Revolade 25 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

revolade 25 mg filmsko obložene tablete

novartis europharm limited - eltrombopag - filmsko obložena tableta - eltrombopag 25 mg / 1 tableta - eltrombopag

Revolade 25 mg prašek za peroralno suspenzijo Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

revolade 25 mg prašek za peroralno suspenzijo

novartis europharm limited - eltrombopag - prašek za peroralno suspenzijo - eltrombopag 25 mg / 1 vrečica - eltrombopag

Revolade 50 mg filmsko obložene tablete Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

revolade 50 mg filmsko obložene tablete

novartis europharm limited - eltrombopag - filmsko obložena tableta - eltrombopag 50 mg / 1 tableta - eltrombopag

Revolade Evropska unija - slovenščina - EMA (European Medicines Agency)

revolade

novartis europharm limited - eltrombopag - purpura, trombocitopenična, idiopatska - other systemic hemostatics, antihemorrhagics - revolade is indicated for the treatment of adult patients with primary immune thrombocytopenia (itp) who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 in 5. revolade is indicated for the treatment of paediatric patients aged 1 year and above with primary immune thrombocytopenia (itp) lasting 6 months or longer from diagnosis and who are refractory to other treatments (e. corticosteroids, immunoglobulins) (see sections 4. 2 in 5. 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. 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.