Drug Safety Research Unit (DSRU)

Drug Safety Research Unit (DSRU) The Drug Safety Research Unit (DSRU) is the UK’s leading pharmacovigilance and pharmacoepidemiology unit, conducting a broad range of drug safety studies.

We are also the leading provider of pharmacovigilance training courses in Europe.

Shaping vaccine safety evidence across EuropeDSRU colleagues have contributed to a major VAC4EU study examining thrombos...
22/06/2026

Shaping vaccine safety evidence across Europe

DSRU colleagues have contributed to a major VAC4EU study examining thrombosis with thrombocytopaenia syndrome (TTS) — a rare blood clotting condition — following the Oxford-AstraZeneca COVID-19 vaccine. The findings are published in Vaccine.

The UK arm of the study drew on CPRD Aurum, the UK's database of anonymised primary care records. Across the UK, Spain and the Netherlands, the study included more than 5.3 million people who received the AstraZeneca vaccine.

Key findings:

- Possible increased risk of TTS after vaccination, particularly after the first dose
- Higher risk observed in people aged under 60
- Risk window: 1–42 days after vaccination
- Results varied between countries and data sources

This underlines why collaborative, real-world evidence matters in vaccine safety monitoring.

We're proud to contribute to this important European collaboration.

Read the full paper here: https://www.sciencedirect.com/science/article/pii/S0264410X26005323?dgcid=coauthor

https://www.dsru.org/dsrunews/shaping-vaccine-safety-evidence-across-europe/

Join our Risk Benefit Assessment in Pharmacovigilance course on 24 – 25 June 2026, where Catherine Fry (DSRU) will demon...
22/06/2026

Join our Risk Benefit Assessment in Pharmacovigilance course on 24 – 25 June 2026, where Catherine Fry (DSRU) will demonstrate how risk can be evaluated using statistical approaches.

Register now: https://bit.ly/3XJ7SIJ

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, led by expert speakers including...
19/06/2026

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, led by expert speakers including Kristina Strutt (Bicycle Therapeutics).

Kristina will present on routine risk minimisation through safety information documents, exploring the role of the SmPC, PIL, and CCSI in supporting effective risk management and clear benefit–risk communication across the product lifecycle.

Register now: https://bit.ly/3XJ7SIJ

One week to go!Last chance to register for our Risk Benefit Assessment in Pharmacovigilance course on 24 -25 June 2026!E...
17/06/2026

One week to go!

Last chance to register for our Risk Benefit Assessment in Pharmacovigilance course on 24 -25 June 2026!

Explore the relationship between risk and benefit and develop your understanding of risk benefit assessments in pharmacovigilance on this engaging course.

Book now: https://bit.ly/3XJ7SIJ

Dr Anne Ruth van Troostenburg de Bruyn (SagePharmaSolutions Ltd) will speak on the practical implications of regulatory ...
16/06/2026

Dr Anne Ruth van Troostenburg de Bruyn (SagePharmaSolutions Ltd) will speak on the practical implications of regulatory requirements at our Risk Benefit Assessment in Pharmacovigilance course, 24–25 June 2026.

Register here: https://bit.ly/3XJ7SIJ

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, featuring expert speakers includ...
15/06/2026

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, featuring expert speakers including Debabrata Roy (DSRU).

Debabrata will present a worked example of the Benefit Risk Action Team (BRAT) methodology, providing practical insight into structured benefit–risk assessment to support regulatory and safety decision making.

Register now: https://bit.ly/3XJ7SIJ

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, led by expert speakers including...
12/06/2026

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, led by expert speakers including Sandeep Dhanda (DSRU).

Sandeep will present Identification and Evaluation of Risk, focusing on how safety risks are identified, assessed, and prioritised using internal and external data sources to support effective risk management.

Register now: https://bit.ly/3XJ7SIJ

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, featuring expert speakers includ...
10/06/2026

Join us on 24–25 June 2026 for our Risk Benefit Assessment in Pharmacovigilance course, featuring expert speakers including Kristina Strutt (Bicycle Therapeutics).

Kristina will present on Taking action - the MAH point of view, covering minimising risks with medicines, regulatory actions, Risk Management Plans, selecting appropriate risk minimisation activities, and effective issue management.

Register now: https://bit.ly/3XJ7SIJ

Join our Risk Benefit Assessment in Pharmacovigilance course on 24–25 June 2026. Miranda Davies (DSRU) and Kristina Stru...
08/06/2026

Join our Risk Benefit Assessment in Pharmacovigilance course on 24–25 June 2026. Miranda Davies (DSRU) and Kristina Strutt (Bicycle Therapeutics) will lead an interactive workshop on communicating drug safety issues using a real‑life case study.

Secure your place now: https://bit.ly/3XJ7SIJ

Join our Risk Benefit Assessment in Pharmacovigilance course on 24–25 June 2026. Miranda Davies (DSRU) and Kristina Stru...
04/06/2026

Join our Risk Benefit Assessment in Pharmacovigilance course on 24–25 June 2026. Miranda Davies (DSRU) and Kristina Strutt (Bicycle Therapeutics) will lead an interactive workshop on crisis management.

Secure your place now: https://bit.ly/3XJ7SIJ

Address

Bursledon Hall
Southampton

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+442380408600

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