This brand name is authorized in Austria, Brazil, Canada, Cyprus, Estonia, Hong Kong SAR China, Ireland, Lithuania, Malta, New Zealand, Poland, Singapore, South Africa.
The drug PRIORIX TETRA contains a combination of these active pharmaceutical ingredients (APIs):
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UNII
52202H034Z - RUBELLA VIRUS STRAIN WISTAR RA 27/3 LIVE ANTIGEN
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Rubella virus vaccine contains live attenuated rubella virus, produced in human diploid (MRC-5) cells. It is a virus vaccine for active immunization against rubella that is subcutaneously administered. |
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UNII
GPV39ZGD8C - VARICELLA-ZOSTER VIRUS STRAIN OKA/MERCK LIVE ANTIGEN
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Natural infection induces a cellular and humoral immune response to the varicella-zoster virus, which can be rapidly detected following infection. IgG, IgM and IgA directed against viral proteins usually appear at the same time that a cellular immune response can be demonstrated, making the relative contribution of humoral and cellular immunity to disease progression difficult to ascertain. Vaccination has been shown to induce both humoral and cell-mediated types of immunity. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| J07BD54 | Measles, combinations with mumps, rubella and varicella, live attenuated | J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BD Measles vaccines |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| BR | Câmara de Regulação do Mercado de Medicamentos | 510611701153411, 510618090060207 |
| CA | Health Products and Food Branch | 02297884 |
| EE | Ravimiamet | 1277489, 1277490, 1277502, 1277513, 1277861, 1277872, 1277883 |
| HK | Department of Health Drug Office | 57798 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1024239, 1024240, 1024466, 1024758, 1026808, 1026809, 1026810, 1026811, 1065761 |
| MT | Medicines Authority | MA170/01002, MA170/01003 |
| NZ | Medicines and Medical Devices Safety Authority | 11761 |
| PL | Rejestru Produktów Leczniczych | 100182334, 100182357 |
| SG | Health Sciences Authority | 13627P |
| ZA | Health Products Regulatory Authority | 43/30.1/0127 |
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