Gly-Coramin

Hauptinformation

  • Handelsname:
  • Gly-Coramin Lutschtabletten
  • Darreichungsform:
  • Lutschtabletten
  • Zusammensetzung:
  • nicethamidum 125 mg, glucose monohydricum 200 mg Glukose-Flüssigkeit, Zucker 1.138 g, excipiens für die Torte.
  • Verwenden für:
  • Menschen
  • Art der Medizin:
  • Biologische Medizin

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Gly-Coramin Lutschtabletten
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Synthetika
  • Therapiebereich:
  • Tonikum

Weitere Informationen

Status

  • Quelle:
  • Swissmedic - Swiss Agency for Therapeutic Products
  • Zulassungsnummer:
  • 25385
  • Berechtigungsdatum:
  • 10-06-1959
  • Letzte Änderung:
  • 24-10-2018

Packungsbeilage: zusammensetzung, kinische angaben, nebenwirkungen, wechselwirkungen, dosierung, schwangerschaft, stillzeit

Patienteninformation

Gly-Coramin®

HÄNSELER

Was ist Gly-Coramin und wann wird es angewendet?

Gly-Coramin enthält Traubenzucker (Glucose), der Energie spendet, und Nikethamid, das die

Atmung anregend beeinflussen kann. Gly-Coramin kann angewendet werden bei:

Ermüdungserscheinungen bei körperlichen Anstrengungen sowie bei Beschwerden, die durch einen

Höhenaufenthalt oder Luftdruckveränderungen wie z.B. beim Berggehen hervorgerufen werden.

Was sollte dazu beachtet werden?

Hinweis für Diabetiker: Gly-Coramin enthält Rohrzucker (Saccharose) und ist deshalb für Diabetiker

nicht geeignet.

Hinweis für Sportler: Die Einnahme von Gly-Coramin kann eine positive Reaktion bei Antidoping-

Kontrollen zur Folge haben.

1 Lutschtablette enthält 2,7 g Kohlenhydrate (= 0,27 Brotwerte).

Wann darf Gly-Coramin nicht angewendet werden?

Bei bekannter Überempfindlichkeit gegenüber in Gly-Coramin enthaltenen Substanzen sowie bei

Epilepsie, Porphyrie (eine Stoffwechselerkrankung) und Bluthochdruck.

Wann ist bei der Einnahme von Gly-Coramin Vorsicht geboten?

Gly-Coramin enthält Traubenzucker (Glucose) sowie Rohrzucker (Saccharose) und ist deshalb für

Diabetiker nicht geeignet.

Informieren Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin, Apothekerin oder Drogistin,

wenn Sie an anderen Krankheiten leiden, Allergien haben oder andere Arzneimittel (auch

selbstgekaufte!) einnehmen oder äusserlich anwenden.

Darf Gly-Coramin während einer Schwangerschaft oder in der Stillzeit eingenommen werden?

Wenn Sie schwanger sind oder es werden möchten und während der Stillzeit sollten Sie Gly-

Coramin nicht einnehmen. Schwangerschaftsbedingte Ermüdungserscheinungen sollen nicht mit

Gly-Coramin behandelt werden.

Wie verwenden Sie Gly-Coramin?

Die Wirkung von Gly-Coramin wird rasch verspürt.

Erwachsene und Jugendliche ab 16 Jahren: 1 Lutschtablette im Munde zergehen lassen. In der Regel

können auf den Tag verteilt bis zu ca. 10 Lutschtabletten eingenommen werden. Gly-Coramin soll

bei Kindern und Jugendlichen unter 16 Jahren nicht angewendet werden.

Halten Sie sich an die in der Packungsbeilage angegebene oder vom Arzt oder der Ärztin

verschriebene Dosierung. Wenn Sie glauben, das Arzneimittel wirke zu schwach oder zu stark, so

sprechen Sie mit Ihrem Arzt, Apotheker oder Drogisten bzw. mit Ihrer Ärztin, Apothekerin oder

Drogistin.

Welche Nebenwirkungen kann Gly-Coramin haben?

Für Gly-Coramin sind bisher keine Nebenwirkungen beobachtet worden. Wenn Sie dennoch

Nebenwirkungen bemerken, sollten Sie Ihren Arzt, Apotheker oder Drogisten bzw. Ihre Ärztin,

Apothekerin oder Drogistin informieren.

Was ist ferner zu beachten?

Arzneimittel sollen für Kinder unerreichbar aufbewahrt werden, Gly-Coramin insbesondere wegen

der Verwechslungsgefahr mit Bonbons.

Vor Feuchtigkeit schützen und bei Raumtemperatur (15–25 °C) lagern. Das Arzneimittel darf nur bis

zu dem auf dem Behälter mit «EXP» bezeichneten Datum verwendet werden.

Weitere Auskünfte erteilt Ihnen Ihr Arzt, Apotheker oder Drogist bzw. Ihre Ärztin, Apothekerin oder

Drogistin.

Was ist in Gly-Coramin enthalten?

1 Lutschtablette enthält: 125 mg Nikethamid, 200 mg Glucose in Form von Stärkesirup, 1,1 g

Saccharose sowie Aromastoffe.

Zulassungsnummer

25385 (Swissmedic).

Wo erhalten Sie Gly-Coramin? Welche Packungen sind erhältlich?

In Apotheken und Drogerien, ohne ärztliche Verschreibung.

Packung zu 30 Lutschtabletten.

Zulassungsinhaberin

Hänseler AG, 9101 Herisau.

Diese Packungsbeilage wurde im April 2012 letztmals durch die Arzneimittelbehörde (Swissmedic)

geprüft.

14-12-2018

Project DEMETER: Concept Note for an Emerging Risks Knowledge Exchange Platform (ERKEP) Framework

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Published on: Thu, 13 Dec 2018 Researchers, governments, agencies, food producers and the civil society are increasingly concerned about ‘emerging food risks’. It is recognised that the successful identification of emerging risks is at the heart of protecting public health and the environment, and that this requires worldwide cooperation between all parties involved in the food supply chain. The objectives and research proposed in the DEMETER project are designed to support current (and future) EFSA pro...

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Assessment of genetically modified maize MZHG0JG for food and feed uses, import and processing under Regulation (EC) No 1829/2003 (application EFSA‐GMO‐DE‐2016‐133)

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Risk assessment of substances used in food supplements: the example of the botanical Gymnema sylvestre

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Published on: Tue, 28 Aug 2018 00:00:00 +0200 Botanicals and preparations derived from these are among the substances frequently added to foods and food supplements, yet the safety of many botanicals has not been systematically assessed. In the context of the EU‐FORA fellowship programme, the fellow performed an assessment on the safety of the botanical Gymnema sylvestre, in accordance with EFSA's guidance on the assessment of safety of botanicals. Although preparations of G. sylvestre are marketed as f...

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Seaweed consumption: remain vigilant to the risk of excess iodine intake

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Over the last few years, seaweed has become increasingly common on our plates. Fresh, dried or as a food supplement, its iodine content varies and can sometimes be high. ANSES assessed the risk of excess iodine intake from the consumption of seaweed-based products. In view of the non-negligible risk of exceeding the upper limit of safe intake for iodine, the Agency advises against the consumption of seaweed and seaweed-based food supplements by certain at-risk populations, and recommends that regular con...

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Apricot kernels pose a risk of cyanide poisoning

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A familiar ingredient for jam-makers, apricot kernels are increasingly being consumed as a natural remedy for their claimed "anti-cancer" properties. While one kernel added to perfume several jars of jam is not a problem, ingesting them in large quantities exposes consumers to the risk of cyanide poisoning. ANSES has identified several cases of apricot kernel poisoning in France through its toxicovigilance scheme, and encourages consumers to exercise caution.

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Orphan designation: Glucagon, Treatment of noninsulinoma pancreatogenous hypoglycaemia syndrome, 19/11/2018, Positive

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14-2-2019

EU/3/16/1656 (Sellas Life Sciences Limited)

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EU/3/16/1656 (Active substance: Tyr-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu, Ser-Gly-Gln-Ala-Tyr-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu-Pro-Ser-Cys-Leu-Glu-Ser, Arg-Ser-Asp-Glu-Leu-Val-Arg-His-His-Asn-Met-His-Gln-Arg-Asn-Met-Thr-Lys-Leu and Pro-Gly-Cys-Asn-Lys-Arg-Tyr-Phe-Lys-Leu-Ser-His-Leu-Gln-Met-His-Ser-Arg-Lys-His-Thr-Gly) - Transfer of orphan designation - Commission Decision (2019)1346 of Thu, 14 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003557

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14-2-2019

EU/3/16/1655 (Sellas Life Sciences Limited)

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EU/3/16/1655 (Active substance: Tyr-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu, Ser-Gly-Gln-Ala-Tyr-Met-Phe-Pro-Asn-Ala-Pro-Tyr-Leu-Pro-Ser-Cys-Leu-Glu-Ser, Arg-Ser-Asp-Glu-Leu-Val-Arg-His-His-Asn-Met-His-Gln-Arg-Asn-Met-Thr-Lys-Leu and Pro-Gly-Cys-Asn-Lys-Arg-Tyr-Phe-Lys-Leu-Ser-His-Leu-Gln-Met-His-Ser-Arg-Lys-His-Thr-Gly) - Transfer of orphan designation - Commission Decision (2019)1345 of Thu, 14 Feb 2019 European Medicines Agency (EMA) procedure number: EMA/OD/0000003572

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14-2-2019

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14-2-2019

EU/3/15/1529 (DLRC Pharma Services Ltd)

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17-1-2019


Opinion/decision on a Paediatric investigation plan (PIP): His-Ser-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Lys(γ-Glu-palmitoyl)-Ser-Glu-Tyr-Leu-Asp-Ser-Glu-Arg-Ala-Arg-Asp-Phe-Val-Ala-Trp-Leu-Glu-Ala-Gly-Gly-OH (MEDI0382), decision type: , therapeutic area: , PIP nu

Opinion/decision on a Paediatric investigation plan (PIP): His-Ser-Gln-Gly-Thr-Phe-Thr-Ser-Asp-Lys(γ-Glu-palmitoyl)-Ser-Glu-Tyr-Leu-Asp-Ser-Glu-Arg-Ala-Arg-Asp-Phe-Val-Ala-Trp-Leu-Glu-Ala-Gly-Gly-OH (MEDI0382), decision type: , therapeutic area: , PIP nu

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26-11-2018

A hemodialysis system, which has modernized through miniaturization; and a patient monitoring system that can monitor more patients and/or more parameters and which are increasingly becoming networked in healthcare facilities increasing the risk for cyber

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FDA - U.S. Food and Drug Administration

26-11-2018

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FDA - U.S. Food and Drug Administration

21-11-2018

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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

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21-8-2018

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