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The Safe Use of the COVID -19 Vaccine: Focusing on Allergic Reactions

Kim SR, Lee JHn

As treatment options for the COVID-19 pandemic are limited, the most effective strategy so far is to obtain herd immunity through vaccination; however, the fear of adverse reactions following immunization...
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Paradigm Shift of Pharmacovigilance: 10 Years’ Experience of Active Surveillance by One Regional Pharmacovigilance Center

Lee MG

21st century pharmacovigilance is not merely about the identification of adverse events but also includes systemic preand post-market surveillance and a complete understanding of the risks associated with certain drugs....
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Comparison of Postmarket Surveillance Strategies of Implantable Medical Devices in the United States, European Union, and South Korea

Cho Yo, Lee JYe, Shim DaYo, Park SJ, Rhee HE, Sung HG, Kim HJ, Choi NK, Song HJ, K im JA, Park Sm, Shin JY

The biomedical industry is making rapid progresses like never before, and the number of adverse events caused by implantable medical devices is also increasing. As such, there is an ever-growing...
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Adverse Reactions after the Second Dose of ChAdOx1 COVID-19 Vaccine in H ealthcare Workers

Kim HJ, Kim HH, Park S, Yeom HJ, Jang JY, Park Gy, Kang HR, Kang DY

Objective: The Seoul National University Hospital Drug Safety Monitoring Center performed a prospective survey regarding adverse reactions after the second dose of the adenovirus-vectored vaccine (ChAdOx1 nCoV-19) in healthcare workers....
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Surveillance of Adverse Drug Reactions to First-line Antitu berculosis Drugs Using Common Data Model

Byeon Sj, Park HA, Kang DY, Choi IY, Choi JH

Objective: Tuberculosis (TB) remains a major health problem with high rates of mortality in Korea. Adverse drug reactions (ADRs) to anti-TB drugs negatively affect drug compliance, lead to poor prognosis,...
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Drug Labeling Status of Culprit Drugs Inducing Severe Cutaneous Adverse Reactions

Yeom HJ, Kim HHw, Kim HJ, Park S, Jang JY, Park GY, Kang DY, Kang HR

Objective: The labeling status of culprit drugs of Severe Cutaneous Adverse Reactions (SCAR) was evaluated by comparing the labeling status of the US Food and Drug Administration (FDA) to the...
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