Ichtholan 20% Zugsalbe

Informazioni principali

  • Nome commerciale:
  • Ichtholan 20% Zugsalbe Salbe
  • Forma farmaceutica:
  • Salbe
  • Composizione:
  • ichthammolum 200 mg, adeps lanae, excipiens annuncio unguentum pro 1 g.
  • Utilizzare per:
  • Esseri umani
  • Tipo di medicina:
  • Farmaco biologico

Documenti

  • per i professionisti:
  • Il foglio illustrativo per questo prodotto non è al momento disponibile, é possibile inviare una richiesta al nostro Servizio Clienti ed essere avvisati nel momento in cui è disponibile sulla nostra piattaforma.


    Richiedi il foglio illustrativo per i professionisti.

Localizzazione

  • Disponibile in:
  • Ichtholan 20% Zugsalbe Salbe
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • Entzündliche Hautleiden

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 10751
  • Data dell'autorizzazione:
  • 18-06-1941
  • Ultimo aggiornamento:
  • 19-10-2018

Foglio illustrativo: composizione, posologia, indicazioni, interazioni, gravidanza, allattamento, effetti indesiderati, controindicazioni

Patienteninformation

Ichtholan® Pomata revulsiva 10%, 20%, 50%

Medinova AG

Che cos'è Ichtholan 10%, 20%, 50% e quando si usa?

Grazie allo scisto sulfobituminato (sulfobituminato di ammonio, Ichthammolum) in essa contenuto,

Ichtholan svolge un'azione antibatterica, antinfiammatoria e antipruriginosa. Nei casi di affezioni

cutanee purulente, accelera, nello stadio avanzato dell'infiammazione, la colliquazione del focolaio e

la fuoriuscita del pus.

La pomata revulsiva Ichtholan 10%, 20% e 50% viene impiegata nelle sue diverse concentrazioni per

il trattamento di infiammazioni cutanee di varia natura:

Ichtholan 10%: pomata revulsiva da impiegare in caso di infiammazioni cutanee facciali (stati

infiammatori e pustole dolorose nella zona degli angoli della bocca, della bocca, delle guance, della

fronte e delle palpebre)

Ichtholan 20%: pomata revulsiva da impiegare in caso di infiammazioni cutanee di natura più

profonda come ascessi, infiammazioni del letto ungueale, infiammazioni ed ascessi delle ghiandole

sudoripare.

Ichtholan 50%: pomata revulsiva per la maturazione di foruncoli.

Ichtholan 50% può essere inoltre anche impiegata, applicando fasciatura apposita per un periodo di

3-5 giorni, per il trattamento di infiammazioni dell'apparato locomotore e in presenza di lesioni non

penetranti (casi di infiammazioni articolari, tenosinoviti, borsiti, gomito del tennista e lesioni non

penetranti quali distorsioni, schiacciamenti, contusioni o lesioni per attività sportiva).

L'uso di Ichtholan 50% come fasciatura fissa produce un effetto analgesico, un miglioramento della

mobilità delle articolazioni e la regressione di versamenti articolari.

Quando non si può usare la pomata revulsiva Ichtholan 10%, 20%, 50%?

In caso d'ipersensibilità al sulfobituminato di ammonio (Ichthammolum), alla lanolina anidra o ad un

altro ingrediente.

Fino ad ora non è stata testata l'applicazione e la sicurezza della pomata revulsiva Ichtholan 10%,

20% su bambini di età inferiore ai 12 anni.

Quando è richiesta prudenza nell'uso della pomata revulsiva Ichtholan 10%, 20%, 50%?

Se si assiste ad un peggioramento locale o se non si constata guarigione nel giro di due o tre

settimane, occorre recarsi dal medico o dal farmacista. Se lo stato generale della salute peggiora (per

es. comparsa di febbre), occorre consultare immediatamente un medico.

Informi il suo medico, il suo farmacista o il suo droghiere se soffre di altre malattie, soffre di allergie

o assume o applica (medicamento per uso esterno) altri medicamenti (anche se acquistati di sua

iniziativa).

Si può usare la pomata revulsiva Ichtholan 10%, 20%, 50% durante la gravidanza o l'allattamento?

Non si è a conoscenza di effetti dannosi durante il periodo della gravidanza e dell'allattamento.

Qualora sia incinta o se desideri diventarlo, consulti il suo medico prima di utilizzare Ichtholan.

Come usare la pomata revulsiva Ichtholan 10%, 20%, 50%?

Ichtholan 10%

Salvo diversa prescrizione medica, la pomata revulsiva Ichtholan 10% viene applicata 1 volta al

giorno sulle regioni cutanee interessate dall'infiammazione. Il trattamento può durare fino alla

regressione dell'infiammazione cutanea.

Ichtholan 20% e 50%

Salvo diversa prescrizione medica, Ichtholan 20% o Ichtholan 50% viene applicata abbondantemente

sulle regioni cutanee interessate e quindi coperta. A questo scopo consigliamo di posare un batuffolo

di ovatta sulla pomata applicata e poi di coprirlo ampiamente con cerotto. Se si impiega pomata

revulsiva Ichtholan 50% in fasciatura fissa, badare ad applicare prima la pomata e poi a coprirla

ampiamente con una fascia di garza. Facendo attenzione ad una sufficiente traspirazione si deve

quindi applicare la fasciatura che andrà cambiata dopo massimo 3 giorni. La durata dell'applicazione

dipende dal successo del trattamento. Ogni volta che si cambia la fasciatura, prima di passare ad un

nuovo trattamento con pomata revulsiva Ichtholan 20% o 50%, si deve provvedere ad eliminare i

residui di pomata lavandoli con acqua tiepida e sapone.

Fino ad ora non è stata testata l'applicazione e la sicurezza della pomata revulsiva Ichtholan 10%,

20% su bambini di età inferiore ai 12 anni.

In presenza di infiammazioni cutanee, sopratutto di foruncoli, sussiste il pericolo di propagare

l'infezione e che possa quindi insorgere una foruncolosi (comparsa, anche ripetitiva, di foruncoli)

difficilmente controllabile.

Per questo è necessaria una tecnica di fasciatura accurata:

·pulizia rigorosa, disinfezione della cute sana adiacente

·applicazione di una fasciatura che copra bene, senza scivolare o sfregare

·eventualmente fare un bagno con un additivo disinfettante.

Si attenga alla posologia indicata nel foglietto illustrativo o prescritta dal medico. Se ritiene che

l'azione del medicamento sia troppo debole o troppo forte ne parli al suo medico, al suo farmacista o

al suo droghiere.

Quali effetti collaterali può avere la pomata revulsiva Ichtholan 10%, 20%, 50%?

Con l'applicazione della pomata revulsiva Ichtholan 10%, 20%, 50% possono manifestarsi i seguenti

effetti collaterali.

In casi eccezionali, durante il trattamento con pomata revulsiva Ichtholan, possono verificarsi delle

reazioni cutanee di incompatibilità che si manifestano con pruriti, bruciori e arrossamenti della cute.

Una fasciatura chiusa può dar luogo, in casi estremamente rari, a forti reazioni cutanee, come ad

esempio, la formazione di vescicole. Alla comparsa di questi fenomeni occorre consultare

immediatamente il medico.

Se osserva effetti collaterali qui non descritti dovrebbe informare il suo medico, il suo farmacista o il

suo droghiere.

Di che altro occorre tener conto?

Conservare il medicamento fuori dalla portata dei bambini.

Richiudere bene il tubetto dopo l'uso.

Eventuali macchie possono essere facilmente eliminate utilizzando prima un solvente organico (per

es. benzina rettificata) e poi un normale detersivo.

Il medicamento non deve essere utilizzato oltre la data indicata con «EXP» sulla confezione.

Conservare a temperatura ambiente (15-25 °C) e in luogo asciutto.

Cosa contiene la pomata revulsiva Ichtholan 10%, 20%, 50%?

10% e 20%:

1 g di pomata contiene: sulfobituminato di ammonio (Ichthammolum) 100 mg/200 mg. Sostanze

ausiliarie: vaselina gialla, lanolina anidra, acqua depurata.

50%:

1 g di pomata contiene: sulfobituminato di ammonio (Ichthammolum) 500 mg. Sostanze ausiliarie:

vaselina gialla, lanolina anidra, paraffina microcristallina, acqua depurata.

Numero dell'omologazione

10751 (Swissmedic).

Dov'è ottenibile la pomata revulsiva Ichtholan 10%, 20%, 50%? Quali confezioni sono disponibili?

In farmacia e in drogheria senza prescrizione medica.

Tubetti da 40 g di pomata Ichtholan 10%, 20%, 50%.

Titolare dell’omologazione

Medinova AG, 8050 Zürich.

Fabbricante

Ichthyol-Gesellschaft Cordes, Hermanni & Co. (GmbH & Co.) KG, Hamburg, Deutschland.

Questo foglietto illustrativo è stato controllato l'ultima volta nel novembre 2010 dall'autorità

competente in materia di medicamenti (Swissmedic).

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Europe - EMA - European Medicines Agency

21-9-2018

Pending EC decision:  Luxturna, voretigene neparvovec, Opinion date: 20-Sep-2018

Pending EC decision: Luxturna, voretigene neparvovec, Opinion date: 20-Sep-2018

Europe - EMA - European Medicines Agency

21-9-2018

Pending EC decision:  Fulphila, pegfilgrastim, Opinion date: 20-Sep-2018

Pending EC decision: Fulphila, pegfilgrastim, Opinion date: 20-Sep-2018

Europe - EMA - European Medicines Agency

21-9-2018

Pending EC decision:  Pelmeg, pegfilgrastim, Opinion date: 20-Sep-2018

Pending EC decision: Pelmeg, pegfilgrastim, Opinion date: 20-Sep-2018

Europe - EMA - European Medicines Agency

21-9-2018

Pending EC decision:  Ziextenzo, pegfilgrastim, Opinion date: 20-Sep-2018

Pending EC decision: Ziextenzo, pegfilgrastim, Opinion date: 20-Sep-2018

Europe - EMA - European Medicines Agency

21-9-2018

Pending EC decision:  Poteligeo, mogamulizumab, Opinion date: 20-Sep-2018

Pending EC decision: Poteligeo, mogamulizumab, Opinion date: 20-Sep-2018

Europe - EMA - European Medicines Agency

21-9-2018

Pending EC decision:  Pifeltro, doravirine, Opinion date: 20-Sep-2018

Pending EC decision: Pifeltro, doravirine, Opinion date: 20-Sep-2018

Europe - EMA - European Medicines Agency

21-9-2018

Outcome of the consultation with Member States, the applicant and EFSA on the pesticide risk assessment for sulfoxaflor in light of confirmatory data

Outcome of the consultation with Member States, the applicant and EFSA on the pesticide risk assessment for sulfoxaflor in light of confirmatory data

Published on: Thu, 20 Sep 2018 00:00:00 +0200 The European Food Safety Authority (EFSA) was asked by the European Commission to provide scientific assistance with respect to the risk assessment for an active substance in light of confirmatory data requested following approval in accordance with Article 6(1) of Directive 91/414/EEC and Article 6(f) of Regulation (EC) No 1107/2009. In this context EFSA's scientific views on the specific points raised during the commenting phase conducted with Member State...

Europe - EFSA - European Food Safety Authority Publications

21-9-2018

Modification of the existing maximum residue level for clothianidin in potatoes

Modification of the existing maximum residue level for clothianidin in potatoes

Published on: Thu, 20 Sep 2018 00:00:00 +0200 In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Bayer CropScience AG submitted a request to the competent national authority in Germany to modify the existing maximum residue level (MRL) for the active substance clothianidin to accommodate the use on potatoes imported from Canada. The data submitted in support of the request were found to be sufficient to derive a MRL proposal. Adequate analytical methods for enforcement are availa...

Europe - EFSA - European Food Safety Authority Publications

20-9-2018

Pending EC decision:  Xtandi, enzalutamide, Opinion date: 20-Sep-2019

Pending EC decision: Xtandi, enzalutamide, Opinion date: 20-Sep-2019

Europe - EMA - European Medicines Agency

24-12-2018

ACCM meeting statement, Meeting 20, 16 November 2018

ACCM meeting statement, Meeting 20, 16 November 2018

ACCM meeting statement for 16 November 2018 published

Therapeutic Goods Administration - Australia

21-12-2018

Consultation: Fees and charges proposal 2019-20

Consultation: Fees and charges proposal 2019-20

The TGA is seeking comments from interested parties on the proposed changes in fees and charges for 2019-2020. Closing date: 8 February 2018

Therapeutic Goods Administration - Australia

20-12-2018

Namuscla (Lupin Europe GmbH)

Namuscla (Lupin Europe GmbH)

Namuscla (Active substance: Mexiletine) - New authorisation - Commission Decision (2018)9133 of Thu, 20 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4584

Europe -DG Health and Food Safety

20-12-2018

Bevespi Aerosphere (AstraZeneca AB)

Bevespi Aerosphere (AstraZeneca AB)

Bevespi Aerosphere (Active substance: glycopyrronium bromide / formoterol) - New authorisation - Commission Decision (2018)9127 of Thu, 20 Dec 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4245

Europe -DG Health and Food Safety

18-12-2018


Human medicines European public assessment report (EPAR): Vabomere, meropenem / vaborbactam, Urinary Tract Infections,Bacteremia,Bacterial Infections,Respiratory Tract Infections,Pneumonia,Pneumonia, Ventilator-Associated, Date of authorisation: 20/11/20

Human medicines European public assessment report (EPAR): Vabomere, meropenem / vaborbactam, Urinary Tract Infections,Bacteremia,Bacterial Infections,Respiratory Tract Infections,Pneumonia,Pneumonia, Ventilator-Associated, Date of authorisation: 20/11/20

Human medicines European public assessment report (EPAR): Vabomere, meropenem / vaborbactam, Urinary Tract Infections,Bacteremia,Bacterial Infections,Respiratory Tract Infections,Pneumonia,Pneumonia, Ventilator-Associated, Date of authorisation: 20/11/2018, Status: Authorised

Europe - EMA - European Medicines Agency

18-12-2018


Human medicines European public assessment report (EPAR): Buvidal, buprenorphine, Opioid-Related Disorders, Date of authorisation: 20/11/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Buvidal, buprenorphine, Opioid-Related Disorders, Date of authorisation: 20/11/2018, Status: Authorised

Human medicines European public assessment report (EPAR): Buvidal, buprenorphine, Opioid-Related Disorders, Date of authorisation: 20/11/2018, Status: Authorised

Europe - EMA - European Medicines Agency

12-12-2018


Human medicines European public assessment report (EPAR): Exondys, eteplirsen, Muscular Dystrophy, Duchenne, Date of refusal: 20/09/2018, Status: Refused

Human medicines European public assessment report (EPAR): Exondys, eteplirsen, Muscular Dystrophy, Duchenne, Date of refusal: 20/09/2018, Status: Refused

Human medicines European public assessment report (EPAR): Exondys, eteplirsen, Muscular Dystrophy, Duchenne, Date of refusal: 20/09/2018, Status: Refused

Europe - EMA - European Medicines Agency

5-12-2018

TGA presentation: Webinar: Advertising therapeutic goods in 2019: The Code basics – 20 November

TGA presentation: Webinar: Advertising therapeutic goods in 2019: The Code basics – 20 November

The slides from TGA's webinar on Advertising Code Basics have been published

Therapeutic Goods Administration - Australia

28-11-2018

PHEBURANE (Eurocept International BV)

PHEBURANE (Eurocept International BV)

PHEBURANE (Active substance: Sodium Phenylbutyrate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8043 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2500/T/20

Europe -DG Health and Food Safety

26-11-2018

Data show that nearly 20% of current 510(k)s are cleared based on a predicate that’s more than 10 years old. That doesn’t mean the products are unsafe. But it does mean that some devices may not be continually improving, which is the hallmark of health te

Data show that nearly 20% of current 510(k)s are cleared based on a predicate that’s more than 10 years old. That doesn’t mean the products are unsafe. But it does mean that some devices may not be continually improving, which is the hallmark of health te

Data show that nearly 20% of current 510(k)s are cleared based on a predicate that’s more than 10 years old. That doesn’t mean the products are unsafe. But it does mean that some devices may not be continually improving, which is the hallmark of health technologies.

FDA - U.S. Food and Drug Administration

16-11-2018

Latuda (Aziende Chimiche Riunite Angelini Francesco - A.C.R.A.F. S.p.A.)

Latuda (Aziende Chimiche Riunite Angelini Francesco - A.C.R.A.F. S.p.A.)

Latuda (Active substance: lurasidone) - Centralised - Renewal - Commission Decision (2018)7674 of Fri, 16 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2713/R/20

Europe -DG Health and Food Safety

14-11-2018

Jinarc (Otsuka Pharmaceutical Netherlands B.V.)

Jinarc (Otsuka Pharmaceutical Netherlands B.V.)

Jinarc (Active substance: tolvaptan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7604 of Wed, 14 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2788/T/20

Europe -DG Health and Food Safety

1-10-2018

EU/3/05/328 (Celgene Europe B.V.)

EU/3/05/328 (Celgene Europe B.V.)

EU/3/05/328 (Active substance: (E)-(1S,4S,10S,21R)-7-[(Z)-ethylidene]-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23- tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone) - Transfer of orphan designation - Commission Decision (2018)6434 of Mon, 01 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/056/05/T/03

Europe -DG Health and Food Safety

1-10-2018

EU/3/05/279 (Celgene Europe B.V.)

EU/3/05/279 (Celgene Europe B.V.)

EU/3/05/279 (Active substance: (E)-(1S,4S,10S,21R)-7-[(Z)-ethylidene]-4,21-diisopropyl-2-oxa-12,13-dithia-5,8,20,23- tetraazabicyclo[8.7.6]tricos-16-ene-3,6,9,19,22-pentone) - Transfer of orphan designation - Commission Decision (2018)6433 of Mon, 01 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/001/05/T/03

Europe -DG Health and Food Safety

17-9-2018

Agenda:  Agenda - CHMP agenda of the 17-20 September 2018 meeting

Agenda: Agenda - CHMP agenda of the 17-20 September 2018 meeting

Europe - EMA - European Medicines Agency