Probenecid "Medic"

Primær information

  • Handelsnavn:
  • Probenecid "Medic" 250 mg tabletter
  • Dosering:
  • 250 mg
  • Lægemiddelform:
  • tabletter
  • Brugt til:
  • Mennesker
  • Medicin typen:
  • Allopatiske stof

Dokumenter

Lokation

  • Fås i:
  • Probenecid "Medic" 250 mg tabletter
    Danmark
  • Sprog:
  • dansk

Andre oplysninger

Status

  • Kilde:
  • Lægemiddelstyrelsen - Danish Medicines Agency
  • Autorisation status:
  • Markedsført
  • Autorisationsnummer:
  • 07448
  • Sidste ændring:
  • 17-07-2018

Indlægsseddel

INDLÆGSSEDDEL: INFORMATION TIL BRUGEREN

Probenecid ”medic” 250 mg, tabletter

Probenecid

Læs denne indlægsseddel grundigt, inden du begynder at tage dette lægemiddel, da den

indeholder vigtige oplysninger.

Gem indlægssedlen. Du kan få brug for at læse den igen.

Spørg lægen eller på apotekspersonalet, hvis der mere du vil vide.

Lægen har ordineret Probenecid “medic” til dig personligt. Lad derfor være med at give det til

andre. Det kan være skadeligt for andre, selvom de har de samme symptomer, som du har.

Tal med lægen eller apotekspersonalet, hvis en bivirkning bliver værre, eller hvis du får

bivirkninger der ikke er nævnt her.

Den nyeste indlægsseddel for dette produkt kan findes på www.indlaegsseddel.dk.

Oversigt over indlægssedlen

Virkning og anvendelse

Det skal du vide, før du begynder at tage Probenecid ”medic”

Sådan skal du tage Probenecid ”medic”

Bivirkninger

Opbevaring

Pakningsstørrelser og yderligere oplysninger

1.

VIRKNING OG ANVENDELSE

Probenecid ”medic” mindsker gigtbesvær ved at øge udskillelsen af urinsyre. Herved falder

mængden af urinsyre i blodet. Der kommer færre anfald, fordi der aflejres mindre urinsyre i

leddene.

Probenecid nedsætter udskillelsen af penicillin i urinen. Herved bliver mængden af penicillin i

blodet større.

Du kan bruge Probenecid ”medic” til behandling af:

Urinsur gigt (podagra).

Infektioner, når der ønskes større virkning af penicillin.

Probenecid ”medic” hjælper ikke mod betændelse eller ved akutte anfald af podagra.

Lægen kan have foreskrevet anden anvendelse. Følg altid lægens anvisning.

2.

DET SKAL DU VIDE FØR DU BEGYNDER AT TAGE PROBENECID ”MEDIC”

Lægen kan have foreskrevet anden anvendelse eller dosering end angivet i denne information.

Følg altid lægens anvisning og oplysningerne på doseringsetiketten.

Tag ikke Probenecid “medic”, hvis du:

er allergisk overfor probenecid eller et af de øvrige indholdsstoffer i Probenecid ”medic”

(angivet i pkt. 6).

har meget dårlige nyrer

Advarsler og forsigtighedsregler

Kontakt lægen eller apoteket, før du tager Probenecid ”medic”, hvis du har:

dårlige nyrer

mavesår

porfyri, en sjælden, arvelig stofskiftesygdom, med bl.a. mørkfarvning af urinen og voldsomme

anfald af mavesmerter

Fund af Probenicid i urinen kan medføre diskvalifikation ved en dopingtest.

Brug af anden medicin

Fortæl det altid til lægen eller på apoteket, hvis du bruger anden medicin eller har gjort det for

nylig. Det gælder også medicin, som ikke er købt på recept, f.eks. naturlægemidler, vitaminer og

mineraler.

Tal med din læge, hvis du tager:

smertestillende medicin (acetylsalicylsyre, indometacin, ketoprofen, naproxen, diflunisal)

anden medicin til behandling af urinsyregigt (allopurinol)

medicin mod gigtlidelser og cancer (methotrexat)

antibiotika (penicillin, cefalosporiner)

medicin mod virus (zidovudin og ganciclovir)

medicin mod epilepsi (carbamazepin)

Brug af Probenecid ”medic” sammen med mad og drikke

Drik rigelig væske under behandlingen for at modvirke udfældninger i urinvejene.

Graviditet og amning

Spørg din læge eller apoteket til råds før du tager nogen form for medicin.

Graviditet

Hvis du er gravid, må du kun tage Probenecid “medic” efter aftale med lægen.

Amning

Hvis du ammer, må du kun tage Probenecid “medic” efter aftale med lægen.

Trafik- og arbejdssikkerhed

Probenecid “medic” påvirker ikke arbejdssikkerhed eller evnen til at færdes sikkert i trafikken.

3.

SÅDAN SKAL DU TAGE PROBENECID “MEDIC”

Tag altid Probenecid ”medic” nøjagtig efter lægens anvisning. Er du i tvivl, så spørg lægen eller

apotekspersonalet.

Det er vigtigt at drikke rigeligt med væske under behandlingen.

Synk tabletterne hele med et glas vand. Du kan eventuelt dele, knuse eller tygge tabletterne.

Den sædvanlige dosis er

Urinsur gigt:

Voksne: Startdosis: 1 tablet 2 gange dagligt, stigende i løbet af en uge til 2 tabletter 2 gange

dagligt. Følg lægens anvisninger.

Har du taget for meget Probenecid “medic”

Kontakt lægen, skadestuen eller apoteket, hvis du har taget mere af Probenecid “medic” end der

står i denne information, eller mere end lægen har foreskrevet og du føler dig utilpas.

Tag pakningen med.

Symptomer på overdosering kan være kvalme, opkastning, hovedpine, koma, voldsomme og

langvarige kramper og leverskader.

Hvis du har glemt at tage Probenecid ”medic”

Du må ikke tage en dobbeltdosis som erstatning for den glemte tablet.

4.

BIVIRKNINGER

Dette lægemiddel kan som al anden medicin give bivirkninger, men ikke alle får bivirkninger.

Alvorlige bivirkninger

Sjældne bivirkninger: Det sker hos mellem 1 og 10 ud af 10.000 patienter:

Smerter, feber, blod i urinen og skummende urin, evt. hævelser i ansigt, på hænder og fødder,

pga. nyreskade. Kontakt læge eller skadestue.

Leversvigt med voldsom gulsot og bevidstløshed. Kontakt straks læge eller skadestue.

Bivirkninger, hvor hyppigheden ikke er kendt:

Almen sløjhed, bleghed, blødninger fra hud og slimhinder, blå mærker samt tendens til

betændelse (infektioner) især halsbetændelse og feber pga. forandringer i blodet (for få røde

og hvide blodlegemer og blodplader). Kontakt straks læge eller skadestue.

Voldsomme, ofte turevise smerter i lænden og evt. blod i urinen pga. nyresten. Kontakt læge

eller skadestue.

Mørkerød urin, kraftige mavesmerter, psykiske forstyrrelser pga. en sjælden, arvelig sygdom

(porfyri). Kontakt straks læge eller skadestue.

Blæreformet udslæt og betændelse i huden, især på hænder og fødder samt i og omkring

munden ledsaget af feber. Kontakt læge eller skadestue.

Ikke alvorlige bivirkninger

Almindelige bivirkninger: Det sker hos mellem 1 og 10 ud af 100 patienter:

Kvalme og mavegener

Sjældne – meget sjældne bivirkninger: Det sker hos færre end 1 ud af 1000 patienter:

Hududslæt

Bivirkninger, hvor hyppigheden ikke er kendt

:

:

Hovedpine, svimmelhed

Hårtab, rødme

Risiko for anfald af urinsur gigt i begyndelsen af behandlingen

Overfølsomhedsreaktioner med feber, betændelse i huden, kløe og nældefeber

Tal med lægen eller apotekspersonalet, hvis du får bivirkninger, herunder bivirkninger, som ikke

fremgår af denne indlægsseddel.

Indberetning af bivirkninger

Hvis du oplever bivirkninger, bør du tale med din læge, sygeplejerske eller apoteket. Dette gælder

også mulige bivirkninger, som ikke er medtaget i denne indlægsseddel. Du eller dine pårørende

kan også indberette bivirkninger direkte til Sundhedsstyrelsen på www.meldenbivirkning.dk, ved at

kontakte Sundhedsstyrelsen via mail på sst@sst.dk eller med almindeligt brev til

Sundhedsstyrelsen, Axel Heides Gade 1, 2300 København S. Ved at indrapportere bivirkninger

kan du hjælpe med at fremskaffe mere information om sikkerheden af dette lægemiddel.

5.

SÅDAN OPBEVARER DU PROBENECID ”MEDIC”

Opbevar Probenecid “medic” utilgængeligt for børn.

Du kan opbevare Probenecid “medic” ved almindelig temperatur.

Brug ikke Probenecid “medic” efter den udløbsdato, der står på pakningen. Udløbsdatoen er den

sidste dag i den nævnte måned.

Spørg på apoteket, hvordan du skal bortskaffe medicinrester. Af hensyn til miljøet må du ikke

smide medicinrester i afløbet, toilettet eller skraldespanden.

6.

PAKNINGSSTØRRELSER OG YDERLIGERE OPLYSNINGER

Probenecid “medic” indeholder:

Aktivt stof: Probenecid.

Øvrige indholdsstoffer: Gelatine, kartoffelstivelse, silica kolloid vandfri,

magnesiumstearat og mikrokrystallinsk cellulose (E460).

Udseende og pakningsstørrelser

Udseende

Probenecid ”medic” er runde hvide tabletter med delekærv.

Pakningsstørrelse

100 stk.

Indehaver af markedsføringstilladelsen og fremstiller

Indehaver af markedsføringstilladelsen

Meda AS

Solvang 8

3450 Allerød

Tlf.: 45 52 88 88 / Fax.: 45 52 88 99

E-mail: info@meda.dk

Fremstiller

Viminco A/S,

Lodshusvej 11

4230 Skælskør

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24-9-2018

Renvela (Genzyme Europe B.V.)

Renvela (Genzyme Europe B.V.)

Renvela (Active substance: sevelamer (carbonate)) - Centralised - Variation - Commission Decision (2018)6225 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/993/X/39

Europe -DG Health and Food Safety

24-9-2018

Deferiprone Lipomed (Lipomed GmbH)

Deferiprone Lipomed (Lipomed GmbH)

Deferiprone Lipomed (Active substance: Deferiprone) - Centralised - Authorisation - Commission Decision (2018)6233 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4710

Europe -DG Health and Food Safety

24-9-2018

Inhixa (Techdow Europe AB)

Inhixa (Techdow Europe AB)

Inhixa (Active substance: enoxaparin sodium) - Centralised - Variation - Commission Decision (2018)6101 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4264/X/18, 26

Europe -DG Health and Food Safety

24-9-2018

Sevelamer carbonate Zentiva (Genzyme Europe B.V.)

Sevelamer carbonate Zentiva (Genzyme Europe B.V.)

Sevelamer carbonate Zentiva (Active substance: Sevelamer carbonate) - Centralised - Variation - Commission Decision (2018)6214 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3971/X/11

Europe -DG Health and Food Safety

24-9-2018

Cinqaero (Teva B.V.)

Cinqaero (Teva B.V.)

Cinqaero (Active substance: reslizumab) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6218 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3912T/18

Europe -DG Health and Food Safety

24-9-2018

Kigabeq (ORPHELIA Pharma SAS)

Kigabeq (ORPHELIA Pharma SAS)

Kigabeq (Active substance: vigabatrin) - Centralised - Authorisation - Commission Decision (2018)6224 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4534

Europe -DG Health and Food Safety

24-9-2018

Mektovi (Pierre Fabre MEdicament)

Mektovi (Pierre Fabre MEdicament)

Mektovi (Active substance: binimetinib) - Centralised - Authorisation - Commission Decision (2018)6217 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004579/0000

Europe -DG Health and Food Safety

24-9-2018

Braftovi (Pierre Fabre MEdicament)

Braftovi (Pierre Fabre MEdicament)

Braftovi (Active substance: encorafenib) - Centralised - Authorisation - Commission Decision (2018)6216 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004580/0000

Europe -DG Health and Food Safety

24-9-2018

Lenalidomide Accord (Accord Healthcare Limited)

Lenalidomide Accord (Accord Healthcare Limited)

Lenalidomide Accord (Active substance: lenalidomide) - Centralised - Authorisation - Commission Decision (2018)6237 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4857

Europe -DG Health and Food Safety

24-9-2018

Diacomit (Biocodex)

Diacomit (Biocodex)

Diacomit (Active substance: Stiripentol) - Centralised - Renewal - Commission Decision (2018)6254 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/664/R/21

Europe -DG Health and Food Safety

24-9-2018

EndolucinBeta (ITG Isotope Technologies Garching GmbH)

EndolucinBeta (ITG Isotope Technologies Garching GmbH)

EndolucinBeta (Active substance: Lutetium (177 Lu) chloride) - PSUSA - Modification - Commission Decision (2018)6236 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3999/PSUSA/10391/201712

Europe -DG Health and Food Safety

24-9-2018

Topotecan Hospira (Pfizer Europe MA EEIG)

Topotecan Hospira (Pfizer Europe MA EEIG)

Topotecan Hospira (Active substance: topotecan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6238 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1192/T/33

Europe -DG Health and Food Safety

24-9-2018

Zoledronic acid Hospira (Pfizer Europe MA EEIG)

Zoledronic acid Hospira (Pfizer Europe MA EEIG)

Zoledronic acid Hospira (Active substance: zoledronic acid) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6243 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2365/T/33

Europe -DG Health and Food Safety

24-9-2018

Xerava (Tetraphase Pharmaceuticals Ireland Limited)

Xerava (Tetraphase Pharmaceuticals Ireland Limited)

Xerava (Active substance: Eravacycline) - Centralised - Authorisation - Commission Decision (2018)6231 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4237

Europe -DG Health and Food Safety

24-9-2018

Ovitrelle (Merck Europe B.V.)

Ovitrelle (Merck Europe B.V.)

Ovitrelle (Active substance: Choriogonadotrophin alfa) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6220 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/320/T/75

Europe -DG Health and Food Safety

24-9-2018

Cosentyx (Novartis Europharm Limited)

Cosentyx (Novartis Europharm Limited)

Cosentyx (Active substance: secukinumab) - PSUSA - Modification - Commission Decision (2018)6213 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/00010341/201712

Europe -DG Health and Food Safety

24-9-2018

Lumark (IDB Holland B.V.)

Lumark (IDB Holland B.V.)

Lumark (Active substance: lutetium, isotope of mass 177) - PSUSA - Modification - Commission Decision (2018)6212 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/00010391/201712

Europe -DG Health and Food Safety

21-9-2018

Click the link for a handy list of #FDA’s recommendations for using and  caring for your medical devices during a #hurricane.   https://go.usa.gov/xPbgc  #MedicalDevice

Click the link for a handy list of #FDA’s recommendations for using and caring for your medical devices during a #hurricane. https://go.usa.gov/xPbgc  #MedicalDevice

Click the link for a handy list of #FDA’s recommendations for using and caring for your medical devices during a #hurricane. https://go.usa.gov/xPbgc  #MedicalDevice

FDA - U.S. Food and Drug Administration

21-9-2018

#DYK #hurricane season is active through November. Be prepared & stay informed of #MedicalDevice safety. Click the link to find a useful planning booklet from the #FDA that can help u prepare & handle power outages for medical devices that use electricity

#DYK #hurricane season is active through November. Be prepared & stay informed of #MedicalDevice safety. Click the link to find a useful planning booklet from the #FDA that can help u prepare & handle power outages for medical devices that use electricity

#DYK #hurricane season is active through November. Be prepared & stay informed of #MedicalDevice safety. Click the link to find a useful planning booklet from the #FDA that can help u prepare & handle power outages for medical devices that use electricity: https://go.usa.gov/xPbYt 

FDA - U.S. Food and Drug Administration

21-9-2018

Regulatory and procedural guideline:  Draft guideline on the summary of product characteristics (SPC) for veterinary medicinal products containing antimicrobial substances - Revision 1, draft: consultation open

Regulatory and procedural guideline: Draft guideline on the summary of product characteristics (SPC) for veterinary medicinal products containing antimicrobial substances - Revision 1, draft: consultation open

The guideline, which was developed to encourage optimal use and to minimise selection of antimicrobial resistance (AMR), was revised in order to improve consistency of the summary of product characteristics (SPCs) for antimicrobial products in the EU Member States.

Europe - EMA - European Medicines Agency

21-9-2018

Scientific guideline:  Reflection paper on resistance in ectoparasites, draft: consultation open

Scientific guideline: Reflection paper on resistance in ectoparasites, draft: consultation open

The Committee adopted a new draft reflection paper on ectoparasitic resistance (EMA/CVMP/EWP/310225/2014) for a 11-month period of public consultation. The reflection paper aims to give an overview of the currently known resistance situation in ectoparasites to active substances used in veterinary medicinal products with a special focus on Europe, and to provide a review of the current knowledge on resistance mechanisms.

Europe - EMA - European Medicines Agency

21-9-2018

Scientific guideline:  Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

Scientific guideline: Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

The objective of this document is to review available information on the use of aminopenicillins and their beta-lactamase inhibitor combinations in veterinary medicines in the EU, their effect on the emergence of antimicrobial resistance (AMR) and the potential impact of resistance on human and animal health. The document provides information for the risk profiling, as recommended by the Antimicrobial Advice ad hoc Expert Group (AMEG) of the EMA.

Europe - EMA - European Medicines Agency