Ferrum Hausmann

Informazioni principali

  • Nome commerciale:
  • Ferrum Hausmann Kapseln
  • Forma farmaceutica:
  • Kapseln
  • Composizione:
  • ferro(II) 100 mg ut ferrosi fumaras, colore.: E 133, excipiens pro il capsula.
  • 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:
  • Ferrum Hausmann Kapseln
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • Eisenmangelanämie bei nachgewiesenem Eisenmangel

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 35102
  • Data dell'autorizzazione:
  • 19-01-1970
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Ferrum Hausmann® Capsule

VIFOR (INTERNATIONAL)

Che cos'è Ferrum Hausmann Capsule e quando si usa?

Le capsule Ferrum Hausmann contengono come principio attivo il ferro (sotto forma di sale di

ferro(II)-fumarato) di cui l'organismo ha bisogno per produrre l'emoglobina dei globuli rossi. Le

capsule Ferrum Hausmann servono ad eliminare una carenza di ferro dell'organismo, che può

verificarsi ad es. durante la gravidanza, nel puerperio, in caso di mestrui frequenti e copiosi, in

presenza di perdite di sangue dovute a malattie gastroenteriche o dopo operazioni a livello

gastrointestinale, in caso di alterazioni dell'assorbimento di ferro dai cibi, in tarda età o durante le

fasi di crescita dei bambini.

Pallore dovuto a tasso troppo basso d'emoglobina (anemia), stanchezza insolita, respiro affannoso o

riduzione dell'efficienza fisica fanno parte dei sintomi di una carenza di ferro.

Di che cosa occorre inoltre tener conto durante il trattamento?

Prima di iniziare il trattamento con le capsule Ferrum Hausmann, è opportuno che il tasso troppo

basso di ferro e d'emoglobina nel sangue sia confermato dal medico mediante esami appropriati. Se

l'anemia non è dovuta a carenza di ferro, il preparato non solo è privo d'efficacia ma può anche

indurre un sovraccarico di ferro.

Il medico seguirà con analisi del sangue i progressi della terapia.

Se i disturbi non migliorano nel giro di 3 settimane, consultare il medico.

Quando non si può usare le capsule Ferrum Hausmann?

Se soffre di emocromatosi, sovraccarico di ferro, disturbi del metabolismo del ferro (ad es. anemia

dovuta ad alterato assorbimento del ferro nell'intestino), intolleranza al ferro (ad es. gravi processi

infiammatori a livello gastrico e intestinale) o gravi malattie epatiche e renali, non deve prendere le

capsule Ferrum Hausmann. Il medico curante sa cosa occorre fare in casi del genere. I bambini al

disotto dei 6 anni non devono essere curati con le capsule Ferrum Hausmann, ma solo con un

preparato che contenga meno ferro. Il medico sa quale preparato è adatto per i bambini al disotto dei

6 anni.

Quando è richiesta prudenza nella somministrazione delle capsule Ferrum Hausmann?

In presenza di gastropatie o enteropatie a carattere infiammatorio o di altre affezioni del tratto

gastroenterico, è opportuno prendere preparati a base di ferro solo con prudenza e dopo aver

consultato il medico. La contemporanea assunzione dell'antibiotico tetraciclina riduce l'efficacia delle

capsule Ferrum Hausmann. Per questo stesso motivo, le capsule non devono essere assunte

contemporaneamente a cibi o generi voluttuari (tè, caffè) contenenti tannini.

In caso di assunzione concomitante quando devono essere assunti sia Ferrum Hausmann Capsule sia

ormoni tiroidei, dovrebbero trascorrere almeno 2 ore tra le due assunzioni per evitare di

compromettere l'assorbimento dell'ormone tiroideo.

Alcuni farmaci contro l'iperacidità di stomaco (se contengono calcio carbonato) o farmaci

ipolipidemizzanti (a base di colestiramina) possono ridurre l'efficacia delle capsule Ferrum

Hausmann pregiudicando l'assorbimento intestinale del ferro. Tra l'assunzione dei suddetti farmaci e

quella di un preparato a base di ferro, è quindi opportuno frapporre un intervallo di diverse ore.

Informi il suo medico il suo farmacista nel caso in cui

·soffre di altre malattie,

·soffre di allergie o

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

L'abuso cronico di alcool può indurre un sovraccarico di ferro a causa di un incremento

dell'assorbimento del ferro.

Si può assumere le capsule Ferrum Hausmann 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 le capsule Ferrum Hausmann?

Adulti:

Salvo diversa prescrizione medica, si assume solitamente 1 capsula al giorno, 10-15 minuti prima di

fare colazione con una quantità di liquido sufficiente. Per ridurre la comparsa di disturbi gastrici in

pazienti sensibili, si possono prendere le capsule anche con il pasto o subito dopo un pasto, benché la

loro efficacia possa risultare compromessa se assunte secondo questa modalità.

Le capsule Ferrum Hausmann vanno preso per lo più per parecchie settimane o mesi. Circa l'esatta

durata del trattamento sarà il medico a decidere in ogni caso singolo. 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 o al suo farmacista.

Bambini e ragazzi:

L'impiego e la sicurezza nei bambini e nei ragazzi finora non sono stati sperimentati in modo

metodico e sistematico.

Quali effetti collaterali possono avere le capsule Ferrum Hausmann?

Con l'assunzione delle capsule Ferrum Hausmann possono manifestarsi i seguenti effetti collaterali:

dolori addominali, diarrea, stitichezza e nausea (occasionalmente vomito), bruciore di stomaco, calo

dell'appetito e reazioni cutanee (ad es. arrossamento, prurito, esantema).

Tali effetti collaterali sono per lo più innocui e di natura transitoria. Se dovessero perdurare e dare

problemi, dovrà rivolgersi al medico.

Dato che le capsule Ferrum Hausmann contengono ferro, le feci possono assumere una colorazione

scura. Questo fenomeno è dovuto al fatto che non tutto il ferro è stato assorbito nell'intestino e

solitamente non ha alcuna importanza dal punto di vista medico. Tuttavia, in rari casi, possono

presentarsi feci nerastre e collose insieme ad altri effetti collaterali, in particolare feci striate di rosso,

crampi, dolori gastro-addominali. Se si osservano questi effetti collaterali, bisogna rivolgersi al

medico senza indugi.

Se inavvertitamente viene assunta una quantità maggiore (ad es. nei bambini) può verificarsi

un'intossicazione da ferro. I primi sintomi sono diarrea, nausea, vomito e dolori gastrici. In questi

casi è necessario informare immediatamente il medico che potrà stabilire come procedere.

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

Di che altro occorre tener conto?

Le capsule Ferrum Hausmann devono essere conservate assolutamente al di fuori della portata dei

bambini. Già una piccola confezione da 30 capsule contiene una dose complessiva di ferro che, se

assunta in una sola volta specie dai bambini piccoli, può causare una intossicazione da ferro grave e

potenzialmente fatale.

Conservare il medicamento in un luogo asciutto e a temperatura ambiente (15–25 °C). Il

medicamento non dev'essere utilizzato oltre la data indicata con «EXP» sulla confezione. Le capsule

eventualmente scadute vanno riportate in farmacia affinché vengano eliminate. Il medico o il

farmacista, che sono in possesso di documentazione professionale dettagliata, possono darle ulteriori

informazioni.

Che cosa contengono le capsule Ferrum Hausmann?

1 capsula di Ferrum Hausmann contiene come principio attivo 304 mg di ferro(II)-fumarato che

corrispondono a 100 mg di ferro (II).

Sostanze ausiliarie: coloranti Brilliant Blue FCF (E133) e titanio biossido (E171), sodio laurilsolfato

e altre sostanze ausiliarie.

Numero dell'omologazione

35102 (Swissmedic).

Dove sono ottenibili le capsule Ferrum Hausmann? Quali confezioni sono disponibili?

In farmacia senza prescrizione medica, confezioni da 30 e 100 capsule.

Titolare dell’omologazione

Vifor (International) AG, 9001 San Gallo.

Questo foglietto illustrativo è stato controllato l’ultima volta nell'aprile 2017 dall'autorità competente

in materia di medicamenti (Swissmedic).

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Opdivo (Bristol-Myers Squibb Pharma EEIG)

Opdivo (Bristol-Myers Squibb Pharma EEIG)

Opdivo (Active substance: nivolumab) - Centralised - 2-Monthly update - Commission Decision (2018)5204 of Wed, 01 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3985/II/41

Europe -DG Health and Food Safety

30-7-2018

NovoEight (Novo Nordisk A/S)

NovoEight (Novo Nordisk A/S)

NovoEight (Active substance: turoctocog alfa) - Centralised - 2-Monthly update - Commission Decision (2018)5093 of Mon, 30 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2719/II/23

Europe -DG Health and Food Safety

13-7-2018

Briviact (UCB Pharma S.A.)

Briviact (UCB Pharma S.A.)

Briviact (Active substance: brivaracetam) - Centralised - 2-Monthly update - Commission Decision (2018)4715 of Fri, 13 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3898/II/10/G

Europe -DG Health and Food Safety

9-7-2018

Pexion (Boehringer Ingelheim Vetmedica GmbH)

Pexion (Boehringer Ingelheim Vetmedica GmbH)

Pexion (Active substance: Imepitoin) - Centralised - 2-Monthly update - Commission Decision (2018)4433 of Mon, 09 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/2543/II/11/G

Europe -DG Health and Food Safety

4-7-2018

Tecentriq (Roche Registration GmbH)

Tecentriq (Roche Registration GmbH)

Tecentriq (Active substance: atezolizumab) - Centralised - 2-Monthly update - Commission Decision (2018)4336 of Wed, 04 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4143/II/10

Europe -DG Health and Food Safety

4-7-2018

Simponi (Janssen Biologics B.V.)

Simponi (Janssen Biologics B.V.)

Simponi (Active substance: golimumab) - Centralised - 2-Monthly update - Commission Decision (2018) 4350 of Wed, 04 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/992/II/79

Europe -DG Health and Food Safety

3-7-2018

Samsca (Otsuka Pharmaceutical Europe Ltd)

Samsca (Otsuka Pharmaceutical Europe Ltd)

Samsca (Active substance: tolvaptan) - Centralised - 2-Monthly update - Commission Decision (2018) 4250 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/980/II/31

Europe -DG Health and Food Safety

3-7-2018

Jinarc (Otsuka Pharmaceutical Europe Ltd)

Jinarc (Otsuka Pharmaceutical Europe Ltd)

Jinarc (Active substance: tolvaptan) - Centralised - 2-Monthly update - Commission Decision (2018)4243 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2788/II/16

Europe -DG Health and Food Safety

29-6-2018

Porcilis PCV M Hyo (Intervet International B.V.)

Porcilis PCV M Hyo (Intervet International B.V.)

Porcilis PCV M Hyo (Active substance: Porcine circovirus and Mycoplasma hyopneumoniae vaccine (inactivated)) - Centralised - 2-Monthly update - Commission Decision (2018)4166 of Fri, 29 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/3796/II/7

Europe -DG Health and Food Safety

20-6-2018

Blincyto (Amgen Europe B.V.)

Blincyto (Amgen Europe B.V.)

Blincyto (Active substance: blinatumomab) - Centralised - Authorisation - Switch to non-conditional - Commission Decision (2018)3953 of Wed, 20 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3731/II/9

Europe -DG Health and Food Safety

11-6-2018

Cimzia (UCB Pharma S.A.)

Cimzia (UCB Pharma S.A.)

Cimzia (Active substance: certolizumab pegol ) - Centralised - 2-Monthly update - Commission Decision (2018)3768 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1037/II/65

Europe -DG Health and Food Safety

11-6-2018

Cerdelga (Genzyme Europe B.V.)

Cerdelga (Genzyme Europe B.V.)

Cerdelga (Active substance: eliglustat) - Centralised - 2-Monthly update - Commission Decision (2018)3754 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3724/II/15/G

Europe -DG Health and Food Safety

11-6-2018

TAGRISSO (AstraZeneca AB)

TAGRISSO (AstraZeneca AB)

TAGRISSO (Active substance: osimertinib) - Centralised - 2-Monthly update - Commission Decision (2018)3757 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4124/II/19

Europe -DG Health and Food Safety

11-6-2018

Pradaxa (Boehringer Ingelheim International GmbH)

Pradaxa (Boehringer Ingelheim International GmbH)

Pradaxa (Active substance: dabigatran etexilate mesilate) - Centralised - 2-Monthly update - Commission Decision (2018)3755 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/829/II/108

Europe -DG Health and Food Safety

11-6-2018

Xultophy (Novo Nordisk A/S)

Xultophy (Novo Nordisk A/S)

Xultophy (Active substance: insulin degludec / liraglutide) - Centralised - 2-Monthly update - Commission Decision (2018)3779 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2647/II/23

Europe -DG Health and Food Safety

11-6-2018

Bexsero (GlaxoSmithKline Vaccines S.r.l.)

Bexsero (GlaxoSmithKline Vaccines S.r.l.)

Bexsero (Active substance: Meningococcal group B Vaccine (rDNA, component, adsorbed)) - Centralised - 2-Monthly update - Commission Decision (2018)3769 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2333/II/59

Europe -DG Health and Food Safety

6-6-2018

Prolia (Amgen Europe B.V.)

Prolia (Amgen Europe B.V.)

Prolia (Active substance: denosumab) - Centralised - 2-Monthly update - Commission Decision (2018) 3685 of Wed, 06 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1120/II/68

Europe -DG Health and Food Safety

4-6-2018

Yervoy (Bristol-Myers Squibb Pharma EEIG)

Yervoy (Bristol-Myers Squibb Pharma EEIG)

Yervoy (Active substance: ipilimumab) - Centralised - 2-Monthly update - Commission Decision (2018)3618 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2213/II/55

Europe -DG Health and Food Safety

4-6-2018

Eliquis (Bristol-Myers Squibb/Pfizer EEIG)

Eliquis (Bristol-Myers Squibb/Pfizer EEIG)

Eliquis (Active substance: apixaban) - Centralised - 2-Monthly update - Commission Decision (2018)3616 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2148/II/50

Europe -DG Health and Food Safety

4-6-2018

Alecensa (Roche Registration GmbH)

Alecensa (Roche Registration GmbH)

Alecensa (Active substance: alectinib) - Centralised - 2-Monthly update - Commission Decision (2018)3621 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4164/II/10

Europe -DG Health and Food Safety

30-5-2018

Avvio del procedimento di Pay-Back convenzionata 1.83% - 2° semestre 2017 (30/05/2018)

Avvio del procedimento di Pay-Back convenzionata 1.83% - 2° semestre 2017 (30/05/2018)

Si informano le aziende farmaceutiche che dalle ore 18,00 della data odierna sarà attiva la piattaforma Servizi Online dedicata al procedimento di Pay-back convenzionata 1,83% II semestre 2017.

Italia - AIFA - Agenzia Italiana del Farmaco

25-5-2018

Dirigenti di II Fascia - aggiornamento sezione

Dirigenti di II Fascia - aggiornamento sezione

L'Agenzia Italiana del Farmaco, ai sensi del d.lgs. 33/2013, rende disponibili aggiornamenti della sezione "Dirigenti di II Fascia".

Italia - AIFA - Agenzia Italiana del Farmaco

15-5-2018

CABOMETYX (Ipsen Pharma)

CABOMETYX (Ipsen Pharma)

CABOMETYX (Active substance: cabozantinib) - Centralised - 2-Monthly update - Commission Decision (2018)3015 of Tue, 15 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4163/II/3

Europe -DG Health and Food Safety

15-5-2018

Repatha (Amgen Europe B.V.)

Repatha (Amgen Europe B.V.)

Repatha (Active substance: evolocumab) - Centralised - 2-Monthly update - Commission Decision (2018)3014 of Tue, 15 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3766/II/17/G

Europe -DG Health and Food Safety