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Este documento fornece informações detalhadas sobre o produto medicinal Comirnaty, um vacina de mRNA COVID-19 indicada para imunização ativa contra o COVID-19 em crianças de 5 a 11 anos. Inclui composição, indicações, posologia, método de administração, contraindicações, advertências, efeitos indesejáveis, propriedades farmacológicas e considerações sobre armazenamento e manuseio.
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01
Ensure you have the necessary supplies: vaccine vial, syringes, and alcohol swabs.
02
Check the vaccine vial for expiration date and any visible particles.
03
Clean the vial's rubber stopper with an alcohol swab.
04
Use a sterile syringe to withdraw the required dosage of 0.1 mL of Comirnaty 10 mcg EUA.
05
Administer the vaccine intramuscularly, typically in the deltoid muscle of the upper arm.
06
Dispose of used syringes and vials according to biohazard regulations.
07
Monitor the recipient for any immediate adverse reactions following vaccination.

Who needs comirnaty 10 mcg eua?

01
Individuals aged 5 years and older who are eligible for vaccination.
02
People who have not yet received a complete COVID-19 vaccination series.
03
Those recommended by public health guidelines for COVID-19 vaccination.
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Comirnaty 10 mcg EUA refers to the 10 microgram formulation of the Pfizer-BioNTech COVID-19 vaccine that has received Emergency Use Authorization (EUA) from regulatory authorities for use in certain populations.
Healthcare providers and organizations administering the vaccine are required to file the Comirnaty 10 mcg EUA to report on vaccine usage and adverse events associated with the vaccine.
To fill out the Comirnaty 10 mcg EUA, healthcare providers should follow the instructions provided by the regulatory authority, ensuring to include patient information, administration details, and any adverse effects observed.
The purpose of Comirnaty 10 mcg EUA is to provide a safe and effective vaccine option to help control the spread of COVID-19 in the population, particularly among younger individuals or as part of a booster regimen.
Information that must be reported on Comirnaty 10 mcg EUA includes patient demographics, vaccination date, vaccine lot number, healthcare provider details, any adverse events or side effects, and follow-up actions taken.
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