HOW TO ADMINISTER AND STORE SHINGRIX

SHINGRIX is administered intramuscularly as a 2-dose series

  • Administer the second dose 2 to 6 months after the first
  • It is important to receive both doses. The efficacy results of SHINGRIX were demonstrated in clinical trials when administered as a 2-dose series
Doctor follow up icon

Follow up on the second dose

Your patients count on you and your staff to help them complete their 2-dose series of SHINGRIX

 

How to help your patients stay accountable:

  • Document your discussion
  • Encourage them to schedule their second dose appointment at your practice or at a pharmacy by visiting ScheduleSHINGRIX.com
  • Follow up to ensure they received both doses of SHINGRIX

What you should know about the storage and handling of SHINGRIX before vaccinating your patients

SHINGRIX is supplied as an adjuvant and antigen for reconstitution

  • Prepare SHINGRIX by reconstituting the lyophilized gE antigen component (powder) with the accompanying ASO1B  adjuvant suspension component (liquid)
  • SHINGRIX is a vaccine for intramuscular injection only
SHINGRIX reconstitution image

Storage and administration

Prior to reconstitution

Store both the antigen (powder) and adjuvant (liquid) components refrigerated between 2°C and 8°C (36°F and 46°F). Do not freeze; discard if frozen and protect from light.

 

After reconstitution

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

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    gE=glycoprotein E

Watch the reconstitution video for SHINGRIX

How to reconstitute SHINGRIX

Review reconstitution instructions for SHINGRIX.

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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