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  2. 2-Bromopyridine - Wikipedia

    en.wikipedia.org/wiki/2-Bromopyridine

    2-Bromopyridine reacts with butyllithium to give 2-lithiopyridine, [2] which is a versatile reagent. [3] Pyrithione can be prepared in a two-step synthesis from 2-bromopyridine by oxidation to the N-oxide with a suitable peracid followed by substitution using either sodium dithionite or sodium sulfide with sodium hydroxide to introduce the thiol functional group.

  3. Over-the-counter drug - Wikipedia

    en.wikipedia.org/wiki/Over-the-counter_drug

    Examples of these include some sleep aid tablets such as diphenhydramine, human deworming tablets such as mebendazole, painkillers with small amounts of codeine (up to 12.8 mg per tablet), and pseudoephedrine. Medication available only with a prescription is marked somewhere on the box/container with [POM].

  4. Bromocriptine - Wikipedia

    en.wikipedia.org/wiki/Bromocriptine

    Bromocriptine, originally marketed as Parlodel and subsequently under many brand names, [1] is an ergoline derivative and dopamine agonist that is used in the treatment of pituitary tumors, Parkinson's disease, hyperprolactinaemia, neuroleptic malignant syndrome, and, as an adjunct, type 2 diabetes.

  5. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    2-Phenethyl bromide (C 6 H 5 CH 2 CH 2 Br) is produced via this route from styrene. Hydrogen bromide can also be used to convert alcohols to alkyl bromides. This reaction, that must be done under low temperature conditions, is employed in the industrial synthesis of allyl bromide: HOCH 2 CH=CH 2 + HBr → BrCH 2 CH=CH 2 + H 2 O

  6. Urinary anti-infective agent - Wikipedia

    en.wikipedia.org/wiki/Urinary_anti-infective_agent

    Some drugs need to be used with caution in patients with renal dysfunction. The use of nitrofurantoin is contraindicated in patients with an estimated GFR of less than 30 mL/min/1.73m 2 as drug accumulation can lead to increased side effects and impaired recovery of the urinary tract, increasing the risk of treatment failure. [29]

  7. Idoxuridine - Wikipedia

    en.wikipedia.org/wiki/Idoxuridine

    Idoxuridine is available as either a 0.5% ophthalmic ointment or as a 0.1% ophthalmic solution. [3] The dosage of the ointment is every 4 hours during day and once before bedtime. [ 3 ] The dosage of the solution is 1 drop in the conjunctival sac hourly during the day and every 2 hours during the night until definitive improvement, then 1 drop ...

  8. Red Dye 3 Just Got Banned. These Are the Foods to Avoid If ...

    www.aol.com/red-dye-3-just-got-134800003.html

    The petition filed by over 20 consumer advocacy groups in 2022 that argued for the removal of Red Dye No. 3 from food and dietary supplements cited studies, the FDA's prior use of the Delaney ...

  9. Sonidegib - Wikipedia

    en.wikipedia.org/wiki/Sonidegib

    Sonidegib is administered by mouth.Common side effects include muscle spasms, hair loss, fatigue, abdominal pain, nausea, headache, and weight loss. [1]Sonidegib binds to and inhibits smoothened to inhibit activation of the Hedgehog pathway.