EVEROLIMUS TARO 10 MG

Země: Izrael

Jazyk: angličtina

Zdroj: Ministry of Health

Koupit nyní

Aktivní složka:

EVEROLIMUS

Dostupné s:

TARO INTERNATIONAL LTD, ISRAEL

ATC kód:

L04AA18

Léková forma:

TABLETS

Složení:

EVEROLIMUS 10 MG

Podání:

PER OS

Druh předpisu:

Required

Výrobce:

SYNTHON CHILE LTDA, CHILE

Terapeutické oblasti:

EVEROLIMUS

Terapeutické indikace:

- For the treatment of patients with SEGA associated with tuberous sclerosis complex (TSC) who require therapeutic intervention but are not candidates for curative surgical resection. The effectiveness of Everolimus Taro is based on an analysis of change in SEGA volume. Clinical benefit such as improvement in disease-related symptoms or increase in overall survival has not been demonstrated.- Treatment of progressive neuroendocrine tumors of pancreatic origin (PNET) in patients with unresectable, locally advanced or metastatic disease.The safety and effectiveness of Everolimus Taro in the treatment of patients with carcinoid tumors have not been established.- For the treatment of hormone receptor – positive, HER2/neu negative advanced breast cancer, in combination with exemestane, in postmenopausal women without symptomatic visceral disease after recurrence or progression follwing a non – steroidal aromatase inhibitor.- Everolimus Taro is indicated for the treatment of adult patients with renal angiomyolipoma and tuberous sclerosis complex (TSC), not requiring immediate surgery. The effectiveness of Everolimus Taro in treatment of renal angiomyolipoma is based on an analysis of durable objective responses in patients treated for a median of 8.3 months. Further follow-up of patients is required to determine long-term outcomes.- Everolimus Taro is indicated for the treatment of patients with advanced renal cell carcinoma, whose disease has progressed on or after treatment with VEGF-targeted therapy.- Treatment of unresectable, locally advanced or metastatic, well-differentiated (Grade 1 or Grade 2) non-functional neuroendocrine tumours of gastrointestinal or lung origin in adults with progressive disease.

Datum autorizace:

2021-08-04

Informace pro uživatele

                                Page 1 of 10
PATIENT LEAFLET IN ACCORDANCE WITH THE PHARMACISTS' REGULATIONS
(PREPARATIONS) - 1986
The medicine is dispensed with a doctor’s prescription only
EVEROLIMUS TARO 2.5 MG,
EVEROLIMUS TARO 5 MG, EVEROLIMUS TARO 10 MG
TABLETS
TABLETS
TABLETS
ACTIVE INGREDIENT:
ACTIVE INGREDIENT:
ACTIVE INGREDIENT:
Each tablet contains:
Each tablet contains:
Each tablet contains:
everolimus 2.5 mg
everolimus 5 mg
everolimus 10 mg
Inactive ingredients and allergens: See section 2 under 'Important
information regarding
some of this medicine's ingredients' and section 6 'Further
Information'.
READ THE ENTIRE LEAFLET CAREFULLY BEFORE YOU START USING THIS
MEDICINE. This leaflet
contains concise information about this medicine. If you have further
questions, consult your
doctor or pharmacist.
This medicine has been prescribed to treat your illness. Do not pass
it on to others. It may
harm them, even if it seems to you that their illness is similar to
yours.
1.
WHAT IS THIS MEDICINE INTENDED FOR?
Everolimus Taro 2.5, 5 and 10 mg tablets are intended for:
•
Treatment of patients with a subependymal giant cell astrocytoma
(SEGA), a type of
brain tumor associated with tuberous sclerosis complex (TSC) for whom
surgery is
not appropriate.
•
Treatment of adult patients with a kidney tumor known as
angiomyolipoma (AML)
when the kidney tumor does not require immediate surgery. This type of
tumor is
associated with a genetic condition known as tuberous sclerosis
complex.
•
Treatment of advanced hormone receptor-positive and HER2-negative
breast cancer,
in conjunction with exemestane, in postmenopausal women without
symptomatic
metastatic disease spread to internal organs, after recurrence or
progression of the
disease following treatment with nonsteroidal aromatase inhibitors.
•
Treatment of advanced kidney cancer [advanced renal cell carcinoma
(RCC)], where
other treatments that target vascular endothelial growth factor
(VEGF-targeted
therapy) have not helped stop your disease.
•
Treatment of locally advanced, metastatic or 
                                
                                Přečtěte si celý dokument
                                
                            

Dokumenty v jiných jazycích

Informace pro uživatele Informace pro uživatele arabština 27-02-2023
Informace pro uživatele Informace pro uživatele hebrejština 27-02-2023

Vyhledávejte upozornění související s tímto produktem

Zobrazit historii dokumentů