RECONSTITUTION & ADMINISTRATION

Watch the video and follow the step-by-step instructions to reconstitute and administer SHINGRIX.

SHINGRIX is a suspension for intramuscular injection only.

Reconstitution

Watch the reconstitution video for SHINGRIX. Please refer to the full Prescribing Information for SHINGRIX for full details.

Please refer to the full Prescribing Information for SHINGRIX for full details. 

Reconstitution Step by Step

Image of Reconstitution Vial 1 of 2

Vial 1 of 2

AS01B Adjuvant Suspension Component (liquid)

Image of SHINGRIX Reconstitution: Step 1

STEP 1

Cleanse both vial stoppers. Using a sterile needle and sterile syringe, withdraw the entire contents of the vial containing the adjuvant suspension component (liquid) by slightly tilting the vial. Vial 1 of 2.

Image of Reconstitution Vial 2 of 2

Vial 2 of 2

Lyophilized VZV gE Antigen Component (powder)

Image of SHINGRIX Reconstitution: Step 2

STEP 2

Slowly transfer entire contents of syringe into the lyophilized gE antigen component vial (powder). Vial 2 of 2.

 

VZV=varicella zoster virus; gE=glycoprotein E.

Image of SHINGRIX Reconstitution: Step 3

STEP 3

Gently swirl the vial until powder is completely dissolved. Do not shake vigorously. The reconstituted vaccine should be an opalescent, colorless to pale brownish liquid.

Image of SHINGRIX Reconstitution: Step 4

STEP 4

After reconstitution, withdraw 0.5 mL from the vial containing the reconstituted vaccine and administer intramuscularly. The preferred site for intramuscular injection is the deltoid region of the upper arm.  

Storage

Before reconstitution:

Refrigerate both vials between 2°C and 8°C (36°F to 46°F). Protect vials from light. Do not freeze; discard if frozen.

 

After reconstitution: 

Administer immediately or store refrigerated between 2°C and 8°C (36°F and 46°F) for up to 6 hours. Do not freeze; discard if frozen. Discard if not used within 6 hours.

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Storage & Dosing

Learn how to store and properly dose SHINGRIX.

CDC Recommendations

See what CDC says about SHINGRIX. 

Safety Profile

Learn about the safety profile of SHINGRIX in immunocompromised patients aged 18 years and older.

CDC=Centers for Disease Control and Prevention.

Indication & Important Safety Info

Indication

Important Safety Information

Indication

SHINGRIX is a vaccine indicated for prevention of herpes zoster (HZ) (shingles):

  • in adults aged 50 years and older.
  • in adults aged 18 years and older who are or will be at increased risk of HZ due to immunodeficiency or immunosuppression caused by known disease or therapy.

SHINGRIX is not indicated for prevention of primary varicella infection (chickenpox).

Important Safety Information

  • SHINGRIX is contraindicated in anyone with a history of a severe allergic reaction (eg, anaphylaxis) to any component of the vaccine or after a previous dose of SHINGRIX
  • Review immunization history for possible vaccine sensitivity and previous vaccination-related adverse reactions. Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of SHINGRIX
  • In a postmarketing observational study, an increased risk of Guillain-Barré syndrome was observed during the 42 days following vaccination with SHINGRIX
  • Syncope (fainting) can be associated with the administration of injectable vaccines, including SHINGRIX. Procedures should be in place to avoid falling injury and to restore cerebral perfusion following syncope
  • Solicited local adverse reactions reported in individuals aged 50 years and older were pain (78%), redness (38%), and swelling (26%)
  • Solicited general adverse reactions reported in individuals aged 50 years and older were myalgia (45%), fatigue (45%), headache (38%), shivering (27%), fever (21%), and gastrointestinal symptoms (17%)  
  • Solicited local adverse reactions reported in autologous hematopoietic stem cell transplant recipients (aged 18 to 49 and ≥50 years of age) were pain (88% and 83%), redness (30% and 35%), and swelling (21% and 18%)  
  • Solicited general adverse reactions reported in autologous hematopoietic stem cell transplant recipients (aged 18 to 49 and ≥50 years of age) were fatigue (64% and 54%), myalgia (58% and 52%), headache (44% and 30%), gastrointestinal symptoms (21% and 28%), shivering (31% and 25%), and fever (28% and 18%)
  • The data are insufficient to establish if there is vaccine-associated risk with SHINGRIX in pregnant women
  • It is not known whether SHINGRIX is excreted in human milk. Data are not available to assess the effects of SHINGRIX on the breastfed infant or on milk production/excretion
  • Vaccination with SHINGRIX may not result in protection of all vaccine recipients

 

Please see full Prescribing Information.

To report SUSPECTED ADVERSE REACTIONS, contact GSK at https://gsk.public.reportum.com or
1-888-825-5249 or VAERS at 1-800-822-7967 or www.vaers.hhs.gov.

References

  1. Prescribing Information for SHINGRIX.

    Questions About SHINGRIX?

    Call: 1-800-772-9292

    Available Monday - Friday

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