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Hazel Melia
Medical Advisor, Haematology
NOW AVAILABLE
Want to know more about OMJJARA▼ (momelotinib)?
Get in touch with your local GSK Ireland Team today to learn more.
Adverse event reporting information can be found at the bottom of this page
Summary of product characteristics & Patient information leaflet for 100 mg, 150 mg and 200 mg film coated tablets
INDICATION
OMJJARA is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with moderate to severe anaemia who have primary myelofibrosis, post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis and who are Janus Kinase (JAK) inhibitor naïve or have been treated with ruxolitinib.
Reference
- OMJJARA Summary of Product Characteristics (SPC), available on www.medicines.ie/medicines/omjjara-100-150-200-mg-film-coated-tablets-36329/spc. Last accessed: September 2024.
▼This medicine is subject to additional monitoring. This will allow quick identification of new safety information.
Adverse events should be reported directly to the Health Products Regulatory Authority (HPRA) on their website: www.hpra.ie.
Adverse events should also be reported to GlaxoSmithKline on 1800 244 255.
Omjjara is a registered trademark of the GlaxoSmithKline group of companies.
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September 2024 | PM-IE-MML-WCNT-240002
