Vermox 100 mg

Informazioni principali

  • Nome commerciale:
  • Vermox 100 mg Tabletten
  • Forma farmaceutica:
  • Tabletten
  • Composizione:
  • mebendazolum 100mg, gossypii oleum hydrogenatum, aromatica, saccharinum natricum, colore.: E 110, 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:
  • Vermox 100 mg Tabletten
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • Anthelmintikum

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 38853
  • Data dell'autorizzazione:
  • 18-12-1974
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Informazioni destinata ai pazienti

Legga attentamente il foglietto illustrativo, che contiene importanti informazioni.

Questo medicamento le è stato prescritto dal suo medico o le è stato consegnato senza prescrizione

medica in farmacia. Per ottenere il maggior beneficio, usi il medicamento conformemente al foglietto

illustrativo o segua le indicazioni del suo medico o del suo farmacista.

Conservi il foglietto illustrativo per poterlo rileggere all’occorrenza.

Vermox® 100 mg

Che cos’è Vermox 100 mg e quando si usa?

Il Vermox 100 mg è un preparato contro le elmintiasi (malattie da vermi) intestinali dovuto ad

ossiuri, ascaridi, tricocefali, strongili e/o anchilostomi.

Il Vermox 100 mg è efficace anche contro certe specie di tenia (tenia del bue e tenia del maiale).

Il Vermox 100 mg altera il metabolismo dei parassiti che, di conseguenza, muoiono e vengono

eliminati con le feci dopo alcuni giorni.

Dato che gli ossiuri sono facilmente trasmissibili, è senz’altro possibile che anche altri membri della

famiglia abbiano contratto senza saperlo l’infezione. In questi casi, si consiglia di curare tutti i

membri di una famiglia o di un gruppo di persone.

Di che cosa occorre inoltre tener conto durante il trattamento?

Per evitare una trasmissione dei parassiti, occorrono misure igieniche rigorose. Bisogna evitare di

toccare direttamente l’ano con le mani. Dopo ogni defecazione, si devono lavare le mani (comprese

le unghie) scrupolosamente. La biancheria intima va cambiata sovente.

Il Vermox 100 mg non macchia la biancheria.

Quando non si può assumere Vermox 100 mg?

Il paziente non deve prendere il Vermox 100 mg in caso di ipersensibilità nota al principio attivo o

ad uno degli eccipienti contenuti nel preparato.

Quando è richiesta prudenza nella somministrazione di Vermox 100 mg?

Nei bambini minori di 2 anni, il Vermox 100 mg può essere somministrato esclusivamente su

prescrizione medica.

I pazienti ipersensibili alle sostanze coloranti azoiche, agli acidi acetilsalicilici nonché agli

antireumatici ed analgesici (inibitore della prostaglandina), devono astenersi dall’uso di Vermox 100

Se il paziente deve prendere contemporaneamente un preparato contenente cimetidina (un

medicamento contro la secrezione eccessiva di acido gastrico), carbamazepina o fentoina per

precauzione dovrebbe segnalarlo al medico o al farmacista.

Va evitata la somministrazione di Vermox insieme a preparati che contengono metronidazolo.

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

assume altri medicamenti (anche se acquistati di sua iniziativa!).

Si può somministrare Vermox 100 mg durante la gravidanza o l’allattamento?

Se è in corso o in programma una gravidanza o se allatta, la paziente dovrebbe prendere il Vermox

100 mg soltanto dopo avere consultato il medico.

Negli esperimenti condotti su animali, Vermox ha provocato malformazioni congenite nei topi e nei

ratti. Per quanto concerne l’uomo, si dispone finora di scarse esperienze. Per questo motivo le donne

in età fertile possono prendere Vermox 100 mg solamente se è esclusa una gravidanza. Se una

gravidanza non può essere esclusa, Vermox 100 mg non deve essere preso, salvo diversa

prescrizione medica.

Non è noto se il mebendazolo passi nel latte materno. In caso di assunzione di Vermox 100 mg è

consigliato lo svezzamento per le madri che allattano.

Come usare Vermox 100 mg?

Salvo diversa prescrizione del medico, il Vermox 100 mg va utilizzato nel seguente modo:

Le compresse di Vermox 100 mg possono essere ingerite intere o masticate. Le compresse vanno

prese con un po’ di cibo o di liquido; ai bambini si possono dare anche triturate.

Le seguenti posologie valgono sia per gli adulti che per i bambini maggiori di 1 anno,

indipendentemente dal peso corporeo:

Parassitosi da ossiuri: 1 compressa come dose unica. Si consiglia di ripetere il trattamento dopo 2

settimane.

Parassitosi da diverse specie di vermi, ascaridi, tricocefali, strongili e anchilostomi: 1 compressa al

mattino ad 1 alla sera per 3 giorni consecutivi.

Teniasi: 2 x 1-2 compresse al giorno per 3 giorni.

Non occorrono ulteriori misure dietetiche o l’assunzione di lassativi.

Si attenga alla posologia indicata nel foglietto illustrativo o prescritta dal suo 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 Vermox 100 mg?

Sono stati osservati i seguenti effetti collaterali che possono comparire a seguito dell’assunzione di

Vermox 100 mg:

Occasionalmente possono manifestarsi capogiri, diarrea, flatulenze, dolori addominali, nausea e

vomito (tali effetti possono derivare anche dall’infestazione da vermi stessa), nonché cefalea e

vertigini. Le patologie cutanee di forma allergica (inclusa la sindrome di Stevens-Johnsons) e le

reazioni di ipersensibilità al principio attivo non possono essere completamente escluse; queste

compaiono soprattutto all’inizio del trattamento e si manifestano con eruzioni cutanee, prurito,

orticaria e gonfiori localmente circoscritti al viso, alla bocca o alla gola (angioedema). In questo caso

informare immediatamente il medico, il quale deciderà se proseguire il trattamento.

In casi molto rari sono stati osservati caduta di capelli, alterazioni del quadro ematico, che possono

manifestarsi con febbre, mal di gola e altri sintomi di angina. In questi casi si deve consultare

immediatamente il medico prima di proseguire il trattamento. Molto raramente possono inoltre

manifestarsi epatiti che possono manifestarsi con dolore nell'addome superiore, soprattutto sotto

l’arco costale destro, perdita di appetito, nausea, vomito, febbre, ingiallimento degli occhi e della

pelle, colorazione scura delle urine e colorazione chiara delle feci.

Nei bambini e nei neonati possono verificarsi molto raramente crampi.

Inoltre il colorante E 110 (giallo-arancio S) può provocare reazioni di ipersensibilità della pelle e del

sistema respiratorio, in particolare nei pazienti affetti da asma, orticaria (orticaria cronica),

ipersensibilità agli acidi acetilsalicilici e ad altri antireumatici o analgesici.

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

Sovradosaggio

Se Vermox viene assunto in quantità superiori alle dosi raccomandate o per periodi prolungati, può

causare come conseguenze patologie ematiche, renali ed epatiche, che in alcuni casi possono

assumere forme gravi. Può inoltre verificarsi la caduta di capelli, che in alcuni casi può protrarsi a

lungo.

Se ha ingerito una dose troppo elevata di Vermox, possono presentarsi gastrospasmi, nausea, vomito

e diarrea. In questo caso si rivolga al medico che le potrà consigliare di assumere del carbone

vegetale che è in grado di assorbire il quantitativo di Vermox ancora presente nello stomaco.

Informazioni per il medico in caso di sovradosaggio

-Non c’è un antidoto specifico.

-Se si ritiene opportuno, è possibile somministrare carbone vegetale.

Di che altro occorre tener conto?

Tenere fuori dalla portata dei bambini!

Il Vermox 100 mg deve essere conservato nella confezione originale chiusa, in luogo asciutto a

temperatura ambiente (15 – 25 °C).

Il medicamento non dev’essere utilizzato oltre la data indicata con “EXP” sul contenitore.

Terminato il trattamento, riporti il farmaco col contenuto residuo dove le è stato consegnato, per lo

smaltimento specializzato.

Il medico o il farmacista, che sono in possesso di un’informazione professionale dettagliata, possono

darle ulteriori informazioni.

Cosa contiene Vermox 100 mg?

Compresse di colore arancio chiaro, rotonde e piatte, da 100 mg di mebendazolum per compressa.

1 compressa di Vermox 100 mg contiene 100 mg di mebendazolo (principio attivo); aromi ed

edulcoranti (saccarina); colorante: giallo arancio S (E 110), olio di semi di cotone idrogenato (da

semi di cotone modificato con tecnologia genetica) ed eccipienti.

Numero dell’omologazione

38853 (Swissmedic)

Dov'è ottenibile Vermox 100 mg? Quali confezioni sono disponibili?

In farmacia, senza prescrizione medica.

Confezioni da 6 compresse.

Titolare dell’omologazione

Janssen-Cilag AG, Zug, ZG

Questo foglietto illustrativo è stato controllato l'ultima volta nel luglio 2017 dall'autorità competente

in materia di medicamenti (Swissmedic).

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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