For the treatment of mild to moderate COVID-19 in adult patients
700 mg bamlanivimab and 1,400 mg etesevimab administered together as a single intravenous infusion
Bamlanivimab and etesevimab are supplied in individual single-dose vials
Each dose required 1 bamlanivimab vial and 2 etesevimab vials
Prior to dilution, the product must be stored under refrigeration at 2 to 8 degrees C (36 to 46 degrees F)
Dilute dose in a 50 mL, 100 mL, 150 mL, or 250 mL 0.9% Sodium Chloride Injection prefilled infusion bag
Administer together as a single intravenous infusion as soon as possible after positive test for SARS-CoV-2
Minimum infusion time depends on size of infusion bag used as follows:
50 mL bag: Infuse over at least 21 minutes
100 mL bag: Infuse over at least 31 minutes
150 mL bag: Infuse over at least 41 minutes
250 mL bag: Infuse over at least 70 minutes if patient weighs less than 50 kg and over at least 60 minutes if patient weighs 50 kg or more
Infusion-related reactions have been observed and may be severe or life-threatening
Signs include: fever, chills, nausea, headache, bronchospasm, dyspnea, reduced oxygen saturation, fatigue, arrhythmia exacerbation (e.g., atrial fibrillation, sinus tachycardia, bradycardia), chest pain or discomfort, weakness, altered mental status, hypotension, hypertension, angioedema, throat irritation, rash, urticaria, pruritus, myalgia, dizziness, and diaphoresis
Consider slowing/stopping the infusion and administering supportive care
Serious hypersensitivity reactions, including anaphylaxis, have been observed
If a clinically significant reaction develops, immediately discontinue treatment and administer supportive care
Pregnancy:
Only use during pregnancy if potential benefits outweigh potential risk
No adequate data regarding treatment of pregnant women
Infusion-related reactions: dizziness, nausea, pruritus
Hypersensitivity reactions: anaphylaxis
COVID-19 vaccines:
Defer COVID-19 vaccination for at least 90 days as a precaution to avoid interference with vaccine-induced immune responses
Conversely, use/timing of bamlanivimab; etesevimab should not be affected by prior vaccinations in patients who develop COVID-19 after receiving the vaccine
Timesnownews.com. DCGI gives emergency use approval to Eli Lilly’s antibody drug to treat COVID-19 patients. Retrieved June 7, 2021. Available on the World Wide Web at: https://www.timesnownews.com/india/article/eli-lilly-gets-dcgi-emergency-use-approval-for-its-monoclonal-antibody-drugs-for-treatment-of-covid-patients/764729
Reuters. Eli Lilly gets Indian emergency use nod for COVID-19 antibody drug combination. Retrieved June 7, 2021. Available on the World Wide Web at: https://www.reuters.com/world/india/eli-lilly-gets-indian-emergency-use-nod-antibody-drug-combination-2021-06-01/
Eli Lilly. Emergency Use Authorization (EUA) for the treatment of COVID-19. Retrieved June 7, 2021. Available on the World Wide Web at: https://www.covid19.lilly.com/bam-ete/hcp
Food and Drug Administration (FDA). Fact sheet for health care providers: emergency use authorization (EUA) of bamlanivimab and etesevimab. Retrieved May 19, 2021. Available on the World Wide Web at: https://www.fda.gov/media/145802/download
COVID-19 Treatment Guidelines Panel. Coronavirus Diseases 2019 (COVID-19) Treatment Guidelines. National Institutes of Health. Accessed April 21, 2021. Available on the World Wide Web at: https://covid19treatmentguidelines.nih.gov/
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