Parenteral Manual

Sotrovimab

Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Alternate Name(s): 
Xevudy
Classification: 
Anti-SARS-CoV-2 spike protein monoclonal antibody
Original Date: 
January 2022
Indications: 
  • Treatment of mild to moderate Covid-19 in patients ≥12 years weighing ≥40 kg who are at high risk fop regressing to hospitalization and/or death
Reconstitution and Stability: 
  • Available as a 500mg/8mL solution
  • Store undiluted vials in refrigerator and protect from light
  • Allow vial to equilibrate to room temperature for 15 minutes prior to use
  • Gently swirl the vial several times before use without creating air bubbles. Do not shake or vigorously agitate the vial.
  • From a 100 mL bag of 0.9% NaCl, remove 18 mL(8mL + 10mL overfill) for a final volume of 92 mL
  • Withdraw 8 mL from the vial of sotrovimab.
  • Inject the 8 mL of sotrovimab into the infusion bag
  • Prior to the infusion, gently rock the infusion bag back and forth 3 to 5 times. Do not invert the infusion bag. Avoid forming air bubbles.
  • Vial stability once diluted: 6 hours room temperature OR 24 hours refrigerated
Compatibility: 
  • Solutions Compatible: 0.9% Sodium Chloride, Dextrose 5%
  • Additives/Above Cassette Compatible: No information
  • Y-site Compatible: No information

Administration: 

(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)

SC NO
IM NO
IV Direct NO
IV Intermittent Infusion

YES

Infusion Time: 60 minutes

IV Continuous Infusion NO

 

Dosage: 

(For neonatal dosages, refer to Neonatal IV Drug Manual.)

  • Patients ≥12 years and weighing ≥40 kg: 500mg IV dose once  
Potential hazards of parenteral administration: 
  • Hypersensitivity, including anaphylaxis, reactions
  • Infusion related reactions
Notes: 
  • Contraindicated in patients with hypersensitivity to sotrovimab or any non-medicinal ingredients in the formulation
  • Not authorized for treatment of patients younger than 12 years old or those weighing less than 40 kg
  • Sotrovimab may diminish the effects of the COVID-19 Vaccine.  If patient is due a vaccine, wait at least 90 days after receiving sotrovimab or other monoclonal antibodies used for the treatment of COVID-19.
References: 
  • Sotrovimab Health Canada drug product monograph

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