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  2. Clindamycin - Wikipedia

    en.wikipedia.org/wiki/Clindamycin

    Clindamycin phosphate topical solution. For the treatment of acne, in the long term, the combined use of topical clindamycin and benzoyl peroxide was similar to salicylic acid plus benzoyl peroxide. [22] [23] Topical clindamycin plus topical benzoyl peroxide is more effective than topical clindamycin alone. [22] [23]

  3. Clindamycin/benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Clindamycin/benzoyl_peroxide

    It is a fixed-dose combination of clindamycin, as the phosphate, an antibiotic; and benzoyl peroxide, an antiseptic. [7] Common side effects include peeling, itching, and dryness of the skin where the gel was applied. [7] Clindamycin/benzoyl peroxide was approved for medical use in the United States in December 2000.

  4. Clindamycin/tretinoin - Wikipedia

    en.wikipedia.org/wiki/Clindamycin/tretinoin

    Clindamycin/tretinoin is a topical gel used in the treatment of acne. The two active ingredients are the antibiotic clindamycin phosphate (1.2%) and tretinoin (0.025%), a retinoid . [ 1 ] The two active ingredients perform different functions, the clindamycin is active against gram-positive bacteria, including streptococci and penicillin ...

  5. Clindamycin/adapalene/benzoyl peroxide - Wikipedia

    en.wikipedia.org/wiki/Clindamycin/adapalene/...

    It contains clindamycin, as the phosphate, a lincosamide antibacterial; adapalene, a synthetic retinoid; and benzoyl peroxide, an oxidizing agent. [2] It is applied to the skin . [ 2 ]

  6. Lincosamides - Wikipedia

    en.wikipedia.org/wiki/Lincosamides

    Of the lincosamides, clindamycin is most commonly used within the clinic due to its higher bioavailability, higher oral absorption and efficacy within the target organism spectrum. [23] Lincosamides are generally the first-choice use antibiotic class in veterinary microbiology, most commonly used to combat skin infections. [7]

  7. Lincomycin - Wikipedia

    en.wikipedia.org/wiki/Lincomycin

    A related compound, clindamycin, is derived from lincomycin by using thionyl chloride to replace the 7-hydroxy group with a chlorine atom with inversion of chirality. [4] It was released for medical use in September 1964. [5]

  8. Mueller–Hinton agar - Wikipedia

    en.wikipedia.org/wiki/Mueller–Hinton_agar

    Mueller Hinton agar is a type of growth medium used in microbiology to culture bacterial isolates and test their susceptibility to antibiotics. This medium was first developed in 1941 by John Howard Mueller and Jane Hinton, who were microbiologists working at Harvard University.

  9. Antimalarial medication - Wikipedia

    en.wikipedia.org/wiki/Antimalarial_medication

    Clindamycin should be given in conjunction with quinine as a 300 mg dose (in adults) four times a day for five days. The only side effects recorded in patients taking clindamycin are nausea, vomiting and abdominal pains and cramps. However these can be alleviated by consuming large quantities of water and food when taking the drug.