Skip to content

eletriptan

As the list published 23 Sept 2026 has it, binding since 20 Apr 2022. Each entry binds six months after its own publication date (Article 107c(7) of Directive 2001/83/EC).

What the list says

EU reference date
20 Jan 2000
PSUR frequency
5 years
Data lock point
19 Feb 2026
Submission date
20 May 2026
Next data lock point
Not stated
Next submission date
Not stated
Products covered
Nationally authorised (NAP)

Are PSURs required for products referred to in Articles 10(1), 10a and 16a of Directive 2001/83/EC?

No — the list does not require PSURs for these products.

The list asks this as one question for Articles 10(1), 10a and 16a together, and does not answer it for Article 14 at all. A PSUR may in any case be required at the request of a competent authority or as a condition of the marketing authorisation.

Notes in the list

DLP was updated on 20/10/2021 PRAC Rapporteur name updated on 27/06/2017 Next DLP was updated on 18/11/2016 The DLP amended on 30/09/2015 Lead MS was added on 13/07/2015

Track dates like these for your own products: a sample workspace, read-only, no account needed.

Try the demo

The next three reports

  • Data lock point 19 Feb 2031Submission by 20 May 2031
  • Data lock point 19 Feb 2036Submission by 19 May 2036
  • Data lock point 19 Feb 2041Submission by 20 May 2041

Counted from the data lock point the list gives, on the cycle it states: the submission date is 90 days after the data lock point — 70 days for a cycle of twelve months or less, 90 days for a longer one, as GVP Module VII sets out.

In earlier versions of the list

  • EMA/630645/2012 Rev.164 · published 23 Sept 2026

    eletriptan — every 5 years, data lock point 19 Feb 2026

  • EMA/630645/2012 Rev.156 · published 4 Feb 2026

    eletriptan — every 5 years, data lock point 19 Feb 2026

Source: European Medicines Agency, list of EU reference dates and frequency of submission of periodic safety update reports, EMA/630645/2012 Rev.164, published 23 Sept 2026. Open the published file

Kreastel is a planning and oversight aid for pharmacovigilance obligations. It tracks dates like these for a marketing authorisation holder's own products.

Report a discrepancy — if this page and the published file disagree, the file is right and we want to know.

Kreastel