Mixtard

Country: European Union

Language: Maltese

Source: EMA (European Medicines Agency)

Active ingredient:

Insulin human

Available from:

Novo Nordisk A/S

ATC code:

A10AD01

INN (International Name):

insulin human (rDNA)

Therapeutic group:

Drogi użati fid-dijabete

Therapeutic area:

Diabetes Mellitus

Therapeutic indications:

Trattament tad-dijabete mellitus.

Product summary:

Revision: 19

Authorization status:

Awtorizzat

Authorization date:

2002-10-07

Patient Information leaflet

                                53
B. FULJETT TA' TAGĦRIF
54
FULJETT TA’ TAGĦRIF: INFORMAZZJONI GĦALL-UTENT
MIXTARD 30 40 UI/ML (UNITÀ INTERNAZZJONALI/ML) SUSPENSJONI
GĦALL-INJEZZJONI F'KUNJETT
insulina umana
AQRA SEW DAN IL-FULJETT KOLLU QABEL TIBDA TUŻA DIN IL-MEDIĊINA
PERESS LI FIH INFORMAZZJONI
IMPORTANTI GĦALIK.
-
Żomm dan il-fuljett. Jista’ jkollok bżonn terġa’ taqrah.
-
Jekk ikollok aktar mistoqsijiet, staqsi lit-tabib, lill-ispiżjar jew
lill-infermier tiegħek.
-
Din il-mediċina ġiet mogħtija lilek biss. M’għandekx tgħaddiha
lil persuni oħra. Tista’
tagħmlilhom il-ħsara, anke jekk għandhom l-istess sinjali ta’
mard bħal tiegħek.
-
Jekk ikollok xi effett sekondarju kellem lit-tabib, lill-ispiżjar jew
lill-infermier tiegħek. Dan
jinkludi xi effett sekondarju possibbli li mhuwiex elenkat f’dan
il-fuljett. Ara sezzjoni 4.
1.
X’INHU MIXTARD U GЋALXIEX JINTUŻA
Mixtard hu insulina umana li għandu effett kemm li jaħdem malajr kif
ukoll li jibqa’ jaħdem fit-tul.
Mixtard jintuża biex inaqqas il-livell għoli ta’ zokkor fid-demm
f’pazjenti bid-dijabete mellitus (id-
dijabete). Id-dijabete hija marda fejn il-ġisem tiegħek ma jagħmilx
biżżejjed insulina biex jikkontrolla
l-livell taz-zokkor fid-demm tiegħek. Il-kura b’Mixtard tgħin biex
tippreveni kumplikazzjonijiet mid-
dijabete tiegħek.
Mixtard se jibda jbaxxilek il-livell taz-zokkor fid-demm madwar 30
minuta wara li tinjettah u l-effett
idum għal madwar 24 siegħa.
2.
X'GĦANDEK TKUN TAF QABEL MA TUŻA MIXTARD
TUŻAX MIXTARD
►
Jekk inti allerġiku/a għall-insulina umana jew għal xi sustanza
oħra ta’ din il-mediċina, ara
sezzjoni 6.
►
Jekk qiegħed/qiegħda tissusspetta bidu ta' ipogliċemija (livell
baxx ta’ zokkor fid-demm), ara_ _a)
Sommarju ta’ effetti sekondarji serji u komuni ħafna f’sezzjoni
4.
►
F’pompi tal-infużjoni tal-insulina
►
Jekk l-għatu protettiv huwa laxk jew nieqes. Kull kunjett għandu
għatu protettiv tal-plastik
magħmul apposta kontra t-tbagħbis. Jekk mhuwiex f’kundizzjoni
perfetta met
                                
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Summary of Product characteristics

                                ANNESS I
SOMMARJU TAL-KARATTERISTIĊI TAL-PRODOTT
2
1.
ISEM IL-PRODOTT MEDIĊINALI
Mixtard 30 40 unità internazzjonali/ml suspensjoni għall-injezzjoni
f’kunjett.
Mixtard 30 100 unità internazzjonali/ml suspensjoni għall-injezzjoni
f’kunjett.
Mixtard 30 Penfill 100 unità internazzjonali/ml suspensjoni
għall-injezzjoni f’skartoċċ.
Mixtard 30 InnoLet 100 unità internazzjonali/ml suspensjoni
għall-injezzjoni f’pinna mimlija għal-
lest.
Mixtard 30 FlexPen 100 unità internazzjonali/ml suspensjoni
għall-injezzjoni f’pinna mimlija għal-
lest.
2.
GĦAMLA KWALITATTIVA U KWANTITATTIVA
_ _
Mixtard 30 f’kunjett (40 unità intern
azzjonali/ml)
Kunjett fih 10 ml ekwivalenti għal 400 unità internazzjonali.
Millilitru ta’ suspensjoni fih 40 unità
internazzjonali ta’ insulina umana li tinħall*/insulina isophane
(NPH) umana* f’proporzjon ta’ 30/70
(ekwivalenti għal 1.4 mg).
Mixtard 30 f’kunjett (100 unità internazzjonali/ml)
Kunjett fih 10 ml ekwivalenti għal 1,000 unità internazzjonali.
Millilitru ta’ suspensjoni fih 100 unità
internazzjonali ta’ insulina umana li tinħall*/insulina isophane
(NPH) umana* f’proporzjon ta’ 30/70
(ekwivalenti għal 3.5 mg).
Mixtard 30 Penfill
Skartoċċ fih 3 ml ekwivalenti għal 300 unità internazzjonali.
Millilitru ta’ suspensjoni fih 100 unità
internazzjonali ta’ insulina umana li tinħall*/insulina isophane
(NPH) umana* f’proporzjon ta’ 30/70
(ekwivalenti għal 3.5 mg).
Mixtard 30 InnoLet/Mixtard 30 FlexPen
Pinna mimlija għal-lest fiha 3 ml ekwivalenti għal 300 unità
internazzjonali. Millilitru ta’ suspensjoni
fih 100 unità internazzjonali ta’ insulina umana li
tinħall*/insulina isophane (NPH) umana*
f’proporzjon ta’ 30/70 (ekwivalenti għal 3.5 mg).
*L-insulina umana hija magħmula f'_Saccharomyces cerevisiae_ permezz
tat-teknoloġija tad-DNA
rikombinanti
Eċċipjent b’effett magħruf:
Mixtard 30 fih inqas minn mmol 1 ta’ sodium (23 mg) għal kull
doża, i.e Mixtard 30 huwa
essenzjalment ‘bla sodium’.
Għal-lista
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 24-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 24-01-2024
Public Assessment Report Public Assessment Report Bulgarian 19-09-2014
Patient Information leaflet Patient Information leaflet Spanish 24-01-2024
Public Assessment Report Public Assessment Report Spanish 19-09-2014
Patient Information leaflet Patient Information leaflet Czech 24-01-2024
Public Assessment Report Public Assessment Report Czech 19-09-2014
Patient Information leaflet Patient Information leaflet Danish 24-01-2024
Public Assessment Report Public Assessment Report Danish 19-09-2014
Patient Information leaflet Patient Information leaflet German 24-01-2024
Public Assessment Report Public Assessment Report German 19-09-2014
Patient Information leaflet Patient Information leaflet Estonian 24-01-2024
Public Assessment Report Public Assessment Report Estonian 19-09-2014
Patient Information leaflet Patient Information leaflet Greek 24-01-2024
Public Assessment Report Public Assessment Report Greek 19-09-2014
Patient Information leaflet Patient Information leaflet English 24-01-2024
Public Assessment Report Public Assessment Report English 19-09-2014
Patient Information leaflet Patient Information leaflet French 24-01-2024
Public Assessment Report Public Assessment Report French 19-09-2014
Patient Information leaflet Patient Information leaflet Italian 24-01-2024
Public Assessment Report Public Assessment Report Italian 19-09-2014
Patient Information leaflet Patient Information leaflet Latvian 24-01-2024
Public Assessment Report Public Assessment Report Latvian 19-09-2014
Patient Information leaflet Patient Information leaflet Lithuanian 24-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 24-01-2024
Public Assessment Report Public Assessment Report Lithuanian 19-09-2014
Patient Information leaflet Patient Information leaflet Hungarian 24-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 24-01-2024
Public Assessment Report Public Assessment Report Hungarian 19-09-2014
Patient Information leaflet Patient Information leaflet Dutch 24-01-2024
Public Assessment Report Public Assessment Report Dutch 19-09-2014
Patient Information leaflet Patient Information leaflet Polish 24-01-2024
Public Assessment Report Public Assessment Report Polish 19-09-2014
Patient Information leaflet Patient Information leaflet Portuguese 24-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 24-01-2024
Public Assessment Report Public Assessment Report Portuguese 19-09-2014
Patient Information leaflet Patient Information leaflet Romanian 24-01-2024
Public Assessment Report Public Assessment Report Romanian 19-09-2014
Patient Information leaflet Patient Information leaflet Slovak 24-01-2024
Public Assessment Report Public Assessment Report Slovak 19-09-2014
Patient Information leaflet Patient Information leaflet Slovenian 24-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 24-01-2024
Public Assessment Report Public Assessment Report Slovenian 19-09-2014
Patient Information leaflet Patient Information leaflet Finnish 24-01-2024
Public Assessment Report Public Assessment Report Finnish 19-09-2014
Patient Information leaflet Patient Information leaflet Swedish 24-01-2024
Public Assessment Report Public Assessment Report Swedish 19-09-2014
Patient Information leaflet Patient Information leaflet Norwegian 24-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 24-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 24-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 24-01-2024
Patient Information leaflet Patient Information leaflet Croatian 24-01-2024

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