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  2. File:Promethazine.svg - Wikipedia

    en.wikipedia.org/wiki/File:Promethazine.svg

    The following other wikis use this file: Usage on ar.wikipedia.org بروميثازين; Usage on azb.wikipedia.org پرومتازین; Usage on bn.wikipedia.org

  3. Promethazine - Wikipedia

    en.wikipedia.org/wiki/Promethazine

    Promethazine has a variety of medical uses, including: Sedation [13] In Germany, it is approved for the treatment of agitation and agitation associated with underlying psychiatric disorders with a maximum daily dose of 200 mg. [14] For nausea and vomiting associated with anesthesia or chemotherapy. It is commonly used postoperatively as an ...

  4. List of benzodiazepines - Wikipedia

    en.wikipedia.org/wiki/List_of_benzodiazepines

    0.125, 0.25 0.5: 0.5–2: 2: hypnotic: Drug Name Common Trade Names Year Approved Typical Dosages of Oral Tablets (mg) Approx. Equivalent Oral Dose to 10mg Diazepam (mg) Peak onset of action (hours) Elimination Half-life of Active Metabolite (hours) Primary Therapeutic Use

  5. File:Promethazine synthesis.svg - Wikipedia

    en.wikipedia.org/wiki/File:Promethazine...

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  6. Teva Pharmaceuticals - Wikipedia

    en.wikipedia.org/wiki/Teva_Pharmaceuticals

    [24] [25] In 2008, sales totalled $11.08 billion, $13.9 billion in 2009, and in 2010 total sales rose to $16.1 billion, of which a major portion was in Europe and North America. On December 23, 2008, Teva acquired Barr Pharmaceuticals for $7.5 billion, making Barr and Pliva (which Barr bought earlier) part of Teva.

  7. Chlorpromazine - Wikipedia

    en.wikipedia.org/wiki/Chlorpromazine

    In 1947, it synthesized promethazine, a phenothiazine derivative, which was found to have more pronounced sedative and antihistaminic effects than earlier drugs. [ 59 ] : 77 A year later, the French surgeon Pierre Huguenard used promethazine together with pethidine as part of a cocktail to induce relaxation and indifference in surgical patients.

  8. Brotizolam - Wikipedia

    en.wikipedia.org/wiki/Brotizolam

    Brotizolam [3] (marketed under brand name Lendormin) is a sedative-hypnotic [4] thienotriazolodiazepine [5] drug which is a benzodiazepine analog. [6] It possesses anxiolytic, anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties, and is considered to be similar in effect to other short-acting hypnotic benzodiazepines such as triazolam or midazolam. [7]

  9. Amitriptyline/perphenazine - Wikipedia

    en.wikipedia.org/wiki/Amitriptyline/perphenazine

    25.9: 50: 1848: This receptor is believed to be partly responsible for the metabolic adverse effects of the atypical antipsychotics. σ: 300: 2000: 31.5: All three values are for binding to the guinea pig brain receptors.