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Bamlanivimab Emergency Use Authorization Order Patient Name: Date of Birth: Address: Height (in.): Phone#: Weight (Kg): Ordering Provider: Phone: Address: Patient has a confirmed positive test and
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Prepare the casirivimab and imdevimab emergency by gently swirling the vial. Do not shake.
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Administer the casirivimab and imdevimab emergency through a slow intravenous infusion over a specified period of time.
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Monitor the patient for any adverse reactions during and after the infusion.
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Dispose of all used materials in a proper biohazard waste container.
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Keep track of the administration and report any side effects to healthcare professionals.
Who needs casirivimab and imdevimab emergency?
01
Casirivimab and imdevimab emergency is intended for individuals aged 12 years and above, weighing at least 40 kg.
02
It is recommended for patients who have tested positive for COVID-19 and are at high risk of developing severe symptoms or requiring hospitalization.
03
Specific eligibility criteria may be determined by healthcare professionals.
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What is casirivimab and imdevimab emergency?
Casirivimab and imdevimab are monoclonal antibody treatments authorized for emergency use to prevent and treat COVID-19 in certain patients at high risk of severe disease.
Who is required to file casirivimab and imdevimab emergency?
Healthcare providers who administer casirivimab and imdevimab treatments are required to file emergency use documentation with the appropriate health authorities.
How to fill out casirivimab and imdevimab emergency?
To fill out the emergency use documentation, providers must provide patient information, treatment details, and any adverse effects observed during administration.
What is the purpose of casirivimab and imdevimab emergency?
The purpose is to enable rapid access to these monoclonal antibodies for at-risk patients during the COVID-19 pandemic to reduce the risk of severe disease.
What information must be reported on casirivimab and imdevimab emergency?
Providers must report patient demographics, treatment dates, dosage administered, any adverse events, and outcomes following treatment.
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