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PLEASE READ AND REVIEW THE FOLLOWING TERMS AND CONDITIONS OF USE CAREFULLY BEFORE USING THIS WEB SITE.

General.

Welcome to Veltassa.com (the "Website"). This Website is owned by Vifor Fresenius Medical Care Renal Pharma Ltd., with registered offices at Flughofstrasse 61, CH-8152 Glattbrugg, Switzerland ("Vifor Fresenius Medical Care Renal Pharma Ltd."). This Website is hosted in Germany and is governed by Swiss law without respect to its conflict of laws principles. Your access and use of the information contained herein is subject to the following terms and conditions of use and all applicable laws.

By accessing and browsing this Website, you accept, without limitation or qualification, these terms and conditions of use and acknowledge that (i) they constitute the entire agreement between you and Vifor Fresenius Medical Care Renal Pharma Ltd. with respect to the use of this Website and (ii) they supersede any other agreement between you and Vifor Fresenius Medical Care Renal Pharma Ltd.. You agree to indemnify Vifor Fresenius Medical Care Renal Pharma Ltd. for any claims or damages resulting from your failure to abide by these terms and conditions. If you do not agree to all of these Terms and Conditions of Use, please leave the Website.

The information on this Website was developed by Vifor Fresenius Medical Care Renal Pharma Ltd. as a resource for healthcare professionals (“HCPs”). The Website is not intended for use by US HCPs. If you are not a healthcare professional, please refrain from using this site. 

Some information on this Website may relate to medical, health or fitness conditions, their prevention and treatment. Any references to products or services on the Website do not imply that Vifor Fresenius Medical Care Renal Pharma Ltd. offers or intends to offer these products or services in your country. Please always refer to local prescribing information before making any prescribing decisions.  THE INFORMATION CONTAINED ON THIS WEBSITE IS NOT INTENDED TO PROVIDE OR REPLACE MEDICAL ADVICE. VIFOR FRESENIUS MEDICAL CARE RENAL PHARMA LTD. HEREBY PROHIBITS YOU FROM USING THE INFORMATION ON THIS WEBSITE FOR DIAGNOSING A HEALTH OR FITNESS PROBLEM OR DISEASE. 

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Vifor Fresenius Medical Care Renal Pharma Ltd. will use reasonable efforts to include accurate, complete and up-to-date information on this Website. Information and related materials are subject to change without notice. This Website, and all information and related materials it contains, are provided "as is." Vifor Fresenius Medical Care Renal Pharma Ltd. makes no representation or warranty whatsoever regarding the completeness, accuracy, "up-to-dateness", or adequacy of, or the suitability, functionality, availability, or operation of this Website or the information or materials it contains. By using this Website, you assume the risk that the information and materials on this Website may be incomplete, inaccurate, out of date, or may not meet your needs and requirements. Vifor Fresenius Medical Care Renal Pharma Ltd. does not warrant that access to the Website will be available at all times or that the Website or the server that makes it available are free of viruses or other harmful components. Vifor Fresenius Medical Care Renal Pharma Ltd. specifically disclaims all warranties, express or implied, including without limitation, the warranties or merchantability, fitness for a particular purpose, and non-infringement with respect to this Website and information, graphics and materials contained herein.

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Vifor Fresenius Medical Care Renal Pharma Ltd. reserves the right to alter or delete material from this Website at any time. Vifor Fresenius Medical Care Renal Pharma Ltd. may, at any time, revise these terms and conditions of use by updating this posting. You are bound by any such revisions and should, therefore, periodically review these terms to review the then current Website terms of use.

If any provision herein is held to be unlawful, void, or for any reason unenforceable, then that provision shall be eliminated or limited to the minimum extent necessary and such elimination or limitation shall not affect the validity and enforceability of any remaining provisions.

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Date of last revision: 18.02.2021

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  • What is Hyperkalaemia?
    • K+ Homeostasis is critical
    • What causes hyperkalaemia?
    • HK is a serious medical condition
    • CKD and HF patients are at Risk of HK
  • HK Challenge in CKD
    • RAASI therapy is vital
    • HK Risk is exacerbated by RAASI
    • HK leads to suboptimal RAASI use
    • Current treatment options are limited
  • HK Challenge in HF
    • RAASI therapy is vital
    • HK Risk is exacerbated by RAASI
    • HK leads to suboptimal RAASI use
    • Current treatment options are limited
  • About Veltassa
    • What is Veltassa
    • Mechanism of action of Veltassa
    • Easy to use
  • Clinical Experience
    • Reliable K+ Control
    • RAASI enablement
    • Favourable safety and tolerability
    • Clinical programme
  • Resources
    • For you
    • For your patients

VELTASSA 8,4 g ja 16,8 g jauhe oraalisuspensiota varten
PATIROMEERI

 Tähän lääkkeeseen kohdistuu lisäseuranta.
Käyttöaihe: Aikuisten hyperkalemian hoito. Annostus ja antotapa: Annostus: Suositeltu aloitusannos on 8,4 g patiromeeria kerran vuorokaudessa. Vuorokausiannosta voidaan sovittaa viikon välein tai harvemmin seerumin kaliumpitoisuuden ja halutun tavoitealueen perusteella. Vuorokausiannosta voidaan suurentaa tai pienentää 8,4 g:lla tarvittaessa 25,2 g:n enimmäisvuorokausiannokseen asti. Jos seerumin kaliumpitoisuus laskee halutun alueen alapuolelle, annosta pitää pienentää tai valmisteen käyttö lopettaa. Veltassa-valmisteen ja muiden suun kautta otettavien lääkevalmisteiden annon välissä on oltava 3 tuntia. Valmisteen turvallisuutta ja tehoa alle 18 vuoden ikäisten lasten hoidossa ei ole vielä varmistettu. Antotapa: Suun kautta. Annos kaadetaan lasiin, jossa on noin 40 ml vettä ja sekoitetaan, sitten lisätään 40 ml vettä, ja suspensiota sekoitetaan huolellisesti. Jauhe ei liukene. Tarvittaessa lisätään vettä halutun koostumuksen saavuttamiseksi. Seoksen valmistamiseen voi käyttää veden sijasta omena- tai karpalomehua. Karpalomehun runsasta nauttimista (yli 400 ml) pitää välttää, koska sillä voi olla yhteisvaikutuksia muiden lääkevalmisteiden kanssa. Veltassa otetaan ruoan kanssa tai ilman ruokaa. Sitä ei pidä kuumentaa tai lisätä kuumiin ruokiin tai nesteisiin eikä ottaa kuivassa muodossa. Vasta-aiheet: Yliherkkyys vaikuttavalle aineelle tai apuaineille. Varoitukset ja käyttöön liittyvät varotoimet: Seerumin magnesiumpitoisuutta on seurattava vähintään kuukauden ajan hoidon aloittamisesta. Muiden kaliumin sitojien kanssa on raportoitu ruoansulatuskanavan iskemiaa, nekroosia ja/tai suolten puhkeamista. Patiromeerin annon hyötyjä ja riskejä on harkittava tarkoin ennen hoitoa ja hoidon aikana potilailla, joilla on tai on ollut vakavia ruoansulatuselimistön häiriöitä.

Kun hoito lopetetaan, seerumin kaliumpitoisuus voi nousta, erityisesti jos RAA-järjestelmää estävää hoitoa jatketaan. Seerumin kaliumpitoisuutta on seurattava erityisesti, kun on muutettu seerumin kaliumpitoisuuteen vaikuttavien lääkkeiden tai patiromeerin annoksia. Veltassa sisältää sorbitolia noin 4 g (10,4 kcal)/8,4 g patiromeeria. Ei sovi potilaille, joilla on harvinainen perinnöllinen fruktoosi-intoleranssi. Veltassa sisältää kalsiumia, joten annon hyötyjä ja riskejä on harkittava tarkoin potilailla, joilla on hyperkalsemian riski. Yhteisvaikutukset: Patiromeeri voi sitoa joitakin suun kautta samanaikaisesti otettavia lääkevalmisteita, mikä voi heikentää niiden imeytymistä ruoansulatuskanavasta. Hedelmällisyys, raskaus ja imetys: Raskaus: Varmuuden vuoksi patiromeerin käyttöä on suositeltavaa välttää raskauden aikana. Imetys: Ei ole odotettavissa vaikutuksia vastasyntyneisiin tai imeväisiin. Haittavaikutukset: Yleiset: Ummetus, ripuli, vatsakipu, ilmavaivat ja hypomagnesemia. Tarkemmat tiedot: katso valmisteyhteenveto. Pakkaukset ja hinnat (VMH+alv) 1/2020: Veltassa 8,4 g 30 annospussia 320,79 euroa, Veltassa 16,8 g 30 annospussia 320,79 euroa. Korvattavuus: Rajoitettu peruskorvaus lääkärin lausunnolla (40 %). Valmiste on rajoitetusti peruskorvattava hyperkalemian hoitoon kroonista munuaissairautta sairastaville aikuispotilaille, joiden sairaus on hoitoa aloitettaessa vaiheessa 3 - 4 ja jotka käyttävät ACE-estäjää tai ATR-salpaajaa, eivät ole dialyysihoidossa ja joille hoito natriumpolystyreenisulfonaatilla ei sovi, peruskorvausoikeusnumero 3020. Reseptilääke. Huom. Tutustu valmisteyhteenvetoon ennen lääkkeen määräämistä. Tämä teksti perustuu valmisteyhteenvetoon 15.10.2020. Lisätiedot: Pharmaca Fennica ja Vifor Pharma Nordiska AB, puh +46 8 558 066 00, info.nordic@viforpharma.com, www.viforpharma.se

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FI-PAT-2100006 | Date of preparation: November 2021