Tenormin mite

Informazioni principali

  • Nome commerciale:
  • Tenormin mite Tabletten
  • Forma farmaceutica:
  • Tabletten
  • Composizione:
  • atenololum 50 mg, 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:
  • Tenormin mite Tabletten
    Svizzera
  • Lingua:
  • italiano

Informazioni terapeutiche

  • Gruppo terapeutico:
  • Synthetika
  • Area terapeutica:
  • Beta-Rezeptorenblocker

Altre informazioni

Status

  • Fonte:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Numero dell'autorizzazione:
  • 39879
  • Data dell'autorizzazione:
  • 19-08-1976
  • Ultimo aggiornamento:
  • 19-10-2018

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

Patienteninformation

Tenormin®/- mite/- submite

ASTRAZENECA

Che cos’ è Tenormin e quando si usa?

Tenormin protegge il cuore da stimolazioni eccessive. Il lavoro del muscolo cardiaco viene ridotto e

la reazione cardiaca al carico fisico e psichico è attenuata. Tenormin diminuisce la pressione

sanguigna elevata. L'angina pectoris (forti dolori al petto con eventuale propagazione al braccio

sinistro) è dovuta a una ossigenazione insufficiente del cuore sotto sforzo. Tenormin evita gli attacchi

anginosi o ne diminuisce la frequenza e il dolore. Tenormin può normalizzare il ritmo cardiaco

alterato o ridurre le pulsazioni originate da malattia o dallo stress.

L'atenololo, principio attivo del Tenormin, appartiene ad una generazione di betabloccanti ad azione

specifica sul cuore. Esso riduce la pressione sanguigna elevata e calma l'attività cardiaca senza effetti

sulla muscolatura delle vie respiratorie. Pertanto, con la dovuta prudenza, anche i pazienti con

malattie respiratorie (respirazione difficile, asma) possono assumere Tenormin.

Il medico prescrive Tenormin:

·per ridurre la pressione sanguigna elevata (ipertensione),

·per proteggere il muscolo cardiaco da sforzi eccessivi (angina pectoris),

·per curare i disturbi del ritmo cardiaco,

·dopo infarto cardiaco,

·per prevenire un infarto cardiaco ulteriore.

Tenormin si può usare soltanto su prescrizione medica.

Quando non si può usare Tenormin?

In caso di una delle malattie seguenti rinunci a prendere Tenormin: se ha già avuto in precedenza una

reazione allergica al Tenormin od al principio attivo atenololo, se soffre d’insufficienza cardiaca o

blocco cardiaco (pulsazioni al disotto di 50 al minuto), nel caso Lei abbia avuto un polso molto lento

o molto irregolare, una pressione arteriosa molto bassa o molto cattiva irrorazione sanguigna, se in

Lei è stata constatata la presenza di un feocromocitoma o dopo un digiuno prolungato.

Tenormin non è adatto ai bambini.

Quando è richiesta prudenza nella somministrazione dell’Tenormin?

Questo medicamento può ridurre la capacità di reazione, la capacità di condurre un veicolo e la

capacità di utilizzare attrezzi o macchine! A causa dei possibili effetti indesiderati di Tenormin

(stanchezza, vertigini) occorre prudenza alla guida di veicoli e utilizzando delle macchine. Informi il

medico o il farmacista se soffre di asma, disturbi respiratori, disturbi dell’irrorazione sanguigna,

problemi al cuore, malattie dei reni o della tiroide. Comunichi al medico se usa altri medicamenti

quali, ad esempio disopiramide o amiodarone contro un polso irregolare, l’ipertensione o l’angina

pectoris, l’insufficienza cardiaca o contro i dolori.

Parli col medico se usa degli spray nasali decongestionanti o dei medicamenti contro le infreddature.

Se assume clonidina per la terapia di ipertensione o di emicrania, non deve sospendere né la

clonidina né il Tenormin senza averne prima parlato con il Suo medico.

Il suo polso si può rallentare durante il trattamento. Questa è una reazione normale al principio

attivo. Avverta il medico se le pulsazioni, a riposo, scendono al disotto di 50 al minuto.

Se durante il trattamento avverte vertigini o sensazione di stanchezza, Lei non deve guidare veicoli

ne usare macchinari.

Chieda consiglio al medico in caso di diabete, glicemia sovente troppo bassa, o se assume

contemporaneamente altri farmaci (e in particolare farmaci per il cuore). Prima d’intervento

chirurgico si devono elencare al medico anestesista i farmaci assunti.

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

o assuma o applichi altri medicamenti (anche acquistati di sua iniziativa).

Si può somministrare Tenormin durante la gavidanza o l’allattamento?

Durante la gravidanza o l’allattamento è opportuno evitare ogni farmaco e questa norma prudenziale

vale anche per Tenormin. In casi particolari il medico deciderà se e quando Tenormin va assunto

durante la gravidanza o l’allattamento.

Come usare Tenormin?

Come ogni farmaco, Tenormin si assume attenendosi strettamente alla prescrizione medica.

Generalmente la dose per l'adulto è di 1 compressa al giorno di Tenormin mite o 1 compressa al

giorno di Tenormin. Il medico adatterà la dose ai pazienti con malattia renale e turbe

dell'eliminazione. Ingerire la compressa con un poco di liquido, senza masticarla, di preferenza

sempre alla stessa ora, durante o dopo i pasti. Se una volta ha dimenticato di assumere una

compressa, la prenda appena se ne ricorda. Tuttavia, non si devono prendere due compresse

contemporaneamente. La pressione sanguina troppo alta può avere conseguenze gravi. Evitare in

ogni caso di interrompere la cura bruscamente e farlo gradualmente. Per rafforzare l’effetto di

Tenormin il medico può aggiungere un altro farmaco. Per evitare di interrompere la cura ci si accerti

di avere sempre una scorta adeguata di Tenormin. 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 Tenormin?

Con l’assunzione o l’applicazione di Tenormin possono manifestarsi i seguenti effetti collaterali:

Spesso sono stati riferiti stanchezza, rallentamento del battito cardiaco, sensazione di freddo nelle

dita delle mani e dei piedi, nausea, vomito e diarrea. Occasionalmente possono manifestarsi dei

disturbi del sonno. Rari sono piccole emorragie nella pelle o nelle mucose (porpora), confusione,

vertigini, mal di testa, cambiamenti d’umore, incubi, psicosi, allucinazioni, formicolio alle mani,

disturbi della vista, “occhi secchi”, aggravamento di disturbi dell’irrorazione sanguigna, blocco

cardiaco (ne sono sintomi battito cardiaco irregolare, stanchezza e vertigini alzandosi troppo

rapidamente), peggioramento di un’insufficienza cardiaca, pressione sanguigna bassa (ipotensione),

peggioramento dei disturbi respiratori negli asmatici, secchezza della bocca, aggravamento di una

psoriasi, eruzioni sulla pelle, caduta dei capelli e impotenza. Avverta immediatamente il medico se le

pulsazioni, a riposo, scendono al disotto di 50 al minuto o se la pressione sanguigna è troppo bassa.

Come tutti i farmaci regolatori della frequenza cardiaca, anche Tenormin può determinare alterazioni

del ritmo cardiaco.

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

Di che altro occorre tener conto?

Conservare le compresse nel loro imballaggio originale a temperatura ambiente (15-25 °C), al riparo

da luce e da umidità, in luogo inaccessibile ai bambini. Il medicamento non deve 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 Tenormin ?

Tenormin: compresse da 100 mg di atenololo e eccipienti.

Tenormin mite: compresse da 50 mg di atenololo e eccipienti.

Tenormin submite: compresse da 25 mg di atenololo e eccipienti.

Numero dell'omologazione

39879 (Swissmedic).

Dov’è ottenibile Tenormin? Quali confezioni sono disponibili?

Tenormin, Tenormin mite e Tenormin submite sono ottenibili in farmacia solo su ricetta medica.

Confezioni da 30 e 100 compresse.

Titolare dell’omologazione

AstraZeneca AG, 6340 Baar.

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

competente in materia di medicamenti (Swissmedic).

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Nyxoid (Mundipharma Corporation (Ireland) Limited)

Nyxoid (Mundipharma Corporation (Ireland) Limited)

Nyxoid (Active substance: naloxone) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7966 of Mon, 26 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4325/T/04

Europe -DG Health and Food Safety

26-11-2018

TAKHZYRO (Shire Pharmaceuticals Ireland Limited)

TAKHZYRO (Shire Pharmaceuticals Ireland Limited)

TAKHZYRO (Active substance: lanadelumab) - Centralised - Authorisation - Commission Decision (2018)7971 of Mon, 26 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004806/0000

Europe -DG Health and Food Safety

22-11-2018

Brineura (BioMarin International Limited)

Brineura (BioMarin International Limited)

Brineura (Active substance: cerliponase alfa) - Centralised - Yearly update - Commission Decision (2018)7885 of Thu, 22 Nov 2018

Europe -DG Health and Food Safety

22-11-2018

Incruse Ellipta (GlaxoSmithKline (Ireland) Limited)

Incruse Ellipta (GlaxoSmithKline (Ireland) Limited)

Incruse Ellipta (Active substance: umeclidinium bromide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7876 of Thu, 22 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2809/T/22

Europe -DG Health and Food Safety

22-11-2018

Levetiracetam Hospira (Hospira UK Limited)

Levetiracetam Hospira (Hospira UK Limited)

Levetiracetam Hospira (Active substance: levetiracetam) - Centralised - Renewal - Commission Decision (2018)7895 of Thu, 22 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2783/R/18

Europe -DG Health and Food Safety

22-11-2018

Vabomere (Rempex London Limited)

Vabomere (Rempex London Limited)

Vabomere (Active substance: meropenem/vaborbactam) - Centralised - Authorisation - Commission Decision (2018)7888 of Thu, 22 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4669/00

Europe -DG Health and Food Safety

21-11-2018

Rheumocam (Chanelle Pharmaceuticals Manufacturing Limited)

Rheumocam (Chanelle Pharmaceuticals Manufacturing Limited)

Rheumocam (Active substance: Meloxicam) - Centralised - Variation - Commission Decision (2018)7841 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/121/X/22

Europe -DG Health and Food Safety

21-11-2018

EU/3/15/1567 (TMC Pharma (EU) Limited)

EU/3/15/1567 (TMC Pharma (EU) Limited)

EU/3/15/1567 (Active substance: Recombinant human interleukin-3 truncated diphtheria toxin fusion protein) - Transfer of orphan designation - Commission Decision (2018)7816 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/064/15/T/02

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2102 (IQVIA RDS Ireland Limited)

EU/3/18/2102 (IQVIA RDS Ireland Limited)

EU/3/18/2102 (Active substance: Apraglutide) - Orphan designation - Commission Decision (2018)7812 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/115/18

Europe -DG Health and Food Safety

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

21-11-2018

EU/3/18/2099 (Celgene Europe Limited)

EU/3/18/2099 (Celgene Europe Limited)

EU/3/18/2099 (Active substance: Lisocabtagene maraleucel) - Orphan designation - Commission Decision (2018)7809 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/124/18

Europe -DG Health and Food Safety

21-11-2018

EU/3/18/2095 (United Neuroscience Limited)

EU/3/18/2095 (United Neuroscience Limited)

EU/3/18/2095 (Active substance: Ile-Ser-Ile-Thr-Glu-Ile-Lys-Gly-Val-Ile-Val-His-Arg-Ile-Glu-Thr-Ile-Leu-Phe-Lys-Lys-Lys-Lys-Glu-Met-Pro-Ser-Glu-Glu-Gly-Tyr-Gln-Asp) - Orphan designation - Commission Decision (2018)7805 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/146/18

Europe -DG Health and Food Safety

21-11-2018

EU/3/08/556 (Vertex Pharmaceuticals (Ireland) Limited)

EU/3/08/556 (Vertex Pharmaceuticals (Ireland) Limited)

EU/3/08/556 (Active substance: N-(2,4-Di-tert-butyl-5-hydroxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxamide) - Transfer of orphan designation - Commission Decision (2018)7814 of Wed, 21 Nov 2018 European Medicines Agency (EMA) procedure number: EMA/OD/010/08/T/03

Europe -DG Health and Food Safety

16-11-2018

Daptomycin Hospira (Hospira UK Limited)

Daptomycin Hospira (Hospira UK Limited)

Daptomycin Hospira (Active substance: daptomycin) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7678 of Fri, 16 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/004310/T/0008

Europe -DG Health and Food Safety

16-11-2018

Benlysta (GlaxoSmithKline (Ireland) Limited)

Benlysta (GlaxoSmithKline (Ireland) Limited)

Benlysta (Active substance: belimumab) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7679 of Fri, 16 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2015/T/60

Europe -DG Health and Food Safety

16-11-2018

Laventair Ellipta (GlaxoSmithKline (Ireland) Limited)

Laventair Ellipta (GlaxoSmithKline (Ireland) Limited)

Laventair Ellipta (Active substance: umeclidinium bromide / vilanterol trifenatate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7673 of Fri, 16 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3754/T/26

Europe -DG Health and Food Safety

9-11-2018

Recent Ebola outbreaks in remote areas with limited resources can benefit from rapid diagnostic tools, and the issuance of today’s EUA is an important step in addressing these outbreaks.  http://go.usa.gov/xPvs4 pic.twitter.com/o2I1dYUQCx

Recent Ebola outbreaks in remote areas with limited resources can benefit from rapid diagnostic tools, and the issuance of today’s EUA is an important step in addressing these outbreaks. http://go.usa.gov/xPvs4 pic.twitter.com/o2I1dYUQCx

Recent Ebola outbreaks in remote areas with limited resources can benefit from rapid diagnostic tools, and the issuance of today’s EUA is an important step in addressing these outbreaks. http://go.usa.gov/xPvs4  pic.twitter.com/o2I1dYUQCx

FDA - U.S. Food and Drug Administration

6-11-2018

Symkevi (Vertex Pharmaceuticals (Europe) Limited)

Symkevi (Vertex Pharmaceuticals (Europe) Limited)

Symkevi (Active substance: tezacaftor/ivacaftor) - Centralised - Authorisation - Commission Decision (2018)7415 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4682

Europe -DG Health and Food Safety

6-11-2018

Trelegy Ellipta (GlaxoSmithKline Trading Services Limited)

Trelegy Ellipta (GlaxoSmithKline Trading Services Limited)

Trelegy Ellipta (Active substance: fluticasone furoate/umeclidinium/vilanterol) - Centralised - 2-Monthly update - Commission Decision (2018)7416 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4363/WS/1369

Europe -DG Health and Food Safety

6-11-2018

Elebrato Ellipta (GlaxoSmithKline Trading Services Limited)

Elebrato Ellipta (GlaxoSmithKline Trading Services Limited)

Elebrato Ellipta (Active substance: fluticasone furoate/umeclidinium/vilanterol) - Centralised - 2-Monthly update - Commission Decision (2018)7417 of Tue, 06 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4781/WS/1369

Europe -DG Health and Food Safety

1-11-2018

Taxespira (Hospira UK Limited)

Taxespira (Hospira UK Limited)

Taxespira (Active substance: docetaxel) - Centralised - Withdrawal - Commission Decision (2018)7368 of Thu, 01 Nov 2018

Europe -DG Health and Food Safety

31-10-2018

Integrilin (GlaxoSmithKline (Ireland) Limited)

Integrilin (GlaxoSmithKline (Ireland) Limited)

Integrilin (Active substance: Eptifibatide) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7340 of Wed, 31 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/230/T/79

Europe -DG Health and Food Safety

31-10-2018

Volibris (GlaxoSmithKline (Ireland) Limited)

Volibris (GlaxoSmithKline (Ireland) Limited)

Volibris (Active substance: Ambrisentan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)7339 of Wed, 31 Oct 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/839/T/56

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Sellas Life Sciences Limited)

EU/3/18/2078 (Active substance: Peptides YMFPNAPYL, SGQAYMFPNAPYLPSCLES, RSDELVRHHNMHQRNMTKL and PGCNKRYFKLSHLQMHSRKHTG) - Orphan designation - Commission Decision (2018)7279 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/091/18

Europe -DG Health and Food Safety

30-10-2018

EU/3/18/2071 (Loxo Oncology Limited)

EU/3/18/2071 (Loxo Oncology Limited)

EU/3/18/2071 (Active substance: 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazabicyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile) - Orphan designation - Commission Decision (2018)7272 of Tue, 30 Oct 2018 European Medicines Agency (EMA) procedure number: EMA/OD/125/18

Europe -DG Health and Food Safety

22-10-2018

EU/3/17/1966 (Sirius Regulatory Consulting EU Limited)

EU/3/17/1966 (Sirius Regulatory Consulting EU Limited)

EU/3/17/1966 (Active substance: N-(bromoacetyl)-3,3-dinitroazetidine) - Transfer of orphan designation - Commission Decision (2018)6986 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety

22-10-2018

EU/3/15/1532 (Sirius Regulatory Consulting EU Limited)

EU/3/15/1532 (Sirius Regulatory Consulting EU Limited)

EU/3/15/1532 (Active substance: Insulin human) - Transfer of orphan designation - Commission Decision (2018)6985 of Mon, 22 Oct 2018

Europe -DG Health and Food Safety