Froben 100 mg

Informazioni principali

  • Nome commerciale:
  • Froben 100 mg Confetti
  • Forma farmaceutica:
  • Confetti
  • Composizione:
  • flurbiprofenum 100 mg, excipiens pro compresso obducto.
  • 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:
  • Froben 100 mg Confetti
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • Antiphlogisticum

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 40795
  • Data dell'autorizzazione:
  • 13-09-1977
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Froben®

BGP Products GmbH

Che cos’è Froben e quando si usa?

Il Froben è un medicamento altamente efficace capace di ridurre notevolmente le infiammazioni e di

combattere il dolore. Abbassa inoltre la febbre.

Il Froben viene applicato su prescrizione medica per il trattamento di dolori reumatici, come per

esempio malattie delle articolazioni, della schiena e dei muscoli, poliartrite, malattia di Bechterew ed

altri processi morbosi in cui è indicato combattere il dolore e l'infiammazione.

Froben confetti possono essere impiegati anche per lenire i dolori mestruali.

Quando non si può usare il Froben?

Froben non può essere assunto

·qualora abbia una reazione allergica ai componenti oppure abbia avuto dispnea o una reazione

dermica simile ad una allergia in seguito all'assunzione di acido acetilsalicilico o di altri analgesici o

antireumatici, i cosiddetti farmaci anti-infiammatori non steroidei;

·nell'ultimo trimestre della gravidanza;

·in caso di ulcere gastriche e/o duodenali o emorragie gastrointestinali attive;

·in caso di enteriti croniche (Malattia di Crohn, colite ulcerosa);

·in caso di una funzionalità epatica e renale fortemente limitata;

·in caso di grave debolezza cardiaca;

·nel trattamento di dolori in seguito ad interventi di bypass coronarico al cuore (o impiego di una

macchina cuore-polmone).

Quando è richiesta prudenza nella somministrazione di Froben?

Durante il trattamento con Froben possono manifestarsi nel tratto gastrointestinale superiore ulcere

alla mucosa, raramente emorragie o in singoli casi perforazioni gastro-intestinali. Tali complicazioni

possono manifestarsi durante il trattamento anche senza sintomi di avvertimento. Per ridurre il

rischio il Suo medico Le prescrive la dose minima efficace da assumere nell'arco di una durata del

trattamento più breve possibile. Si rivolga al Suo medico qualora accusi dolori allo stomaco o

qualora sospetti che vi sia un legame con l'assunzione del medicamento.

Questo medicamento può limitare la capacità di reazione, l'idoneità alla guida e la capacità di usare

attrezzi o macchine.

Per determinati analgesici, i cosiddetti inibitori COX-2, è stato accertato, nel caso vengano assunte

elevate dosi e/o in caso di un trattamento prolungato, un maggior rischio di infarto cardiaco e di

apoplessia. Se tale aumento del rischio vale anche per Froben non è ancora noto. Qualora abbia già

avuto un infarto cardiaco, un'apoplessia o una trombosi venosa, o qualora abbia i fattori di rischio

(come pressione sanguigna alta, diabete, elevata lipemia, fumo), il Suo medico deciderà se potrà

usare comunque Froben. Informi in ogni caso il Suo medico di tali circostanze. Non superare la dose

o la durata del trattamento consigliata.

L'assunzione di Froben può compromettere la funzione dei reni, comportando un possibile aumento

della pressione sanguigna e/o accumuli di liquidi (edemi). Informi il Suo medico qualora soffra di

cuore, di fegato o di reni, se assume medicamenti per l'ipertensione (per es. diuretici, ACE-inibitori)

o se vi è un aumento della perdita di liquidi, per es. attraverso una forte sudorazione.

Durante una terapia a base di analgesici sono state riscontrate molto raramente gravi reazioni

dermiche con arrossamenti e formazione di vescicole (dermatite esfoliativa, sindrome di Stevens-

Johnson e necrolisi tossica epidermica/sindrome di Lyell). Il maggior rischio per reazioni di questo

tipo sembra manifestarsi all'inizio della terapia, poiché nella maggior parte dei casi queste reazioni si

sono manifestate nel primo mese di trattamento. Al primo segno di eruzione cutanea, lesioni alla

mucosa o altri segni di una reazione di ipersensibilità la terapia con Froben dovrebbe essere interrotta

e dovrebbe essere consultato immediatamente un medico.

Informi il Suo medico se assume medicamenti, come anticoagulanti, diuretici, ACE-inibitori

(preparati contro la pressione alta e l'insufficienza cardiaca), antibiotici, immunosoppressivi

(preparati contro i rifiuti di trapianti), farmaci contro l'aumento di glicemia, contro l'AIDS, l'epilessia

e le depressioni. Informi il Suo medico, nel caso in cui Lei sia stata da poco curata per

un'interruzione di gravidanza. I farmaci antireumatici non steroidei, come l'Ibuprofene, e i farmaci

citati sopra possono influenzarsi reciprocamente.

L'acido acetilsalicilico o altri analgesici non devono essere assunti contemporaneamente a Froben,

poiché in tal caso il rischio che si manifestino effetti collaterali aumenta.

I pazienti ipersensibili alle sostanze coloranti azoiche, all'acido acetilsalicilico nonché ad

antireumatici e analgesici (inibitore di prostaglandina), devono astenersi dall'uso di Froben.

Pazienti anziani:

nei pazienti anziani si manifestano più spesso effetti collaterali in seguito all'uso di farmaci anti-

infiammatori non steroidei, in particolare emorragie e perforazioni nel tratto gastro-intestinale. Per

tale motivo, nel caso di una somministrazione a pazienti anziani, è necessario un monitoraggio

medico particolarmente accurato.

Informi il Suo medico o il Suo farmacista nel caso in cui

·soffre di asma,

·soffre di malattie cardiache, epatiche o renali,

·se in passato ha avuto una grave malattia dello stomaco o degli intestini,

·se soffre di disturbi di coagulazione,

·soffre di ipertensione arteriosa,

·soffre di altre malattie,

·se è allergico,

·se prende altri medicamenti (anche di propria iniziativa!) o li usa esternamente.

Si può somministrare il Froben durante la gravidanza o l’allattamento?

Gravidanza

Nel caso sia incinta o progetti di avere un bambino, consulti il Suo medico prima di prendere Froben.

Froben non deve essere assunto nell'ultimo trimestre di gravidanza.

Allattamento

Froben non deve essere assunto durante l'allattamento, a meno che Le sia espressamente consentito

dal Suo medico.

Come usare il Froben?

Froben Confetti

Adulti: 3–4 volte al giorno 1 confetto Froben 50 mg o 2 volte al giorno 1 confetto Froben 100 mg. In

casi severi il medico può prescrivere un dosaggio più alto (massimo 6 confetti Froben 50 mg o 3

confetti Froben 100 mg).

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 il Froben?

Con l'assunzione o l'applicazione di Froben possono manifestarsi i seguenti effetti collaterali:

Con il trattamento con Froben possono presentarsi spesso disturbi gastrointestinali come diarrea,

costipazione, disturbi digestivi, mal di pancia, flatulenza, bruciori di stomaco, nausea, feci scure e

vomito. Possono inoltre presentarsi spesso cefalea, capogiri, malessere, stanchezza, ritenzione idrica,

edemi, prolungamento del tempo di sanguinamento.

Ulcere gastriche possono presentarsi occasionalmente ma repentinamente e senza sintomi

premonitori. Ne possono conseguire emorragie gastriche. In casi rari possono manifestarsi eruzioni

cutanee o gonfiori nel viso, ai piedi o alle gambe.

Froben può causare occasionalmente reazioni di ipersensibilità a carico della cute e degli organi della

respirazione, in particolare nei pazienti affetti da asma, orticaria cronica o con ipersensibilità nota

all'acido acetilsalicilico o ad altri analgesici o antireumatici.

Molto raramente possono verificarsi reazioni dermiche gravi con arrossamento e formazione di

vescicole.

Se si dovessero osservare dei sintomi di tonsillite, come per esempio febbre alta, ingrossamento delle

ghiandole linfatiche nella regione del collo (in casi molto rari), dolori nell'addome, o se si notasse

una colorazione nera delle feci, allora si dovrebbe interrompere la somministrazione e consultare il

medico.

Occasionalmente possono presentarsi anemia, disturbi sensoriali, disturbi della vista, ipersensibilità

alla luce, tinnito, ipertensione, ridotta efficienza cardiaca, e raramente stati confusionali, depressioni,

disturbi del sonno e ridotta funzionalità renale.

Molto raramente sono state osservate allucinazioni, ittero e infiammazioni del pancreas.

L'uso di medicamenti come Froben può essere legato ad un rischio lievemente maggiore di infarti

cardiaci o apoplessie.

In caso di comparsa di altri effetti collaterali non riportati qui, informi il medico o il farmacista.

Di che altro occorre tener conto?

Froben deve essere conservato in luogo asciutto, non esposto alla luce ed a temperatura ambiente

(15-25 °C). Tenere fuori dalla 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.

Che cosa contiene il Froben?

Principio attivo: Flurbiprofene.

Froben confetti contengono: 50 mg rispett. 100 mg del principio attivo flurbiprofene nonché altri

eccipienti.

Numero dell’omologazione

40795 (Swissmedic).

Dov’è ottenibile Froben? Quali confezioni sono disponibili?

In farmacia dietro presentazione della prescrizione medica.

Froben Confetti da 50 mg/100 mg: 20 e 100.

Titolare dell’omologazione

BGP Products GmbH, 6341 Baar.

Questo foglietto illustrativo è stato controllato l'ultima volta nel settembre 2015 dall'autorità

competente in materia di medicamenti (Swissmedic).

[Version 206 I]

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Compounded Products Containing Triamcinolone-Moxifloxacin by Guardian Pharmacy Services (Dallas, Texas): Alert to Health Professionals - Adverse Events Reported After Receiving Eye Injections

Compounded Products Containing Triamcinolone-Moxifloxacin by Guardian Pharmacy Services (Dallas, Texas): Alert to Health Professionals - Adverse Events Reported After Receiving Eye Injections

At least 43 patient reported adverse event after receiving eye injections of Guardian’s Pharmacy Services compounded triamcinolone-moxifloxacin product during cataract surgery. The patients reportedly experienced various symptoms, including vision impairment, poor night vision, loss of color perception, and significant reductions in best-corrected visual acuity and visual fields. FDA identified multiple substances in Guardian’s product, including poloxamer 407 and poloxamer 407 degradants. FDA prepared i...

FDA - U.S. Food and Drug Administration

12-6-2018

Blokhuis: harde feiten gif in sigaretten zeer zorgelijk

Blokhuis: harde feiten gif in sigaretten zeer zorgelijk

Teer, nicotine en koolmonoxide gehalten in sigaretten die gemeten worden volgens de Canadian Intense (CI) methode zijn minimaal twee keer zo hoog als de gehalten gemeten met de wettelijke voorgeschreven ISO methode waarmee de EU en dus ook Nederland werkt. In sommige gevallen liggen de gehaltes zelfs tot meer dan 20 keer hoger. Dat blijkt uit onderzoek van het RIVM, dat 100 sigaretten onder de loep nam. Staatssecretaris Paul Blokhuis (VWS) heeft als opdrachtgever het onderzoek vandaag in ontvangst genome...

Netherlands - Ministerie van Volksgezondheid, Welzijn en Sport

3-5-2018

CVM eSubmitter Webinar 1 Agenda

CVM eSubmitter Webinar 1 Agenda

CVM will host the first of a three-part webinar series to provide information on the use of CVM’s electronic submission tool, eSubmitter, in the new animal drug application approval process. These webinars will support the use of eSubmitter as we move to 100% electronic submission.

FDA - U.S. Food and Drug Administration

28-2-2018

Help 100% & Pure Natural & Body Slim capsules

Help 100% & Pure Natural & Body Slim capsules

Help 100% & Pure Natural & Body Slim Capsules pose a serious risk to your health and should not be taken

Therapeutic Goods Administration - Australia

8-9-2017

The Icelandic Medicines Agency advertises a vacancy for an inspector in its Inspection Unit

The Icelandic Medicines Agency advertises a vacancy for an inspector in its Inspection Unit

The Icelandic Medicines Agency advertises a vacancy for an inspector. The Agency is looking for a candidate who is willing and able to work on demanding and interesting tasks, including travels in Iceland and abroad on behalf of the Agency. The vacancy is a full post (100%).

IMA - Icelandic Medicines Agency

3-7-2017

The Icelandic Medicines Agency wishes to recruit experts to its Licencing Unit

The Icelandic Medicines Agency wishes to recruit experts to its Licencing Unit

The Agency advertises two vacancies for experts in its Quality Assessment Team. The Agency is looking for strong candidates who are willing to work on challenging and interesting tasks. Each vacancy is a full position (100%). Application deadline is up to and including 16 July 2017.

IMA - Icelandic Medicines Agency

12-12-2018

Therapeutic Goods (Microbiological Standards for Medicines) (TGO 100) Order 2018

Therapeutic Goods (Microbiological Standards for Medicines) (TGO 100) Order 2018

TGO 100 has been registered on the Federal Register of Legislation. It commences on 8 December 2018, repealing and replacing TGO 98

Therapeutic Goods Administration - Australia

22-11-2018


Opinion/decision on a Paediatric investigation plan (PIP): Bempedoic acid (ETC-1002), decision type: , therapeutic area: , PIP number: P/0185/2018

Opinion/decision on a Paediatric investigation plan (PIP): Bempedoic acid (ETC-1002), decision type: , therapeutic area: , PIP number: P/0185/2018

Opinion/decision on a Paediatric investigation plan (PIP): Bempedoic acid (ETC-1002), decision type: , therapeutic area: , PIP number: P/0185/2018

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