{
  "url": "https://openlegislation.uk/veterinary-medicines-regulations-2007/schedule-6/paragraph-9",
  "json_url": "https://openlegislation.uk/veterinary-medicines-regulations-2007/schedule-6/paragraph-9.json",
  "legislation": "uksi/2007/2539",
  "legislation_title": "The Veterinary Medicines Regulations 2007",
  "legislation_url": "https://openlegislation.uk/veterinary-medicines-regulations-2007",
  "path": "schedule/6/paragraph/9",
  "kind": "paragraph",
  "number": "9",
  "heading": "Adverse reactions",
  "text": "(1) The manufacturer, importer or retailer of a veterinary medicinal product must notify the Secretary of State of any serious adverse reactions (as defined in paragraph 57 of Schedule 1) of which he becomes aware within 15 days of learning of the reaction.\n(2) It is an offence to fail to comply with this paragraph.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/2007/2539/schedule/6/paragraph/9",
    "retrieved_at": "2026-10-29T03:44:29.692897+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}