We encourage healthcare professionals and patients to report any information about the safety, quality or performance of a Vitra Pharmaceuticals product. This includes potential adverse events, reports on certain circumstances that may increase a patient’s risk of developing an adverse event, as well as other reportable information, including product complaints and unexpected therapeutic effects.

All Vitra Pharmaceuticals employees play a critical role in meeting our legal and ethical responsibilities to collect and analyse reports and are fully trained in how to recognize and report an adverse event. We have to report all such events to the regulatory bodies, whether or not we can confirm their accuracy.