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"fda"

  • Paneer or substitute? Maharashtra govt makes disclosure mandatory for restaurants, eateries

    Food and Drug Administration Maharashtra has mandated restaurants across Maharashtra to disclose whether paneer dishes use real dairy or substitutes. The rule aims to ensure transparency, prevent consumer deception, and standardize labelling across menus and food outlets
  • Methylene Blue: From a fabric dye to biohacking tool, but doctors warn of fatal risks

    Methylene blue, a synthetic dye now touted by influencers for its alleged cognitive and anti-ageing benefits, is being consumed despite lacking clinical proof. Doctors warn it can cause fatal serotonin syndrome when combined with common medications like antidepressants or sleep aids
  • Ixchiq: World’s First Chikungunya Vaccine Approved By FDA | Vaccine For Chikungunya | US News

    This single-dose vaccine is intended for individuals aged 18 and older at a heightened risk of Chikungunya virus exposure, transmitted primarily through infected mosquitoes.
  • AI-powered Google Pixel 8 phones bring new camera tools, 7 yrs of key update

    The new Google Pixel 8 starts at $699.99 for the 128GB storage model. Pixel 8 Pro with in-built temperature sensor starts from $999
  • USFDA issues warning letter to Intas Pharma for Sanand plant

    The letter also makes clear that the company must correct the problem and provides directions and a timeframe for its plans for correction.
  • First oral pill for postpartum depression approved by US FDA

    The label carries a boxed warning indicating that Zurzuvae may impair driving and other hazardous activities.
  • Study reveals potential to repurpose existing cancer drugs for combating aggressive forms of cancer

    This cancer category, making up 15% of all cancers, is especially prevalent in aggressive tumors like osteosarcomas and glioblastomas in the brain.
  • New blood test to predict preeclampsia earlier in pregnant women

    The new test works by detecting sFlt1 and PIGF -- two proteins in the blood that predict poor outcomes from preeclampsia with substantially better accuracy than the current methods.
  • GlaxoSmithKline launches Shingles vaccine in India

    Shingrix is the world’s first non-live, recombinant subunit vaccine to be given intramuscularly in two doses
  • Telangana only region in world with 200-plus FDA approved pharma sites: KT Rama Rao

    The Minister said the State’s capability would be further strengthened with the launch of Hyderabad Pharma City, which will be the world’s largest and sustainable integrated pharma park
  • MIT develops new test to quantify immunity against Covid-19

    Hyderabad: In general, an antibody test (serological test) for Covid-19 is performed in specialized labs, and to get results it takes anywhere from 24 hours to several days. But a new paper test developed by researchers from the Massachusetts Institute of Technology (MIT) has shown that it takes only 10 minutes to find the level of neutralizing antibodies […]
  • FDA bans Juul e-cigarettes from US market

    Washington: The US Food and Drug Administration (FDA) has issued marketing denial orders (MDOs) to JUUL Labs for all of their products currently marketed in the country. The products include the JUUL device and four types of JUULpods: Virginia tobacco flavoured pods at nicotine concentrations of 5.0 per cent and 3.0 per cent and menthol […]
  • Indigenously developed blood test to detect early breast cancer gets USFDA breakthrough status

    Hyderabad: A Nashik-based cancer diagnostic research facility Datar Cancer Genetics has announced that US Food and Drug Administration (FDA) has granted ‘breakthrough designation’ for its blood test to detect early-stage breast cancer. The proprietary diagnostic test, developed by the cancer genetics research facility, can ‘detect Circulating Tumor Cells and Clusters specific to Breast Cancer with very high […]
  • Dr Batra’s launch bio-engineered hair fall treatment

    Combining homeopathy and biological growth factors, this bio-engineered treatment is a non-invasive, natural, Platelet Rich Plasma treatment and has also been approved by the FDA
  • Pfizer, Moderna Covid shots generate lasting immunity

    Even 15 weeks after the first dose, eight of 10 people still had detectable germinal centers containing B cells targeting the virus.
  • Study identifies possible Covid drugs

    The study, published in the journal Cell Reports, screened thousands of existing drugs and drug-like molecules for their ability to inhibit the replication of the Covid-19-causing coronavirus, SARS-CoV-2.
  • US Food and Drug Administration authorises Amazon’s Covid-19 test kit

    Amazon plans to use the real-time RT-PCR Test for detecting SARS-CoV-2 as part of the company's overall preparedness and response programme.
  • US FDA approves emergency use of J&J Covid-19 vaccine

    The authorisation allows the vaccine to be distributed in the US for use in individuals 18 years of age and older, the FDA said on Saturday.
  • People should overcome vaccine hesitancy: FDA official

    “Many people wonder how we’ve done in less than a year what usually takes at least 4-5 years. It is through getting rid of the dead space," said Dr Peter Marks, director of CBER, FDA
  • Philippines approves emergency use of Sinovac’s Covid vaccine

    China's Sinovac Biotech is the third vaccine maker that was given the green light by the FDA, Xinhua reported.
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