness of AM among HCPs, patients or their careers in EU countries
• Outcomes:
  To assess (a) attitudes towards ADR reporting and reasons for not reporting an ADR and (b) awareness of AM among HCPs, patients or their careers in EU countries
• Data analysis plan:
  Survey responses analysis