I think a lot more are positive pa kasi mostly rapid test na lang at home at hindi na nag RT PCR
Sent from my SM-N960F using Tapatalk
I think a lot more are positive pa kasi mostly rapid test na lang at home at hindi na nag RT PCR
Sent from my SM-N960F using Tapatalk
kaya hindi reliable ang PCR numbers
-
even if madami talaga nagkakacovid ngayon, hindi na pareho sa covid ng 2021
it's now an upper respiratory tract infection
people recover after a few days with OTC meds
no need for alarmism
So I tested positive June 5 (June 4 I was still negative) I checked again and I am negative naCovid the second time around was NOTHING compared to delta. Sore throat and cough pero hindi naka affect ng o2 sat and pulse rate. I did not even drink any covid medicine (just regular meds for fever and cough)
Sa US daw pag covid positive Paxlovid agad. My Tita was asking me why I'm not taking it hehe
Anyone got vaccinated with J&J vaccine?
US FDA already planning for the next vaccine specific formulation vs XBB...
And WHO recommending countries to ditch the "newer" bivalent vaccine boosters, wa epek versus XBB variant. Eh halos wala pa nga yung bivalent vaccine dito sa pinas, except yung expiring donation from Lithuania.
J&J’s COVID vaccine is dead in the US; FDA revokes authorization | Ars Technica
The Food and Drug Administration has withdrawn authorization for Johnson & Johnson's COVID-19 vaccine, ending its short-lived but troubled existence amid the pandemic.
In a letter last week, the FDA's top vaccine regulator, Peter Marks, wrote to Janssen Biotech—the Johnson & Johnson-owned, Belgium-based company responsible for the vaccine—saying that the agency was revoking authorization. Marks opened the letter by noting that the withdrawal was at the request of the company.
The complete withdrawal this month comes as the FDA prepares to discuss new formulations of COVID-19 vaccines for this fall. The FDA has long held to the idea of updating COVID shots much like annual flu shots—reassessing vaccine formulas in the late spring/early summer in order to prompt manufacturers to have updated formulas ready for rollout in the fall. The agency's vaccine advisory committee will meet on June 15 to discuss the best formula for this fall.
Already, the World Health Organization's vaccine advisory committee has advised that countries this year should switch to monovalent vaccines that target the XBB lineage, the latest omicron sublineage to dominate transmission. In a statement released May 18, WHO advisers recommended that countries ditch the current bivalent formulas—which target both the ancestral SARS-CoV-2 virus and an omicron subvariant—because continuing to target the ancestral strain doesn't seem to boost protection against current strains. Moreover, keeping the ancestral strain in the shots "reduces the concentration of the new target antigen(s) as compared to monovalent vaccines."
The FDA advisers meeting on June 15 will discuss reformulations that will apply to mRNA vaccines made by Pfizer-BioNTech and Moderna. Novavax, which makes a protein-based vaccine available in the US, is also working on an updated COVID-19 shot against XBB strains.
Last edited by Monseratto; June 13th, 2023 at 01:28 PM.
Virus which kills one person a second likely to be heading to UK, scientists say - Wales Online
lol, MSM back at its game again!
1person per second haha!
... there's something ... weird with that headline...
googling,
there were only 514 suspected cases,
and only 27 reported deaths...
even malaria, had only an annual rate of one death per 55 seconds... (annual fatality numbers, reported in number of deaths per unit time).
i pray for explanation.
heh heh.