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  2. Linezolid - Wikipedia

    en.wikipedia.org/wiki/Linezolid

    Linezolid is a member of the oxazolidinone class of medications. [10] Linezolid was discovered in the mid-1990s, and was approved for commercial use in 2000. [16] [17] It is on the World Health Organization's List of Essential Medicines. [18] The World Health Organization classifies linezolid as critically important for human medicine. [19]

  3. Quinupristin/dalfopristin - Wikipedia

    en.wikipedia.org/wiki/Quinupristin/dalfopristin

    Quinupristin and dalfopristin are protein synthesis inhibitors in a synergistic manner. While each of the two is only a bacteriostatic agent, the combination shows bactericidal activity.

  4. Pretomanid - Wikipedia

    en.wikipedia.org/wiki/Pretomanid

    Pretomanid was approved for medical use in the United States in August 2019, [4] [7] and in the European Union in July 2020. [2] Pretomanid was developed by TB Alliance. [8] [4] [9] The US Food and Drug Administration (FDA) considers it to be a first-in-class medication. [10] It is on the World Health Organization's List of Essential Medicines ...

  5. Escitalopram (Lexapro): Everything You Need to Know Before ...

    www.aol.com/escitalopram-lexapro-everything-know...

    Linezolid. Over-the-counter treatments for depression such as St. John’s wort. ... To avoid any dangerous interactions, be sure to disclose all of your current medications to your medical provider.

  6. Pristinamycin - Wikipedia

    en.wikipedia.org/wiki/Pristinamycin

    The pristinamycin biosynthetic gene cluster is the largest antibiotic supercluster known so far, with a size of ~210 kb, wherein the PI and PII biosynthetic genes are not clustered individually but are scattered across the complete sequence region. [2] Furthermore, this biosynthetic gene region is interrupted by a cryptic type II PKS gene cluster.

  7. Amikacin - Wikipedia

    en.wikipedia.org/wiki/Amikacin

    Around 16% of amikacin crosses the placenta; while the half-life of amikacin in the mother is 2 hours, it is 3.7 hours in the fetus. [14] A pregnant woman taking amikacin with another aminoglycoside has a possibility of causing congenital deafness in her child. While it is known to cross the placenta, amikacin is only partially secreted in ...

  8. Monoamine oxidase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Monoamine_oxidase_inhibitor

    While safer than general MAOIs, RIMAs still possess significant and potentially serious drug interactions with many common drugs; in particular, they can cause serotonin syndrome or hypertensive crisis when combined with almost any antidepressant or stimulant, common migraine medications, certain herbs, or most cold medicines (including ...

  9. Rasagiline - Wikipedia

    en.wikipedia.org/wiki/Rasagiline

    Rasagiline inhibits platelet MAO-B activity with single doses by 35% one-hour after 1 mg, 55% after 2 mg, 79% after 5 mg, and 99% after 10 mg in healthy young people. [ 1 ] [ 55 ] [ 2 ] [ 54 ] With all dose levels, maximum inhibition is maintained for at least 48 hours after the dose.