Let us know if you have an adverse event
If things go wrong when you use an ACVM, let us know. Examples of adverse events are:
- side effects or a reaction to a product
- a product not working
- detection of residues in food
- human exposure to a product
- a possible interaction with other products.
How to report an event
If you are an end user of a product such as a grower, farmer, veterinarian, or animal owner, you can report an adverse event by:
- reporting it directly to the Ministry for Primary Industries (MPI) by filling in a form
- telling the product registrant or distributor – check for their contact details on the label. (Registrants must tell MPI about any adverse events reported to them).
To report an event directly to MPI
There are different reporting forms for different product types.
For the product you’ve used:
- download the relevant reporting form and guideline below
- use the guideline to help you fill out the form
- email the completed form to ACVMfirstname.lastname@example.org
Adverse event forms and guidelines
For agricultural chemicals
- Guideline: Adverse event reporting for agricultural chemicals [PDF, 261 KB]
- Form: Adverse event report for agricultural chemicals [DOC, 426 KB]
For animal feeds
- Form: Adverse event report for animal feeds [DOC, 445 KB]
For vertebrate toxic agents
- Guideline: Adverse event reporting for vertebrate toxic agents [PDF, 258 KB]
- Form: Adverse event report vertebrate toxic agents [DOC, 442 KB]
For veterinary medicines
- Guidelines for vets and animal owners: Adverse event reporting for veterinary medicines [DOC, 346 KB]
- Guidelines for registrants: Adverse event reporting for veterinary medicines [PDF, 381 KB]
- Form: Adverse event report for veterinary medicines [DOC, 445 KB]
After you report an event to MPI
We'll send a copy of your report to the product registrant or distributor for immediate investigation. The registrant may contact you to discuss the issue.
The registrant then sends us an investigation report. We assess this and may also refer to scientific information. We’ll decide whether:
- the product was used according to label directions
- further investigation is required.
You will be advised of the outcome, including whether the adverse effects were likely to be related to the use of, or exposure to, the product.
Actions we may take
We will decide if any regulatory action is required, such as:
- additional label warning statements
- product recalls
- formulation or manufacturing process changes
- education of product users
- changes to the conditions of registration (such as restrictions on off-label use).
In cases where there isn’t a clear link or there’s insufficient information to make a definite conclusion, we may take no action.