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HomeClinical InformationClinical InformationACIP RecommendationsWhat is TicoVac®?What is TBE?Symptoms & Risk FactorsDemonstrated EffectivenessDosing & Administration ScheduleResourcesResourcesMaterialsVideosOrder TicoVac®
Prescribing Information Indication Patient Site
Dosing & Administration Schedule TicoVac® Dosing Schedule

The TicoVac® primary dose series is recommended to be completed at least 1 week prior to potential exposure to TBEV.1

Primary Vaccination
The primary TicoVac® dosage consists of:
  • three 0.25 mL doses for individuals 1 to 15 years of age1;
  • three 0.5 mL doses for individuals 16 years of age and older.1
Primary Vaccination Schedule – TicoVac®1

A booster dose (fourth dose) may be given at least 3 years after completion of the primary immunization series if ongoing exposure or re-exposure to TBEV is expected.1

Learn more about Dosing, Schedule and Administration from the CDC

Dosing, Schedule and Administration Primary Vaccination Series

The vaccination dose and timing for the 3-dose primary TBE vaccine series vary by age (Box 2).

1–15 years: 3 doses (0.25 mL each) administered intramuscularly (IM) with the first 2 doses administered 1 to 3 months apart and the third dose administered 5 to 12 months after dose 2.

16 years and older: 3 doses (0.5 mL each) administered IM with the first 2 doses administered 14 days to 3 months apart and the third dose administered 5 to 12 months after dose 2.

For all age groups, the 3-dose primary immunization series should be completed at least 1 week before potential exposure to TBE virus. 

For persons (e.g., travelers) who cannot complete the 3-dose primary series, see section “Immunologic Response After an Incomplete Primary Series (1 or 2 Doses) in Adults and Children” of the ACIP Recommendations for additional information.

Booster Dose

For all age groups, a booster dose (i.e., fourth dose) can be administered at least 3 years after completion of the primary 3-dose TBE vaccine series if ongoing exposure or re-exposure to TBE virus is expected.

No ACIP recommendations are made on the need for subsequent booster doses.

1–15 years: 0.25 mL dose administered IM at ≥3 years after completion of primary series.

16 years and older: 0.5 mL dose administered IM at ≥3 years after completion of primary series.

There are currently no U.S. recommendations on the need for subsequent booster doses.

Contact your Pfizer Customer Service Representative at
​​​​​​​1-800-666-7248.
Reference:TicoVac® (Tick-Borne Encephalitis Vaccine). Prescribing Information. New York, NY: Pfizer Inc. 2021.
Clinical Information
RESOURCES FOR YOU & YOUR PATIENTS

Discover more about TBE with these helpful resources. You can access HCP and patient materials via the Resources tab.

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To report an adverse event, please call 1-800-438-1985

Pfizer for Professionals 1-800-505-4426

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PP-TCV-USA-0190
INDICATION AND USAGE TicoVac® is a vaccine indicated for active immunization to prevent tick-borne encephalitis (TBE) and is approved for use in individuals 1 year of age and older.
IMPORTANT SAFETY INFORMATION
  • TicoVac® should not be given to anyone with a severe allergic reaction (e.g. anaphylaxis) to any component of TicoVac®.
  • Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of TicoVac®.
  • TicoVac® may not protect all individuals against TBE.
  • Some individuals with altered immunocompetence may have a reduced response to TicoVac®.
  • TicoVac® contains albumin, a derivative of human blood, and based on effective donor screening and product manufacturing processes carries an extremely remote and theoretical risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD).
  • In clinical studies, the most common adverse reactions in subjects 1 through 15 years of age who received TicoVac® were local tenderness (18.1%), local pain (11.2%), headache (11.1%), fever (9.6%), and restlessness (9.1%).
  • In clinical studies, the most common adverse reactions in subjects 16 through 65 years of age who received TicoVac® were local tenderness (29.9%), local pain (13.2%), fatigue (6.6%), headache (6.3%), and muscle pain (5.1%).
  • Safety and effectiveness have not been established in pregnant women.​​​
Patients should always ask their healthcare providers for medical advice about adverse events.You are encouraged to report negative side effects of vaccines to the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). Visit http://www.vaers.hhs.gov or call 1-800-822-7967.
Please see full prescribing information for TicoVac® here.
Indication TicoVac® is a vaccine indicated for active immunization to prevent tick-borne encephalitis (TBE) and is approved for use in individuals 1 year of age and older.
Important Safety Information
  • TicoVac® should not be given to anyone with a severe allergic reaction (e.g. anaphylaxis) to any component of TicoVac®.
  • Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of TicoVac®.
  • TicoVac® may not protect all individuals against TBE.
  • Some individuals with altered immunocompetence may have a reduced response to TicoVac®.
  • TicoVac® contains albumin, a derivative of human blood, and based on effective donor screening and product manufacturing processes carries an extremely remote and theoretical risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD).
  • In clinical studies, the most common adverse reactions in subjects 1 through 15 years of age who received TicoVac® were local tenderness (18.1%), local pain (11.2%), headache (11.1%), fever (9.6%), and restlessness (9.1%).
  • In clinical studies, the most common adverse reactions in subjects 16 through 65 years of age who received TicoVac® were local tenderness (29.9%), local pain (13.2%), fatigue (6.6%), headache (6.3%), and muscle pain (5.1%).
  • Safety and effectiveness have not been established in pregnant women.​​​
Patients should always ask their healthcare providers for medical advice about adverse events. You are encouraged to report negative side effects of vaccines to the US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). Visit http://www.vaers.hhs.gov or call 1-800-822-7967. Please see full prescribing information for TicoVac® here. Indication
TicoVac® is a vaccine indicated for active immunization to prevent tick-borne encephalitis (TBE) and is approved for use in individuals 1 year of age and older.
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