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REVOLADE 25MG contains Eltrombopag which belongs to the group of medicines called thrombopoietin receptor agonists

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Revolade is indicated for chronic immune (idiopathic)
thrombocytopenic purpura (ITP) patients aged 1 year and above who are
refractory to other treatments (e.g. corticosteroids, immunoglobulins)
(see sections 4.2 and 5.1).

Revolade is indicated in adult patients with chronic hepatitis C
virus (HCV) infection for the treatment of thrombocytopenia, where the
degree of thrombocytopenia is the main factor preventing the initiation
or limiting the ability to maintain optimal interferon-based therapy
(see sections 4.4 and 5.1).

Revolade is indicated in adult patients with acquired severe aplastic
anaemia (SAA) who were either refractory to prior immunosuppressive
therapy or heavily pretreated and are unsuitable for haematopoietic stem
cell transplantation (see section 5.1).

How is Revolade used?

Revolade(Eltrombopag) is available as tablets (12.5, 25, 50
and 75 mg) and as a powder (25 mg) to prepare a suspension (a liquid to
be taken by mouth). The medicine can only be obtained with a
prescription and treatment should be started and supervised by a doctor
who has experience in treating blood diseases or chronic hepatitis C and
its complications.

The dose depends on the patient’s age and the disease Revolade is
being used to treat; it is adjusted as needed to maintain the
appropriate platelet level. For ITP and aplastic anaemia, a lower
starting dose may be needed in patients of East Asian descent (such as
Chinese, Japanese, Korean or Taiwanese).

Patients should not take any antacids, dairy products or mineral
supplements in the four hours before and in the two hours after taking
Revolade. For more information, see the package leaflet.

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