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This document provides instructions on how to report nonviable vaccines received through the Minnesota Department of Health (MDH), detailing the steps to take in case the vaccine is spoiled or expired,
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How to fill out Nonviable MDH Vaccine

01
Gather all necessary patient information including medical history.
02
Ensure to have the correct dosage information for the specific age group.
03
Prepare the vaccine by checking the expiration date and storage conditions.
04
Clean the injection site with an antiseptic wipe.
05
Draw the appropriate dose of the Nonviable MDH Vaccine into a syringe.
06
Administer the vaccine intramuscularly or subcutaneously as directed.
07
Dispose of the syringe and needle in a proper sharps container.
08
Record the administration details in the patient's medical record.

Who needs Nonviable MDH Vaccine?

01
Individuals at risk of disease that the Nonviable MDH Vaccine prevents.
02
Children and adults based on vaccination schedules and recommendations.
03
People with specific health conditions that warrant the use of the vaccine.
04
Travelers to areas where diseases prevented by the vaccine are prevalent.
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Any non-viable vaccine that cannot be returned to McKesson is considered waste. Terms used in vaccine accountability: OPENED: a partially used multi-dose vial; a vial that has been punctured; a syringe with an opened safety cap; or a vial missing the plastic cap.
All expired or wasted VFC vaccine must be returned to McKesson by providers, with the exception of broken vials/syringes, open vials or drawn but not used syringes. Broken/open vials and drawn but not used syringes should be recorded as wastage in MCIR VIM and then discarded in a sharps container.

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Nonviable MDH Vaccine refers to a type of vaccine that does not contain live pathogens but instead includes components that stimulate the immune system to provide protection against diseases.
Healthcare providers and institutions that administer the Nonviable MDH Vaccine are typically required to file documentation regarding its use, including vaccination records and reporting to health authorities.
To fill out the Nonviable MDH Vaccine documentation, providers must include the patient's information, vaccine details, administration date, lot number, and any adverse reactions observed.
The purpose of the Nonviable MDH Vaccine is to provide immunity against specific infectious diseases without the risk of causing the disease itself, thereby safeguarding public health.
Information that must be reported includes the vaccine type, lot number, expiration date, administration details, patient demographics, and any noted side effects or adverse reactions.
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