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  2. Clindamycin - Wikipedia

    en.wikipedia.org/wiki/Clindamycin

    Clindamycin may prolong the effects of neuromuscular-blocking drugs, such as succinylcholine and vecuronium. [55] [56] [57] Its similarity to the mechanism of action of macrolides and chloramphenicol means they should not be given simultaneously, as this causes antagonism [26] and possible cross-resistance. [medical citation needed]

  3. Macrolide - Wikipedia

    en.wikipedia.org/wiki/Macrolide

    Macrolides belong to the polyketide class of natural products. Some macrolides have antibiotic or antifungal activity and are used as pharmaceutical drugs. Rapamycin is also a macrolide and was originally developed as an antifungal, but has since been used as an immunosuppressant drug and is being investigated as a potential longevity ...

  4. Lincosamides - Wikipedia

    en.wikipedia.org/wiki/Lincosamides

    Clindamycin alone has been shown to be efficacious in the treatment of acne, [24] toxic shock syndrome [25] and malaria, [26] and to decrease the risk of premature births in women with bacterial vaginosis. [27] Lincosamide antibiotics may also be useful in the treatment of methicillin-resistant S. aureus. [28]

  5. Ketolide - Wikipedia

    en.wikipedia.org/wiki/Ketolide

    Ketolides are antibiotics belonging to the macrolide group. Ketolides are derived from erythromycin by substituting the cladinose sugar with a keto-group and attaching a cyclic carbamate group in the lactone ring. [1] These modifications give ketolides much broader spectrum than other macrolides.

  6. Dangerous side effect of popular antibiotic - AOL

    www.aol.com/lifestyle/dangerous-side-effect...

    Bottom line: Most drugs carry a risk, but if you've been prescribed an oral or injected fluoroquinolone and you're concerned about side effects, be sure to talk to your doctor about switching.

  7. Protein synthesis inhibitor - Wikipedia

    en.wikipedia.org/wiki/Protein_synthesis_inhibitor

    Macrolides [15] [16] and clindamycin [15] [16] (both also having other potential mechanisms) cause premature dissociation of the peptidyl-tRNA from the ribosome. Puromycin has a structure similar to that of the tyrosinyl aminoacyl-tRNA. Thus, it binds to the ribosomal A site and participates in peptide bond formation, producing peptidyl-puromycin.

  8. Aminoglycoside - Wikipedia

    en.wikipedia.org/wiki/Aminoglycoside

    The incidence of inner ear toxicity varies from 7 to 90%, depending on the types of antibiotics used, susceptibility of the patient to such antibiotics, and the duration of antibiotic administration. [20] Another serious and disabling side effect of aminoglycoside use is vestibular ototoxicity. [19]

  9. But in 2024, after four months on Zepbound, I was forced to stop taking it. ... I didn’t have any adverse physical side effects after stopping, but the food noise came back immediately.

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