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Package Leaflet: Information for the user Prevent 13 suspension for injection Pneumococcal polysaccharide conjugate vaccine (13 talent, adsorbed) Read all of this leaflet carefully before you or your
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How to fill out prevenar 13 suspension for

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How to fill out prevenar 13 suspension for:

01
Carefully read and follow the instructions provided with the prevenar 13 suspension package.
02
Shake the suspension well before use to ensure the proper mixing of the vaccine.
03
Use a sterile syringe or needle to draw the correct dose of prevenar 13 suspension.
04
Administer the vaccine through intramuscular injection, usually in the thigh or upper arm.
05
Dispose of any unused vaccine and needles properly according to local regulations.

Who needs prevenar 13 suspension:

01
Infants and children: Prevenar 13 suspension is recommended for infants and children aged 6 weeks to 5 years as a protection against diseases caused by Streptococcus pneumoniae bacteria. This includes pneumococcal meningitis, pneumonia, ear infections, and bloodstream infections.
02
Immunocompromised individuals: Prevenar 13 suspension may also be recommended for individuals with weakened immune systems, such as those undergoing chemotherapy or with HIV, to reduce the risk of pneumococcal infections.
03
Healthcare workers: In some cases, healthcare workers who have direct contact with high-risk populations may be recommended to receive the prevenar 13 vaccination to prevent the spread of pneumococcal infections.
It is important to consult with a healthcare professional to determine if prevenar 13 suspension is appropriate for you or your child and to receive proper guidance on how to administer the vaccine.
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Prevenar 13 suspension is a vaccine used to prevent infections caused by Streptococcus pneumoniae bacteria, such as pneumonia, meningitis, and sepsis.
Healthcare providers or facilities administering the vaccine are required to file prevenar 13 suspension reports.
The prevenar 13 suspension form can be filled out online or submitted through the Vaccine Adverse Event Reporting System (VAERS) website.
The purpose of prevenar 13 suspension reports is to monitor and track any adverse events or side effects associated with the vaccine.
Information such as the patient's demographics, vaccine lot number, date of administration, and any adverse reactions must be reported on prevenar 13 suspension forms.
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