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241por Frank, Mayu O., Blachere, Nathalie E., Parveen, Salina, Hacisuleyman, Ezgi, Fak, John, Luna, Joseph M., Michailidis, Eleftherios, Wright, Samara, Stark, Pamela, Campbell, Ann, Foo, Ashley, Sakmar, Thomas P., Huffman, Virginia, Bergh, Marissa, Goldfarb, Audrey, Mansisidor, Andres, Patriotis, Agata L., Palmquist, Karl H., Poulton, Nicolas, Leicher, Rachel, Vargas, César D. M., Duba, Irene, Hurley, Arlene, Colagreco, Joseph, Pagane, Nicole, Orange, Dana E., Mora, Kevin, Rakeman, Jennifer L., Fowler, Randal C., Fernandes, Helen, Lamendola-Essel, Michelle F., Didkovsky, Nicholas, Silvera, Leopolda, Masci, Joseph, Allen, Machelle, Rice, Charles M., Darnell, Robert B.“…Direct comparison of results from 162 individuals tested by FDA EUA oropharyngeal (OP) or NP swabs with co-collected saliva samples identified four otherwise unidentified positive cases in DRUL buffer. …”
Publicado 2021
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242por Schuler, Charles F., Gherasim, Carmen, O’Shea, Kelly, Manthei, David M., Chen, Jesse, Zettel, Cristyn, Troost, Jonathan P., Kennedy, Andrew A., Tai, Andrew W., Giacherio, Donald A., Valdez, Riccardo, Baldwin, James L., Baker, James R.“…Adults with and without COVID-19, verified by FDA EUA-approved SARS-CoV-2 RT-PCR assays, were screened for spike and nucleocapsid antibody responses using FDA EUA-approved immunoassays and for pseudoviral neutralization activity. …”
Publicado 2021
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243por Song, Tae, Hayanga, Jeremiah, Durham, Lucian, Garrison, Lawrence, McCarthy, Paul, Barksdale, Andy, Smith, Deane, Bartlett, Robert, Jaros, Mark, Nelson, Peter, Molnar, Zsolt, Deliargyris, Efthymios, Moazami, Nader“…Introduction: CytoSorb extracorporeal blood purification therapy received FDA Emergency Use Authorization (EUA) to suppress hyperinflammation in critically ill COVID-19 patients. …”
Publicado 2021
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244por Cooper, Megan H, Christensen, Paul A, Salazar, Eric, Perez, Katherine K, Graviss, Edward A, Nguyen, Duc, Musser, James M, Huang, Howard J, Liebl, Michael G“…The objective of this study was to report the outcomes of high-risk, SARS-CoV-2-positive patients infused with 1 of the 3 mAb therapies available through Food and Drug Administration Emergency Use Authorization (EUA). METHODS: A total of 4328 SARS-CoV-2-positive patients who satisfied EUA criteria for eligibility for receiving mAb therapy were infused with bamlanivimab or the combination therapies bamlanivimab-etesevimab or casirivimab-imdevimab from November 22, 2020, to May 31, 2021, at 6 infusion clinics and multiple emergency departments within the 8 Houston Methodist Hospitals in Houston, Texas. …”
Publicado 2021
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245por Hubbard, Michael J, Polega, James, Haggerty, Diana K, Andersen, Nicholas A, Simeunovic, Gordana“…The Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for MAB within 10 days from the symptom onset. …”
Publicado 2022
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246por de Canecaude, Claire, Montastruc, François, Bergeron, Sandrine, Sanchez-Pena, Paola, Grandvuillemin, Aurélie“…In March 2021, this drug was granted emergency use authorisation (EUA) in France for early treatment of COVID-19 in patients at increased risk of progression to severe COVID-19. …”
Publicado 2023
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247“…BACKGROUND: Multidisciplinary care involving surgical drainage via examinations under anesthesia (EUA) and anti-tumor necrosis factor (TNF) therapy is recommended for perianal Crohn’s disease (PCD). …”
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248“…Pfizer’s Paxlovid has recently been approved for the emergency use authorization (EUA) from the US Food and Drug Administration (FDA) for the treatment of mild-to-moderate COVID-19. …”
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249por Casey, Bradley, Vernick, Robert C, Bahekar, Amol, Patel, Divyang, Ncogo Alene, Inmaculada“…An Emergency Use Authorization (EUA) was issued by the FDA on December 22, 2021 for the investigational antiviral drug nirmatrelvir copackaged with the HIV-1 protease inhibitor ritonavir (Paxlovid - Pfizer) for outpatient treatment of mild to moderate COVID-19 in children 12 years and old that are high risk of severe disease. …”
Publicado 2023
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250Publicado 2023“…The American Urological Association (AUA), European Association of Urology (EUA) and International Urological Society (SIU) annual meetings were held in 2022. …”
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251“…Safety monitoring is of paramount importance for vaccines authorized for emergent use (EUA) by the US Food and Drug Administration (FDA) against SARS-CoV-2. …”
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252“…Molecular assays and serological tests have been approved under EUA (emergency use authorization) by the FDA (food and drug administration), given these unprecedented times. …”
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253por Smith, Katherine, Hegazy, Karim, Cai, Miranda R., McKnight, Irene, Rousculp, Matthew D., Alves, Katia“…BACKGROUND: NVX-CoV2373 (Nuvaxovid™ or the Novavax COVID-19 Vaccine, Adjuvanted), the first protein-based COVID-19 vaccine, received emergency use authorization (EUA) as a primary series/booster and is available globally. …”
Publicado 2023
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254por Degli-Angeli, Emily, Dragavon, Joan, Huang, Meei-Li, Lucic, Danijela, Cloherty, Gavin, Jerome, Keith R., Greninger, Alexander L., Coombs, Robert W.“…Abbott Molecular developed and received emergency use authorization (EUA) to deploy the new RealTime SARS-CoV-2 assay, run on the automated m2000sp/rt system. …”
Publicado 2020
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255por Kwong, Cheryl H.T., Mu, Jingfang, Li, Shengke, Fang, Yaohui, Liu, Qianyun, Zhang, Xiangjun, Kam, Hiotong, Lee, Simon M.Y., Chen, Yu, Deng, Fei, Zhou, Xi, Wang, Ruibing“…Chloroquine (CQ), an antimalarial drug, was found to exhibit promising antiviral activity in vitro and in vivo at a high dosage, thus CQ was approved by the FDA for the emergency use authorization (EUA) in the fight against COVID-19 in the US, but later was revoked the EUA status due to the severe clinical toxicity. …”
Publicado 2021
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256por Munoz, Flor M., Beigi, Richard H., Posavad, Christine M., Richardson, Barbra A., Chu, Helen Y., Bok, Karin, Campbell, James, Cardemil, Cristina, DeFranco, Emily, Frenck, Robert W., Makhene, Mamodikoe, Piper, Jeanna M., Sheffield, Jeanne, Miller, Ashley, Neuzil, Kathleen M.“…Approximately 200 pregnant women and 65 postpartum women will be enrolled per EUA or licensed COVID-19 vaccine formulation in the U.S. …”
Publicado 2022
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257“…However, becuase the EUA had limited indications for inpatients, data on their use in hospitalized patients are limited. …”
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258por Gdoura, Mariem, Halouani, Habib, Sahli, Donia, Mrad, Mehdi, Chamsa, Wafa, Mabrouk, Manel, Hogga, Nahed, Ben-Salem, Kamel, Triki, Henda“…Conclusion: Although using an FDA-EUA approved serology test, each laboratory should carry out its own evaluation. …”
Publicado 2022
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259por Amanam, Idoroenyi, Yao, Janny M., Puing, Alfredo, Tsai, Ni-Chun, Samuels, Diana, Ngo, Dat, Ho, Stephanie, Ali, Haris, Aribi, Ahmed, Arslan, Shukaib, Artz, Andrew S., Htut, Myo, Koller, Paul, Salhotra, Amandeep, Sandhu, Karamjeet S., Nikolaenko, Liana, Pawlowska, Anna B, Shouse, Geoffrey, Stein, Anthony S., Marcucci, Guido, Forman, Stephen J, Nakamura, Ryotaro, Dadwal, Sanjeet S, Al Malki, Monzr M.“…Food and Drug Administration (FDA) issued emergency use authorization (EUA) for monoclonal antibody (mAb) therapy in patients with mild to moderate COVID-19 who are at high risk for disease progression. …”
Publicado 2021
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260por Mohamed, Sarah, Reda Mostafa, Mostafa, Magdi Eid, Mohamed, AbdelQadir, Yossef Hassan, Abdelghafar, Yomna Ali, Swed, Sarya, Jahshan, Bishara, El‐Radi, Waddah Abd“…The Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for ritonavir‐nirmatrelvir on December 22, 2021, to treat COVID‐19. …”
Publicado 2023
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