Teva – Tolvaptan

Tolvaptan Teva Training Portal

This website is intended for UK registered healthcare professionals (HCPs) only. Adverse event reporting can be found at the bottom.

As agreed with the Medicines and Healthcare Products Regulatory Agency (MHRA), a register of prescribers who have reviewed the additional Risk Minimisation Materials (aRMM) on the safety aspects of Tolvaptan Teva is being maintained. Teva UK Limited will also issue annual reminders to re-review the aRMM.

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I have read and understood the aRMM for Tolvaptan Teva

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Please report suspected adverse drug reactions (ADRs) to the MHRA through the Yellow Card scheme. You can report via: the Yellow Card website, the free Yellow Card app available from the Apple App Store or Google Play Store and also some clinical IT systems (EMIS/SystmOne/Vision/MiDatabank) for healthcare professionals.

Alternatively you can report a suspected side effect to the Yellow Card scheme by calling 0800 731 6789 for free, Monday to Friday between 9am and 5pm. You can leave a message outside of these hours.

When reporting please provide as much information as possible. By reporting side effects, you can help provide more information on the safety of this medicine.

Adverse events should also be reported to Teva using our online reporting form, via email to uk.safety@tevauk.com or by calling 0207 540 7117.

D: TOL-GB-NP-00008 (V3.0) / T: TOL-GB-NP-00006 (V3.0) / M: TOL-GB-NP-00007 (V3.0)
Date of Preparation: January 2026

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