dc.contributor.author |
Petousis-Harris, Helen |
|
dc.coverage.spatial |
New Zealand |
|
dc.date.accessioned |
2023-03-08T20:58:29Z |
|
dc.date.available |
2023-03-08T20:58:29Z |
|
dc.date.issued |
2020-12 |
|
dc.identifier.citation |
(2020). Drug Safety, 43(12), 1205-1210. |
|
dc.identifier.issn |
0114-5916 |
|
dc.identifier.uri |
https://hdl.handle.net/2292/63232 |
|
dc.description.abstract |
Vaccines against COVID-19 are being developed at speeds not previously achieved. With this unprecedented effort comes challenges for post-marketing safety monitoring and challenges for vaccine safety communication. To deploy these new vaccines fast across diverse populations, it is vital that robust pharmacovigilance and active surveillance systems are in place. Not all countries have the capability or resources to undertake adequate surveillance and will rely on data from those who can. The tools exist to assess COVID-19 vaccines as they are deployed such as surveillance systems, administrative data and case definitions for adverse events of special interest. However, stitching these all together and using them effectively requires investment and collaboration. This paper provides a high-level overview of some of the facets of modern vaccine safety assessment and how they are, or can be, applied to COVID-19 vaccines. |
|
dc.format.medium |
Print-Electronic |
|
dc.language |
eng |
|
dc.publisher |
Springer Nature |
|
dc.relation.ispartofseries |
Drug safety |
|
dc.rights |
Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. |
|
dc.rights.uri |
https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm |
|
dc.subject |
Humans |
|
dc.subject |
Drug Approval |
|
dc.subject |
Product Surveillance, Postmarketing |
|
dc.subject |
Pharmacoepidemiology |
|
dc.subject |
Clinical Trials, Phase IV as Topic |
|
dc.subject |
Pharmacovigilance |
|
dc.subject |
Drug Development |
|
dc.subject |
COVID-19 |
|
dc.subject |
SARS-CoV-2 |
|
dc.subject |
COVID-19 Vaccines |
|
dc.subject |
Vaccine Related |
|
dc.subject |
Prevention |
|
dc.subject |
Patient Safety |
|
dc.subject |
Immunization |
|
dc.subject |
3 Prevention of disease and conditions, and promotion of well-being |
|
dc.subject |
3.4 Vaccines |
|
dc.subject |
3 Good Health and Well Being |
|
dc.subject |
Science & Technology |
|
dc.subject |
Life Sciences & Biomedicine |
|
dc.subject |
Public, Environmental & Occupational Health |
|
dc.subject |
Pharmacology & Pharmacy |
|
dc.subject |
Toxicology |
|
dc.subject |
COLLABORATION STANDARDIZED TEMPLATE |
|
dc.subject |
BENEFIT-RISK ASSESSMENT |
|
dc.subject |
BRIGHTON COLLABORATION |
|
dc.subject |
KEY INFORMATION |
|
dc.subject |
COLLECTION |
|
dc.subject |
EPIDEMIC |
|
dc.subject |
DISEASE |
|
dc.subject |
1115 Pharmacology and Pharmaceutical Sciences |
|
dc.title |
Assessing the Safety of COVID-19 Vaccines: A Primer. |
|
dc.type |
Journal Article |
|
dc.identifier.doi |
10.1007/s40264-020-01002-6 |
|
pubs.issue |
12 |
|
pubs.begin-page |
1205 |
|
pubs.volume |
43 |
|
dc.date.updated |
2023-02-08T08:25:48Z |
|
dc.rights.holder |
Copyright: The authors |
en |
dc.identifier.pmid |
32997318 (pubmed) |
|
pubs.author-url |
https://www.ncbi.nlm.nih.gov/pubmed/32997318 |
|
pubs.end-page |
1210 |
|
pubs.publication-status |
Published |
|
dc.rights.accessrights |
http://purl.org/eprint/accessRights/RetrictedAccess |
en |
pubs.subtype |
research-article |
|
pubs.subtype |
Journal Article |
|
pubs.elements-id |
817688 |
|
pubs.org-id |
Medical and Health Sciences |
|
pubs.org-id |
Population Health |
|
pubs.org-id |
Gen.Practice& Primary Hlthcare |
|
dc.identifier.eissn |
1179-1942 |
|
dc.identifier.pii |
10.1007/s40264-020-01002-6 |
|
pubs.record-created-at-source-date |
2023-02-08 |
|
pubs.online-publication-date |
2020-09-30 |
|