GNH USA

Europe — EMA

Jakavi

GNH USA supplies Jakavi (Ruxolitinib), a Janus kinase inhibitor for myelofibrosis, polycythemia vera and acute graft‑versus‑host disease.

Ruxolitinib

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What is Ruxolitinib?

Ruxolitinib, the active ingredient in Jakavi, is a Janus kinase (JAK) inhibitor presented as a tablet for oral use. It treats certain hematologic malignancies, specifically myelofibrosis, polycythemia vera, and acute graft‑versus‑host disease, in adult patients, and can improve disease‑related symptoms and quality of life.

GNH USA supplies Jakavi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide. The company follows stringent quality standards and provides full regulatory documentation to facilitate import, registration and clinical use in multiple regions.

What is Ruxolitinib used for?

Jakavi (ruxolitinib) is indicated for several myeloproliferative disorders and immune‑mediated conditions where JAK‑STAT signaling contributes to disease pathology.

Myelofibrosis: reduces spleen size, improves blood counts and alleviates constitutional symptoms such as fatigue and night sweats. Polycythemia vera: helps control elevated hematocrit, reduces thrombotic risk and decreases the frequency of therapeutic phlebotomy. Acute graft‑versus‑host disease: moderates donor‑derived immune response, leading to improvement in skin rash, liver enzyme elevation and gastrointestinal inflammation.

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 - Thrombocytopenia - Diarrhea

Serious or Rare Side Effects: - Severe infections, including opportunistic pathogens - Reactivation of hepatitis B virus - Pulmonary hypertension

What precautions apply to Ruxolitinib?

Before and during treatment, clinicians should observe several safety measures. - Monitor blood counts: regular CBC testing to detect cytopenias. - Assess infection risk: screen for active infections before initiating therapy. - Liver function: evaluate hepatic enzymes periodically. - Pregnancy: avoid use unless benefits outweigh potential risks, as safety is unknown. - Drug interactions: avoid concomitant strong CYP3A4 inhibitors without dose adjustment. - Store at ambient temperature: keep tablets in original container, protect from moisture and light.

What does Ruxolitinib interact with?

Ruxolitinib can interact with other medicines, requiring careful management.

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase ruxolitinib exposure. - Potent CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce efficacy. - Live vaccines: increased risk of infection.

Moderate Interactions (Monitor Closely): - Moderate CYP3A4 inhibitors (e.g., fluconazole): may require dose adjustment. - Anticoagulants (e.g., warfarin): may enhance bleeding risk, monitor INR. - Antiplatelet agents (e.g., aspirin): monitor for thrombocytopenia.

Frequently asked questions

What conditions is Jakavi used to treat?+
Jakavi (ruxolitinib) is approved for the treatment of myelofibrosis, polycythemia vera, and acute graft‑versus‑host disease. In each case the drug targets abnormal JAK‑STAT signaling that drives disease progression, helping to control blood counts, reduce organ enlargement, and mitigate immune‑mediated tissue damage.
How does ruxolitinib work in the body?+
Ruxolitinib blocks the activity of Janus kinase 1 and 2 (JAK1/JAK2), enzymes that transmit signals from cytokine receptors to the nucleus via the STAT pathway. By inhibiting this cascade, the drug reduces abnormal cell proliferation and dampens inflammatory signaling that underlies the listed hematologic and immune disorders.
What is the usual dose of Jakavi?+
The dose of Jakavi is individualized by the prescribing physician based on the specific indication, patient weight, blood‑count parameters and tolerability. Dosing may be adjusted over time, and any changes should be made only under medical supervision.
Is Jakavi safe to use during pregnancy or breastfeeding?+
Safety of ruxolitinib in pregnancy and lactation has not been established. The product is classified as pregnancy category unknown, and it is generally advised to avoid use unless the potential benefit justifies the potential risk to the fetus or infant.
How do I order Jakavi from GNH USA?+
To request 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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.
How does Jakavi compare with other JAK inhibitors?+
Jakavi (ruxolitinib) is a first‑generation JAK1/JAK2 inhibitor, whereas alternatives such as fedratinib target JAK2 more selectively. Clinical data suggest comparable efficacy in myelofibrosis, but safety profiles differ; for example, fedratinib has a higher reported incidence of gastrointestinal toxicity, while ruxolitinib is more associated with cytopenias.
What are the recommended storage conditions for Jakavi?+
Jakavi tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from excess moisture, heat and direct sunlight to maintain product stability throughout its shelf life.
How is Jakavi administered to patients?+
Jakavi is taken orally as a tablet, usually with water. It can be swallowed with or without food, but patients should follow the dosing schedule prescribed by their clinician and avoid crushing or chewing the tablet.
What are the most serious risks associated with Jakavi?+
The most serious risks include severe or opportunistic infections, reactivation of hepatitis B, pulmonary hypertension, significant liver enzyme elevations, and the possible development of secondary malignancies. Patients should be monitored closely for signs of infection, respiratory symptoms, and abnormal laboratory values.
Who should not use Jakavi?+
Jakavi is contraindicated in patients with severe hepatic impairment, active uncontrolled infections, and in pregnant women unless the benefit outweighs the risk. Caution is also advised for individuals with a history of severe cardiovascular disease or known hypersensitivity to ruxolitinib.
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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