Rafinlar 75mg Capsule contains dabrafenib 75mg, a prescription targeted anticancer medicine belonging to the BRAF inhibitor class. It is used for selected cancers carrying specific BRAF V600 mutations, including unresectable or metastatic melanoma and, in combination with trametinib, certain BRAF V600 mutation-positive non-small cell lung cancers and other approved indications depending on the market.
Rafinlar is marketed by Novartis and is available as 50mg and 75mg hard capsules. The 75mg capsule contains dabrafenib equivalent to 75mg of the active drug.
Dabrafenib is a molecularly targeted therapy that inhibits abnormal BRAF signaling involved in cancer-cell growth. Because treatment is dependent on the tumor’s molecular characteristics, appropriate BRAF mutation testing is required before treatment.
Rafinlar 75mg is an oral targeted cancer medicine containing dabrafenib. Rather than broadly suppressing rapidly dividing cells, dabrafenib specifically targets abnormal signaling associated with mutated BRAF proteins.
Rafinlar 75mg is particularly relevant for patients whose tumors have an eligible BRAF V600 mutation, which should be confirmed using an appropriate diagnostic test before treatment.
Rafinlar/dabrafenib is used for specific cancers with qualifying BRAF mutations. Depending on the approved indication and country, uses include:
The exact approved indications differ between regulatory jurisdictions, so treatment should follow the local prescribing information.
Dabrafenib selectively inhibits BRAF kinase, including forms of the BRAF protein containing activating V600 mutations.
BRAF is part of the MAPK signaling pathway, which regulates cellular growth and proliferation. In tumors containing an activating BRAF mutation, this pathway can become abnormally active and contribute to uncontrolled cancer-cell growth.
By inhibiting mutant BRAF signaling, dabrafenib can reduce downstream signaling and help slow the growth and proliferation of eligible cancer cells.
Rafinlar is a biomarker-driven cancer treatment. It is not appropriate for every patient with melanoma or lung cancer.
Before treatment, the tumor generally needs to be tested for the relevant BRAF V600 mutation using an appropriate validated diagnostic method.
This makes the following commercial search relationship particularly important:
Rafinlar 75mg → Dabrafenib 75mg → BRAF Inhibitor → BRAF V600 Mutation Treatment → Targeted Cancer Therapy
Dabrafenib is commonly combined with trametinib for several approved BRAF V600 mutation-positive cancers.
The combination targets two different points in the MAPK pathway: dabrafenib inhibits BRAF, while trametinib inhibits MEK. This dual pathway inhibition can provide greater suppression of abnormal MAPK signaling than BRAF inhibition alone in applicable cancers.
The combination should only be prescribed and monitored by an oncology specialist.
The dose and treatment schedule must be determined by the treating oncologist according to the patient’s cancer type, mutation status, treatment combination, medical history and response to therapy.
Rafinlar capsules should be taken exactly as prescribed. The capsules should be swallowed whole and should not be opened, crushed or chewed.
Do not change the dose or stop treatment without consulting the prescribing oncologist.
Dabrafenib can cause adverse effects, and the risk profile can vary depending on whether it is used alone or together with trametinib.
Potential adverse effects include:
More serious reactions can occur, including severe fever-related reactions, eye problems, bleeding, heart-related effects, liver abnormalities and development of new skin cancers. Patients should promptly report concerning symptoms to their oncology team.
Follow the storage conditions stated on the product packaging and official prescribing information. Keep the capsules in their original container and out of reach of children.
Do not use capsules beyond the expiry date.
The active pharmaceutical ingredient in Rafinlar is dabrafenib.
Where an authorized generic or equivalent dabrafenib product is available, commercially relevant searches may include:
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The term generic Rafinlar should only be used when the specific product has the appropriate generic/equivalent regulatory status in the target market.
Rafinlar 75mg is a prescription oncology medicine and should be obtained through an appropriately licensed pharmacy or authorized pharmaceutical supplier.
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Availability, prescription requirements, importation and dispensing regulations differ across the USA, UK, UAE/Dubai, Australia, Singapore, Thailand, China and Russia.
Rafinlar contains dabrafenib and is used for selected cancers with an eligible BRAF V600 mutation, including unresectable or metastatic melanoma. It is also used with trametinib for certain other approved BRAF V600 mutation-positive cancers.
The generic name is dabrafenib. The capsule contains dabrafenib equivalent to 75mg of active drug.
Yes. Dabrafenib is a targeted BRAF kinase inhibitor that inhibits signaling from mutant BRAF proteins.
Yes. Rafinlar/dabrafenib is used for eligible patients with BRAF V600 mutation-positive unresectable or metastatic melanoma.
Dabrafenib, in combination with trametinib, is approved for certain adults with BRAF V600 mutation-positive advanced non-small cell lung cancer.
Yes. Because dabrafenib is a biomarker-directed treatment, the relevant BRAF mutation should be confirmed with an appropriate diagnostic test before treatment.
Rafinlar is the brand name, while dabrafenib is its active pharmaceutical ingredient.
The treatment regimen depends on the specific cancer and regulatory indication. Dabrafenib may be used alone for certain melanoma indications, while combination therapy with trametinib is required or preferred for several other approved indications.
Rafinlar is a prescription anticancer medicine. It should be purchased only from an appropriately licensed pharmacy or authorized pharmaceutical supplier and used under oncology supervision.
Common adverse effects can include fever, fatigue, nausea, headache, joint pain, diarrhea, vomiting and skin-related reactions. Your oncologist should be informed about persistent or severe symptoms.
Yes. Oncology follow-up and appropriate monitoring are required during treatment. Depending on the treatment regimen, monitoring may include skin examinations, eye assessments, blood tests, liver function and cardiovascular evaluation.
Medical Disclaimer: This product information is provided for educational and informational purposes only and is not a substitute for professional medical advice, diagnosis or treatment. Rafinlar (dabrafenib) is a prescription anticancer medicine that requires specialist oncology supervision. Treatment is dependent on appropriate molecular testing and the specific approved indication. Dabrafenib can cause serious and potentially life-threatening adverse reactions. Always follow the official prescribing information for the specific product and consult a qualified oncologist before starting, stopping or changing treatment.
Last Updated: August 23, 2026
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Estimated delivery: 3–7 business days to UK. 7–10 business days to UAE, Saudi Arabia and Gulf countries. 10–15 days for USA and Asian countries.
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