dr. F.P.A.M. (Florence) van Hunsel, PhD

Telephone:

E-mail:

f.p.a.m.van.hunsel rug.nl

Publications

Comparison of Perceived Adverse Events After COVID-19 Vaccination Between Pregnant and NonPregnant Women Using Two Cohort Studies in the Netherlands

Woestenberg, P. J., Terpstra, A. W., van Hunsel, F., Lieber, T. & Maas, V. Y. F., Jun-2025, In: Birth Defects Research. 117, 6, 10 p., e2490.

Research output: Contribution to journal › Article › Academic › peer-review

General practitioner consultation for postmenopausal bleeding after COVID-19 vaccination—a self-controlled cohort study

Jajou, R., van Puijenbroek, E. P., Veldkamp, R., Overbeek, J. A., van Hunsel, F. P. A. M. & Kant, A. C., 18-Mar-2025, (E-pub ahead of print) In: British Journal of Clinical Pharmacology.

Research output: Contribution to journal › Article › Academic › peer-review

Impact of Regulatory Action on Dose Maximalization for Vitamin B6 Dietary Supplements on the Reporting Pattern for Neuropathy

van Hunsel, F., Scholl, J., Vrolijk, M. & Ekhart, C., Feb-2025, In: Pharmacoepidemiology and Drug Safety. 34, 2, p. e70108 5 p.

Research output: Contribution to journal › Article › Academic › peer-review

Qualitative Interviews with Stakeholders in Herbal Pharmacovigilance and Recommendations for Best Practices to be Applied Worldwide

Ekhart, C., Wiarda, S. H. P., van de Koppel, S., Skalli, S., Alghamdi, W., Menniti-Ippolito, F., Tangchitkhachon, K., Mponda, J. S., Woerdenbag, H. J. & van Hunsel, F., Jan-2025, In: Drug Safety. 48, p. 75-86 12 p.

Research output: Contribution to journal › Article › Academic › peer-review

Quality of Clinical Information in Pregnancy Pharmacovigilance Data Sources: A Contribution of the ConcePTION Project

van Rijt-Weetink, Y. R. J., van Gendt, J., Egberts, T. C. G., van Hunsel, F. P. A. M., Lewis, D. J., Yates, L. M., Winterfeld, U. & van Puijenbroek, E. P., Jul-2025, In: Pharmacoepidemiology and Drug Safety. 34, 7, 10 p., e70182.

Research output: Contribution to journal › Article › Academic › peer-review

The Role of Adverse Event Follow-Up in Advancing the Knowledge of Medicines and Vaccines Safety: A Scoping Review

Kara, V., Van Hunsel, F., Bate, A. & van Puijenbroek, E., 20-May-2025, (E-pub ahead of print) In: Drug Safety.

Research output: Contribution to journal › Review article › peer-review

Timing Matters: Exploring the Role of the Time to Onset in Recall Bias for Adverse Events Following Immunization (AEFIs) of COVID-19 Vaccines from Spontaneous Reports

Scholl, J., van Hunsel, F. & Puijenbroek ,van, E., 7-Apr-2025, In: Pharmacoepidemiology. 4, 2, 11 p.

Research output: Contribution to journal › Article › Academic › peer-review

Achieving patient engagement in pharmacovigilance: from high-income countries to lower and -middle-income countries with focus on Africa

Sabblah, G. T., Taxis, K., Duwiejua, M., Seaneke, S. K., van Puijenbroek, E. & van Hunsel, F., 2024, In: Expert Opinion on Drug Safety. 23, 12, p. 1493-1501 9 p.

Research output: Contribution to journal › Review article › peer-review

Analysis of Adverse Reactions Associated with the Use of Crataegus-Containing Herbal Products

Woerdenbag, H. J., Ursidae, M., Ekhart, C., Schmidt, M., Vitalone, A. & van Hunsel, F. P. A. M., Nov-2024, In: Pharmaceuticals. 17, 11, 27 p., 1490.

Research output: Contribution to journal › Article › Academic › peer-review

An innovative method to strengthen evidence for potential drug safety signals using Electronic Health Records

Abedian Kalkhoran, H., Zwaveling, J., van Hunsel, F. & Kant, A., 16-May-2024, In: Journal of Medical Systems. 48, 1, p. 51

Research output: Contribution to journal › Article › Academic › peer-review

All (150) publications

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