SHINGRIX Vaccination Schedule for Adults
The recommended vaccination schedule for SHINGRIX (recombinant zoster vaccine with AS01B adjuvant) is two doses administered intramuscularly 2 to 6 months apart for adults aged 50 years and older. 1
Recommended Schedule and Administration
- SHINGRIX is administered as a two-dose series with the second dose given 2 to 6 months after the first dose 1
- The vaccine is administered intramuscularly (IM) 1
- The recommended age for vaccination is 50 years and older 1
- The vaccine is also recommended for adults aged ≥18 years who are or will be immunocompromised due to disease or therapy 2
Efficacy and Protection
- SHINGRIX demonstrates high efficacy in preventing herpes zoster (shingles) with vaccine efficacy of:
- Protection against postherpetic neuralgia (PHN) is 88.8% in adults 70 years and older 3
- Vaccine efficacy remains well-preserved across all age groups, including those 80 years and older (89.1%) 3
- Protection persists for at least 8 years with minimal waning, maintaining efficacy above 83.3% during this period 1
Advantages Over Previous Zoster Vaccine
- SHINGRIX (RZV) offers significantly higher efficacy compared to the older live-attenuated Zostavax (ZVL) vaccine 1, 4
- Unlike Zostavax, SHINGRIX is not contraindicated in immunocompromised individuals as it is a non-live recombinant vaccine 4, 2
- SHINGRIX maintains high efficacy across all age groups, while Zostavax efficacy decreased significantly with age (70% in ages 50-59 vs. 18% in those ≥80 years) 1
Special Populations
- For immunocompromised adults, SHINGRIX is now recommended for those aged ≥19 years who are or will be immunodeficient or immunosuppressed due to disease or therapy 2
- For patients with autoimmune inflammatory rheumatic diseases, SHINGRIX is preferred over the live-attenuated vaccine due to safety considerations 1
- Real-world effectiveness studies show that SHINGRIX maintains effectiveness in adults with autoimmune conditions and those with immunosuppressive conditions 5
Common Side Effects
- Injection-site reactions (pain, redness, swelling) are common, with 9.5% experiencing grade 3 injection site reactions compared to 0.4% with placebo 1
- Common systemic reactions include myalgia, fatigue, and headache 6
- Systemic symptoms were reported in 11.4% of vaccine recipients versus 2.4% in placebo recipients 1
- Despite higher reactogenicity compared to placebo, most adverse reactions are transient and mild to moderate in severity 4
Important Considerations
- If the second dose is delayed beyond the recommended 6-month interval, it should still be administered as soon as possible; real-world data shows that delayed second doses maintain effectiveness 5
- The complete two-dose series is important for optimal protection, as single-dose effectiveness (56.9%) is lower than two-dose effectiveness (70.1%) in real-world studies 5
- No serious safety concerns have been identified in large clinical trials, with similar rates of serious adverse events between vaccine and placebo groups 1, 3