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Why testing children has become a focus in Oregon

An update on where Oregon's largest school district stands with its testing program and a doctor's take on why COVID testing kids has become such a focus this year ....

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4 Hot Penny Stocks to Watch With High Volume in August

4 Hot Penny Stocks to Watch With High Volume in August
dailyherald.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from dailyherald.com Daily Mail and Mail on Sunday newspapers.

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Stewardship / Resistance Scan for Jul 27, 2021

Study: Use of restricted antibiotics rose after hospital ASP discontinued
The discontinuation of an antimicrobial stewardship program (ASP) at a South Korean hospital led to a rapid return of antibiotic use patterns observed before the ASP was implemented, researchers reported yesterday in
Clinical Microbiology and Infection.
The interrupted time-series analysis looked at antibiotic use at the 859-bed hospital from September 2015 through August 2019. The hospital ASP, which focused on restricting the use of certain antibiotics, was implemented in September 2016 and discontinued in March 2018 after an infectious disease (ID) specialist resigned. Infection control measures at the hospital remained largely the same throughout the study period. ....

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Trending Reddit Penny Stocks to Buy Now? Take a Look At These 7
dailyherald.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from dailyherald.com Daily Mail and Mail on Sunday newspapers.

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Iterum Therapeutics Provides Regulatory Update

Nachrichtenquelle: globenewswire
| 02.07.2021, 00:30 |
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DUBLIN, Ireland and CHICAGO, July 01, 2021 (GLOBE NEWSWIRE) Iterum Therapeutics plc (Nasdaq: ITRM) (the “Company”), a clinical-stage pharmaceutical company focused on developing next generation
oral and IV antibiotics to treat infections caused by multi-drug resistant pathogens in both community and hospital settings, today announced that the Company received a letter from the U.S. Food
and Drug Administration (“FDA”) stating that, as part of their ongoing review of the Company’s New Drug Application (“NDA”) for sulopenem etzadroxil/probenecid, the agency has identified
deficiencies that preclude the continuation of the discussion of labeling and post marketing requirements/commitments at this time. No details with respect to deficiencies w ....

Corey Fishman , Executive Officer , கோரி மீன் , நிர்வாகி அதிகாரி ,