HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use TICOVAC safely and effectively. See full prescribing information for TICOVAC. TICOVAC (Tick-Borne Encephalitis Vaccine), Suspension for intramuscular injection Initial U.S. Approval: 2021 INDICATIONS AND USAGETICOVAC is a vaccine indicated for active immunization to prevent tick-borne encephalitis (TBE). TICOVAC is approved for use in individuals 1 year of age and older. (1) DOSAGE AND ADMINISTRATIONFor intramuscular use only.
Primary Vaccination: Three doses (2.1)
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 tick-borne encephalitis virus (TBEV) is expected. DOSAGE FORMS AND STRENGTHSSuspension for injection supplied as a 0.25 mL or 0.5 mL single-dose in pre-filled syringes. (3) CONTRAINDICATIONS
ADVERSE REACTIONSThe most common adverse reactions are as follows:
To report SUSPECTED ADVERSE REACTIONS, contact Pfizer Inc. at 1-800-438-1985 or VAERS at 1-800-822-7967 or https://vaers.hhs.gov. See 17 for PATIENT COUNSELING INFORMATION. Revised: 7/2023 |
HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use TICOVAC safely and effectively. See full prescribing information for TICOVAC. TICOVAC (Tick-Borne Encephalitis Vaccine), Suspension for intramuscular injection Initial U.S. Approval: 2021 INDICATIONS AND USAGETICOVAC is a vaccine indicated for active immunization to prevent tick-borne encephalitis (TBE). TICOVAC is approved for use in individuals 1 year of age and older. (1) DOSAGE AND ADMINISTRATIONFor intramuscular use only.
Primary Vaccination: Three doses (2.1)
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 tick-borne encephalitis virus (TBEV) is expected. DOSAGE FORMS AND STRENGTHSSuspension for injection supplied as a 0.25 mL or 0.5 mL single-dose in pre-filled syringes. (3) CONTRAINDICATIONS
ADVERSE REACTIONSThe most common adverse reactions are as follows:
To report SUSPECTED ADVERSE REACTIONS, contact Pfizer Inc. at 1-800-438-1985 or VAERS at 1-800-822-7967 or https://vaers.hhs.gov. See 17 for PATIENT COUNSELING INFORMATION. Revised: 7/2023 |
{{section_body_html_patient}}
Chat online with Pfizer Medical Information regarding your inquiry on a Pfizer medicine.
*Speak with a Pfizer Medical Information Professional regarding your medical inquiry. Available 9AM-5PM ET Monday to Friday; excluding holidays.
Submit a medical question for Pfizer prescription products.
Pfizer Safety
To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:
Pfizer Safety Reporting Site*If you are involved in a clinical trial for this product, adverse events should be reported to your coordinating study site.
If you cannot use the above website, or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at (800) 438-1985.
FDA Medwatch
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or call (800) 822-7967.