Votubia

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

everolimus

Available from:

Novartis Europharm Limited

ATC code:

L01XE10

INN (International Name):

everolimus

Therapeutic group:

Antineoplastic agents

Therapeutic area:

Tuberous Sclerosis

Therapeutic indications:

Renal angiomyolipoma associated with tuberous sclerosis complex (TSC)Votubia is indicated for the treatment of adult patients with renal angiomyolipoma associated with tuberous sclerosis complex (TSC) who are at risk of complications (based on factors such as tumour size or presence of aneurysm, or presence of multiple or bilateral tumours) but who do not require immediate surgery.The evidence is based on analysis of change in sum of angiomyolipoma volume.Subependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis complex (TSC)Votubia is indicated for the treatment of patients with subependymal giant cell astrocytoma (SEGA) associated with tuberous sclerosis complex (TSC) who require therapeutic intervention but are not amenable to surgery.The evidence is based on analysis of change in SEGA volume. Further clinical benefit, such as improvement in disease‑related symptoms, has not been demonstrated.

Product summary:

Revision: 30

Authorization status:

Authorised

Authorization date:

2011-09-02

Patient Information leaflet

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Votubia 2.5 mg tablets
Votubia 5 mg tablets
Votubia 10 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Votubia 2.5 mg tablets
Each tablet contains 2.5 mg everolimus.
_Excipient with known effect _
Each tablet contains 74 mg lactose.
Votubia 5 mg tablets
Each tablet contains 5 mg everolimus.
_Excipient with known effect _
Each tablet contains 149 mg lactose.
Votubia 10 mg tablets
Each tablet contains 10 mg everolimus.
_Excipient with known effect _
Each tablet contains 297 mg lactose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet.
Votubia 2.5 mg tablets
White to slightly yellow, elongated tablets of approximately 10.1 mm
in length and 4.1 mm in width,
with a bevelled edge and no score, engraved with “LCL” on one side
and “NVR” on the other.
Votubia 5 mg tablets
White to slightly yellow, elongated tablets of approximately 12.1 mm
in length and 4.9 mm in width,
with a bevelled edge and no score, engraved with “5” on one side
and “NVR” on the other.
Votubia 10 mg tablets
White to slightly yellow, elongated tablets of approximately 15.1 mm
in length and 6.0 mm in width,
with a bevelled edge and no score, engraved with “UHE” on one side
and “NVR” on the other.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Renal angiomyolipoma associated with tuberous sclerosis complex (TSC)
Votubia is indicated for the treatment of adult patients with renal
angiomyolipoma associated with
TSC who are at risk of complications (based on factors such as tumour
size or presence of aneurysm,
or presence of multiple or bilateral tumours) but who do not require
immediate surgery.
The evidence is based on analysis of change in sum of angiomyolipoma
volume.
Subependymal giant cell astrocytoma (SEGA) associated with TSC
Votubia is indicated for the treatment of adult and paediatric
patients with SEGA associated with TSC
who require therapeutic intervention but are not amenable to surgery.
The evi
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Votubia 2.5 mg tablets
Votubia 5 mg tablets
Votubia 10 mg tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Votubia 2.5 mg tablets
Each tablet contains 2.5 mg everolimus.
_Excipient with known effect _
Each tablet contains 74 mg lactose.
Votubia 5 mg tablets
Each tablet contains 5 mg everolimus.
_Excipient with known effect _
Each tablet contains 149 mg lactose.
Votubia 10 mg tablets
Each tablet contains 10 mg everolimus.
_Excipient with known effect _
Each tablet contains 297 mg lactose.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Tablet.
Votubia 2.5 mg tablets
White to slightly yellow, elongated tablets of approximately 10.1 mm
in length and 4.1 mm in width,
with a bevelled edge and no score, engraved with “LCL” on one side
and “NVR” on the other.
Votubia 5 mg tablets
White to slightly yellow, elongated tablets of approximately 12.1 mm
in length and 4.9 mm in width,
with a bevelled edge and no score, engraved with “5” on one side
and “NVR” on the other.
Votubia 10 mg tablets
White to slightly yellow, elongated tablets of approximately 15.1 mm
in length and 6.0 mm in width,
with a bevelled edge and no score, engraved with “UHE” on one side
and “NVR” on the other.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Renal angiomyolipoma associated with tuberous sclerosis complex (TSC)
Votubia is indicated for the treatment of adult patients with renal
angiomyolipoma associated with
TSC who are at risk of complications (based on factors such as tumour
size or presence of aneurysm,
or presence of multiple or bilateral tumours) but who do not require
immediate surgery.
The evidence is based on analysis of change in sum of angiomyolipoma
volume.
Subependymal giant cell astrocytoma (SEGA) associated with TSC
Votubia is indicated for the treatment of adult and paediatric
patients with SEGA associated with TSC
who require therapeutic intervention but are not amenable to surgery.
The evi
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 27-06-2022
Summary of Product characteristics Summary of Product characteristics Bulgarian 27-06-2022
Public Assessment Report Public Assessment Report Bulgarian 15-06-2018
Patient Information leaflet Patient Information leaflet Spanish 27-06-2022
Public Assessment Report Public Assessment Report Spanish 15-06-2018
Patient Information leaflet Patient Information leaflet Czech 27-06-2022
Public Assessment Report Public Assessment Report Czech 15-06-2018
Patient Information leaflet Patient Information leaflet Danish 27-06-2022
Public Assessment Report Public Assessment Report Danish 15-06-2018
Patient Information leaflet Patient Information leaflet German 27-06-2022
Public Assessment Report Public Assessment Report German 15-06-2018
Patient Information leaflet Patient Information leaflet Estonian 27-06-2022
Public Assessment Report Public Assessment Report Estonian 15-06-2018
Patient Information leaflet Patient Information leaflet Greek 27-06-2022
Public Assessment Report Public Assessment Report Greek 15-06-2018
Patient Information leaflet Patient Information leaflet French 27-06-2022
Public Assessment Report Public Assessment Report French 15-06-2018
Patient Information leaflet Patient Information leaflet Italian 27-06-2022
Public Assessment Report Public Assessment Report Italian 15-06-2018
Patient Information leaflet Patient Information leaflet Latvian 27-06-2022
Public Assessment Report Public Assessment Report Latvian 15-06-2018
Patient Information leaflet Patient Information leaflet Lithuanian 27-06-2022
Summary of Product characteristics Summary of Product characteristics Lithuanian 27-06-2022
Public Assessment Report Public Assessment Report Lithuanian 15-06-2018
Patient Information leaflet Patient Information leaflet Hungarian 27-06-2022
Summary of Product characteristics Summary of Product characteristics Hungarian 27-06-2022
Public Assessment Report Public Assessment Report Hungarian 15-06-2018
Patient Information leaflet Patient Information leaflet Maltese 27-06-2022
Public Assessment Report Public Assessment Report Maltese 15-06-2018
Patient Information leaflet Patient Information leaflet Dutch 27-06-2022
Public Assessment Report Public Assessment Report Dutch 15-06-2018
Patient Information leaflet Patient Information leaflet Polish 27-06-2022
Public Assessment Report Public Assessment Report Polish 15-06-2018
Patient Information leaflet Patient Information leaflet Portuguese 27-06-2022
Summary of Product characteristics Summary of Product characteristics Portuguese 27-06-2022
Public Assessment Report Public Assessment Report Portuguese 15-06-2018
Patient Information leaflet Patient Information leaflet Romanian 27-06-2022
Public Assessment Report Public Assessment Report Romanian 15-06-2018
Patient Information leaflet Patient Information leaflet Slovak 27-06-2022
Public Assessment Report Public Assessment Report Slovak 15-06-2018
Patient Information leaflet Patient Information leaflet Slovenian 27-06-2022
Summary of Product characteristics Summary of Product characteristics Slovenian 27-06-2022
Public Assessment Report Public Assessment Report Slovenian 15-06-2018
Patient Information leaflet Patient Information leaflet Finnish 27-06-2022
Public Assessment Report Public Assessment Report Finnish 15-06-2018
Patient Information leaflet Patient Information leaflet Swedish 27-06-2022
Public Assessment Report Public Assessment Report Swedish 15-06-2018
Patient Information leaflet Patient Information leaflet Norwegian 27-06-2022
Summary of Product characteristics Summary of Product characteristics Norwegian 27-06-2022
Patient Information leaflet Patient Information leaflet Icelandic 27-06-2022
Summary of Product characteristics Summary of Product characteristics Icelandic 27-06-2022
Patient Information leaflet Patient Information leaflet Croatian 27-06-2022
Public Assessment Report Public Assessment Report Croatian 15-06-2018

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