VP Ma’ ruf supervises vaccination dry run in Bekasi regency

Vice President Ma’ ruf Amin checked out a community health center (Puskesmas) in North Cikarang, Bekasi regency, West Java, on Thursday morning to monitor a simulation for the upcoming COVID-19 mass vaccination drive.

Throughout the go to, Ma’ ruf witnessed the treatments for the vaccination program. He was accompanied by Health Minister Terawan Agus Putranto, West Java Guv Ridwan Kamil and Bekasi Regent Eka Supriatmaja.

” The simulation belongs to the total preparation ahead of the [COVID-19] immunization, which has actually been set by the federal government,” stated Ma’ ruf during the check out as priced estimate by antaranews.com

He went on to state that a series of preparations prior to the vaccination consisted of the list of vaccine receivers, phases of injection, vaccine circulation system and vaccine waste management.

Ma’ ruf arrived at the Puskesmas at 8: 50 a.m. and he immediately visited the area for the simulation, along with Bekasi regency Health Company head Sri Enny.

The simulation belongs to the federal government’s efforts to promote the importance of the upcoming vaccination, which is thought to be essential in suppressing the COVID-19 pandemic.

President Joko “Jokowi” Widodo had actually supervised a comparable simulation held at the Puskesmas Tanah Sareal in Bogor, West Java, on Wednesday.

Throughout the Bogor visit, the President said he expected the COVID-19 vaccination to be carried out in late December or early January 2021, depending on the schedule of the vaccines and the ability of the country to organize the immunization effort.

Jokowi ' prepared ' to get first COVID-19 vaccine shot

Nevertheless, the nation might not be able to start the mass vaccination program this year due to the fact that of effectiveness issues.

The Indonesian Food and Drug Monitoring Firm (BPOM) has said it will not license the emergency situation usage of a COVID-19 prospect vaccine in December since of a lack of data on its effectiveness.

However, the agency has used an alternative restricted vaccination program through a “caring usage” provision, where a vaccine might be used in a minimal capability although its effectiveness has actually not been shown.

BPOM head Penny Kusumastuti Lukito told lawmakers on Tuesday that, throughout an assessment of Sinovac Biotech centers in China, her company had actually obtained data from the very first 2 stages of the candidate vaccine’s scientific trials. Data from the last of testing, happening in Indonesia, would be readily available in late November.

The Sinovac candidate vaccine is one of a number of prospective COVID-19 vaccines in final-stage screening internationally. Sinovac has stated it is positive about the safety of the prospective vaccine.

Nevertheless, according to Cent, last information on the prospect vaccine’s effectiveness will show up behind anticipated. This information is required for the vaccine’s approval for emergency situation usage, as agreed in a World Health Company online forum on vaccine assessment on Nov. 6.

The online forum was participated in by world drug regulators, including the United States Fda (FDA) and the European Medicines Firm (EMA).

An interim analysis of the clinical trials would be gotten after 3 months of observation, Cent said. An effectiveness rate of a minimum of 50 percent would be needed for the vaccine’s approval. (nkn)

Editor’s note: This post is part of a public project by the COVID-19 task force to raise individuals’s awareness about the pandemic.

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