This brand name is authorized in Estonia, Ireland, Lithuania, Netherlands, Poland, Romania
The drug ZERIT contains one active pharmaceutical ingredient (API):
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1
Stavudine
UNII BO9LE4QFZF - STAVUDINE
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Stavudine, a thymidine analogue, is phosphorylated by cellular kinases to stavudine triphosphate which inhibits HIV reverse transcriptase by competing with the natural substrate, thymidine triphosphate. It also inhibits viral DNA synthesis by causing DNA chain termination due to a lack of the 3'-hydroxyl group necessary for DNA elongation. Cellular DNA polymerase γ is also sensitive to inhibition by stavudine triphosphate, while cellular polymerases α and β are inhibited at concentrations 4,000-fold and 40-fold higher, respectively, than that needed to inhibit HIV reverse transcriptase. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| ZERIT Powder for oral solution | European Medicines Agency (EU) | MPI, EU: SmPC | |
| ZERIT Hard capsule | European Medicines Agency (EU) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| J05AF04 | Stavudine | J Antiinfectives for systemic use → J05 Antivirals for systemic use → J05A Direct acting antivirals → J05AF Nucleoside and nucleotide reverse transcriptase inhibitors |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: EE | Ravimiamet | Identifier(s): 1032400, 1032411, 1032422, 1032433, 1032444, 1073472, 1073528, 1073539, 1073540 |
| Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1015967, 1015968, 1015969, 1015970, 1015971, 1015972, 1015973, 1015974, 1015975 |
| Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 44776 |
| Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100000480, 100000965, 100082963, 100083098, 100084092 |
| Country: RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | Identifier(s): W52738001 |
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