Christine Erikstrup Hallgreen

Søgeresultater

• 2024

  Implementation of electronic distribution of Direct Healthcare Professional Communications (DHPCs) by the Danish Medicines Agency: A survey study of physicians’ experiences and preferences

  Sindahl, P., Møllebæk, M., Gardarsdottir, H., De Bruin, M. L., Hallgreen, C. E. & Clemmensen, M. H., 2024, (Accepteret/In press) I: Therapeutic Advances in Drug Safety.

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• The life cycle of vaccines evaluated by the European Medicines Agency

  Gräf, D. D., Westphal, L. & Hallgreen, C. E., 2024, I: Vaccine. 42, 21, 12 s., 126186.

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• 2023

  Clinical evidence and use of extrapolation in European biosimilar marketing authorizations

  Druedahl, L. C., Vive Nielsen, C. & Hallgreen, C. E., 2023, (Under udarbejdelse) I: BioDrugs.

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• Impact of 2018 EU Risk Minimisation Measures and Revised Pregnancy Prevention Programme on Utilisation and Prescribing Trends of Medicinal Products Containing Valproate: An Interrupted Time Series Study

  Abtahi, S., Pajouheshnia, R., Durán, C. E., Riera-Arnau, J., Gamba, M., Alsina, E., Hoxhaj, V., Andersen, M., Bartolini, C., Kristiansen, S. B., Brown, J., Hallgreen, C. E., Garcia-Poza, P., Gardarsdottir, H., Gini, R., Girardi, A., Holthuis, E., Huerta, C., Ibánez, L., Limoncella, G. & 8 flere, Martín-Pérez, M., Paoletti, O., Roberto, G., Souverein, P., Swart, K. M. A., Wing, K., Sturkenboom, M. & Klungel, O., 2023, I: Drug Safety. 46, 7, s. 689-702

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  7 Citationer (Scopus)

  23 Downloads (Pure)

• Impact of the 2018 revised Pregnancy Prevention Programme by the European Medicines Agency on the use of oral retinoids in females of childbearing age in Denmark, Italy, Netherlands, and Spain: an interrupted time series analysis

  Durán, C. E., Riera-Arnau, J., Abtahi, S., Pajouheshnia, R., Hoxhaj, V., Gamba, M., Alsina, E., Martin-Perez, M., Garcia-Poza, P., Llorente-Garcia, A., Gonzalez-Bermejo, D., Ibánez, L., Sabaté, M., Vidal, X., Ballarín, E., Sanfélix-Gimeno, G., Rodríguez-Bernal, C., Peiró, S., García-Sempere, A., Sanchez-Saez, F. & 22 flere, Ientile, V., Ingrasciotta, Y., Guarneri, C., Tanaglia, M., Tari, M., Herings, R., Houben, E., Swart-Polinder, K., Holthuis, E., Huerta, C., Gini, R., Roberto, G., Bartolini, C., Paoletti, O., Limoncella, G., Girardi, A., Hyeraci, G., Andersen, M., Kristiansen, S. B., Hallgreen, C. E., Klungel, O. & Sturkenboom, M., 2023, I: Frontiers in Pharmacology. 14, 12 s., 1207976.

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  3 Citationer (Scopus)

  18 Downloads (Pure)

• Regional Disparity in First-in-Class Anticancer Drug Development in the US, EU, and Japan

  Hino, Y., Okada, M., Hallgreen, C. E., De Bruin, M. L., Doty, R. E., Matsumaru, N. & Tsukamoto, K., 2023, I: Biological and Pharmaceutical Bulletin. 46, 5, s. 700-706

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• 2022

  Guidance for pediatric use in prescription information for novel medicinal products in the EU and the US

  Christiansen, H., De Bruin, M. L., Frokjaer, S. & Hallgreen, C. E., 2022, I: PLoS ONE. 17, 4, 19 s., e0266353.

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  3 Citationer (Scopus)

  50 Downloads (Pure)

• Hydroxyzine Initiation Following Drug Safety Advisories on Cardiac Arrhythmias in the UK and Canada: A Longitudinal Cohort Study

  Morrow, R. L., Mintzes, B., Souverein, P. C., Hallgreen, C. E., Ahmed, B., Roughead, E. E., De Bruin, M. L., Kristiansen, S. B., Lexchin, J., Kemp-Casey, A., Sketris, I., Mangin, D., Pearson, S. A., Puil, L., Lopert, R., Bero, L., Gnjidic, D., Sarpatwari, A. & Dormuth, C. R., 2022, I: Drug Safety. 45, s. 623–638

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  1 Citationer (Scopus)

  35 Downloads (Pure)

• Impact of regulatory interventions to restrict the combined use of renin-angiotensin system-acting agents: A Danish nationwide drug utilisation study

  Sindahl, P., Ofori-Asenso, R., Hallgreen, C. E., Kemp, K., Gardarsdottir, H. & Bruin, M. L. D., 2022, I: British Journal of Clinical Pharmacology. 88, 3, s. 1379-1384

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• Influence of drug safety advisories on drug utilisation: an international interrupted time series and meta-analysis

  Morrow, R. L., Mintzes, B., Souverein, P. C., De Bruin, M. L., Roughead, E. E., Lexchin, J., Kemp-Casey, A., Puil, L., Sketris, I., Mangin, D., Hallgreen, C. E., Pearson, S-A., Lopert, R., Bero, L., Ofori-Asenso, R., Gnjidic, D., Sarpatwari, A., Perry, L. T. & Dormuth, C. R., 2022, I: BMJ quality & safety. 31, 3, s. 179–190

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  6 Citationer (Scopus)

  44 Downloads (Pure)

• Mandatory requirements for pediatric drug development in the EU and the US for novel drugs: A comparative study

  Christiansen, H., De Bruin, M. L. & Hallgreen, C. E., 2022, I: Frontiers in Medicine. 9, 11 s., 1009432.

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  2 Citationer (Scopus)

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• Medication Adherence Measurement Methods in Registration Trials Supporting the Approval of New Medicines: A Cross-Sectional Analysis of Centralized Procedures in the European Union 2010–2020

  Mantila, K. M., Pasmooij, A. M. G., Hallgreen, C. E., Mol, P. G. M. & van Boven, J. F. M., 2022, I: Clinical Pharmacology and Therapeutics. 112, 5, s. 1051-1060

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  7 Citationer (Scopus)

  19 Downloads (Pure)

• New Information on Old Medicinal Products: A Cross-Sectional Analysis of Guidance for Paediatric Use for Substances on the European Priority List of Off-Patent Medicinal Products

  Mogensen, A. K. B., Christiansen, H., De Bruin, M. L. & Hallgreen, C. E., 2022, I: Pediatric Drugs. 24, s. 679–687

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• Status of Planned and Ongoing Paediatric Trials Investigating COVID-19 Vaccines: A Cross-Sectional Study of Paediatric Clinical Trials Planned in Agreed PIPs and/or Registered in Clinical Trial Databases

  Christiansen, H., Thirstrup, S. & Hallgreen, C. E., 2022, I: Therapeutic Innovation & Regulatory Science. 56, s. 474–482

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• 2020

  Are monitoring instructions provided in direct healthcare professional communications (DHPCs) of sufficient quality? A retrospective analysis of DHPCs sent out between 2007 and 2018

  Højer, M-M. G., De Bruin, M. L., Boskovic, A. & Hallgreen, C. E., 2020, I: BMJ Open. 10, 5, 9 s., e036498.

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  10 Citationer (Scopus)

  22 Downloads (Pure)

• Comparison of electronic self-reported prescription medication use during pregnancy with the national prescription register in Denmark

  Laursen, M., Hallgreen, C. E., Dreyer, N., Bourke, A., Mt-Isa, S. & Blackburn, S., 2020, I: Pharmacoepidemiology and Drug Safety. 29, 3, s. 328-336

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  8 Citationer (Scopus)

• How and Why to Involve Patients in Drug Development: Perspectives from the Pharmaceutical Industry, Regulatory Authorities and Patient Organizations

  Hansen, M. B., Nørgaard, L. S. & Hallgreen, C. E., 2020, I: Therapeutic Innovation & Regulatory Science. 54, s. 577-585 9 s.

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  9 Citationer (Scopus)
• 2017

  Differences and similarities in medicine use, perceptions and sharing among adolescents in two different educational settings

  Vestergaard, S. K., Hallgreen, C. E., Ravn, P. & Kaae, S., 2017, I: International Journal of Adolescent Medicine and Health. DOI: https://doi.org/10.1515/ijamh-2017-0097, 9 s., 0097.

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• 2016

  Literature review of visual representation of the results of benefit-risk assessments of medicinal products

  Hallgreen, C. E., Mt-Isa, S., Lieftucht, A., Phillips, L. D., Hughes, D., Talbot, S., Asiimwe, A., Downey, G., Genov, G., Hermann, R., Noel, R., Peters, R., Micaleff, A., Tzoulaki, I., Ashby, D. & PROTECT Benefit-Risk Group, mar. 2016, I: Pharmacoepidemiology and Drug Safety. 25, 3, s. 238-50 13 s.

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  24 Citationer (Scopus)

• Recommendations for benefit-risk assessment methodologies and visual representations

  Hughes, D., Waddingham, E., Mt-Isa, S., Goginsky, A., Chan, E., Downey, G. F., Hallgreen, C. E., Hockley, K. S., Juhaeri, J., Lieftucht, A., Metcalf, M. A., Noel, R. A., Phillips, L. D., Ashby, D., Micaleff, A. & PROTECT Benefit-Risk Group, mar. 2016, I: Pharmacoepidemiology and Drug Safety. 25, 3, s. 251-62 12 s.

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  58 Citationer (Scopus)

• Serious adverse events reported for antiobesity medicines: postmarketing experiences from the EU adverse event reporting system EudraVigilance

  Aagaard, L., Hallgreen, C. E. & Hansen, E. H., nov. 2016, I: International journal of obesity (2005). 40, 11, s. 1742-1747 6 s.

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  16 Citationer (Scopus)
• 2014

  Balancing benefit and risk of medicines: a systematic review and classification of available methodologies

  Mt-Isa, S., Hallgreen, C. E., Wang, N., Callréus, T., Genov, G., Hirsch, I., Hobbiger, S. F., Hockley, K. S., Luciani, D., Phillips, L. D., Quartey, G., Sarac, S. B., Stoeckert, I., Tzoulaki, I., Micaleff, A., Ashby, D. & IMI-PROTECT benefit-risk participants, jul. 2014, I: Pharmacoepidemiology and Drug Safety. 23, 7, s. 667-78 12 s.

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  106 Citationer (Scopus)

• Benefit-risk assessment in a post-market setting: a case study integrating real-life experience into benefit-risk methodology

  Hallgreen, C. E., van den Ham, H. A., Mt-Isa, S., Ashworth, S., Hermann, R., Hobbiger, S., Luciani, D., Micaleff, A., Thomson, A., Wang, N., van Staa, T. P., Downey, G., Hirsch, I., Hockley, K., Juhaeri, J., Metcalf, M., Mwangi, J., Nixon, R., Peters, R., Stoeckert, I. & 4 flere, Waddingham, E., Tzoulaki, I., Ashby, D. & Wise, L., sep. 2014, I: Pharmacoepidemiology and Drug Safety. 23, 9, s. 974-983 10 s.

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  20 Citationer (Scopus)
• 2009

  A model of NEFA dynamics with focus on the postprandial state

  Jelic, K., Hallgreen, C. E. & Colding-Jørgensen, M., sep. 2009, I: Annals of Biomedical Engineering. 37, 9, s. 1897-1909 13 s.

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  31 Citationer (Scopus)
• 2008

  Allometric relationship between changes of visceral fat and total fat mass

  Hallgreen, C. E. & Hall, K. D., maj 2008, I: International Journal of Obesity. 32, 5, s. 845-852 8 s.

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  43 Citationer (Scopus)