Change description : 2025-07-17 15:41:00: Table updated to include Zermex 100 mg/ml LA Solution for Injection for Cattle and Zermex 20 mg/ml LA Solution for Injection for Sheep – SPC change and StromEase 25 mg/ml Eye Drops, Solution for Dogs and Cats – SPC change. [Guidance and regulation]
Urgent and clinically significant safety updates for veterinary medicines
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
An adverse event is any observation in animals, whether or not considered to be product-related, that is unfavourable and unintended and that occurs after any use of a veterinary medicine, whether off-label or on-label use. This include events related to a suspected lack of expected efficacy according to approved labelling or noxious reactions in humans after being exposed to a veterinary medicine.
If anyone becomes aware of an adverse event involving a veterinary medicine they can report this to the Marketing Authorisation Holder (MAH or pharmaceutical company).
The MAH for a UK-authorised medicine can be found on the product leaflet or by searching for the product on the Product Information Database.
To report a suspected adverse event to a human medicine or a product that you know is not an authorised veterinary medicine, please request a form from adverse.events@vmd.gov.uk, stating within your email that you are requesting the form in order to report an adverse event to a human medicine or to a product that you know is not an authorised veterinary medicinal product, as applicable.
The VMD’s pharmacovigilance team continuously monitors all adverse event reports that are submitted to the VMD and reports submitted directly to the MAH.
List of urgent and/or clinically significant safety updates
Urgent and/or clinically significant safety updates published by the VMD in the last 12 months.
SPC changes listed on this page may have been made as a result of routine rather than urgent pharmacovigilance processes. They include additions of Medically Important Terms (MITs), however. SPC changes involving non-MITs assessed as having a significant beneficial clinical impact may also be included. More detail can be found in our adverse event reporting guidance.
Section 4.6 has been amended to clarify that irritation or inflammation of the eye and/or its adnexa have been reported in very rare cases, especially blinking of the eyelids or even closure of the eye, eye redness or conjunctival oedema, particularly in dogs.
Information relating to the occurrence of eye disorders, despite no direct ocular contact, has been removed from section 4.5 and section 4.6 (adverse reactions) has been updated.
Section 4.6 now states Pruritus, bloody diarrhoea, urinary incontinence, inappropriate urination, polyuria and polydipsia can occur very rarely following the administration of the veterinary medicinal product.
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Further guidance on what veterinary pharmacovigilance is and who is responsible can be found in the guidance documents on gov.uk.
You will find the Summary of Product Characteristics (SPC) for all veterinary medicinal products authorised for marketing in the UK on our Product Information Database
No medicine is 100% risk free, the SPC includes information on what adverse events have been known to occur following administration of a particular product, these can be found in the section ‘Adverse events’ (3.6) or ‘Adverse reactions’ (4.6).
A rolling 6-month list of SPC changes for veterinary medicinal products is published on the Veterinary Practice and Supply page under the Medicine Updates section of VMD Connect.
Additional updates on veterinary pharmacovigilance in the UK can also be found on the adverse events page of VMD Connect.
Table updated to include Zermex 100 mg/ml LA Solution for Injection for Cattle and Zermex 20 mg/ml LA Solution for Injection for Sheep - SPC change and StromEase 25 mg/ml Eye Drops, Solution for Dogs and Cats – SPC change.
Further update: Genta-Equine 100 mg/ml Solution for Injection for Horses – Adverse events added to table.