Alcohol Consumption Emerges as a Key Risk Factor for Buccal Cancer in India
December 24, 2025
Brand Name :
Kimyrsa, Orbactiv
Synonyms :
oritavancin
Class :
Glycopeptides
Dosage forms & Strengths:
Adult:
Lyophilized powder for injection
400 mg/vial
1200 mg/vial
Safety and efficacy are not seen in pediatrics
Refer to the adult dosing
may decrease the therapeutic effect when combined with heparin
it may enhance the metabolism when combined with aripiprazole lauroxil
oritavancin is a semisynthetic lipoglycopeptide antibiotic used to treat certain bacterial infections. It is classified as a glycopeptide antibiotic and works by inhibiting the synthesis of the bacterial cell wall. oritavancin has a broad spectrum of activity. It is effective against a range of gram-positive bacteria. It includes methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci.
1-10%:
Nausea (9.9%)
Vomiting (4.6%)
Headache (7.1%)
Diarrhea (3.7%)
Dizziness (2.7%)
Tachycardia (2.5%)
Infusion site reactions (1.9%)
Increased ALT (2.8%)
Increased AST (1.8%)
Infusion site reactions (1.9%)
oritavancin should not be used in people hypersensitive to oritavancin or other glycopeptide antibiotics. People with kidney or liver problems should use the drug cautiously.
Pregnancy consideration:
No data is available regarding the use of the drug during pregnancy.
Breastfeeding warnings:
No data is available regarding the secretion of the drug in breast milk.
Pregnancy category:
Pharmacology
Oritavancin is a semisynthetic lipoglycopeptide antibiotic used to treat certain bacterial infections. It is classified as a glycopeptide antibiotic and works by inhibiting the synthesis of the bacterial cell wall. oritavancin has a broad spectrum of activity, and it is effective against a range of gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci.
Pharmacodynamics
oritavancin has a long half-life, which allows it to be given as a single dose and helps to prevent the development of resistance to the antibiotic. It is metabolized by the liver and eliminated in the urine and feces.
Pharmacokinetics
After intravenous administration, oritavancin is rapidly absorbed and reaches peak plasma concentrations within 1-2 hours.
Absorption
The absorption of oritavancin is achieved in 1-2 hours. The peak plasma concentration is 138 mcg/ml. The value of the area under the curve for 0-24 hours is around 1110 mcg×hr/ml.
Distribution
Protein is bound at 85%, and the volume of distribution is 87.6L which is extensively distributed into tissues.
Metabolism
The drug is not metabolized due to weak inhibitors of CYP2C19 and CYP2C9
Elimination and excretion
The drug’s half-life is 2.29 hours, 13.4 hours, and 245 hours for an alpha, beta, and terminal, respectively.
Patient information leaflet
Generic Name: oritavancin
Pronounced: or-ita-van-cin
Why do we use oritavancin?
oritavancin helps treat skin structure infections.