Microplastics and Misinformation: What Science Really Says
November 12, 2025
Brand Name :
Kimyrsa, Orbactiv
Synonyms :
oritavancin
Class :
Glycopeptides
Dosage forms & Strengths:Â
Adult:Â
Lyophilized powder for injectionÂ
400 mg/vialÂ
1200 mg/vialÂ
Safety and efficacy are not seen in pediatricsÂ
Refer to the adult dosingÂ
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.Â
1-10%:Â
Nausea (9.9%)Â Â
Vomiting (4.6%)Â Â
Headache (7.1%)Â
Diarrhea (3.7%)Â
Dizziness (2.7%)Â
Tachycardia (2.5%)Â
Infusion site reactions (1.9%)Â
Increased ALT (2.8%)Â
Increased AST (1.8%)Â
Infusion site reactions (1.9%)Â Â
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.Â
Pregnancy consideration:Â Â
No data is available regarding the use of the drug during pregnancy.Â
Breastfeeding warnings:Â Â
No data is available regarding the secretion of the drug in breast milk.Â
Pregnancy category:Â
PharmacologyÂ
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.Â
PharmacodynamicsÂ
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. Â
PharmacokineticsÂ
After intravenous administration, oritavancin is rapidly absorbed and reaches peak plasma concentrations within 1-2 hours.Â
AbsorptionÂ
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 mcgĂ—hr/ml.Â
DistributionÂ
Protein is bound at 85%, and the volume of distribution is 87.6L which is extensively distributed into tissues.Â
MetabolismÂ
The drug is not metabolized due to weak inhibitors of CYP2C19 and CYP2C9Â
Elimination and excretionÂ
The drug’s half-life is 2.29 hours, 13.4 hours, and 245 hours for an alpha, beta, and terminal, respectively.Â
Patient information leafletÂ
Generic Name: oritavancinÂ
Pronounced: or-ita-van-cinÂ
Why do we use oritavancin?Â
oritavancin helps treat skin structure infections. Â