de Vries ST - Search Results

1

Patient-Reported Adverse Events of Radiopharmaceuticals: Development and Validation of a Questionnaire.

Schreuder N, de Hoog Q, de Vries ST, Jager PL, Kosterink JGW, van Puijenbroek EP. Schreuder N, et al. Among authors: de vries st, de hoog q. Drug Saf. 2020 Apr;43(4):319-328. doi: 10.1007/s40264-019-00895-2. Drug Saf. 2020. PMID: 31916082 Free PMC article.

2

Development and Initial Validation of a Patient-Reported Adverse Drug Event Questionnaire.

de Vries ST, Mol PG, de Zeeuw D, Haaijer-Ruskamp FM, Denig P. de Vries ST, et al. Among authors: de zeeuw d. Drug Saf. 2013 Sep;36(9):765-77. doi: 10.1007/s40264-013-0036-8. Drug Saf. 2013. PMID: 23553447 Clinical Trial.

3

The validity of a patient-reported adverse drug event questionnaire using different recall periods.

de Vries ST, Haaijer-Ruskamp FM, de Zeeuw D, Denig P. de Vries ST, et al. Among authors: de zeeuw d. Qual Life Res. 2014 Nov;23(9):2439-45. doi: 10.1007/s11136-014-0715-7. Epub 2014 May 22. Qual Life Res. 2014. PMID: 24848596

4

Factors Influencing the Use of a Mobile App for Reporting Adverse Drug Reactions and Receiving Safety Information: A Qualitative Study.

de Vries ST, Wong L, Sutcliffe A, Houÿez F, Ruiz CL, Mol PG; IMI Web-RADR Work Package 3b Consortium. de Vries ST, et al. Drug Saf. 2017 May;40(5):443-455. doi: 10.1007/s40264-016-0494-x. Drug Saf. 2017. PMID: 28035492 Free PMC article.

5

Sex Differences in Reported Adverse Drug Reactions of Selective Serotonin Reuptake Inhibitors.

Ekhart C, van Hunsel F, Scholl J, de Vries S, van Puijenbroek E. Ekhart C, et al. Drug Saf. 2018 Jul;41(7):677-683. doi: 10.1007/s40264-018-0646-2. Drug Saf. 2018. PMID: 29484612

6

Safety Communication Tools and Healthcare Professionals' Awareness of Specific Drug Safety Issues in Europe: A Survey Study.

de Vries ST, van der Sar MJM, Coleman AM, Escudero Y, Rodríguez Pascual A, Maciá Martínez MÁ, Cupelli A, Baldelli I, Šipić I, Andrić A, Michan L, Denig P, Mol PGM; SCOPE work package 6. de Vries ST, et al. Drug Saf. 2018 Jul;41(7):713-724. doi: 10.1007/s40264-018-0643-5. Drug Saf. 2018. PMID: 29500798 Free PMC article.

7

Interest in a Mobile App for Two-Way Risk Communication: A Survey Study Among European Healthcare Professionals and Patients.

de Vries ST, Denig P, Lasheras Ruiz C, Houÿez F, Wong L, Sutcliffe A, Mol PGM; IMI Web-RADR Work Package 3b Consortium. de Vries ST, et al. Drug Saf. 2018 Jul;41(7):697-712. doi: 10.1007/s40264-018-0648-0. Drug Saf. 2018. PMID: 29500800 Free PMC article.

8

Use of a Patient-Friendly Terms List in the Adverse Drug Reaction Report Form: A Database Study.

de Vries ST, Harrison J, Revelle P, Ptaszynska-Neophytou A, Radecka A, Ragunathan G, Tregunno P, Denig P, Mol PGM. de Vries ST, et al. Drug Saf. 2019 Jul;42(7):881-886. doi: 10.1007/s40264-019-00800-x. Drug Saf. 2019. PMID: 30725337 Free PMC article.

9

Recommendations on the Use of Mobile Applications for the Collection and Communication of Pharmaceutical Product Safety Information: Lessons from IMI WEB-RADR.

Pierce CE, de Vries ST, Bodin-Parssinen S, Härmark L, Tregunno P, Lewis DJ, Maskell S, Van Eemeren R, Ptaszynska-Neophytou A, Newbould V, Dasgupta N, Wisniewski AFZ, Gama S, Mol PGM. Pierce CE, et al. Among authors: de vries st. Drug Saf. 2019 Apr;42(4):477-489. doi: 10.1007/s40264-019-00813-6. Drug Saf. 2019. PMID: 30911975 Free PMC article.

10

Sex differences in adverse drug reactions reported to the National Pharmacovigilance Centre in the Netherlands: An explorative observational study.

de Vries ST, Denig P, Ekhart C, Burgers JS, Kleefstra N, Mol PGM, van Puijenbroek EP. de Vries ST, et al. Br J Clin Pharmacol. 2019 Jul;85(7):1507-1515. doi: 10.1111/bcp.13923. Epub 2019 Apr 29. Br J Clin Pharmacol. 2019. PMID: 30941789 Free PMC article.

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