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Tillotts Global

We focus on gastroenterology

General Terms and Conditions for Supplier

General Terms and Conditions for the Supply of Goods and Services to Tillotts Pharma AG

1. Sole application
1.1. These General Terms and Conditions for the Supply of Goods and Services to Tillotts Pharma AG (“GTC”) apply to any supplies of goods (including, without limitation, under article 184 et seqq. of the Swiss Code of Obligations (“CO”) and article 363 et seqq. CO) and services (including, without limitation, under article 363 CO et seqq. and article 394 et seqq. CO) to Tillotts Pharma AG (“Tillotts”) by third parties.
1.2. These GTC form an integral part of any agreements between the Supplier and Tillotts (together “Parties”).
1.3. Any alternative or supplementary terms and conditions apply only if expressly agreed in writing. The application of any general terms and conditions of the Supplier is excluded, even if the Supplier refers to such general terms and conditions in any correspondence.

2. Offers
2.1. The Supplier shall submit offers to Tillotts free of charge. A remuneration for offers is due only if the Supplier has informed Tillotts in advance in writing about such remuneration (including the amount thereof) and Tillotts approved such remuneration in writing. Nonetheless, even if a remuneration has been validly agreed between the Parties, the offer will be free of charge if Tillotts accept it.
2.2. Offers remain binding for a period of 90 days, unless it is apparent for the Supplier from the circumstances that Tillotts requires an offer with a longer validity.

3. Acceptance of an offer
3.1. The acceptance of any offer by Tillotts is binding only if in writing.  With the submission of an acceptance of an offer by Tillotts, an agreement is concluded.
3.2. If Tillotts accepts an offer other than on the terms specified therein, an agreement is concluded once the Supplier has agreed to the different terms by confirming the order. If the Supplier supplies the goods or services without such prior confirmation, the terms specified by Tillotts are deemed accepted by the Supplier.
3.3. If an order confirmation following the acceptance of an offer by Tillotts differs in any material respect from the offer accepted by Tillotts, including, without limitation, in terms of pricing, dates or performance, such order confirmation shall not be binding upon Tillotts to the extent such variations are not favorable to Tillotts, unless Tillotts has agreed to the variations in writing.
3.4. Without prejudice to clause 11, Tillotts has the right to request changes to the goods or services to be supplied, including the quantities thereof, at any time. The Supplier shall advise Tillotts if any such changes have cost, timing or other material implications. Insofar as there are such implications, no instructions may be carried out without the prior written consent of Tillotts.

4. Prices
4.1. The prices indicated in an offer are fixed.
4.2. Prices quoted by the Supplier include any additional charges, fees, customs, taxes (including, without limitation, VAT) etc.
4.3. If the Supplier reduces its prices for goods and services which were ordered, but not yet supplied to Tillotts, the price payable by Tillotts shall automatically be reduced accordingly.

5. Billing and payment
5.1. Invoices shall be submitted by the Supplier to Tillotts by invoice@tillotts.com and addressed as follows: Tillotts Pharma AG, Baslerstrasse 15, 4310 Rheinfelden, Switzerland.
5.2. Invoices received by Tillotts shall be paid 60 days after the invoice was received. In any event the invoices will not be paid earlier than the acceptance of the goods or services supplied.
5.3. Payment of any invoice does constitute acknowledgement of any terms and conditions, prices and/or compliance of the goods and services with all contractual requirements.

6. Documentation
6.1. Prior to supplying the final goods or services, the Supplier shall, upon request, present any relevant documents (plans, drafts, concepts etc.) to Tillotts for approval. Such approval by Tillotts shall not relieve the Supplier from its responsibility to ensure fitness for the intended purpose.
6.2. When supplying the goods or services, the Supplier shall provide Tillotts free of charge with any documents (plans, instructions, manuals etc.) which may be reasonably required by Tillotts.

7. Testing
7.1. If testing is specified in respect of goods or services to be supplied, the Supplier shall pay all technical costs and any costs associated with its own personnel. Tillotts pays the costs associated with its own infrastructure and personnel.
7.2. The Supplier shall notify Tillotts not less than one week in advance of the date on which the goods or services will be ready for testing and shall agree with Tillotts on a date for the tests.
7.3. If goods or services are not presented for testing on this date, any technical and personnel costs incurred by Tillotts in connection with the tests shall be refunded by the Supplier to Tillotts. If any defects are found in the goods or services which make it necessary to repeat the tests or conduct further tests, the Supplier shall bear any additional technical and personnel costs incurred by Tillotts.

8. Timing of the supply and consequences of delay
8.1. Goods and services shall be supplied on the agreed delivery date, which is deemed to be a default date (“Verfalltag“).
8.2. The Supplier shall inform Tillotts immediately if it has reason to believe that it will be unable to deliver any or all of the goods or services on the agreed date, indicating the reasons for and likely duration of the delay. In such a case, the Supplier shall at its own cost accelerate the supply of the good and services to the extent possible, including, without limitation, by choosing faster means of transports.
8.3. If an agreement provides for liquidated damages in the event of any delay in delivery, the liquidated damages are payable by the Supplier even if the goods or services supplied are accepted unconditionally. The payment of liquidated damages does not release the Supplier from the underlying contractual obligations. However, any liquidated damages paid will be offset against any damages that may be due.
8.4. Deliveries before the agreed delivery date and/or or partial supplies are permissible with the prior written consent of Tillotts only.
8.5. If it is impossible to supply the goods or services for reasons beyond the Supplier’s control, the supply shall be temporarily suspended until the supply is possible again. Goods to be supplied shall be safely stored by the Supplier at its own costs and risk. If in the event of default of acceptance by Tillotts, the goods shall be safely stored by the Supplier free of charge for a period of one month and against a reasonable fee thereafter, whereby such storage will be at the risk of Tillotts.

9. Specific provisions for the supply of goods
9.1. Goods shall be supplied DDP, Incoterms® 2020, Baslerstrasse 15, CH-4310 Rheinfelden or Hauptstrasse 27, CH-4417 Ziefen (as indicated by Tillotts).
9.2. On the day on which the goods are dispatched, the Supplier shall  send a dispatch note to Tillotts. A delivery note and any other reasonably required documents (e.g., shipping papers, pro-forma invoice etc.) shall be provided together with the goods.
9.3. Tillotts is not obliged to inspect the goods upon delivery, with the exception of the quantity of the goods supplied. Defects, whether apparent or hidden, can be notified to the Supplier at any time during the warranty period. Negative differences in quantities shall be notified within two weeks as from the delivery.

10. Warranties and liability
10.1. The Supplier warrants, without limitation, that any goods (including, without limitation, their packaging and any documentation) and/or services supplied
a.) are free from any defects;
b.) are fit for their intended purpose;
c.) have all the attributes and meet all performance requirements and specifications indicated;
d.) do not vary in any other respect from the provisions of the agreement;
e.) comply with all applicable laws and best industry practices; and
f.) if goods with an expiry date are supplied, no more than 20% of the entire period of time between the manufacturing date and the expiry date has lapsed upon delivery of the goods.
In case of services supplied under article 394 et seqq. CO, these warranties shall apply by analogy to the extent possible. The Supplier warrants, without limitation, that such services are performed with all due skill, care and diligence and in accordance with best industry practices.
10.2. If, at any time during the warranty period, it becomes evident that the goods or services supplied, or any component thereof, are not as warranted in clause 10.1, the Supplier shall at its own cost rectify the defects onsite, or if it is impossible to do this within a reasonable period of time, supply replacement goods or services in accordance with clause 10.1, provided that Tillotts can be reasonably expected to accept such rectification or replacement goods or services. Until a successful rectification and replacement supply has taken place, any liquidated damages agreed between the Parties for a delay in delivery shall be due.
10.3. If the Supplier fails to proceed as aforesaid, even though a reasonable period of time has been granted, or Tillotts cannot be reasonably expected to accept a rectification or the supply of replacement good or services, Tillotts is at its discretion entitled to
a.) rescind the agreement partly or in full;
b.) rectify the defects itself or have them rectified by a third party at the Supplier’s expense; or
c.) procure replacement goods and services at the Supplier’s expense.
The right of Tillotts to claim additional damages remains reserved.
10.4. Upon request of the Supplier, Tillotts shall return defective goods to the Supplier at the Supplier’s cost.
10.5. In case of goods or services supplied under article 184 et seqq. of the Swiss Code of Obligations (“CO”) and article 363 et seqq. CO, the warranty period is two years as from the date on which the goods or services are delivered to Tillotts. In case of other services including, without limitation, under article 394 et seqq. CO, the ordinary statutory limitations periods apply. Where a formal acceptance process takes place, the warranty period commence once the acceptance process has been successfully completed.
10.6. The warranties applying to goods and services supplied shall apply equally to any replacement goods or services and in respect of any work performed to rectify defects.
10.7. The Supplier shall indemnify and hold Tillotts harmless in full (including costs of legal representation) from and against any claims and damages that may result from any breach of the warranties pursuant to clause 10.1.

11. Termination of an agreement by Tillotts at will
11.1. Tillotts is entitled to terminate at will any agreement, whether for goods or services, and waive future performance at any time with immediate effect.
11.2. In case of no fault of the Supplier, Tillotts shall:
a.) in case of the supply of goods: compensate the Supplier for  the proven negative interests (“negatives Vertragsinteresse“), namely the costs incurred by the Supplier in view of the supply of the goods to Tillotts, provided that the Supplier shall be obliged to minimize such negative interests to the extent possible, including, without limitation, by making commercially reasonable efforts to find another purchaser for the relevant goods;
b.) in case of the supply of services: compensate the Supplier on a pro rata basis for the services already rendered until receipt of the termination with immediate effect and compensate the Supplier for the proven negative interests (“negatives Vertragsinteresse“), namely the allocation of resources for the future provision of the services to Tillotts, provided that the Supplier shall be obliged to minimize such negative interests to the extent possible, including, without limitation, by (re-)allocating such resources to other customers.

12. Confidentiality
12.1. Any information which may be provided to the Supplier by Tillotts for the purposes of preparing an offer or executing an order, shall be treated as strictly confidential, adequately protected against any unauthorized access and shall not be used for any purpose other than the supply of the goods and services. All related IP Rights shall exclusively belong to Tillotts.
12.2. Upon request of Tillotts, the Supplier shall immediately return all materials and documents, including any copies, to Tillotts or destroy them irrevocably.
12.3. No reference may be made to the business relationship with Tillotts  in any information or publicity material without its prior written consent.

13. Intellectual property
13.1. The Supplier warrants that no third-party intellectual property rights and/or proprietary know-how (“IP Rights”) are or will be infringed as a result of supplying and using the goods or services.
13.2. The Supplier shall indemnify and hold Tillotts harmless in full (including costs of legal representation) from and against any claims and damages that may result from any infringement of third- party IP Rights.
13.3. If goods or services can no longer be fully used as a result of any infringement of third-party IP Rights, Tillotts is at its discretion entitled to
a.) rescind the agreement partly or in full;
b.) request the Supplier to alter the goods or services at the Supplier’s cost to the extent required, so that they do no longer infringe third-party IP Rights; or request the Supplier to undertake commercially reasonable efforts to acquire a right to use such IP Rights at the Supplier’s cost;
whereby with regard to b.) and c.) above, Tillotts remains free to rescind the agreement if the goods or services are not altered respectively third-party IP Rights are not acquired within a reasonable period of time.
13.4. If any goods or services to be supplied by the Supplier lead to the creation of any IP Rights, any such IP Rights exclusively belong to, and are hereby automatically transferred to Tillotts. The Supplier and its employees (including any subcontractors) shall assist Tillotts in taking any action that may be required to protect its IP Rights and shall sign any documents and make any declarations that may be necessary for such purpose.
13.5. If any work results respectively IP Rights of Tillotts depend on the pre-existing IP Rights of the Supplier, the Supplier grants a non- exclusive, royalty-free and perpetual license to use such IP Rights of the Supplier to the extent required for Tillotts to exploit its work results and IP Rights.

14. Subcontracting
14.1. The Supplier shall not appoint any subcontractors without the prior written consent of Tillotts.
14.2. If Tillotts approves such subcontractors, the Supplier remains fully liable for any acts and omission of such subcontractors, as if such acts and omissions were its own.

15. Insurance, work permits
15.1. The Supplier shall take out and maintain adequate insurance with a reputable insurance company to cover any loss or damage that may be caused by it (including any subcontractors) or its employees or its consultants.
15.2. The Supplier shall insure any machinery and equipment etc. supplied on loan to Tillotts against the usual risks. Any liability on the part of Tillotts in respect of the destruction of or damage caused to such machinery, equipment etc., is hereby excluded, unless such destruction or damage was caused deliberately or through gross negligence.
15.3. The Supplier shall ensure that any employees, including employees of subcontractors, who are assigned to work on the premises of Tillotts hold a valid Swiss work permit respectively a timely notification is filed with the competent authorities and are engaged in accordance with all applicable laws.

16. Data Privacy
16.1. The Parties are aware of the fact that concluding and performing their agreements may result in the processing of personal data in general and the contact details of the other party and its contact persons in particular. The personal data exchanged in the context of the agreements between the Parties shall only be processed by the Parties and their affiliated companies to the extent required for managing the business relationship and executing the agreements between the Parties.
16.2. The Parties warrant that any exchange of personal data with the other party takes place in accordance with the applicable data privacy legislation, including the Swiss Data Protection Act and the EU’s General Data Protection Regulation, to the extent applicable, and that they do not exchange any personal data in violation of such legislation.
16.3. Upon completion of the Services, Supplier shall be obliged to destroy all personal data processed in the course of the Services in Supplier’s possession or control (including personal data processed by Supplier’s subprocessors). This obligation shall not apply to the extent that Supplier is required by any European (or European member state) law to retain all or some of the personal data, in which case Supplier shall isolate and protect the personal data from any further processing except to the extent required by such law.
16.4. Immediately after the destruction of the personal data, Supplier must certify in writing to Tillotts that the destruction of the personal data has been completed, specifying the method used for the true permanent destruction of the personal data.
16.5. For the processing of personal data by Tillotts it is referred to https://www.tillotts.com/privacy-policy/.

17. Business Ethics
17.1. The Supplier shall comply at any time comply by analogy with the Code of Business Ethics (“Ethics Code”) of Tillotts, available at https://www.tillotts.com/ethics-code/.
17.2. The Supplier shall comply at any time with all applicable laws including, without limitation, unfair competition, antitrust, anti-bribery and EHS and non-discrimination laws.

18. Assignment, applicable law and place of jurisdiction
18.1. The Supplier shall not assign any claims against Tillotts to a third party without the prior written consent of Tillotts. Any such assignment is null and void.
18.2. Any agreements between the Parties shall be governed by material Swiss law. The United Nations Convention on Contracts for the International Sale of Goods shall not apply.
18.3. Rheinfelden shall be the exclusive place of jurisdiction.

Version: 01/2021

Please note that if you are a minor (under age 18), for legal reasons we cannot accept your report. An adult (age 18 or older), such as a parent, guardian or healthcare professional, may submit a report on your behalf.

Upozorňujeme, že pokud jste nezletilá osoba (mladší 18 let), ze zákonem daných důvodů nemůžeme vaši zprávu přijmout. Zprávu může vaším jménem odeslat dospělá osoba (starší 18 let), jako je rodič, opatrovník nebo lékař.

Bemærk, hvis du er mindreårig (under 18 år) kan vi af juridiske årsager ikke godtage din indberetning. En voksen (18 år eller ældre), kan være en forælder, en værge eller sundhedspersonale kan indsende en indberetning på dine vegne.

Veuillez noter que, pour des raisons légales, nous ne pouvons accepter votre déclaration si vous êtes mineur(e) (moins de 18 ans). Un adulte (âgé de 18 ans ou plus), tel qu'un parent, tuteur ou professionnel de santé, peut effectuer la déclaration en votre nom.

Huomaa, että jos olet alaikäinen (alle 18-vuotias), emme oikeussyistä voi hyväksyä ilmoitustasi. Täysi-ikäinen (vähintään 18-vuotias) henkilö, kuten vanhempi, huoltaja tai terveydenhuollon ammattilainen, voi tehdä ilmoituksen puolestasi.

Bitte beachten Sie, dass wir aus rechtlichen Gründen Ihren Bericht nicht annehmen können, wenn Sie minderjährig (unter 18 Jahren) sind. Ein Erwachsener (mindestens 18 Jahre alt) wie etwa ein Elternteil, Erziehungsberechtigter oder eine medizinische Fachkraft kann einen Bericht in Ihrem Namen einreichen

Vinsamlegast athugaðu að ef þú ert undir lögaldri (yngri en 18 ára), getum við ekki samþykkt skýrsluna af lagalegum ástæðum. Fullorðinn einstaklingur (18 ára eða eldri), svo sem foreldri, forráðamaður eða heilbrigðisstarfsmaður, má leggja fram skýrslu fyrir þína hönd.

Hvis du er mindreårig (under 18 år), kan vi av juridiske årsaker ikke ta imot rapporten din. En voksen person (18 år eller eldre), for eksempel en forelder, verge eller helsefagperson, kan sende inn rapporten på dine vegne.

Tenga en cuenta que si es menor de edad (menor de 18 años), por motivos legales, no podemos aceptar su reporte.. Un adulto (18 años o más), tales como un progenitor, tutor s o profesional sanitario podría presentar el informe en su nombre.

Observera att om du är minderårig (under 18 år), kan vi inte acceptera din rapport av rättsliga skäl. En vuxen (18 år eller äldre), som en förälder, vårdnadshavare eller sjukvårdspersonal kan skicka in en rapport å dina vägnar.

Nota: se Lei è minorenne (di età inferiore ai 18 anni), per motivi legali non possiamo accettare la Sua segnalazione. Un adulto (di 18 anni di età compiuti), come un genitore, tutore o operatore sanitario, potrà presentare una segnalazione per Suo conto.

Denk eraan dat, als u een minderjarige (jonger dan 18) bent, we om wettelijke redenen uw melding niet kunnen aanvaarden. Een volwassene (18 jaar of ouder), zoals een ouder, voogd of medische zorgverlener, kan namens u een melding indienen.

Ange tähele, kui olete alaealine (alla 18 aasta vanune), ei saa me õiguslikel põhjustel teilt teie teatist vastu võtta. Teie nimel võib teatise esitada täiskasvanu (18-aastane või vanem), näiteks lapsevanem, eestkostja või tervishoiutöötaja.

Σημειώστε ότι εάν είστε ανήλικος (κάτω των 18 ετών), για νομικούς λόγους δεν μπορούμε να δεχτούμε την αναφορά σας. Ένας ενήλικας (ηλικίας 18 ετών και άνω), όπως ένας γονέας, κηδεμόνας ή επαγγελματίας υγείας, μπορεί να υποβάλει μια αναφορά εκ μέρους σας..

Lūdzu, ņemiet vērā, ka, ja Jūs esat nepilngadīgs (jaunāks par 18 gadiem), juridisku iemeslu dēļ mēs nevaram pieņemt Jūsu ziņojumu. Ziņojumu Jūsu vārdā var iesniegt pieaugušais (18 gadus vecs vai vecāks), piemēram, vecāks, aizbildnis vai veselības aprūpes speciālists.

Atkreipkite dėmesį į tai, kad jeigu esate nepilnametis (Jums yra mažiau nei 18 metų), dėl teisinių priežasčių Jūsų pranešimo priimti negalime. Pranešimą Jūsų vardu gali pateikti suaugusysis (18 metų arba vyresnis), pvz., tėvas ar mama, globėjas arba sveikatos priežiūros specialistas.

Ak máte menej ako 18 rokov, Vaše hlásenie nemôžeme z právnych dôvodov akceptovať. Hlásenie vo Vašom mene môže podať dospelá osoba (vo veku od 18 rokov) ako je rodič, právny zástupca alebo zdravotnícky pracovník.

Por favor, note que se for menor (menos de 18 anos), por razões legais, não podemos aceitar a sua notificação. Um adulto (mais de 18 anos), como um pai, tutor ou profissional de saúde, pode apresentar a notificação em seu nome.


Reporter identification *

Identifikace osoby podávající hlášení *

Oplysninger om indberetter *

Identification du déclarant *

Ilmoittajan Tiedot *

Angaben zum Berichterstatter *

Auðkenni tilkynnanda *

Rapportør-ID *

Identificación del notificador *

Uppgifter om rapportören *

Identificativo della persona che effettua la segnalazione *

Identificatie van de melder *

Teate saatja andmed *

Ταυτοποίηση αναφέροντος *

Ziņotāja identifikācija *

Pranešėjo identifikavimas *

Identifikácia nahlasovateľa *

Identificação do notificador *

* At least one has to be filled Je třeba vyplnit alespoň jedno pole Der skal udfyldes mindst én Au moins l'un des champs doit être rempli Ainakin toinen täytettävä Mindestens eines muss ausgefüllt werden Fylla þarf í a.m.k. einn Minst ett felt må krysses ut Al menos debe indicar uno Åtminstone en måste fyllas i Compilare almeno un campo Ten minste één moet worden ingevuld. Vähemalt üks peab olema täidetud. Τουλάχιστον ένα πρέπει να συμπληρωθεί. Jāaizpilda vismaz viens. Turi būti užpildytas bent vienas laukas. Aspoň jedno pole musí byť vyplnené. Pelo menos um deve ser preenchido

** Mandatory fields Povinné pole Obligatoriske felter Champs obligatoires Pakolliset kentät Pflichtfelder Skyldusvæði Obligatoriske felt Campos obligatorios Obligatoriska fält Campi obbligatori Verplichte velden Kohustuslikud väljad Υποχρεωτικά πεδία Obligātais lauks Privalomi laukai Povinné polia Campos obrigatórios


Patient Identification *

Identifikace pacienta *

Oplysninger om patient *

Identification du patient *

Potilaan tiedot *

Angaben zum Patienten *

Auðkenni Sjúklings *

Pasient-ID *

Identificación del paciente *

Uppgifter om patienten *

Identificativo paziente *

Identificatie van de patiënt *

Patsiendi andmed *

Ταυτοποίηση ασθενούς *

Pacienta identifikācija *

Paciento identifikavimas *

Identifikácia pacienta *

Identificação do doente *

* At least one has to be filled Je třeba vyplnit alespoň jedno pole Der skal udfyldes mindst én Au moins l'un des champs doit être rempli Ainakin toinen täytettävä Mindestens eines muss ausgefüllt werden Fylla þarf í a.m.k. einn Minst ett felt må krysses ut Al menos debe indicar uno Åtminstone en måste fyllas i Compilare almeno un campo Ten minste één moet worden ingevuld. Vähemalt üks peab olema täidetud Τουλάχιστον ένα πρέπει να συμπληρωθεί Jāaizpilda vismaz viens Turi būti užpildytas bent vienas laukas Aspoň jedno pole musí byť vyplnené Pelo menos um deve ser preenchido

** Mandatory fields Povinné pole Obligatoriske felter Champs obligatoires Pakolliset kentät Pflichtfelder Skyldusvæði Obligatoriske felt Campos obligatorios Obligatoriska fält Campi obbligatori Verplichte velden Kohustuslikud väljad Υποχρεωτικά πεδία Obligātais lauks Privalomi laukai Povinné polia Campos obrigatórios

Please do NOT provide the full name (neither first nor last name) of the patient Prosím NEUVÁDĚJTE ani jméno ani příjmení pacienta. Patientens fulde navn (fornavn og efternavn) må IKKE oplyses. Veuillez ne PAS indiquer le nom complet du patient (que ce soit le prénom ou le nom de famille). ÄLÄ anna potilaan nimeä (ei etu- eikä sukunimeä). Bitte NICHT den vollständigen Namen des Patienten (weder Vor- noch Nachnamen) angeben. Vinsamlegast EKKI gefa upp fullt nafn (hvorki fornafn né eftirnafn) sjúklingsins. IKKE oppgi pasientens fulle navn (verken fornavn eller etternavn). Por favor, NO indique el nombre completo (ni nombre ni apellido/s) del paciente. Vänligen skriv INTE patientens fullständiga namn ( varken förnamn eller efternamn). NON fornire il nome o il cognome del paziente per intero. Niet de volledige naam (noch de voornaam noch de achternaam) van de patiënt geven. ÄRGE märkige patsiendi täielikku nime (ees- ega perekonnanime). (ΜΗΝ αναφέρετε το πλήρες όνομα (ούτε το όνομα ούτε το επώνυμο) του ασθενούς. Lūdzu, NENORĀDIET pilnu pacienta vārdu (ne vārdu, ne uzvārdu). NEpateikite viso paciento vardo ir pavardės (nei vardo, nei pavardės). NEUVÁDZAJTE celé meno (meno ani priezvisko) pacient. Por favor, não forneça o nome completo (nem primeiro ou último nome) do doente.

Privacy notice:
All the information and personal data you will hereby share with Tillotts Pharma will be protected and kept confidential in line with internal procedures and local regulations. Your information and personal data will be used for the purpose of drug safety surveillance and to enable us to deal with your enquiry appropriately and it may be shared with such other parties with whom Tillotts Pharma shares responsibility for pharmacovigilance (study of drug-related safety information) for Tillotts Pharma’s products in your country of residence, and/or with health authorities. In this context, your personal data may be transferred within your country of residence, the European Economic Area, and/or a country that the European Commission has decided provides adequate protection for personal data. For more information about how we collect and use your personal data, and your rights with respect to your personal data, please see our privacy notice which is available on our website at https://www.tillotts.com/privacy-policy/ Ochrana osobních údajů:
Veškeré informace a osobní údaje, které budete tímto sdílet se společností Tillotts Pharma, budou chráněny a bude s nimi zacházeno jako s důvěrnými v souladu s vnitřními postupy a místními předpisy. Vaše informace a osobní údaje budou používány pro účely sledování bezpečnosti léku a k tomu, abychom mohli řádně odpovídat na vaše dotazy. Tyto informace a osobní údaje mohou být sdíleny se třetími stranami, se kterými společnost Tillotts Pharma sdílí zodpovědnost za sledování bezpečnosti farmaceutických přípravků (klinické hodnocení bezpečnostních informací spojených s léky) u produktů společnosti Tillotts Pharma ve vaší zemi trvalého pobytu a/nebo se zdravotními orgány. V tomto kontextu mohou být vaše osobní údaje převáděny v rámci země vašeho trvalého pobytu, Evropského hospodářského prostoru a/nebo země, o které Evropská komise rozhodla, že má dostatečnou ochranu osobních údajů. Další informace o tom, jak shromažďujeme a používáme vaše osobní údaje a o vašich právech týkajících se vašich osobních údajů naleznete v našem prohlášení o ochraně osobních údajů, které je k dispozici na našich webových stránkách na https://www.tillotts.com/privacy-policy/ Meddelelse om beskyttelse af personlige oplysninger:
Alle de oplysninger og personoplysninger, du hermed deler med Tillotts Pharma, bliver beskyttet og opbevaret fortroligt i overensstemmelse med interne procedurer og lokale bestemmelser. Dine oplysninger og personoplysninger vil blive brugt med henblik på overvågning af lægemiddelsikkerheden og gør det muligt for os at behandle din forespørgsel på passende vis, og kan blive delt med sådanne andre parter, med hvem Tillotts Pharma deler ansvaret for overvågning af lægemiddelrelaterede sikkerhedsoplysninger for Tillotts Pharmas produkter i dit bopælsland, og/eller med sundhedsmyndighederne. I den forbindelse kan dine personoplysninger blive overført inden for dit bopælsland, Det Europæiske Økonomiske Samarbejdsområde og/eller et land, som Europa-Kommissionen har besluttet yder tilstrækkelig beskyttelse af personoplysninger. For yderligere oplysninger om, hvordan vi indsamler og bruger dine personoplysninger, og dine rettigheder med hensyn til dine personoplysninger, kan du se vores meddelelse om beskyttelse af personlige oplysninger, som er tilgængelig på vores hjemmeside på https://www.tillotts.com/privacy-policy/ Déclaration de confidentialité:
Toutes les informations et données personnelles que vous communiquez à Tillotts Pharma seront protégées et tenues confidentielles conformément aux procédures internes et aux réglementations locales. Vos informations et données personnelles seront utilisées à des fins de pharmacovigilance et pour nous permettre de traiter votre demande de manière appropriée. Elles pourront être communiquées aux autres parties avec lesquelles Tillotts Pharma partage la responsabilité de la pharmacovigilance (étude des informations de sécurité relatives aux médicaments) pour les produits de Tillotts Pharma dans votre pays de résidence ou auprès des autorités sanitaires. Dans ce contexte, vos données personnelles peuvent être transférées dans votre pays de résidence, dans l’Espace économique européen ou dans un pays où la Commission européenne a décidé d’assurer une protection adéquate des données personnelles. Pour plus d’informations sur la façon dont nous collectons et utilisons vos données personnelles et vos droits en ce qui les concerne, veuillez consulter notre déclaration de confidentialité disponible sur notre site Web à l’adresse https://www.tillotts.com/privacy-policy/ Tietosuojailmoitus:
Kaikkia Tillotts Pharmalle luovuttamiasi tietoja ja henkilötietoja suojataan ja pidetään luottamuksellisina sisäisten menettelytapojen ja paikallisten määräysten mukaisesti. Tietojasi ja henkilötietojasi käytetään lääketurvallisuuden valvonnan tarkoituksessa, jotta voimme käsitellä ilmoituksesi asianmukaisesti.Niitä voidaan luovuttaa muille sellaisille osapuolille, joiden kanssa Tillotts Pharma on yhdessä vastuussa Tillotts Pharman tuotteiden lääketurvallisuuden valvonnasta (lääkkeisiin liittyvien turvallisuustietojen tutkimus) asuinmaassasi, ja/tai terveysviranomaisille. Tässä yhteydessä henkilötietojasi voidaan siirtää asuinmaasi, Euroopan talousalueen ja/tai sellaisen maan sisällä, joka Euroopan neuvoston päätöksen mukaan tarjoaa riittävän henkilötietojen suojauksen. Lisätietoja siitä, miten keräämme ja käytämme henkilötietojasi, sekä henkilötietojasi koskevat oikeutesi on esitetty tietosuojailmoituksessamme, joka on luettavissa verkkosivullamme https://www.tillotts.com/privacy-policy/ Datenschutz:
Alle Informationen und personenbezogenen Daten, die Sie hiermit mit Tillotts Pharma teilen, werden in Übereinstimmung mit unseren internen Verfahren und den lokalen Vorschriften geschützt und geheim gehalten. Ihre Informationen und personenbezogenen Daten werden zum Zweck der Überwachung der Arzneimittelsicherheit verwendet und um uns in die Lage zu versetzen, Ihre Anfragen angemessen zu bearbeiten. Ihre Informationen werden gegebenenfalls mit den Gesundheitsbehörden und/oder anderen Parteien geteilt, mit denen gemeinsam Tillotts Pharma die Verantwortung für die Pharmakovigilanz (Studien zur Arzneimittelsicherheit) von Tillotts Pharmaprodukten in Ihrem Aufenthaltsland trägt. In diesem Kontext werden Ihre personenbezogenen Daten gegebenenfalls innerhalb Ihres Aufenthaltslandes, des Europäischen Wirtschaftsraums und/oder innerhalb eines Landes, das nach Entscheidung der EU-Kommission einen ausreichenden Schutz Ihrer personenbezogenen Daten gewährleistet, übermittelt. Für weitergehende Informationen darüber, wie wir Ihre personenbezogenen Daten sammeln und verwenden und bezüglich Ihrer Rechte an Ihren personenbezogenen Daten, sehen Sie sich bitte unseren Datenschutzhinweis an, der auf unserer Webseite vorliegt unter Datenschutz Tilkynning um persónuvernd:
Allar upplýsingar og persónuleg gögn sem þú deilir með Tillotts Pharma verða varin og geymd í trúnaði í samræmi við verklagsreglur og gildandi lög. Upplýsingar þínar og persónuleg gögn verða notuð til eftirlits með öryggi við notkun lyfja og til að gera okkur kleift að bregðast rétt við erindi þínu. Einnig gæti þeim verið deilt með aðilum sem bera ásamt Tillotts Pharma ábyrgð á lyfjagát (eftirlit með öryggi við notkun lyfja) fyrir vörur frá Tillotts Pharma í því landi þar sem þú átt heima og/eða með heilbrigðisyfirvöldum. Í því tilfelli gætu persónuleg gögn þín verið send til annarra aðila innan heimalands þíns, Evrópska efnahagssvæðisins og/eða annars lands sem Framkvæmdastjórn Evrópusambandsins hefur ákveðið að veiti fullnægjandi vernd fyrir persónuleg gögn. Frekari upplýsingar um hvernig við söfnum persónulegum gögnum og notum þau og um réttindi þín hvað varðar persónuleg gögn þín er að finna í tilkynningu okkar um persónuvernd á vefsíðu okkar: https://www.tillotts.com/privacy-policy/ Personvernerklæring
All informasjon og personopplysninger du hermed deler med Tillotts Pharma blir beskyttet og behandlet fortrolig i samsvar med interne prosedyrer og lokale forskrifter. Din informasjon og dine personopplysninger vil bli brukt for overvåking av legemiddelsikkerhet og for å sette oss i stand til å håndtere din forespørsel riktig, og de kan deles med andre som Tillotts Pharma deler ansvar med for farmakovigilans (legemiddelrelatert sikkerhetsinformasjon) for Tillotts Pharmas produkter i det landet der du bor og/eller helsemyndigheter. I denne sammenhengen kan dine personopplysninger overføres innenfor det landet du bor i, Det europeiske økonomiske samarbeidsområdet og/eller et land som EU-kommisjonen har besluttet, gir tilstrekkelig beskyttelse av personopplysninger. For mer informasjon om hvordan vi samler inn og bruker dine personopplysninger, og dine rettigheter når det gjelder dine personopplysninger, vennligst se vår personvernerklæring på vårt nettsted: https://www.tillotts.com/privacy-policy/ Aviso de privacidad:
Toda la información y datos personales que usted comparta aquí con Tillotts Pharma estarán protegidos y se mantendrán como confidenciales de acuerdo con los procedimientos internos y las normativas locales. Sus datos personales y su información se utilizarán para controlar la seguridad del fármaco y para que podamos ocuparnos debidamente de su consulta; por lo tanto es posible que se compartan con cualesquiera socios que tengan responsabilidad conjunta con Tillotts Pharma por la farmacovigilancia (el estudio de la información de seguridad relativa al fármaco) de los productos de Tillotts Pharma en su país de residencia, así como con las autoridades sanitarias. En este contexto, sus datos personales pueden ser transferidos dentro de su propio país de residencia, dentro del Espacio Económico Europeo y/o a un país que la Comisión Europea haya decidido que ofrece protección adecuada para los datos personales. Para obtener más información sobre cómo recopilamos y usamos sus datos personales y sobre los derechos que le asisten con respecto a los mismos, vea el aviso de privacidad que figura en nuestro sitio Web https://www.tillotts.com/privacy-policy/ Sekretessmeddelande:
All information och personuppgifter som du härmed delar med Tillotts Pharma kommer att skyddas och behandlas konfidentiellt i enlighet med interna rutiner och lokal lagstiftning. Din information och dina personuppgifter kommer att användas i syfte att övervaka läkemedelssäkerheten, och för att vi ska kunna svara på eventuella frågor från dig. Din information kan komma att delas med tredje part som tillsammans med Tillotts Pharma ansvarar för övervakning av läkemedelsrelaterad säkerhetsinformation gällande Tillotts Pharmas läkemedel som finns tillgängliga i landet där du bor. Din information kan även komma att delas med hälsovårdsmyndigheter. I detta sammanhang kan dina personuppgifter överföras inom landet där du bor, inom det europeiska ekonomiska samarbetsområdet (EES) och/eller till ett land som EU-kommissionen anser har adekvat säkerhet för personuppgifter. För mer information om hur vi samlar in och använder dina personuppgifter, och vilka rättigheter du har med avseende på dina personuppgifter läs vår sekretesspolicy som finns tillgänglig på vår hemsida https://www.tillotts.com/privacy-policy/ Informativa sulla Privacy:
Tutte le informazioni e i dati personali che qui condividerai con Tillotts Pharma saranno protetti e mantenuti riservati in linea con le procedure interne e le normative locali. Le tue informazioni e i dati personali saranno utilizzati ai fini della sorveglianza sulla sicurezza dei farmaci e ci consentiranno di trattare la tua richiesta in modo appropriato e potranno essere condivisi con i soggetti con cui Tillotts Pharma condivide la responsabilità per la farmacovigilanza (studio delle informazioni sulla sicurezza dei farmaci) per i prodotti Tillotts Pharma nel proprio paese di residenza e/o con le autorità sanitarie. In questo contesto, i dati personali possono essere trasferiti all'interno del tuo paese di residenza dello Spazio economico europeo e/o di un paese che, a giudizio della Commissione europea, fornisce una protezione adeguata per i dati personali. Per ulteriori informazioni sulle modalità di raccolta e utilizzo dei tuoi dati personali e relativi diritti connessi a tali dati, potrai consultare la nostra informativa sulla privacy disponibile sul sito web aziendale all'indirizzo https://www.tillotts.com/privacy-policy/ Privacyverklaring:
Alle informatie en persoonsgegevens die u hierbij deelt met Tillotts Pharma, worden beschermd en vertrouwelijk gehouden in overeenstemming met interne procedures en lokale regelgeving. Uw informatie en persoonsgegevens zullen worden gebruikt om de veiligheid van geneesmiddelen te bewaken en om ons in staat te stellen uw verzoek(en) op geschikte wijze in behandeling te nemen. Uw informatie en persoonsgegevens kunnen worden gedeeld met gezondheidsinstanties en/of met andere partijen die de verantwoordelijkheid voor geneesmiddelbewaking (onderzoek naar geneesmiddelgerelateerde veiligheidsinformatie) met Tillotts Pharma delen voor producten van Tillotts Pharma in het land waar u woont. Binnen deze context is het mogelijk dat uw persoonsgegevens worden doorgegeven binnen het land waar u woont, binnen de Europese Economische Ruimte en/of naar een land dat naar het oordeel van de Europese Commissie voldoende bescherming biedt voor persoonsgegevens. Ga voor meer informatie over de wijze waarop we uw persoonsgegevens verzamelen en gebruiken, en over uw rechten met betrekking tot uw persoonsgegevens, naar onze privacyverklaring die beschikbaar is op onze website: https://www.tillotts.com/privacy-policy/ Privaatsusavaldus:
Kogu ettevõttele Tillotts Pharmale edastatav teave ja isikuandmed on kaitstud ja neid hoitakse konfidentsiaalsena kooskõlas ettevõttesiseste protseduurireeglite ja kohalike õigusaktidega. Teie teavet ja isikuandmeid kasutatakse ravimiohutuse järelevalveks ja selleks, et saaksime teie päringut nõuetekohaselt käsitleda, ja neid võib anda ühiskasutusse kolmandatele isikutele, kes vastutavad koos Tillotts Pharmaga Tillotts Pharma ravimite ravimiohutuse järelevalve eest (ravimiga seotud ohutusteabe uuring) teie elukohariigis, ja/või tervishoiu ametiasutustele. Sellega seoses võb teie isikuandmeid edastada teie elukohariigis, Euroopa Majanduspiirkonnas ja/või riigis, kus Euroopa Komisjoni otsuse kohaselt isikuandmete piisav kaitse on tagatud. Lisateabe saamiseks selle kohta, kuidas me isikuandmeid kogume ja kasutame, ning oma isikuandmeid puudutavate õiguste kohta lugege privaatsusavaldust meie veebisaidil: https://www.tillotts.com/privacy-policy/ Δήλωση απορρήτου:
Όλες οι πληροφορίες και τα δεδομένα προσωπικού χαρακτήρα που διά του παρόντος μοιράζεστε με την Tillotts Pharma θα προστατεύονται και θα τηρούνται εμπιστευτικά σύμφωνα με τις εσωτερικές διαδικασίες και τους τοπικούς κανονισμούς. Οι πληροφορίες και τα προσωπικά σας δεδομένα θα χρησιμοποιηθούν για τον σκοπό της επιτήρησης της ασφάλειας των φαρμάκων και για να μπορέσουμε να διεκπεραιώσουμε κατάλληλα το ερώτημά σας και ενδέχεται να κοινοποιηθούν σε άλλα μέρη με τα οποία η Tillotts Pharma μοιράζεται την ευθύνη για τη φαρμακοεπαγρύπνηση (μελέτη πληροφοριών σχετικά με την ασφάλεια των φαρμάκων) για τα προϊόντα της Tillotts Pharma στη χώρα διαμονής σας ή/και στις υγειονομικές αρχές. Στο πλαίσιο αυτό, τα προσωπικά σας δεδομένα ενδέχεται να διαβιβαστούν εντός της χώρας διαμονής σας, του Ευρωπαϊκού Οικονομικού Χώρου ή/και σε χώρα που η Ευρωπαϊκή Επιτροπή έχει αποφασίσει ότι παρέχει επαρκή προστασία για τα δεδομένα προσωπικού χαρακτήρα. Για περισσότερες πληροφορίες σχετικά με τον τρόπο με τον οποίο συλλέγουμε και χρησιμοποιούμε τα προσωπικά σας δεδομένα και τα δικαιώματά σας όσον αφορά τα προσωπικά σας δεδομένα, ανατρέξτε στη δήλωση απορρήτου που είναι διαθέσιμη στον ιστότοπό μας στη διεύθυνση: https://www.tillotts.com/privacy-policy/ Paziņojums par datu privātumu:
Visa informācija un personas dati, ko šeit koplietosiet ar Tillotts Pharma, būs aizsargāta un konfidenciāla atbilstoši iekšējām procedūrām un vietējiem noteikumiem. Jūsu sniegtā informācija un personas dati tiks izmantoti, lai veiktu zāļu drošuma kontroli un lai mēs varētu pareizi apstrādāt Jūsu pieprasījumu, un minētie dati var tikt koplietoti ar citām personām, ar kurām Tillotts Pharma ir kopīgi atbildīgs par farmakovigilanci (ar zāļu saistītas informācijas izpēti) attiecībā uz Jūsu dzīvesvietas valstī pieejamajiem Tillotts Pharma produktiem, un/vai ar veselības aprūpes institūcijām. Šajā kontekstā Jūsu personas dati var tikt nodoti Jūsu dzīvesvietas valstī, Eiropas Ekonomikas Zonas dalībvalstij un/vai valstij, kas saskaņā ar Eiropas Komisijas uzskatiem nodrošina atbilstošu personas datu aizsardzību. Plašāku informāciju par to, kā mēs apkopojam un izmantojam Jūsu personas datus, un Jūsu tiesībām attiecībā uz Jūsu personas datiem, lūdzu, skatiet mūsu privātuma paziņojumā, kas publicēts mūsu tīmekļa vietnē: https://www.tillotts.com/privacy-policy/

Atzīmējot šo lodziņu, es apstiprinu turpmāk minēto: Tillotts Pharma drīkst apkopot un apstrādāt manus personas datus. Šī piekrišana attiecas uz manu personas datu analīzi ar mērķi novērtēt svarīgu drošuma informāciju, kas saistīta ar attiecīgo zāļu lietošanu. Šī piekrišana tāpat attiecas uz citām pusēm, kas kopā ar Tillotts Pharma atbild par manā valstī izmantoto Tillotts Pharma zāļu farmakovigilanci (ar zāļu lietošanu saistītas drošuma informācijas izpēti). Lai sasniegtu šo mērķi, manus personas datus drīkst pārsūtīt manā valstī un Eiropas Ekonomikas zonā. Tillotts Pharma drīkst atklāt manus personas datus veselības aprūpi regulējošām institūcijām, ja to pieprasa likumdošana vai noteikumi. Es saprotu un piekrītu, ka ir piemērojami arī Tillotts Pharma privātuma politikas nosacījumi. Pareiškimas dėl privatumo:
Visa informacija ir asmens duomenys, kuriais pasidalinsite su „Tillotts Pharma“, bus saugomi ir laikomi konfidencialiais, vadovaujantis vidinėmis procedūromis ir vietiniais teisės aktais. Jūsų informacija ir asmens duomenys bus naudojami vaistų saugumo stebėsenos tikslais ir tam, kad galėtume atitinkamai atsakyti į Jūsų užklausą, jais gali būti dalinamasi su kitomis šalimis, su kuriomis „Tillotts Pharma“ dalijasi atsakomybe už „Tillotts Pharma“ vaistinių preparatų farmakologinį budrumą (su vaistu susijusios saugumo informacijos tyrimą) Jūsų gyvenamojoje šalyje, ir (arba) su sveikatos priežiūros institucijomis. Atsižvelgiant į tai, Jūsų asmens duomenys gali būti perduodami Jūsų gyvenamojoje šalyje, Europos ekonominėje erdvėje ir (arba) šalyje, kurioje, Europos Komisijos nuomone, asmens duomenys yra tinkamai saugomi. Daugiau informacijos apie tai, kaip renkame ir naudojame Jūsų asmens duomenis ir apie Jūsų teises, susijusias su Jūsų asmens duomenimis, rasite pareiškime dėl privatumo mūsų svetainėje adresu: https://www.tillotts.com/privacy-policy/ Oznámenie o ochrane osobných údajov:
Všetky informácie a osobné údaje, ktoré týmto poskytujete spoločnosti Tillotts Pharma, budú chránené a uchovávané v dôvernosti v súlade s internými postupmi a miestnymi predpismi. Vaše informácie a osobné údaje sa použijú na účely dohľadu nad bezpečnosťou liekov a príslušného vyriešenia vašej otázky, pričom môžu byť poskytované tretím stranám, s ktorými si spoločnosť Tillotts Pharma delí zodpovednosť v oblasti farmakovigilancie (štúdia informácií súvisiacich s bezpečnosťou liekov) v súvislosti s liekmi spoločnosti Tillotts Pharma v krajine vášho trvalého bydliska, a/alebo zdravotným úradom. V tomto kontexte môžu byť vaše osobné údaje prenášané v rámci krajiny vášho trvalého bydliska, Európskeho hospodárskeho priestoru a/alebo krajiny, ktorej úroveň ochrany osobných údajov Európska Komisia uznala za vhodnú. Viac informácií o našom spôsobe získavania a používania vašich osobných údajov, ako aj o vašich právach v súvislosti s vašimi osobnými údajmi nájdete v našom oznámení o ochrane osobných údajov na adrese: https://www.tillotts.com/privacy-policy/ Aviso de privacidade de dados
Ao marcar esta caixa, confirmo o seguinte: A Tillotts Pharma pode recolher e processar os meus dados pessoais. Este consentimento abrange a análise dos meus dados pessoais para efeitos de avaliação de informações de segurança importantes relacionadas com a minha utilização do produto em questão. Este consentimento estende-se igualmente às outras partes com quem a Tillotts Pharma partilha a responsabilidade de farmacovigilância (estudo das informações de segurança relacionadas com os medicamentos) pelos produtos da Tillotts Pharma no meu país. Os meus dados pessoais podem ser transferidos no meu país e no Espaço Económico Europeu para atingir esse objetivo. A Tillotts Pharma pode divulgar os meus dados pessoais às autoridades de saúde, conforme for exigido por lei ou regulamento. Compreendo e concordo que os termos da Política de Privacidade Tillotts Pharma também se aplicam.


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RE: Suspected Side Effect Dear Reporter, Thank you for filling out our form. Tillotts’ highest priority and responsibility is the safety and well-being of the patients. We have received your message and would like to thank you for reporting a side effect. In addition to your report to us, we recommend that a doctor or another healthcare professional is contacted regarding the side effect. Tillotts Pharma AG Věc: Podezření na vedlejší účinek Vážená paní/pane, Děkujeme Vám za vyplnění našeho formuláře. Bezpečnost a dobrý zdravotní stav pacientů je pro společnost Tillotts nejvyšší prioritou. Obdrželi jsme Vaše hlášení a děkujeme Vám, že jste vedlejší účinek ohlásil/a. Doporučujeme, abyste kvůli vedlejšímu účinku, kromě hlášení naší společnosti, kontaktoval/a také lékaře nebo jiného zdravotnického pracovníka. Tillotts Pharma AG Vedr.: Formodet bivirkning Kære indberetter, Tak fordi du har udfyldt formularen. Tillotts højeste prioritet og ansvar er patientens sikkerhed og velbefindende. Vi har modtaget din meddelelse og vil gerne hermed sige tak, fordi du har indberettet en bivirkning. Ud over indberetningen til os anbefaler vi, at en læge eller en anden sundhedsperson kontaktes angående bivirkningen. Tillotts Pharma AG RE : effet indésirable suspecté Madame, Monsieur, Merci d'avoir rempli notre formulaire. La sécurité et le bien-être des patients sont la priorité absolue de Tillotts et sont au cœur de ses responsabilités. Nous avons bien reçu votre message et nous vous remercions d'avoir déclaré cet effet indésirable. En plus de cette déclaration, nous vous recommandons de prendre contact avec un médecin ou autre professionnel de santé au sujet de cet effet indésirable. Tillotts Pharma AG RE: Epäilty haittavaikutus Hyvä ilmoittaja Kiitos, että täytit haittavaikutuslomakkeen. Vastuu potilaiden turvallisuudesta ja hyvinvoinnista on Tillottsille aina etusijalla. Olemme vastaanottaneet viestisi ja kiitämme haittavaikutuksen ilmoittamisesta. Sen lisäksi, että ilmoitit asiasta meille, suosittelemme haittavaikutuksesta kertomista myös lääkärille tai muulle terveydenhuollon ammattilaiselle. Tillotts Pharma AG Betreff: Verdachtsfall einer Nebenwirkung Sehr geehrter Berichterstatter, vielen Dank für das Ausfüllen unseres Formulars. Tillotts’ höchste Priorität und Verantwortlichkeit ist die Sicherheit und das Wohlergehen der Patienten. Wir haben Ihre Mitteilung erhalten und danken Ihnen, dass Sie eine Nebenwirkung gemeldet haben. Zusätzlich zu dieser Meldung an uns empfehlen wir Ihnen einen Arzt oder einen anderen Angehörigen eines Gesundheitsberufes bezüglich der Nebenwirkung zu kontaktieren. Tillotts Pharma AG Efni: Grunur um aukaverkun Ágæti tilkynnandi Þakka þér fyrir að fylla út eyðublaðið. Tillotts leggur ríka áherslu á og ber ábyrgð á öryggi og velferð sjúklinga. Við höfum móttekið skilaboðin og viljum þakka þér fyrir að tilkynna um aukaverkun. Auk tilkynningarinnar til okkar, mælum við með því að haft verði samband við lækni eða annan heilbrigðisstarfsmann varðandi aukaverkunina. Tillotts Pharma AG RE: mistenkt bivirkning Kjære rapportør Takk for utfyllingen av skjemaet. Tillotts’ høyeste prioritet og ansvar er sikkerheten og velværen til pasientene. Vi har mottatt meldingen din, og ønsker å takke deg for rapporteringen av bivirkningen. I tillegg til å rapportere til oss anbefaler vi at du kontakter lege eller annet helsepersonale med hensyn til bivirkningen. Tillotts Pharma AG RE: Sospecha de reacción adversa Gracias por completar el formulario. La seguridad y bienestar de los pacientes es la mayor prioridad y responsabilidad de Tillotts. Hemos recibido su mensaje y nos gustaría agradecerle que haya reportado un efecto adverso. Asimismo, le recomendamos que contacte también con su médico u otro profesional sanitario respecto al efecto adverso. Tillotts Pharma AG. Angående misstänkt biverkning. Bästa rapportör! Tack för att du fyllde i vår blankett. Tillotts ansvar och högsta prioritet är patienternas säkerhet och välbefinnande. Vi har fått ditt meddelande och vill tacka dig för att du rapporterat en biverkning. I tillägg till din rapport till oss rekommenderar vi att en läkare eller annan sjukvårdspersonal kontaktas beträffande biverkningen. Tillotts Pharma AG Oggetto: Sospetto effetto indesiderato La ringraziamo per aver compliato il formulario. La sicurezza ed il benessere dei pazienti sono la massima priorità per Tillotts. Abbiamo ricevuto il Suo messaggio e vorremmo ringraziarLa per aver segnalato un effetto indesiderato. Le raccomandiamo di informare inoltre anche il Suo medico e farmacista. Tillotts Pharma AG Bedankt voor het invullen van ons formulier. De veiligheid en het welzijn van de patiënten zijn de topprioriteit en de verantwoordelijkheid van Tillotts Pharma. We hebben uw bericht ontvangen en willen u bedanken voor het melden van een bijwerking. Aanvullend op uw melding aan ons bevelen we aan dat u met een arts of met een andere medische zorgverlener contact opneemt voor de bijwerking. Tillotts Pharma AG Täname, et täitsite meie vormi. Tillottsi suurim prioriteet ja vastutus on tagada patsientide ohutus ja heaolu. Oleme teie teatise kätte saanud ja täname, et teatasite kõrvaltoimest. Lisaks meile teate esitamisele soovitame võtta seoses kõrvaltoimega ühendust arsti või muu tervishoiutöötajaga. Tillotts Pharma AG Σας ευχαριστούμε που συμπληρώσατε το έντυπό μας. Η ύψιστη προτεραιότητα και ευθύνη της Tillotts είναι η ασφάλεια και η ευημερία των ασθενών. Έχουμε λάβει το μήνυμά σας και θα θέλαμε να σας ευχαριστήσουμε για την αναφορά της ανεπιθύμητης ενέργειας. Εκτός από την αναφορά σας σε εμάς, συνιστούμε να επικοινωνήσετε με έναν ιατρό ή άλλον επαγγελματία υγείας σχετικά με την ανεπιθύμητη ενέργεια. Tillotts Pharma AG Paldies, ka aizpildījāt šo veidlapu. Tillotts augstākā prioritāte un atbildība ir pacientu drošums un labklājība. Mēs esam saņēmuši Jūsu paziņojumu un vēlamies Jums pateikties, ka ziņojāt par blakusparādību. Papildus tam, ka iesniedzāt mums ziņojumu, mēs Jums iesakām sazināties arī ar ārstu vai citu veselības aprūpes speciālistu saistībā ar blakusparādību. Tillotts Pharma AG. Dėkojame, kad užpildėte mūsų formą. Didžiausias „Tillotts“ prioritetas ir atsakomybė yra pacientų saugumas ir gerovė. Gavome Jūsų pranešimą ir norime Jums padėkoti už tai, kad pranešėte apie šalutinį poveikį. Be šio pranešimo taip pat rekomenduojame, kad dėl šalutinio poveikio kreiptumėtės į gydytoją arba sveikatos priežiūros specialistą. „Tillotts Pharma AG Ďakujeme Vám za vyplnenie formulára. Najvyššou prioritou a zodpovednosťou spoločnosti Tillotts je bezpečnosť a zdravie pacientov. Dostali sme Vašu správu a radi by sme Vám za hlásenie vedľajšieho účinku poďakovali. Okrem nahlásenia nežiaduce účinku našej spoločnosti Vám odporúčame, aby ste sa v tejto súvislosti obrátili na lekára alebo iného zdravotníckeho pracovníka. Tillotts Pharma AG "Obrigado por preencher o nosso formulário. A maior prioridade e responsabilidade da Tillotts é a segurança e o bem-estar dos doentes. Recebemos a sua mensagem e gostaríamos de lhe agradecer por ter notificado um efeito indesejável. Além da sua notificação, recomendamos que um médico ou outro profissional de saúde seja contactado sobre o efeito indesejável. Tillotts Pharma AG "

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