dc.contributor.author |
Ethiopian Food and Drug Authority |
|
dc.date.accessioned |
2024-01-01T05:56:44Z |
|
dc.date.available |
2024-01-01T05:56:44Z |
|
dc.date.issued |
2022 |
|
dc.identifier.uri |
http://repository.iphce.org/xmlui/handle/123456789/2680 |
|
dc.description.abstract |
Adverse Events Following Immunizations (AEFIs) are reported to Ethiopian Food and Drug
Authority (EFDA) by health care providers and vaccine recipients. EFDA investigates and
assesses all AEFI reports and conducts causality analysis where necessary and take appropriate
actions accordingly |
en_US |
dc.language.iso |
English |
en_US |
dc.subject |
Infectious diseases/COVID-19 |
en_US |
dc.title |
Pfizer COVID-19 vaccine safety monitoring and surveillance in Ethiopia |
en_US |
dc.title.alternative |
Adverse Events Following Immunizations (AEFIs) Reports of Pfizer-BioNTech Covid-19 Vaccine in Ethiopia for two round |
en_US |
dc.type |
Report |
en_US |