Nalcrom 100

Informazioni principali

  • Nome commerciale:
  • Nalcrom 100 Sachets
  • Forma farmaceutica:
  • Sachets
  • Composizione:
  • natrii cromoglicas 100 mg, saccharum 1 g, pro charta.
  • Utilizzare per:
  • Esseri umani
  • Tipo di medicina:
  • Farmaco allopatico

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:
  • Nalcrom 100 Sachets
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika human
  • Area terapeutica:
  • Nahrungsmittelallergien

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 46256
  • Data dell'autorizzazione:
  • 04-12-1986
  • Ultimo aggiornamento:
  • 05-02-2018

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

Patienteninformation

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.

Nalcrom®

Che cos’è Nalcrom e quando si usa?

Il Nalcrom è ottenibile su prescrizione medica.Il Nalcrom è una polvere da prendere per bocca,

contenente Natrii cromoglicas quale principio attivo. E’ disponibile sotto forma di capsule ed in

bustine.

Il Nalcrom viene usato per il trattamento profilattico di allergie alimentari, soprattutto in presenza di

un’allergia a parecchi cibi, nelle persone molto sensibili e nei casi in cui appare problematico

ripiegare su altri cibi adeguati.

Eczemi, orticaria, prurito, disturbi gastrointestinali, asma, rinite ed attacchi di emicrania sono sintomi

frequenti di un’allergia alimentare, gli allergeni che scatenano l’allergia possono essere presenti in

molti prodotti alimentari, ad es. nel latte vaccino, nell’albume dell’uovo di gallina, nei cereali, nel

pesce, nel formaggio e nelle noci.

Nella comparsa di disturbi allergici rivestono importanza determinate cellule (mastcellule) presenti

nella mucosa dell’apparato digerente.

A contatto con allergeni, queste cellule liberano sostanze che provocano un’infiammazione della

mucosa dell’apparato digerente. Così la mucosa diventa più permeabile e vengono assorbiti più

allergeni che, in questo caso, possono provocare disturbi anche in altre parti dell’organismo (naso,

polmoni, pelle, ecc.).

Il Nalcrom stabilizza la membrana di queste cellule. Le mastcellule rimangono intatte e non

rilasciano più sostanze irritanti. Il trattamento con il Nalcrom deve essere effettuato sempre prima

dell’assunzione di cibi ed è consigliabile svolgerlo in modo conseguente e regolare.

Di che cosa occorre inoltre tener conto durante il trattamento?

Se in passato ha già avuto un shock anafilattico o una reazione di analoga gravità dopo assunzione di

un determinato cibo, è bene che rinunci per precauzione al consumo del cibo incriminato anche

durante il trattamento con il Nalcrom.

Quando non si può usare Nalcrom?

Nalcrom non va impiegato in presenza di un’ipersensibilità già nota verso il cromoglicato sodico o

verso il saccarosio (compresa l’intolleranza al fruttosio e la sindrome da malassorbimento di

glucosio/galattosio) e nei bambini al di sotto dei 2 anni.

Quando è richiesta prudenza nell’uso di Nalcrom?

Avvertenza per i diabetici

Le bustine Nalcrom contengono zucchero (Nalcrom 100: ca. 1 g di saccarosio, pari a 0,08 unità di

pane; Nalcrom 200: ca. 2 g di saccarosio, pari a 0,16 unità di pane). Se necessario, i diabetici

dovrebbero orientarsi verso le capsule Nalcrom, che sono senza zucchero.

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

o applica altri medicamenti (anche acquistati di sua iniziativa)!

Si può impiegare Nalcrom durante la gravidanza o l’allattamento?

In base alle esperienze fatte finora, non sono noti rischi per il bambino se il medicamento è usato

correttamente. Tuttavia non sono ancora state compiute indagini scientifiche sistematiche. Per

prudenza dovrebbe rinunciare nella misura del possibile ad assumere medicamenti durante la

gravidanza e il periodo d’allattamento o chiedere consiglio al proprio medico o farmacista.

Come usare Nalcrom?

Si consiglia di prendere il Nalcrom 15 – 30 minuti prima dei pasti.

Salvo diversa prescrizione medica, gli adulti devono prendere 4 volte al giorno 2 capsule o 1 bustina

da 200 mg, ed i ragazzi dai 2 ai 14 anni 4 volte al giorno 1 capsula o 1 bustina da 100 mg.

Le capsule si possono inghiottire. E’ però consigliabile ingerirne il contenuto sciolto in 2 – 3 cucchiai

da tavola di acqua calda.

Il contenuto di una bustina va ingerito sciolto in mezzo bicchiere d’acqua.

Poiché gli allergeni possono essere assorbiti attraverso la mucosa orale, è opportuno sciacquarsi la

bocca con la soluzione prima di inghiottirla.

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 Nalcrom?

Con l’assunzione di Nalcrom possono manifestarsi i seguenti effetti collaterali: Sono stati

occasionalmente osservati nausea, vomito, diarrea, mal di ventre, eruzioni cutanee, dolori articolari e

cefalee. In casi molto rari, è stata riportata la comparsa di reazioni d’ipersensibilità (es. con

arrossamento cutaneo e sensazione di calore, orticaria, edemi al volto e difficoltà respiratorie). In

genere questi disturbi scompaiono spontaneamente una volta interrotta l’assunzione del farmaco; se

si presentano in forma piuttosto forte, bisogna consultare il medico.

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

Di che altro occorre tener conto?

Conservare il Nalcrom a temperatura ambiente (15 - 25°C), fuori dalla portata dei bambini ed in

luogo asciutto.

Dopo l’uso, chiudere accuratamente il contenitore.

Il medicamento può essere utilizzato solo fino alla data di scadenza indicata con „EXP“

sull’imballaggio.

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

darle ulteriori informazioni.

Che cosa contiene Nalcrom?

1 capsula di Nalcrom contiene: 100 mg di sodiocromoglicinato.

1 bustina di Nalcrom 100 contiene: 100 mg di sodiocromoglicinato. saccarosio ca. 1 g.

1 bustina di Nalcrom 200 contiene: 200 mg di sodiocromoglicinato. saccarosio ca. 2 g.

Numero dell’omologazione

44778, 46256 (Swissmedic).

Dov’è ottenibile Nalcrom? Quali confezioni sono disponibili?

Ottenibile nelle farmacie, soltanto contro ricetta medica.

Nalcrom capsule: 100.

Nalcrom 100 bustine: 50.

Nalcrom 200 bustine: 50.

Titolare dell’omologazione

Curatis AG, 4410 Liestal

Questo foglietto illustrativo è stato controllato l’ultima volta nel dicembre 2004 dall’autorità

competente in materia di medicamenti (Swissmedic).

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Europe - EMA - European Medicines Agency

21-11-2018

EU/3/18/2100 (Quality Regulatory Clinical Ireland Limited)

EU/3/18/2100 (Quality Regulatory Clinical Ireland Limited)

EU/3/18/2100 (Active substance: Propagermanium) - Orphan designation - Commission Decision (2018)7810 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/103/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Orphan Europe S.A.R.L.)

EU/3/18/2076 (Active substance: Glycine, L-alanine, L-arginine, L-aspartic acid, L-cysteine, L-cystine, L-glutamic acid, L-histidine, L-lysine monohydrate, L-methionine, L-phenylalanine, L-proline, L-serine, L-threonine, L-tryptophan, L-tyrosine, taurine) - Orphan designation - Commission Decision (2018)7277 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/100/18

Europe -DG Health and Food Safety

19-9-2018

Kadcyla (Roche Registration GmbH)

Kadcyla (Roche Registration GmbH)

Kadcyla (Active substance: Trastuzumab emtansine) - Centralised - Renewal - Commission Decision (2018)6100 of Wed, 19 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2389/R/39

Europe -DG Health and Food Safety

23-8-2018

 Minutes of the 100th meeting of the Management Board: 6-7 June 2018

Minutes of the 100th meeting of the Management Board: 6-7 June 2018

Europe - EMA - European Medicines Agency

27-6-2018

PANTOLOC Control (Takeda GmbH)

PANTOLOC Control (Takeda GmbH)

PANTOLOC Control (Active substance: pantoprazole) - PSUSA - Modification - Commission Decision (2018)4105 of Wed, 27 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1100/PSUSA/2285/201708

Europe -DG Health and Food Safety

6-6-2018

Agenda:  Agenda for the 100th meeting of the Management Board

Agenda: Agenda for the 100th meeting of the Management Board

Europe - EMA - European Medicines Agency

5-6-2018

Agenda:  Draft agenda for the 100th meeting of the Management Board

Agenda: Draft agenda for the 100th meeting of the Management Board

Europe - EMA - European Medicines Agency

24-5-2018

Tybost (Gilead Sciences International Limited)

Tybost (Gilead Sciences International Limited)

Tybost (Active substance: cobicistat) - PSUSA - Modification - Commission Decision (2018)3255 of Thu, 24 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10081/201708

Europe -DG Health and Food Safety

24-5-2018

Stribild (Gilead Sciences International Limited)

Stribild (Gilead Sciences International Limited)

Stribild (Active substance: elvitegravir / cobicistat / emtricitabine / tenofovir disoproxil (as fumarate)) - PSUSA - Modification - Commission Decision (2018)3277 of Thu, 24 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2574/PSUSA/10082/201708

Europe -DG Health and Food Safety

18-5-2018

EU/3/14/1328 (Roche Registration GmbH)

EU/3/14/1328 (Roche Registration GmbH)

EU/3/14/1328 (Active substance: 4-{[(2R,3S,4R,5S)-4-(4-chloro-2-fluoro-phenyl)-3-(3-chloro-2-fluoro-phenyl)-4-cyano-5-(2,2-dimethyl-propyl)-pyrrolidine-2-carbonyl]-amino}-3-methoxy-benzoic acid) - Transfer of orphan designation - Commission Decision (2018)3149 of Fri, 18 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/100/14/T/01

Europe -DG Health and Food Safety