GNH USA

Europe — EMA

Jakavi

GNH USA supplies Jakavi (Ruxolitinib), a Janus kinase inhibitor for primary myelofibrosis and polycythemia vera. Request a quote for global supply today.

Ruxolitinib

Request sourcing

1
Pack/s

What is Ruxolitinib?

Ruxolitinib, the active ingredient in Jakavi, is a Janus kinase (JAK) inhibitor presented as an oral tablet for oral use. It is indicated for the treatment of primary myelofibrosis, polycythemia vera, and is used off‑label for graft‑versus‑host disease in appropriate patients. GNH USA supplies Jakavi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Ruxolitinib used for?

Jakavi (ruxolitinib) targets dysregulated JAK‑STAT signaling in myeloproliferative disorders and related conditions. - Primary myelofibrosis: reduces spleen size and alleviates disease‑related symptoms. - Polycythemia vera: helps control hematocrit levels and decreases need for phlebotomy. - Graft‑versus‑host disease (off‑label): may mitigate inflammatory manifestations in affected patients.

What are the side effects of Ruxolitinib?

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

Common Side Effects: - Anemia: reduced red blood cell count leading to fatigue. - Thrombocytopenia: lowered platelet levels increasing bleeding risk. - Diarrhea: loose stools that may affect hydration.

Serious or Rare Side Effects: - Infections: heightened susceptibility to bacterial, viral, or fungal infections. - Reactivation of hepatitis B: potential flare of previously controlled hepatitis B infection. - Severe liver injury: marked elevation of liver enzymes or hepatic failure.

What precautions apply to Ruxolitinib?

When prescribing Ruxolitinib, clinicians should consider several safety and handling precautions. - Monitor blood counts: regular CBC testing to detect anemia, thrombocytopenia, or neutropenia. - Assess infection risk: evaluate for active infections before initiation and monitor during therapy. - Evaluate liver function: periodic liver enzyme tests are recommended. - Avoid use in pregnancy unless benefits outweigh risks: discuss potential fetal effects with a specialist. - Review concomitant medications: check for interactions that may alter drug exposure. - Store at ambient temperature: keep in the original pack, protect from moisture.

What does Ruxolitinib interact with?

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

Major Interactions (Avoid): - Strong CYP3A4 inhibitors (e.g., ketoconazole): may increase ruxolitinib exposure. - Strong CYP3A4 inducers (e.g., rifampicin): may reduce therapeutic levels. - Live vaccines: risk of uncontrolled infection due to immunosuppression.

Moderate Interactions (Monitor Closely): - Anticoagulants (e.g., warfarin): may enhance bleeding tendency. - Immunosuppressants (e.g., azathioprine): additive immunosuppression risk. - CYP2C9 substrates (e.g., warfarin): potential alteration of plasma concentrations.

Frequently asked questions

What is Jakavi used for?+
Jakavi (ruxolitinib) is prescribed for patients with primary myelofibrosis and polycythemia vera to control disease‑related symptoms and blood parameters. It is also employed off‑label for certain cases of graft‑versus‑host disease where cytokine‑driven inflammation is a concern.
How does ruxolitinib work?+
Ruxolitinib blocks the activity of Janus kinase 1 and 2 (JAK1/JAK2), key enzymes in the JAK‑STAT signaling pathway. By inhibiting these kinases, the drug reduces abnormal cell proliferation and inflammatory cytokine signaling that underlie myeloproliferative disorders.
What is the usual dose of Jakavi?+
The dosage of Jakavi is individualized and determined by the prescribing physician based on the specific indication, patient weight, blood counts, and tolerability. Patients should follow the dose and schedule provided by their healthcare professional.
Is Jakavi safe during pregnancy or breastfeeding?+
Safety data for ruxolitinib in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies the potential risk to the fetus or infant, and this decision must be made in consultation with a qualified obstetrician or pediatrician.
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 treatments for myelofibrosis?+
Jakavi is a targeted JAK inhibitor, offering a mechanism‑specific approach compared with conventional therapies such as hydroxyurea or interferon. Clinical studies have shown it can more effectively reduce spleen volume and improve symptom burden, though individual response and side‑effect profiles vary.
How should Jakavi be stored and handled?+
Jakavi tablets should be stored at ambient temperature, below 25 °C, in the original container to protect them from moisture and light. Keep the medication out of reach of children and do not use if the packaging is damaged.
How is Jakavi administered?+
Jakavi is taken orally as a tablet, usually with or without food, according to the schedule prescribed by the treating physician. Patients should swallow the tablet whole and avoid crushing or splitting it unless instructed otherwise.
What are the most serious risks to watch for while taking Jakavi?+
Serious risks include severe infections, reactivation of hepatitis B, and significant liver injury. Patients should promptly report signs of infection, jaundice, or unusual bleeding, and undergo regular monitoring of blood counts and liver function tests.
Who should not use Jakavi?+
Jakavi is contraindicated in patients with known hypersensitivity to ruxolitinib or any tablet excipients. It should be used with caution, or avoided, in individuals with active uncontrolled infections, severe hepatic impairment, or in those who are pregnant without a clear benefit‑risk justification.
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

Related products