It is rapidly absorbed after oral administration, and its bioavailability is 37%. After a single oral dose of 0.5g, the peak time is 2.5 to 2.6 hours, peak plasma concentration (Cmax) is 0.4~0.45mg/L. This product is widely distributed in the body, and concentrations in each tissue are...
However, if it is almost time for your next dose, skip the missed dose and resume your normal dosing schedule. Do not give extra or double doses. Azithromycin Possible Side Effects Azithromycin can cause gastrointestinal side effects such as: Vomiting Diarrhea Inappetence Abdominal pain ...
Arzomicin; Azadose; Azenil; Azimin; Azithral; azithromycinum [INN_la]; Azitromvcin; Aziwok; Aztrin; lpha-D-xylo-hexopyranosyl]oxy]-, (2R,3S,4R,5R,8R,11R,12S,13S,14R)-; MFCD00873574; N-METHYL-11-AZA-10-DEOXO-10-DIHYDROERYTHROMYCIN A; Ribotrex; Setron; Tobil; Ultreon;...
However, single-dose azithromycin and ceftriaxone are suitable for chancroid. Lymphogranuloma venereum, reemergent as a cause of proctitis, is treated with... T Rosen,T Vandergriff,M Harting - 《Dermatologic Clinics》 被引量: 57发表: 2009年 Azithromycin Concentrations in Serum and Bronchial Secre...
Pharmacokinetics, oral bioavailability and tissue distribution of azithromycin in cats Azithromycin is the first of a class of antibiotics classified as azalides. In an initial experiment four cats were given a single dose of azithromycin 5 m... RP Hunter,MJ Lynch,JF Ericson,... - 《Journal of...
were removed surgically at the end of September when he was neutered. The vet did not want to remove the ones on his tongue surgically. He completed a ten day dose of azithromyacin on October 15. The warts appear to be shrinking and turning a beige/brown. When should the warts disappear...
As a result, manufacturers are often limited to using the dry granulation method for formulations containing a low dose of the active ingredient per compressed tablet such that the formulation may accommodate sufficient levels of excipient to make dry granulation practical. In the development of ...
PharmacokineticsIt is rapidly absorbed after oral administration, and its bioavailability is 37%. After a single oral dose of 0.5g, the peak time is 2.5 to 2.6 hours, peak plasma concentration (Cmax) is 0.4~0.45mg/L. This product is widely distributed in the body, and concentrations in each...