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Some of this information is considered by law to be “sensitive personal data” about you. This includes any information that tells us about your:
This information is only processed where relevant and necessary to document your reaction properly and for the purpose of meeting our pharmacovigilance and/or legal requirements. These requirements exist to allow us and competent pharmacovigilance authorities (such as the European Medicines Agency and other authorities) to manage adverse events and make efforts to prevent similar events from happening in the future. ReportersWe collect information about you when you provide us with information in relation to an adverse event you report. Pharmacovigilance laws require us to ensure that adverse events are traceable and available for follow-up. As a result, we must keep sufficient information about reporters to allow us to contact you once we have received the report. The personal data that we may collect about you when you report an adverse event is your:
As part of meeting our pharmacovigilance obligations, we may use and share Personal Data to:
Our pharmacovigilance obligations require us to review patterns across reports received from every country where we market our products. To meet these requirements, information provided as part of an adverse event report is shared within Teva on a worldwide basis through Teva’s Global Database. This database is also the platform through which Teva uploads adverse event reports to various oversight authorities, including the Eudravigilance database (European Medicines Agency corporate system for managing and analysing information on suspected adverse reactions to medicines which have been authorised in the European Economic Area) and other similar databases as required by law.
Because patient safety is so important, we retain all the information we gather about you as a result of an adverse event report to ensure that we can properly assess the safety of our products over time. You may be entitled under applicable law to ask Teva for a copy of your information, to correct it, erase or restrict its processing, or to ask us to transfer some of this information to other organisations. You may also have rights to object to some processing. These rights may be limited in some situations – for example, where we can demonstrate we have a legal requirement to process your personal data. You may exercise these rights by contacting Teva’s Pharmacovigilance team at email@example.com.For legal reasons, we cannot delete information that has been collected as part of an adverse event report unless it is inaccurate.We may require you to provide proper identification before we comply with any request to access or correct Personal Data. Your right to access or correction may be limited by applicable law. We hope that we can satisfy any queries you may have about the way in which we process your personal data.If you have any concerns about how we process your personal data, you can get in touch with Teva’s Pharmacovigilance team at firstname.lastname@example.org. However, if you have unresolved concerns you also have the right to complain to the data protection authority in the location in which you are based.