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Clindamycin Hydrochloride Powder is mainly used clinically for the treatment of infections caused by Gram-positive cocci and various anaerobic bacteria, for the treatment of joint, bone marrow, respiratory and skin soft tissue infections, as well as tonsillitis, pharyngitis, pneumonia, for acne, gynecological inflammation, endocarditis, abscess chest and other various infections.
Clindamycin Hydrochloride Raw Material is easy to dissolve, has a high distribution coefficient in the body, has few adverse effects, and is not affected by daily diet.Clindamycin Hydrochloride CAS 21462-39-5 is a semi-synthetic antibiotic with a broad antibacterial spectrum. Antimicrobial agents. The antimicrobial spectrum is similar to that of Zithromax.
Clindamycin should be given intravenously for severe infections, especially anaerobic infections, and high dose rapid drip is contraindicated. It should not be combined with ampicillin, phenytoin, barbiturates, aminophylline, calcium gluconate, magnesium sulfate, macrolides such as erythromycin, dactinomycin, methicillin and chloramphenicol, or with sodium sulfadiazine and vitamin C in the same container.
Clindamycin Hydrochloride Raw Material has a synergistic effect with gentamicin and can be used in combination with TMP to improve clinical treatment and reduce adverse drug reactions. It can be successfully used in combination with antibacterial drugs such as amikacin, tobramycin, methicillin, cephalosporins and fluoroquinolones. The most serious adverse reaction is pseudomembranous enteritis, which can occur during treatment or several weeks after the drug is administered, and once it occurs, it can be treated with vancomycin. Other gastrointestinal reactions include nausea, bloating, anorexia, diarrhea, etc. The incidence is 2%-20%.
Uses and functions of Clindamycin Hydrochloride Powder.
Pharmacological Effects of Clindamycin Hydrochloride Powder.
Production method of Clindamycin Hydrochloride Powder
Clindamycin is a derivative of jessamycin, which is a semi-synthetic antibiotic obtained by replacing the hydroxyl group at the 7 position of jessamycin with a chlorine atom.
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