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See below for Important Safety Information. See full Prescribing Information for
Flublok® Quadrivalent (Influenza Vaccine), Fluzone® Quadrivalent (Influenza Vaccine), and Fluzone® High-Dose Quadrivalent (Influenza Vaccine).
 
 
Return your Sanofi Pasteur influenza vaccine using VaccineShoppe.com®, which offers you the opportunity to return any unused 2019-2020 season product by July 31, 2020.
 
INFLUENZA VACCINE RETURN INSTRUCTIONS
Generate Your Return Goods Form
Log on to VaccineShoppe.com
Go to the Influenza Vaccine tab
Click on Generate Returns Form
Follow the instructions to generate your Return Goods Form
Save and print the PDFs
Upload Return Goods Form & Generate Return Authorization
Log on to the Inmar Healthcare Management Return Portal https://returns.healthcare.inmar.com
Register for an account if you haven't already
Upload the Return Goods Form you created on VaccineShoppe.com
Generate a Return Authorization
Note: This is not a shipping label
Secure Return Authorization on the outside of the box, and place the Return Goods Form inside the box with your vaccine
Obtain Shipping Label & Send
Obtain a shipping label from your carrier (FedEx or UPS preferred)
Secure the label on the outside of the box (do not cover the Return Authorization)
Send return to: Inmar RX Solutions, Inc. 3845 Grand Lakes Way, Suite 125 Grand Prairie, TX 75050
 
All reservations are subject to Sanofi Pasteur's Terms and Conditions of Sale, including credit review, in effect at the time of reservation confirmation. Copies of which are available upon request or by logging on to VaccineShoppe.com.
 
If you have questions, please visit our website at www.VaccineShoppe.com or call 1-800-VACCINE (1-800-822-2463).
 
Fluzone Quadrivalent, Flublok Quadrivalent, and Fluzone High-Dose Quadrivalent are vaccines indicated for active immunization against disease caused by influenza A subtype viruses and type B viruses contained in the vaccine. Fluzone Quadrivalent is approved for use in persons 6 months of age and older. Flublok Quadrivalent is approved for use in persons 18 years of age and older. Fluzone High-Dose Quadrivalent is approved for use in persons 65 years of age and older.
 
IMPORTANT SAFETY INFORMATION FOR FLUZONE QUADRIVALENT (INFLUENZA VACCINE), FLUBLOK QUADRIVALENT (INFLUENZA VACCINE), AND FLUZONE HIGH-DOSE QUADRIVALENT (INFLUENZA VACCINE)
 
Fluzone Quadrivalent, Flublok Quadrivalent, and Fluzone High-Dose Quadrivalent should not be administered to anyone who has had a severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine (including egg protein for Fluzone Quadrivalent and Fluzone High-Dose Quadrivalent) or after previous dose of the respective vaccine. In addition, Fluzone Quadrivalent and Fluzone High-Dose Quadrivalent should not be administered to anyone who has had a severe allergic reaction after previous dose of any influenza vaccine.
 
Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of the vaccine.
 
If Guillain-Barré syndrome has occurred within 6 weeks following previous influenza vaccination, the decision to give Fluzone Quadrivalent, Flublok Quadrivalent, and Fluzone High-Dose Quadrivalent should be based on careful consideration of the potential benefits and risks.
 
If Fluzone Quadrivalent, Flublok Quadrivalent, and Fluzone High-Dose Quadrivalent are administered to immunocompromised persons, including those receiving immunosuppressive therapy, the immune response may be lower than expected.
 
Vaccination with Fluzone Quadrivalent, Flublok Quadrivalent, and Fluzone High-Dose Quadrivalent may not protect all recipients.
 
For Fluzone Quadrivalent, in children 6 months through 35 months of age, the most common injection-site reactions were pain or tenderness, erythema, and swelling; the most common solicited systemic adverse reactions were irritability, abnormal crying, malaise, drowsiness, appetite loss, myalgia, vomiting, and fever. In children 3 years through 8 years of age, the most common injection-site reactions were pain, erythema, and swelling; the most common solicited systemic adverse reactions were myalgia, malaise, and headache. In adults 18 years and older, the most common injection-site reaction was pain; the most common solicited systemic adverse reactions were myalgia, headache, and malaise.
 
For Flublok Quadrivalent, in adults 18 through 49 years of age, the most common injection-site reactions were tenderness and pain; the most common solicited systemic adverse reactions were headache, fatigue, myalgia, and arthralgia. In adults 50 years of age and older, the most common injection-site reactions were tenderness and pain; the most common solicited systemic adverse reactions were headache, and fatigue.
 
For Fluzone High-Dose Quadrivalent, in adults 65 years of age and older, the most common injection-site reaction was pain; the most common solicited systemic adverse reactions were myalgia, headache, and malaise.
 
For Fluzone Quadrivalent, Flublok Quadrivalent, and Fluzone High-Dose Quadrivalent, other adverse reactions may occur.
 
Before administration, please see the full Prescribing Information for Flublok Quadrivalent, Fluzone Quadrivalent, or Fluzone High-Dose Quadrivalent.
 

 
Should you have any questions,
please contact your Sanofi Pasteur representative
or call 1-800-VACCINE
(1-800-822-2463).
 

 
 
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MAT-US-2000207

05/20