Sars-Cov-2 Nvx-Cov2373 Vaccine, Recomb (Cvx 313) Dosage
Medically reviewed by Drugs.com. Last updated on Sep 17, 2024.
Applies to the following strengths: preservative-free 5 mcg/0.5 mL
Usual Adult Dose for:
Usual Pediatric Dose for:
Additional dosage information:
Usual Adult Dose for COVID-19
FOR INVESTIGATIONAL USE ONLY
No prior history of vaccination: 0.5 mL IM as a series of 2 doses, administered 3 weeks apart
Previously vaccinated with 1 dose of any Novavax vaccine: 0.5 mL IM ONCE to complete the 2-dose series, administered at least 3 weeks after the last dose of Novavax
Previously vaccinated with any COVID-19 vaccine other than Novavax: 0.5 mL IM ONCE, administered at least 2 months after the last dose of COVID-19 vaccine
Comments:
- This drug is not approved by the US FDA to prevent COVID-19. The US FDA has issued an Emergency Use Authorization (EUA) for the use of this drug to prevent COVID-19.
- An additional dose administered at least 2 months following the last dose of this vaccine may be considered for patients who are severely immunocompromised (based on the healthcare provider's discretion).
- No data are available regarding the use of this vaccine to complete a COVID-19 vaccine series initiated with another vaccine.
Use: For active immunization to prevent COVID-19 due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
Usual Pediatric Dose for COVID-19
For investigational use only
12 years and older:
- No prior history of vaccination: 0.5 mL IM as a series of 2 doses, administered 3 weeks apart
- Previously vaccinated with 1 dose of any Novavax vaccine: 0.5 mL IM ONCE to complete the 2-dose series, administered at least 3 weeks after the last dose of Novavax
- Previously vaccinated with any COVID-19 vaccine other than Novavax: 0.5 mL IM ONCE, administered at least 2 months after the last dose of COVID-19 vaccine
Comments:
- This drug is not approved by the US FDA to prevent COVID-19. The US FDA has issued an EUA for the use of this drug to prevent COVID-19.
- An additional dose administered at least 2 months following the last dose of this vaccine may be considered for patients who are severely immunocompromised (based on the healthcare provider's discretion).
- No data are available regarding the use of this vaccine to complete a COVID-19 vaccine series initiated with another vaccine.
Use: For the emergency use for the active immunization to prevent SARS-CoV-2
Renal Dose Adjustments
Data not available
Liver Dose Adjustments
Data not available
Precautions
CONTRAINDICATIONS:
- Patients with a known history of severe allergic reaction to the active component or any of the ingredients.
- Patients with a severe allergic reaction (e.g., anaphylaxis) following administration of a COVID-19 vaccine
Safety and efficacy have not been established in patients younger than 12 years.
Dialysis
Data not available
Other Comments
Administration advice:
- For IM administration only. Do not inject IV, intradermally, or subcutaneously.
Storage requirements:
- During storage, minimize exposure to room light and avoid exposure to direct sunlight and ultraviolet light.
- Store refrigerated between 2C and 8C (36F and 46F).
- Do not freeze.
- Consult the manufacturer product information and/or the Fact Sheet for Health Care Providers.
Reconstitution/preparation techniques:
- Prefilled syringes should not be diluted prior to use.
- The manufacturer product information should be consulted.
General:
- This information pertains only to the vaccine product supplied in a vial with a green label stating "Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula)."
- Prefilled syringes contain a single, 0.5 mL dose of vaccine.
- This vaccine does not contain preservatives.
Patient advice:
- To report suspected adverse reactions, contact the Vaccine Adverse Event Reporting System (VAERS): https://vaers.hhs.gov
More about sars-cov-2 nvx-cov2373 vaccine, recomb (cvx 313)
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.