Fotivda
·
- Prescription status not stated
- Cancer treatments and immune-system medicines
- Active substance
- Tivozanib hydrochloride monohydrate
- Made by
- Recordati Netherlands B.V.
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Fotivda is indicated for the first line treatment of adult patients with advanced renal cell carcinoma (RCC) and for adult patients who are VEGFR and mTOR pathway inhibitor-naïve following disease progression after one prior treatment with cytokine therapy for advanced RCC. Treatment of advanced renal cell carcinoma.
From the official label · 2026-09-30 · European Medicines Agency
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
United StatesNo exact match for this strength and form
SpainNo exact match for this strength and form
NetherlandsNo exact match for this strength and form
Details
| Made by | Recordati Netherlands B.V. |
|---|---|
| Active substance | Tivozanib hydrochloride monohydrate |
| Used in | Cancer treatments and immune-system medicines |
| Classification | L01EK03 · Cancer treatments and immune-system medicines |
| Authorised on | 2017-08-24 |
| Last updated by the regulator | 2023-07-17 |
| EMA product number | EMEA/H/C/004131 |
Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician
Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).