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  2. Doxycycline - Wikipedia

    en.wikipedia.org/wiki/Doxycycline

    Doxycycline, doxycycline monohydrate and doxycycline hyclate are yellow, crystalline powders with a bitter taste. The latter smells faintly of ethanol , a 1% aqueous solution has a pH of 2–3, and the specific rotation is [ α ] D 25 {\displaystyle [\alpha ]_{D}^{25}} −110° cm 3 /dm·g in 0.01 N methanolic hydrochloric acid .

  3. Tetracycline antibiotics - Wikipedia

    en.wikipedia.org/wiki/Tetracycline_antibiotics

    Tetracyclines are generally used in the treatment of infections of the urinary tract, respiratory tract, and the intestines and are also used in the treatment of chlamydia, especially in patients allergic to β-lactams and macrolides; however, their use for these indications is less popular than it once was due to widespread development of resistance in the causative organisms.

  4. Chlamydia trachomatis - Wikipedia

    en.wikipedia.org/wiki/Chlamydia_trachomatis

    Treatment with generic doxycycline 100 mg twice a day for 7 days has equal success with expensive delayed-release doxycycline 200 mg once a day for 7 days. [12] Erythromycin is less preferred as it may cause gastrointestinal side effects, which can lead to non-adherence.

  5. Hyclate - Wikipedia

    en.wikipedia.org/wiki/Hyclate

    A hyclate (Latin: hyclas) is a pharmaceutical term for hydrochloride hemiethanolate hemihydrate [1] [2] (·HCl· ⁠ 1 / 2 ⁠ EtOH· ⁠ 1 / 2 ⁠ H 2 O), e.g ...

  6. Chlamydophila - Wikipedia

    en.wikipedia.org/wiki/Chlamydophila

    Chlamydophila was recognized by a number of scientists in 1999, [3] with six species in Chlamydophila and three in the original genus, Chlamydia. This was immediately seen as controversial. [4] In 2015 the Chlamydophila species were reclassified as Chlamydia. [4] The history of the classification and reclassification is as follows.

  7. Metacycline - Wikipedia

    en.wikipedia.org/wiki/Metacycline

    It is used as a precursor in the industrial synthesis of doxycycline hyclate. [citation needed] It has been found to act as an agonist of the human pregnane X receptor ligand-binding domain and to induce CYP3A4 expression in vitro. [1]