Cite
Personalising drug safety-results from the multi-centre prospective observational study on Adverse Drug Reactions in Emergency Departments (ADRED).
MLA
Just, Katja S., et al. “Personalising Drug Safety-Results from the Multi-Centre Prospective Observational Study on Adverse Drug Reactions in Emergency Departments (ADRED).” European Journal of Clinical Pharmacology, vol. 76, no. 3, Mar. 2020, pp. 439–48. EBSCOhost, https://doi.org/10.1007/s00228-019-02797-9.
APA
Just, K. S., Dormann, H., Böhme, M., Schurig, M., Schneider, K. L., Steffens, M., Dunow, S., Plank-Kiegele, B., Ettrich, K., Seufferlein, T., Gräff, I., Igel, S., Schricker, S., Jaeger, S. U., Schwab, M., & Stingl, J. C. (2020). Personalising drug safety-results from the multi-centre prospective observational study on Adverse Drug Reactions in Emergency Departments (ADRED). European Journal of Clinical Pharmacology, 76(3), 439–448. https://doi.org/10.1007/s00228-019-02797-9
Chicago
Just, Katja S, Harald Dormann, Miriam Böhme, Marlen Schurig, Katharina L Schneider, Michael Steffens, Sandra Dunow, et al. 2020. “Personalising Drug Safety-Results from the Multi-Centre Prospective Observational Study on Adverse Drug Reactions in Emergency Departments (ADRED).” European Journal of Clinical Pharmacology 76 (3): 439–48. doi:10.1007/s00228-019-02797-9.