GNH USA

Europe — EMA

Jakavi

GNH USA supplies Jakavi (Ruxolitinib), a JAK inhibitor for myelofibrosis and polycythemia vera. Request a quote for supply to hospitals and clinics worldwide.

Ruxolitinib

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What is Ruxolitinib?

Ruxolitinib, the active ingredient in Jakavi, is a Janus kinase (JAK) inhibitor presented as an oral tablet for systemic use. It is indicated for the treatment of myelofibrosis and polycythemia vera in adult patients, helping to control disease‑related symptoms and blood counts.

GNH USA supplies Jakavi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides reliable global distribution.

What is Ruxolitinib used for?

Jakavi (ruxolitinib) is used in the management of myeloproliferative neoplasms, targeting abnormal blood cell production.

- Myelofibrosis: reduces spleen size and improves constitutional symptoms. - Polycythemia vera: helps maintain target hematocrit and reduces phlebotomy requirements. - Symptom burden in myeloproliferative disorders: alleviates fatigue, night sweats, and pruritus.

What are the side effects of Ruxolitinib?

Jakavi may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects: - Anemia: decreased red blood cell count. - Thrombocytopenia: reduced platelet levels. - Neutropenia: lowered neutrophil count. - Diarrhea: mild to moderate gastrointestinal upset. - Nausea: occasional feeling of sickness. - Fatigue: general tiredness.

Serious or Rare Side Effects: - Infections: opportunistic or severe infections. - Hepatic dysfunction: elevated liver enzymes or hepatitis. - Pulmonary hypertension: rare increase in pulmonary arterial pressure. - Secondary malignancies: potential development of new cancers.

What precautions apply to Ruxolitinib?

Before prescribing Jakavi, clinicians should consider several safety precautions to minimize risks.

- Baseline blood counts: obtain CBC to assess anemia, platelets, neutrophils. - Infection risk: screen for active infections and monitor for signs during therapy. - Liver function: evaluate hepatic enzymes prior to initiation and periodically. - Cardiovascular assessment: monitor for hypertension or pulmonary hypertension. - Pregnancy and lactation: avoid use unless benefits outweigh risks; discuss with patient. - Store at ambient temperature: keep tablets below 25°C in original packaging, protect from moisture.

What does Ruxolitinib interact with?

Jakavi can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ruxolitinib exposure. - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce therapeutic levels.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): potential for altered bleeding risk. - Vaccines (live attenuated): reduced vaccine efficacy. - Other immunosuppressants: additive risk of infection. - CYP3A4 substrates with narrow therapeutic index: monitor plasma levels.

Frequently asked questions

What is Jakavi used for?+
Jakavi (ruxolitinib) is prescribed for adult patients with myelofibrosis and polycythemia vera, two types of myeloproliferative disorders. In myelofibrosis it helps shrink an enlarged spleen and eases disease‑related symptoms, while in polycythemia vera it assists in controlling hematocrit levels and reduces the need for regular phlebotomy.
How does ruxolitinib work?+
Ruxolitinib works by selectively blocking the activity of Janus kinase 1 and 2 (JAK1/JAK2). These enzymes are central to cytokine signaling that drives abnormal blood cell production and inflammation. Inhibiting JAK1/JAK2 dampens downstream STAT activation, thereby reducing the proliferation of malignant myeloid cells and alleviating inflammatory symptoms.
What is the usual dose of Jakavi?+
The dosage of Jakavi is individualized and determined by the prescribing physician based on the patient’s specific condition, disease severity, and laboratory parameters. Healthcare providers adjust the dose according to response and tolerability, following the approved prescribing information.
Is Jakavi safe during pregnancy or breastfeeding?+
Safety data for Jakavi in pregnancy and lactation are limited, and the product is classified as having an unknown pregnancy category. It should only be used if the potential benefit justifies the potential risk to the fetus or infant. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss alternatives with their healthcare professional.
How do I order Jakavi from GNH USA?+
To order Jakavi, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, and will request verification of trade or institutional credentials. After confirmation, the sales team provides pricing, availability, shipping details (including any cold‑chain requirements), and assists with import documentation.
How does Jakavi compare with the main alternative drug or class?+
The primary alternative to Jakavi in myeloproliferative disorders is fedratinib, another JAK2‑selective inhibitor, and hydroxyurea, a cytoreductive agent. Jakavi targets both JAK1 and JAK2, offering broader cytokine modulation, which can translate into greater spleen volume reduction in myelofibrosis. Fedratinib may be preferred when Jakavi is not tolerated, while hydroxyurea remains a first‑line option for polycythemia vera but does not address splenomegaly as effectively.
How should Jakavi be stored and handled?+
Jakavi tablets should be stored at ambient temperature, below 25 °C, in the original blister pack to protect them from moisture and light. Keep the medication out of reach of children and do not use if the packaging is damaged or the tablets appear discolored.
How is Jakavi administered?+
Jakavi is taken orally as a tablet, usually with water. It can be taken with or without food, but patients should follow the specific timing instructions provided by their prescriber to maintain consistent drug exposure.
What are the most serious risks to watch for while taking Jakavi?+
Serious risks include severe infections (such as opportunistic or bacterial infections), hepatic dysfunction indicated by elevated liver enzymes or hepatitis, pulmonary hypertension, and the possible development of secondary malignancies. Patients should promptly report fever, persistent cough, jaundice, shortness of breath, or unexplained weight loss to their healthcare provider.
Who should not use Jakavi?+
Jakavi should be avoided in patients with known hypersensitivity to ruxolitinib or any tablet excipients. It is also contraindicated in individuals with active, uncontrolled infections, severe hepatic impairment, or those who are pregnant or breastfeeding without a clear medical justification. Clinicians must evaluate each patient’s medical history before initiating therapy.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Ruxolitinib
Route
Oral Use
Manufacturer
Novartis Europharm Limited
Origin
EU

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