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  2. Ruxolitinib - Wikipedia

    en.wikipedia.org/wiki/Ruxolitinib

    Ruxolitinib (sold under the brand names Jakafi and Jakavi among others, and as Opzelura in cream form) is a medication used for the treatment of intermediate or high-risk myelofibrosis, [6] a type of myeloproliferative neoplasm that affects the bone marrow; [11] [12] polycythemia vera, when there has been an inadequate response to or intolerance of hydroxyurea; [6] [13] and steroid-refractory ...

  3. Deuruxolitinib - Wikipedia

    en.wikipedia.org/wiki/Deuruxolitinib

    Deuruxolitinib, sold under the brand name Leqselvi, is a medication used for the treatment of alopecia areata. [1] It is a Janus kinase inhibitor selective for JAK1 and JAK2. [2]

  4. Baricitinib - Wikipedia

    en.wikipedia.org/wiki/Baricitinib

    Then in May 2022, the FDA approved use of baricitinib for the treatment of adults hospitalized with COVID-19 who require supplemental oxygen, non-invasive or invasive mechanical ventilation, or extracorporeal membrane oxygenation with a recommended dose of 4 mg once daily for 14 days or until hospital discharge, whichever happens first.

  5. Nutritionists react to the red food dye ban: 'Took far too long'

    www.aol.com/nutritionists-react-red-food-dye...

    The FDA has banned red dye No. 3, as the synthetic additive is known to cause cancer. ... 800-290-4726 more ways to reach us. Sign in. Mail. 24/7 Help. For premium support please call: 800-290 ...

  6. REACH authorisation procedure - Wikipedia

    en.wikipedia.org/wiki/REACh_authorisation_procedure

    The review period is the duration for which the EU Commission authorises the use of a substance after the Sunset date. Following durations are considered for the review periods: < 7 years : in case the Analysis of Alternatives report is insufficient and/or doubts remain on the impacts of the granting of an authorisation or, alternatively, when ...

  7. Selumetinib - Wikipedia

    en.wikipedia.org/wiki/Selumetinib

    The children received selumetinib 25 mg/m 2 orally twice a day until disease progression or until they experienced unacceptable adverse reactions. [ 14 ] [ 22 ] The clinical trial measured the overall response rate (ORR), defined as the percentage of subjects with a complete response and those who experienced more than a 20% reduction in PN ...

  8. Acceptance (novel) - Wikipedia

    en.wikipedia.org/wiki/Acceptance_(novel)

    Reviews for Acceptance were for the most part favorable. NPR said that the book "is at different times the best haunted lighthouse story ever written, a deeply unsettling tale of first contact, a book about death, a book about obsession and loss, a book about the horrifying experience of confronting an intelligence far greater and far stranger ...

  9. FYI Reviewer - highline.huffingtonpost.com

    highline.huffingtonpost.com/miracleindustry/...

    The 6.6% annual growth allows ro reach the 298 min US$ Risperdal sales in 2000. Here as well, not much room is left for new SDAs. Market growth in Europe as well, however, can be expected to be around 10% (1994-2000). Even with a modest 5-6% annual growth, the Risperdal forecast of 106 mln US$ in 2000 only represents 42% of the value