Locoid

Informazioni principali

  • Nome commerciale:
  • Locoid Crema
  • Forma farmaceutica:
  • Crema
  • Composizione:
  • hydrocortisoni-17 butyras 1 mg, mantenuto.: E 216, butylis parahydroxybenzoas, 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:
  • Locoid Crema
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • Hautkrankheiten ekzematöser, entzündlicher oder allergischer Genese

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 36481
  • Data dell'autorizzazione:
  • 01-11-1973
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Transferiert von Astellas Pharma AG

Informazione destinata ai pazienti

Legga attentamente il foglietto illustrativo prima di far uso del medicamento.

Questo medicamento le è stato prescritto personalmente e quindi non deve essere consegnato ad altre

persone, anche se i sintomi sono gli stessi. Il medicamento potrebbe

nuocere alla loro salute.

Conservi il foglietto illustrativo per poterlo rileggere all’occorrenza.

Locoid®

Che cos’è Locoid e quando si usa?

Su prescrizione medica. Locoid contiene come principio attivo il corticosteroide idrocortisone-17-

butirrato che assomiglia ad un ormone dell’organismo e ha un effetto antiinfiammatorio,

antipruriginioso e antiallergico. Locoid è disponibile nelle forme farmaceutiche di crema, lipocrema,

Scalp Lotion e Locoid Crelo emulsione. Lo stato della pelle varia secondo le malattie. Il trattamento

deve essere effettuato con una forma specifica per i stati della pelle. Questo porta a un essenziale

buon fine. Locoid viene prescritto dal medico per il trattamento di malattie cutanee accompagnate da

prurito, arrossamento, squame o corneificazione della pelle, per esempio eczemi, psoriasi, regioni

cutanee estremamente pruriginose, arrossate e ispessite (neurodermatite).

Quando non si può usare Locoid?

Locoid non va usato in caso di ipersensibilità conosciuta verso i corticosteroidi o verso le sostanze

ausiliarie contenute, su ferite aperte e su infiammazioni purulente come per es. foruncoli, ascessi e

acne; in casi di malattie della pelle causate da virus (per es. varicella, vescicole febbrili, herpes

zoster) e di tubercolosi della pelle. Evitare assolutamente il

contatto di Locoid con gli occhi.

Quando è richiesta prudenza nell’uso di Locoid?

Locoid è un medicamento corticosteroide molto efficace. Il superamento della durata del trattamento

prescritta dal medico (2 a 3 settimane) può causare danni alla pelle. Se la malattia della pelle non

tende a migliorare dopo alcuni giorni di trattamento con Locoid o addirittura peggiora, consulti il suo

medico. Gli comunichi pure se si manifestano prurito e arrossamento, vescicole e ferite, o se la pelle

è diventata estremamente sottile. Malattie della pelle dovute a microrganismi come batteri o funghi

non vengono mai trattate soltanto con corticosteroidi. Se il medico, per questa ragione, le ha

prescritto un secondo medicamento, lei non deve tralasciare di usarlo di propria iniziativa. Locoid

dovrebbe agire soltanto sulla pelle. E tuttavia inevitabile che i corticosteroidi penetrino nella pelle e

raggiungano la circolazione sanguigna. Per questo motivo, Locoid va applicato con molta parsimonia

specialmente sulla pelle del viso, pelle ricoperta da molti peli o danneggiata, pieghe delle pelle, ferite

aperte, le pieghe all’interno delle articolazioni, la pelle tra le dita delle mani e dei piedi, le mucose o

le regioni intime.

Per lo stesso motivo, Locoid non va applicato, senza il controllo del medico, sotto bendaggi occlusivi

(ermetici all’aria), su estese regioni cutanee o nei bambini. I pannolini aderenti o le mutandine di

plastica favoriscono l’assorbimento della sostanza attiva di Locoid nella circolazione del sangue. Per

questo motivo si dovrebbero utilizzare pannolini di stoffa. Locoid va usato per una malattia cutanea

diagnosticata dal Suo medico. Quindi non può essere usato per successive malattie della pelle. Non

dare Locoid ad altre persone.

Informi il suo medico o il suo farmacista nel caso in cui soffre di altre malattie, soffre di allergie o

assume o applica altri medicamenti (anche se acquistati di sua iniziativa).

Si può usare Locoid durante la gravidanza o l’allattamento?

Se non è assolutamente indispensabile, Locoid non dev’essere usato durante la gravidanza.

Durante l’allattamento, l’uso di Locoid potrà essere effettuato unicamente su una piccola superficie

della pelle, per breve tempo e non sui seni. Prima del trattamento bisogna in ogni caso comunicare al

medico una eventuale gravidanza. Gli comunichi pure se dovesse restare incinta durante il

trattamento.

Come usare Locoid?

Se il medico non prescrive altrimenti, Locoid crema, lipocrema e Locoid Crelo emulsione viene

applicato in strato sottile sulle parti della pelle malata 1-2 volte al giorno. Locoid Crelo emulsione è

particolarmente adatto per il trattamento del cuoio capelluto. Si fa gocciolare Locoid Scalp Lotion

sulle parti del cuoio capelluto malato. Una leggera frizione favorisce l’assimilazione nella pelle.

Dopo che si è manifestato un miglioramento, il suo medico le prescriverà eventualmente di applicare

Locoid meno frequentemente.

In caso di malattie gravi, il medico puó prescriverle un’applicazione di Locoid sotto un bendaggio

occlusivo (ermetico all’aria). Dopo la rimozione del bendaggio, la pelle sottostante diventata umida

può emanare un odore sgradevole. Si tratta di un effetto innocuo che scompare lavandosi.

Non modifichi di propria iniziativa la posologia prescritta. Se ritiene che l’azione del medicamento

sia troppo debole o troppo forte ne parli al suo medico o al suo farmacista.

Quali effetti collaterali può avere Locoid?

In seguito all’applicazione di Locoid possono manifestarsi i seguenti effetti collaterali:

In singoli casi possono manifestarsi irritazioni locali della pelle, senso di bruciore, prurito, secchezza,

una irritazione passeggera della pelle o reazioni d’ipersensibilità. L’applicazione di bendaggi

occlusivi favorisce la comparsa di rari effetti collaterali: eruzioni cutanee, pustole e pus.

Raramente, soprattutto dopo trattamenti prolungati, la pelle trattata può diventare estremamente

sottile e i piccoli vasi sanguigni superficiali possono dilatarsi e formare delle strisce rosso-bluastre.

In questi casi bisogna informarne il medico. Nei bambini, specialmente nei lattanti e nei bambini

piccoli, la sostanza attiva di Locoid penetra in quantità maggiori nella circolazione sanguigna e, in

casi molto rari, l’applicazione prolungata può causare disturbi di crescita.

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

Di che altro occorre tener conto?

Conservare Locoid crema, lipocrema e Locoid Crelo emulsione

a temperatura ambiente (15-25ºC). Locoid Scalp Lotion: non conservare a temperatura superiore ai

25°C.

Conservare i medicamenti fuori della portata dei bambini.

Il medicamento non dev’essere utilizzato oltre la data indicata con “EXP” sulla confezione.

Il medico o il farmacista, che sono in possesso di documentazione professionale dettagliata, possono

darle ulteriori informazioni.

Cosa contiene Locoid?

1 g di lipocrema contiene:

Principio attivo: 1 mg di idrocortisone-17-butirrato. Conservante: propile p-ossibenzoato (E 216)

alcool benzilico ed altre sostanze ausiliarie.

1 g di crema contiene:

Principio attivo: 1 mg di idrocortisone- 17-butirrato. Conservante: propile p-ossibenzoato (E 216),

butile p-ossibenzoato e sostanze ausiliarie.

1 g di Locoid Crelo emulsione contiene:

Principio attivo: 1 mg di idrocortisone-17-butirrato, Eccipienti: glicole propilenico, conservante: E

216 (propile p-ossibenzoato), butile p-ossibenzoato; antiossidante:

butilidrossitoluene (E 321) ed altre sostanze ausiliarie.

1 ml di Scalp Lotion contiene:

Principio attivo: 1 mg di idrocortisone-17-butirrato, alcool isopropilico, sostanze ausiliarie.

Numero dell’omologazione

36’481, 36’482, 46’106, 52'585 (Swissmedic)

Dove è ottenibile Locoid? Quali confezioni sono disponibili?

In farmacia dietro presentazione della prescrizione medica.

Locoid lipocrema: Tubo da 30 g.

Locoid crema: Tubo da 30 g.

Locoid Crelo emulsione:

Flacone da 30 g e 100 g.

Locoid Scalp Lotion:

Flacone da 30 ml.

Titolare dell’omologazione

LEO Pharmaceutical Products Sarath Ltd., Regensdorf ZH

Questo foglietto illustrativo è stato controllato l’ultima volta nel marzo 2014 dall’autorità competente

in materia di medicamenti (Swissmedic).

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17-8-2018

EU/3/17/1870 (Pharma Gateway AB)

EU/3/17/1870 (Pharma Gateway AB)

EU/3/17/1870 (Active substance: Thymidine and deoxycytidine) - Transfer of orphan designation - Commission Decision (2018)5403 of Fri, 17 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/317/16/T/01

Europe -DG Health and Food Safety

15-8-2018

EU/3/18/1994 (Quality Regulatory Clinical Ireland Limited)

EU/3/18/1994 (Quality Regulatory Clinical Ireland Limited)

EU/3/18/1994 (Active substance: Ivosidenib) - Transfer of orphan designation - Commission Decision (2018)5555 of Wed, 15 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/172/17/T/01

Europe -DG Health and Food Safety

7-8-2018

EU/3/18/1996 (Worphmed Srl)

EU/3/18/1996 (Worphmed Srl)

EU/3/18/1996 (Active substance: Melatonin) - Transfer of orphan designation - Commission Decision (2018)5409 of Tue, 07 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/227/17/T/01

Europe -DG Health and Food Safety

27-7-2018

EU/3/18/2013 (Roche Registration GmbH)

EU/3/18/2013 (Roche Registration GmbH)

EU/3/18/2013 (Active substance: Polatuzumab vedotin) - Transfer of orphan designation - Commission Decision (2018)5054 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/231/17/T/01

Europe -DG Health and Food Safety

27-7-2018

EU/3/17/1932 (Millendo Therapeutics SAS)

EU/3/17/1932 (Millendo Therapeutics SAS)

EU/3/17/1932 (Active substance: Synthetic cyclic 8 amino acid analogue of human unacylated ghrelin) - Transfer of orphan designation - Commission Decision (2018)5049 of Fri, 27 Jul 2018 European Medicines Agency (EMA) procedure number: EMA/OD/066/17/T/01

Europe -DG Health and Food Safety

26-7-2018

Regulatory and procedural guideline:  EudraVigilance release notes v.1.17

Regulatory and procedural guideline: EudraVigilance release notes v.1.17

This document lists and briefly describes the following areas for the releases of EVWEB starting with the release on 22 November 2017.

Europe - EMA - European Medicines Agency

18-7-2018

Agenda:  Agenda - CVMP agenda of the 17-19 July 2018 meeting

Agenda: Agenda - CVMP agenda of the 17-19 July 2018 meeting

Committee for Medicinal Products for Veterinary Use - Draft agenda of July 2018 meeting

Europe - EMA - European Medicines Agency

17-7-2018

Attivazione nuova piattaforma "OsSC" e progetto “Fast Track” (17/07/2018)

Attivazione nuova piattaforma "OsSC" e progetto “Fast Track” (17/07/2018)

L’Agenzia Italiana del Farmaco comunica l’attivazione della nuova versione dell’Osservatorio sulle Sperimentazioni Cliniche (OsSC), che sarà operativa a partire dal 18 luglio 2018 alle ore 14:00. La nuova versione sarà accessibile al link https://servizionline.aifa.gov.it/, dove apparirà nella sezione “Servizi in Single Sign-On” una voce “Osservatorio sulla sperimentazione clinica - OsSC”, con le utenze già attive con la precedente versione.

Italia - AIFA - Agenzia Italiana del Farmaco

17-7-2018

Agenda:  Agenda - COMP agenda of the 17-19 July 2018 meeting

Agenda: Agenda - COMP agenda of the 17-19 July 2018 meeting

Draft agenda for the meeting on 17-19 July 2018

Europe - EMA - European Medicines Agency

17-7-2018

Rebif (Merck Serono Europe Limited)

Rebif (Merck Serono Europe Limited)

Rebif (Active substance: Interferon beta-1a) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4780 of Tue, 17 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/136/T/135

Europe -DG Health and Food Safety

17-7-2018

Naglazyme (BioMarin International Limited)

Naglazyme (BioMarin International Limited)

Naglazyme (Active substance: galsulfase) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4782 of Tue, 17 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/640/T/72

Europe -DG Health and Food Safety

17-7-2018

Firdapse (BioMarin Europe Ltd)

Firdapse (BioMarin Europe Ltd)

Firdapse (Active substance: amifampridine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 4779 of Tue, 17 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1032/T/57

Europe -DG Health and Food Safety

17-7-2018

Karvea (Sanofi-Aventis groupe)

Karvea (Sanofi-Aventis groupe)

Karvea (Active substance: Irbesartan) - Centralised - Yearly update - Commission Decision (2018)4781 of Tue, 17 Jul 2018

Europe -DG Health and Food Safety

17-7-2018

Comunicazione EMA su medicinali contenenti il principio attivo valsartan (17/07/2018)

Comunicazione EMA su medicinali contenenti il principio attivo valsartan (17/07/2018)

E’ attualmente in corso la revisione da parte dell’ Agenzia Europea dei Medicinali (EMA) dei medicinali a base di valsartan in relazione a un'impurezza riscontrata nella sostanza attiva prodotta da Zhejiang Huahai Pharmaceuticals. L'impurezza - N-nitrosodimetilammina (NDMA) - è classificata come probabile cancerogeno per l'uomo, in base ai risultati di test di laboratorio, e potrebbe causare il cancro nell’uso a lungo termine. Nelle ultime due settimane, le autorità sanitarie nazionali hanno richiamato i...

Italia - AIFA - Agenzia Italiana del Farmaco

17-7-2018

Agenda:  Agenda - Follow up information session on the TransCelerate initiative, 17 July 2018

Agenda: Agenda - Follow up information session on the TransCelerate initiative, 17 July 2018

Follow up information session on the TransCelerate initiative

Europe - EMA - European Medicines Agency

12-7-2018

Tabelle farmaci di classe A e H al 17/04/2018

Tabelle farmaci di classe A e H al 17/04/2018

Al fine di consentire la prescrizione per principio attivo disposta dall’articolo 15, comma 11-bis, del decreto legge 6 luglio 2012 n.95, convertito con modificazioni dalla Legge 7 agosto 2012 n. 135, l’Agenzia Italiana del Farmaco rende disponibili per tutti gli Operatori sanitari, le tabelle contenenti l’elenco dei farmaci di fascia A, dispensati dal Servizio sanitario Nazionale, ordinati rispettivamente per principio attivo e per nome commerciale.

Italia - AIFA - Agenzia Italiana del Farmaco

9-7-2018

 Minutes of the PRAC meeting 14-17 May 2018

Minutes of the PRAC meeting 14-17 May 2018

Europe - EMA - European Medicines Agency

29-6-2018

EU/3/07/505 (Faron Pharmaceuticals Limited)

EU/3/07/505 (Faron Pharmaceuticals Limited)

EU/3/07/505 (Active substance: Interferon beta) - Amendment of orphan designation - Commission Decision (2018)4186 of Fri, 29 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/080/17

Europe -DG Health and Food Safety