This brand name is authorized in Estonia, Finland, France, Ireland, Israel, Lithuania, Malta, UK.
The drug TICOVAC contains one active pharmaceutical ingredient (API):
1
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UNII
42XD79UQQ6 - TICK-BORNE ENCEPHALITIS PURIFIED ANTIGEN (FORMALDEHYDE INACTIVATED)
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Encephalitis, tick borne suspension for injection is indicated for the active (prophylactic) immunization of persons of 16 years of age and older against tick-borne encephalitis (TBE). Its pharmacodynamic effect consists of the induction of a sufficiently high concentration of anti-TBE antibody to provide protection against the TBE virus. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| TICOVAC Suspension for injection in a pre-filled syringe | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BA01 | Encephalitis, tick borne, inactivated, whole virus | J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BA Encephalitis vaccines |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| EE | Ravimiamet | 1201598, 1201600, 1201611, 1201622, 1201677, 1201688, 1201699, 1201701 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 143534, 392228, 421227, 426850 |
| FR | Base de données publique des médicaments | 61440306, 69663909 |
| GB | Medicines & Healthcare Products Regulatory Agency | 135075, 146032 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 8416, 8417 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1021207, 1021208, 1021211, 1021212, 1054244, 1054245, 1072673, 1072674 |
| MT | Medicines Authority | MA505/10501, MA505/10502 |
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