Ferro-Gradumet

Informazioni principali

  • Nome commerciale:
  • Ferro-Gradumet comprimere un rilascio prolungato
  • Forma farmaceutica:
  • comprimere un rilascio prolungato
  • Composizione:
  • ferro(II) 105 mg ut ferrosi zolfo dessiccatus, arom.: saccharinum natricum, colore.: E 127, excipiens pro compresso.
  • 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:
  • Ferro-Gradumet comprimere un rilascio prolungato
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • L'Anemia da carenza di ferro con carenza di ferro accertata

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 31644
  • Data dell'autorizzazione:
  • 22-06-1967
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Ferro-Gradumet®

FARMACEUTICA TEOFARMA

Che cos'è Ferro-Gradumet e quando si usa?

Ferro-Gradumet è un farmaco a base di ferro e viene utilizzato nel trattamento delle carenze di ferro

(anemia da carenza di ferro).

Il ferro è necessario per l’emoglobina contenuta nei globuli rossi e una carenza di ferro può

provocare anemia che si manifesta, per esempio, con un senso insolito d’affaticamento, difficoltà

respiratorie o con una riduzione delle prestazioni fisiche.

Ferro-Gradumet contiene ferro in una forma che libera lentemente il principio attivo nell’intestino

(principio del rilascio prolungato).

Di che cosa occorre inoltre tener conto durante il trattamento?

Prima di iniziare a prendere Ferro-Gradumet, dovrà esservi confermato dal medico il livello troppo

basso di ferro e di pigmento sanguigno (emoglobina) nel sangue tramite esami adeguati. Se l’anemia

non è dovuta a carenza di ferro, Ferro-Gradumet non soltanto è inefficace, ma può perfino condurre a

un sovraccarico di ferro.

Il vostro medico potrà eventualmente voler confermare il progresso del vostro trattamento con esami

ripetuti regolarmente e forse anche procedere a prelievi di sangue. Ciò è assolutamente normale e

non deve preoccuparvi. Se i vostri disturbi non migliorano entro 3 settimane, consultate di nuovo il

vostro medico.

Quando non si può assumere Ferro-Gradumet?

Nei casi di sovraccarico di ferro, di disturbi dell’utilizzo del ferro, di una «anemia» non legata a una

carenza di ferro, di intolleranza accertata (per es. con gravi stati infiammatori gastrointestinali), di

malattie epatiche e renali gravi. In caso di ipersensibilità a uno dei componenti.

A causa dell’alto contenuto di ferro, non somministrare Ferro-Gradumet ai bambini sotto i 12 anni e

con un peso inferiore ai 40 kg.

Quando è richiesta prudenza nell'uso di Ferro-Gradumet?

In presenza di certe malattie gastrointestinali le preparazioni a base di ferro devono essere utilizzate

unicamente dopo aver chiesto consiglio al medico. I medicinali destinati ad alleviare i bruciori

gastrici possono inibire l’assorbimento del ferro.

Inoltre Ferro-Gradumet non deve essere preso simultaneamente a medicinali contro la poliartrite

cronica o a determinati antibiotici (tetracicline e chinoloni), o con alimenti e generi voluttuari

contenenti acido tannico (per esempio, té nero e caffé) perchè questi medicinali/prodotti possono

influenzarsi a vicenda circa l’assorbimento.

Vi dovete perciò preoccupare – e anche il vostro medico ve lo raccomanderà – di lasciar passare

parecchie ore fra l’assunzione di Ferro-Gradumet e di uno di questi medicinali o alimenti.

Tenete presente che il consumo eccessivo e cronico d’alcol può causare un sovraccarico di ferro

attraverso l’aumentato assorbimento del ferro.

Informate il vostro medico o il vostro farmacista se :

·soffrite di altre malattie (in particolare, ulcera gastrica o una malattia intestinale infiammatoria,

come enterite o colite),

·avete un’allergia,

·prendete o usate esternamente altri medicinali (anche in automedicazione!).

Si può assumere/usare Ferro-Gradumet durante la gravidanza o l'allattamento?

Ferro-Gradumet è prescritto anche nei casi di carenza di ferro durante la gravidanza e l’allattamento.

Comunque, prima di iniziare a prendere Ferro-Gradumet, dovete assolutamente parlarne con il vostro

medico.

Come usare Ferro-Gradumet?

Adulti e adolescenti a partire dai 12 anni e di peso superiore ai 40 kg: prendere una compressa al

giorno con un po’ d’acqua, senza masticare, circa mezz’ora prima della colazione del mattino.

Il vostro medico può tuttavia adattare questa indicazione alle necessità del vostro organismo.

Una carenza di ferro necessita un lungo trattamento, vale a dire Ferro-Gradumet deve sovente essere

preso per settimane o mesi. Il successo del trattamento dipende dal vostro uso regolare!

Rispettate la posologia indicata nel foglio illustrativo o prescritta dal vostro medico. Rivolgetevi al

vostro medico o al vostro farmacista se pensate che l’effetto del farmaco sia troppo debole o, al

contrario, troppo forte.

Quali effetti collaterali può avere Ferro-Gradumet?

Si possono talvolta osservare disturbi gastrointestinali come nausea, dolori gastrici, diarrea o

costipazione. Si può osservare una colorazione scura delle feci. In rari casi sono anche state descritte

reazioni allergiche.

Se notate effetti collaterali che non sono citati in questo foglio illustrativo, informate il vostro medico

o il vostro farmacista.

Di che altro occorre tener conto?

Dato che la confezione da 30 compresse di Ferro-Gradumet contiene una dose totale di ferro che, se

presa tutta in una volta, può provocare un’intossicazione che può essere fatale, in particolare nei

bambini piccoli, è indispensabile tenere questo farmaco fuori della portata dei bambini.

Conservate il farmaco a temperatura ambiente (15–25 °C) ed utilizzatelo solo fino alla data riportata

sulla confezione sotto la dicitura «Scadenza».

Per altre informationi, rivolgetevi al vostro medico o al vostro farmacista i quali dispongono di dati

specialistici destinati ai professionisti della sanità.

Cosa contiene Ferro-Gradumet?

1 compressa a rilascio prolungato contiene:

105 mg di ferro (II) sotto forma di solfato di ferro come principio attivo.

Eccipienti: colorante E 127 (eritrosina), saccarina e altri eccipienti.

Numero dell'omologazione

31644 (Swissmedic).

Dov'è ottenibile Ferro-Gradumet? Quali confezioni sono disponibili?

In farmacia, senza ricetta medica.

Confezioni da 30 e 90 compresse.

Titolare dell’omologazione

Farmaceutica Teofarma Svizzera SA, 6901 Lugano.

Questo foglietto illustrativo è stato controllato l’ultima volta nel febbraio 2007 dall’autorità

competente in materia di medicamenti (Swissmedic).

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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