PubMed Biomedical — Article details with structured abstract and MeSH terms
Verified: delivered 1 time
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13 sats · ≈$0.011
Article details with structured abstract and MeSH terms
Example
What agents use this for. Article details with structured abstract and MeSH terms. Category: data/health.
Request
GET https://api.lightningenable.com/l402/proxy/pubmed-biomedical-bc1e/38123456
curl
curl -sS -X GET \ 'https://api.lightningenable.com/l402/proxy/pubmed-biomedical-bc1e/38123456' \ -H 'Accept: application/json' \ # Example only. No L402 token. Sends no sats.
MCP buy
buy({
"sku": "le-de45851f75b1",
"params": {
"pmid": "38123456"
},
"total_cost": "13 sats",
"max_total_sats": 13
})
Example response
Stored from a successful paid delivery. Truncated to a size cap.
{"status":"ok","data":{"pmid":"33301246","title":"Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine.","abstract":"BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the resulting coronavirus disease 2019 (Covid-19) have afflicted tens of millions of people in a worldwide pandemic. Safe and effective vaccines are needed urgently. METHODS: In an ongoing multinational, placebo-controlled, observer-blinded, pivotal efficacy trial, we randomly assigned persons 16 years of age or older in a 1:1 ratio to receive two doses, 21 days apart, of either placebo or the BNT162b2 vaccine candidate (30 μg per dose). BNT162b2 is a lipid nanoparticle-formulated, nucleoside-modified RNA vaccine that encodes a prefusion stabilized, membrane-anchored SARS-CoV-2 full-length spike protein. The primary end points were efficacy of the vaccine against laboratory-confirmed Covid-19 and safety. RESULTS: A total of 43,548 participants underwent randomization, of whom 43,448 received injections: 21,720 with BNT162b2 and 21,728 with placebo. There were 8 cases of Covid-19 with onset at least 7 days after the second dose among participants assigned to receive BNT162b2 and 162 cases among those assigned to placebo; BNT162b2 was 95% effective in preventing Covid-19 (95% credible interval, 90.3 to 97.6). Similar vaccine efficacy (generally 90 to 100%) was observed across subgroups defined by age, sex, race, ethnicity, baseline body-mass index, and the presence of coexisting conditions. Among 10 cases of severe Covid-19 with onset after the first dose, 9 occurred in placebo recipients and 1 in a BNT162b2 recipient. The safety profile of BNT162b2 was characterized by short-term, mild-to-moderate pain at the injection site, fatigue, and headache. The incidence of serious adverse events was low and was similar in the vaccine and placebo groups. CONCLUSIONS: A two-dose regimen of BNT162b2 conferred 95% protection against Covid-19 in persons 16 years of age or older. Safety over a median of 2 months was simila
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