Intrinsa

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Testosterone

Available from:

Warner Chilcott UK Ltd.

ATC code:

G03BA03

INN (International Name):

testosterone

Therapeutic group:

- Ormoni tas-sess u modulaturi ta ' l-ġenitali-sistema,

Therapeutic area:

Disfunzjonijiet Sesswali, Psikoloġiċi

Therapeutic indications:

Intrinsa huwa indikat għall-kura ta ' l-hypoactive sesswali xewqa diżordni (HSDD) fin-nisa (menopause mezz kirurġikament indotti) bilateralment oophorectomised u hysterectomised li tirċievi estrogen konkomittenti terapija.

Product summary:

Revision: 6

Authorization status:

Irtirat

Authorization date:

2006-07-28

Patient Information leaflet

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
Prodott mediċinali li m’għadux awtorizzat
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Intrinsa 300 mikrogramma/24 siegħa garża li tipprovdi mediċina li
tgħaddi minn ġol-ġilda
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
_ _
Kull garża ta’ 28 ċm
2
fiha 8.4 mg ta’ testosterone u tipprovdi 300 mikrogramma ta’
testosterone kull
24 siegħa.
Għal-lista kompleta ta’ sustanzi mhux attivi, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Garża li tipprovdi mediċina li tgħaddi minn ġol-ġilda.
Garża li tipprovdi mediċina li tgħaddi minn ġol-ġilda irqiqa,
ċara, u ovali,
_matrix-type_
, li tikkonsisti fi
tliet saffi: Rita ta’ rinforz fid-dahar, transluċida, b’saff
ta’ mediċina
_matrix_
li twaħħal, u b’inforra li
tipproteġi r-reħi tal-mediċina, li titneħħa qabel ma titwaħħal.
Kull wiċċ tal-garża hu stampat bil-kliem
T001.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Intrinsa hu indikat għat-trattament ta’ mard li fih persuna jkollha
nuqqas ta’ xewqa sesswali
_(hypoactive sexual desire disorder, HSDD)_
f’nisa li kellhom ooforektomija u isterektomija b’mod
bilaterali (menopawsa ikkaġunata b’mod kirurġiku) li kienu qed
jirċievu terapija bl-estroġenu fl-istess
ħin.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Pożoloġija
Id-doża rakkomandata ta’ kuljum ta’ testosterone hi ta’ 300
mikrogramma. Din tinkiseb billi l-garża
tiġi applikata darbtejn f’ġimgħa fuq bażi kontinwa. Il-garża
għandha tinbidel b’garża ġdida kull 3 sa
4 ijiem. Għandha titwaħħal garża waħda biss f’ħin wieħed
_._
_It-trattament bl-estroġenu fl-istess ħin _
L-użu xieraq u restrizzjonijiet marbuta mat-terapija bl-estroġenu
għandhom jiġu kkunsidrati qabel ma
tinbeda t-terapija b’Intrinsa, u matul l-evalwazzjoni mill-ġdid
ta’ rutina tat-trattament. It-tkomplija ta’
l-użu b’Intrinsa hu rakkomandat biss meta l-użu fl-istess ħin
ta’ l-estroġenu hu kkunsidrat li hu adattat
(i.e. l-inqas doża effettiva għa
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
Prodott mediċinali li m’għadux awtorizzat
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Intrinsa 300 mikrogramma/24 siegħa garża li tipprovdi mediċina li
tgħaddi minn ġol-ġilda
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
_ _
Kull garża ta’ 28 ċm
2
fiha 8.4 mg ta’ testosterone u tipprovdi 300 mikrogramma ta’
testosterone kull
24 siegħa.
Għal-lista kompleta ta’ sustanzi mhux attivi, ara sezzjoni 6.1.
3.
GĦAMLA FARMAĊEWTIKA
Garża li tipprovdi mediċina li tgħaddi minn ġol-ġilda.
Garża li tipprovdi mediċina li tgħaddi minn ġol-ġilda irqiqa,
ċara, u ovali,
_matrix-type_
, li tikkonsisti fi
tliet saffi: Rita ta’ rinforz fid-dahar, transluċida, b’saff
ta’ mediċina
_matrix_
li twaħħal, u b’inforra li
tipproteġi r-reħi tal-mediċina, li titneħħa qabel ma titwaħħal.
Kull wiċċ tal-garża hu stampat bil-kliem
T001.
4.
TAGĦRIF KLINIKU
4.1
INDIKAZZJONIJIET TERAPEWTIĊI
Intrinsa hu indikat għat-trattament ta’ mard li fih persuna jkollha
nuqqas ta’ xewqa sesswali
_(hypoactive sexual desire disorder, HSDD)_
f’nisa li kellhom ooforektomija u isterektomija b’mod
bilaterali (menopawsa ikkaġunata b’mod kirurġiku) li kienu qed
jirċievu terapija bl-estroġenu fl-istess
ħin.
4.2
POŻOLOĠIJA U METODU TA’ KIF GĦANDU JINGĦATA
Pożoloġija
Id-doża rakkomandata ta’ kuljum ta’ testosterone hi ta’ 300
mikrogramma. Din tinkiseb billi l-garża
tiġi applikata darbtejn f’ġimgħa fuq bażi kontinwa. Il-garża
għandha tinbidel b’garża ġdida kull 3 sa
4 ijiem. Għandha titwaħħal garża waħda biss f’ħin wieħed
_._
_It-trattament bl-estroġenu fl-istess ħin _
L-użu xieraq u restrizzjonijiet marbuta mat-terapija bl-estroġenu
għandhom jiġu kkunsidrati qabel ma
tinbeda t-terapija b’Intrinsa, u matul l-evalwazzjoni mill-ġdid
ta’ rutina tat-trattament. It-tkomplija ta’
l-użu b’Intrinsa hu rakkomandat biss meta l-użu fl-istess ħin
ta’ l-estroġenu hu kkunsidrat li hu adattat
(i.e. l-inqas doża effettiva għa
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 18-06-2012
Summary of Product characteristics Summary of Product characteristics Bulgarian 18-06-2012
Public Assessment Report Public Assessment Report Bulgarian 18-06-2012
Patient Information leaflet Patient Information leaflet Spanish 18-06-2012
Public Assessment Report Public Assessment Report Spanish 18-06-2012
Patient Information leaflet Patient Information leaflet Czech 18-06-2012
Public Assessment Report Public Assessment Report Czech 18-06-2012
Patient Information leaflet Patient Information leaflet Danish 18-06-2012
Public Assessment Report Public Assessment Report Danish 18-06-2012
Patient Information leaflet Patient Information leaflet German 18-06-2012
Public Assessment Report Public Assessment Report German 18-06-2012
Patient Information leaflet Patient Information leaflet Estonian 18-06-2012
Public Assessment Report Public Assessment Report Estonian 18-06-2012
Patient Information leaflet Patient Information leaflet Greek 18-06-2012
Public Assessment Report Public Assessment Report Greek 18-06-2012
Patient Information leaflet Patient Information leaflet English 18-06-2012
Public Assessment Report Public Assessment Report English 18-06-2012
Patient Information leaflet Patient Information leaflet French 18-06-2012
Public Assessment Report Public Assessment Report French 18-06-2012
Patient Information leaflet Patient Information leaflet Italian 18-06-2012
Public Assessment Report Public Assessment Report Italian 18-06-2012
Patient Information leaflet Patient Information leaflet Latvian 18-06-2012
Public Assessment Report Public Assessment Report Latvian 18-06-2012
Patient Information leaflet Patient Information leaflet Lithuanian 18-06-2012
Summary of Product characteristics Summary of Product characteristics Lithuanian 18-06-2012
Public Assessment Report Public Assessment Report Lithuanian 18-06-2012
Patient Information leaflet Patient Information leaflet Hungarian 18-06-2012
Summary of Product characteristics Summary of Product characteristics Hungarian 18-06-2012
Public Assessment Report Public Assessment Report Hungarian 18-06-2012
Patient Information leaflet Patient Information leaflet Dutch 18-06-2012
Public Assessment Report Public Assessment Report Dutch 18-06-2012
Patient Information leaflet Patient Information leaflet Polish 18-06-2012
Public Assessment Report Public Assessment Report Polish 18-06-2012
Patient Information leaflet Patient Information leaflet Portuguese 18-06-2012
Summary of Product characteristics Summary of Product characteristics Portuguese 18-06-2012
Public Assessment Report Public Assessment Report Portuguese 18-06-2012
Patient Information leaflet Patient Information leaflet Romanian 18-06-2012
Public Assessment Report Public Assessment Report Romanian 18-06-2012
Patient Information leaflet Patient Information leaflet Slovak 18-06-2012
Public Assessment Report Public Assessment Report Slovak 18-06-2012
Patient Information leaflet Patient Information leaflet Slovenian 18-06-2012
Summary of Product characteristics Summary of Product characteristics Slovenian 18-06-2012
Public Assessment Report Public Assessment Report Slovenian 18-06-2012
Patient Information leaflet Patient Information leaflet Finnish 18-06-2012
Public Assessment Report Public Assessment Report Finnish 18-06-2012
Patient Information leaflet Patient Information leaflet Swedish 18-06-2012
Public Assessment Report Public Assessment Report Swedish 18-06-2012
Patient Information leaflet Patient Information leaflet Norwegian 18-06-2012
Summary of Product characteristics Summary of Product characteristics Norwegian 18-06-2012
Patient Information leaflet Patient Information leaflet Icelandic 18-06-2012
Summary of Product characteristics Summary of Product characteristics Icelandic 18-06-2012

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