Aktiferrin

Informazioni principali

  • Nome commerciale:
  • Aktiferrin Suscaps
  • Forma farmaceutica:
  • Suscaps
  • Composizione:
  • ferro(II) (34 mg ut ferrosi zolfo dessiccatus, dl-serinum, 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:
  • Aktiferrin Suscaps
    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:
  • 37840
  • Data dell'autorizzazione:
  • 26-09-1975
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Aktiferrin Suscaps®/Gocce

Mepha Pharma AG

Che cos’è l’Aktiferrin e quando si usa?

L'Aktiferrin è un preparato di ferro usato per il trattamento delle carenze di ferro nel sangue.

Il medicamento è adatto per la somministrazione a lattanti, bambini e adulti dato che è disponibile

sotto forma di gocce e di Suscaps.

Stati di carenza di ferro possono verificarsi

·in caso di perdite di sangue (p.es. a causa di malattie gastrointestinali, dopo operazioni allo stomaco

e all'intestino o in caso di mestruazioni frequenti e forti),

·durante la gravidanza, il puerperio e l'allattamento,

·nei periodi di crescita dei bambini piccoli e dei bambini,

·in caso di disturbi dell'assorbimento del ferro dagli alimenti (p.es. per insufficiente produzione di

acido nello stomaco, nella vecchiaia).

Di che cosa occorre inoltre tener conto durante il trattamento?

Se l'anemia non è dovuta a carenza di ferro l'Aktiferrin non è efficace. In questi casi la sua

somministrazione può portare a un eccesso di ferro nell'organismo.

Prima di iniziare la terapia il medico deve aver confermato con esami adatti che esiste una carenza di

ferro e di emoglobina nel sangue.

Quando non si può assumere l’Aktiferrin?

L'Aktiferrin non si può assumere in caso di eccesso di ferro nell'organismo, in presenza di

determinate forme di disturbi dell'utilizzazione del ferro (quando l'anemia dipende p.es. da un

disturbo dell'utilizzazione del ferro), in caso di anemia non dovuta a carenza di ferro, in caso di

giustificata intolleranza (p.es. per gravi alterazioni infiammatorie dello stomaco e dell'intestino),

dopo trasfusioni di sangue come pure in presenza di gravi malattie del fegato e dei reni. In caso di

ipersensibilità conosciuta a uno dei suoi costituenti.

Il medico sa cosa si deve fare in tali casi.

Quando è richiesta prudenza nella somministrazione dell’Aktiferrin?

Le carenze di ferro dovrebbero sempre essere curate sotto controllo medico. In presenza di malattie

infiammatorie dello stomaco o dell'intestino, in caso di evacuazione patologicamente ritardata dello

stomaco e in presenza di certe altre malattie del tratto gastrointestinale i preparati di ferro si devono

assumere con prudenza e solo dopo aver consultato il medico.

Certi medicamenti contro l'iperacidità gastrica (antiacidi) o contro tassi sanguigni troppo elevati dei

lipidi (colestiramina), certi analgesici e preparati a base di oro possono pregiudicare l'assorbimento

del ferro.

L'assunzione concomitante di preparati di ferro e di certi antibiotici (tetracicline, chinoloni),

dell'ormone tiroideo tiroxina, di medicamenti contro l'artrite reumatoide (penicillamina),

dell'antiipertensivo metildopa o di certi farmaci contro il morbo di Parkinson (levodopa, carbidopa)

ne pregiudica l'assorbimento.

Perciò tra l'assunzione di uno dei medicamenti suddetti e quella del preparato di ferro dev'esserci un

intervallo di alcune ore.

L'effetto irritante dei preparati di ferro sulle mucose dello stomaco e dell'intestino può essere

potenziato dall'assunzione concomitante di certi medicamenti antiinfiammatori. L'abuso cronico

d'alcool, aumentando l'assorbimento del ferro, può causare un eccesso di ferro nell'organismo.

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

o assuma o applichi esternamente altri medicamenti (anche se acquistati di sua iniziativa),

specialmente antibiotici.

Si può assumere l’Aktiferrin durante la gravidanza o l’allattamento?

Durante la gravidanza e l'allattamento l'Aktiferrin va assunto soltanto dopo aver consultato il medico.

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

correttamente. Tuttavia non sono mai state eseguite indagini scientifiche sistematiche. Per prudenza

dovrebbe rinunciare nella misura del possibile ad assumere medicamenti durante la gravidanza e

l'allattamento o chiedere consiglio al suo medico o al suo farmacista.

Come usare l’Aktiferrin?

Aktiferrin Suscaps

Salvo diversa prescrizione del medico, la posologia per adulti e per bambini oltre i 3 anni è di

1 Suscaps 1 volta al giorno.

Aktiferrin gocce

Salvo diversa prescrizione del medico, la posologia per bambini piccoli da 1 a 3 anni è di 18 gocce 2-

3 volte al giorno, per lattanti da 6 a 12 mesi di 13 gocce 2-3 volte al giorno e per lattanti fino ai

6 mesi di 10 gocce 1-3 volte al giorno.

Dopo l'assunzione delle gocce Aktiferrin bisogna lavare subito i denti o sciacquare la bocca con

abbondante liquido, perché altrimenti può verificarsi una colorazione dei denti. Questa colorazione è

innocua e regredisce di nuovo con una normale igiene dentale.

L'effetto di un preparato di ferro viene fortemente ridotto se lo si prende contemporaneamente a certi

alimenti e bevande (p.es. certe verdure, caffè, tè nero). Perciò, se possibile, l'Aktiferrin va preso

prima dei pasti. Se si manifestano dei disturbi di stomaco lo si può prendere anche durante o dopo i

pasti.

Quando si contano le gocce tenere il flaconcino verticalmente.

Generalmente l'Aktiferrin si deve assumere per un periodo di tempo abbastanza lungo; il medico

decide per ogni singolo caso la durata precisa della terapia.

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.

Quali effetti collaterali può avere l’Aktiferrin?

Occasionalmente possono manifestarsi lievi disturbi digestivi quali sensazione di pienezza,

pesantezza di stomaco, vomito, stitichezza o diarrea, che di solito scompaiono dopo aver ridotto la

dose. Però la dose si dovrebbe ridurre solo col consenso del medico.

Una occasionale colorazione nera delle feci non ha nessuna importanza. Quando si assumono dei

medicamenti contenenti ferro le feci si colorano di nero a causa della porzione di ferro non

completamente assorbita dall'organismo. Si può evitare una colorazione dei denti lavandoli e

sciacquando la bocca subito dopo l'assunzione del farmaco.

Raramente sono state constatate anche delle reazioni allergiche.

Un iperdosaggio può provocare i seguenti disturbi: nausea, vomito, dolori di ventre, diarrea e, dopo

un certo tempo, polso accelerato, vertigini, difficoltà di respirazione (dispnea) e cianosi delle labbra e

del viso, in casi gravi respirazione irregolare, convulsioni e fenomeni di paralisi.

In questi casi bisogna avvertire subito il medico e cercare di provocare il vomito.

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

Di che altro occorre tener conto?

Le gocce Aktiferrin contengono 2 vol.% d'alcool.

Siccome una confezione intatta di Aktiferrin (Suscaps o gocce) contiene una dose totale di ferro che

ingerita in una sola volta può causare una grave intossicazione soprattutto nei bambini piccoli, questo

medicamento va assolutamente tenuto fuori dalla portata dei bambini.

Il medicamento non dev'essere utilizzato oltre la data indicata con «EXP» sul contenitore.

Aktiferrin Suscaps

Non conservare a temperatura superiore ai 30 °C. Conservare al riparo dall'umidità. Non congelare e

non conservare in frigorifero.

Tenere fuori dalla portata dei bambini.

Aktiferrin gocce

Non conservare a temperatura superiore ai 25 °C. Conservare al riparo dalla luce. Non congelare e

non conservare in frigorifero.

Dopo l'apertura della confezione, conservare in frigorifero e consumare entro 30 giorni.

Tenere fuori dalla portata dei bambini.

Le macchie lasciate dalle gocce sui tessuti si possono togliere con un prodotto per togliere le macchie

di ruggine.

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

darle ulteriori informazioni.

Cosa contiene l'Aktiferrin?

Aktiferrin Suscaps

1 Suscaps contiene:

Principi attivi: ferro (Fe++) 34 mg (sotto forma di ferroso solfato). DL-serina 129 mg e sostanze

ausiliarie.

Aktiferrin gocce

1 ml (= 13 gocce) contiene:

Principi attivi: ferro (Fe++) 10 mg (sotto forma di ferroso solfato), DL-serina 38 mg.

Sostanze ausiliarie: conservante: potassio sorbato (E 202).

colorante: caramello (E 150) aromatizzanti, alcool (2 vol.%).

Numero dell'omologazione

37840, 40203 (Swissmedic).

Dov'è ottenibile l'Aktiferrin? Quali confezioni sono disponibili?

In farmacia senza prescrizione medica.

Aktiferrin Suscaps: confezioni da 30 Suscaps.

Aktiferrin gocce: confezioni da 30 ml.

Titolare dell’omologazione

Mepha Pharma AG, Basel.

Questo foglietto illustrativo è stato controllato l'ultima volta nel settembre 2016 dall'autorità

competente in materia di medicamenti (Swissmedic).

Numero interno della versione: 4.2

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Coagadex (Bio Products Laboratory Ltd)

Coagadex (Bio Products Laboratory Ltd)

Coagadex (Active substance: human coagulation factor X) - Centralised - 2-Monthly update - Commission Decision (2018)5772 of Wed, 29 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3855/II/07

Europe -DG Health and Food Safety

29-8-2018

Nucala (GlaxoSmithKline Trading Services Limited)

Nucala (GlaxoSmithKline Trading Services Limited)

Nucala (Active substance: mepolizumab) - Centralised - 2-Monthly update - Commission Decision (2018)5770 of Wed, 29 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3860/II/13/G

Europe -DG Health and Food Safety

27-8-2018

RoActemra (Roche Registration GmbH)

RoActemra (Roche Registration GmbH)

RoActemra (Active substance: tocilizumab) - Centralised - 2-Monthly update - Commission Decision (2018)5687 of Mon, 27 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/955/II/78

Europe -DG Health and Food Safety

22-8-2018

Lenvima (Eisai Europe Limited)

Lenvima (Eisai Europe Limited)

Lenvima (Active substance: lenvatinib) - Centralised - 2-Monthly update - Commission Decision (2018)5627 of Wed, 22 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3727/II/11/G

Europe -DG Health and Food Safety

22-8-2018

BTVPUR (Merial)

BTVPUR (Merial)

BTVPUR (Active substance: Bluetongue virus vaccine (inactivated) (multistrain: 1-2 strains out of a set of 4)) - Centralised - 2-Monthly update - Commission Decision (2018)5630 of Wed, 22 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/2231/II/10

Europe -DG Health and Food Safety

7-8-2018

Inovelon (Eisai Limited)

Inovelon (Eisai Limited)

Inovelon (Active substance: Rufinamide) - Centralised - 2-Monthly update - Commission Decision (2018)5424 of Tue, 07 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/660/II/45

Europe -DG Health and Food Safety

6-8-2018

Rapamune (Pfizer Limited)

Rapamune (Pfizer Limited)

Rapamune (Active substance: sirolimus) - Centralised - 2-Monthly update - Commission Decision (2018)5384 of Mon, 06 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/273/II/164

Europe -DG Health and Food Safety

6-8-2018

Dexdor (Orion Corporation)

Dexdor (Orion Corporation)

Dexdor (Active substance: dexmedetomidine) - Centralised - 2-Monthly update - Commission Decision (2018)5377 of Mon, 06 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2268/II/26

Europe -DG Health and Food Safety

3-8-2018

EU/3/18/2042 (MeiraGTx UK II Limited)

EU/3/18/2042 (MeiraGTx UK II Limited)

EU/3/18/2042 (Active substance: Adenovirus associated viral vector serotype 2/8 containing the human CNGA3 gene) - Orphan designation - Commission Decision (2018)5274 of Fri, 03 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/048/18

Europe -DG Health and Food Safety

1-8-2018

Eylea (Bayer AG)

Eylea (Bayer AG)

Eylea (Active substance: aflibercept) - Centralised - 2-Monthly update - Commission Decision (2018)5222 of Wed, 01 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2392/II/45

Europe -DG Health and Food Safety

1-8-2018

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