Voranidenib (Voranigo) is a novel targeted therapy approved for marketing by the U.S. Food and Drug Administration (FDA) in 2024. It is indicated for the treatment of grade 2 gliomas (astrocytoma or oligodendroglioma) with specific IDH1 or IDH2 mutations.
What Are the Purchase Channels for Voranidenib (Voranigo)?
Overseas Purchase
Patients may choose to consult and purchase the drug at hospital pharmacies or licensed pharmacies in countries or regions where voranidenib has been approved for marketing.
As drug prices may be affected by factors such as regional differences and exchange rate fluctuations, patients need to make a budget and plan in advance before purchasing.
Purchase via Medical Service Institutions
Patients can consult domestic overseas medical service institutions that cooperate with international pharmacies or pharmaceutical companies.
These institutions can usually provide legal import channels, as well as professional consultation and guidance services.
Precautions for Purchasing Voranidenib (Voranigo)
Mandatory Medical Evaluation and Prescription Requirement
Confirmation of Gene Mutation: Prior to the administration of voranidenib, the presence of IDH1 or IDH2 mutations must be confirmed through tumor tissue sample testing, which is a fundamental prerequisite for medication use.
Comprehensive Health Assessment: Physicians will evaluate the patient’s overall health status, including liver and kidney function. Due to the risk of hepatotoxicity associated with this drug, regular monitoring is required before and during treatment.
Prescription-only Purchase: Do not attempt to purchase the drug without a prescription. Legal channels will definitely require a valid prescription issued by a licensed physician.
Storage Conditions
Voranidenib tablets should be stored at room temperature between 20°C and 25°C (68°F and 77°F).
Short-term storage within the temperature range of 15°C to 30°C is permitted.
Upon receiving the drug, check whether the package is intact and undamaged, and store it immediately in accordance with the instructions.
How to Distinguish the Authenticity of Voranidenib (Voranigo)?
Verify Outer Packaging and Labels
Brand and Trademark: Check whether the package bears the clear registered trademark “VORANIGO®” and the company information of Servier Pharmaceuticals LLC.
Approval Number and Traceability Code: In countries or regions where the drug is marketed, the package of genuine medicine should carry a specific mark or traceability code approved by the local drug regulatory authority. The authenticity of the code can be verified through official channels.
Anti-counterfeiting Features: Many original drug packages adopt anti-counterfeiting technologies such as holographic labels, special inks, and embossed printing. Examine these features carefully and compare them with the official packaging images.
Check Physical Characteristics of the Tablets
10 mg Tablets: Round, film-coated tablets, white to off-white in color. One side is imprinted with the black number “10”, and the other side is plain.
40 mg Tablets: Oval, film-coated tablets, white to off-white in color. One side is imprinted with the black number “40”, and the other side is plain.
After receiving the drug, verify that the shape, color, and imprint of the tablets are consistent with the official description. Any tablets with uneven color, blurred markings, damage, or unusual odor should be highly suspected as counterfeit products.
