{"topic_id":"ade_romifidine_adverse_events","category":"ade","context":"---\ntopic_id: ade_romifidine_adverse_events\ncategory: ade\ntitle: \"FDA ADE reports for Romifidine Hydrochloride (active ingredient) — total reports, species & reaction breakdown\"\nlang: en\nsource: \"openFDA animalandveterinary/event.json (FDA CVM adverse event reports), pulled 2026-07-22\"\nsource_file: pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json\ndate_parsed: 2026-07-22\ntokens_estimated: 376\nverification:\n  method: substring_match\n  claims: 32\n  passed: 32\n  date: 2026-07-22\n---\n\n# Romifidine Hydrochloride — FDA Animal & Veterinary Adverse Event (ADE) Reports\n\nSource: openFDA `animalandveterinary/event.json`, the FDA Center for Veterinary Medicine (CVM) adverse event report database. Data pulled 2026-07-22. Counts are report-level: one report may list multiple reactions and multiple animals, so figures are not additive and do not imply causation. Romifidine Hydrochloride is a active ingredient.\n\n## Total reports\nRomifidine Hydrochloride: 43\n\n## Reports by species (top entries)\n- Horse 36\n- Dog 1\n- Donkey 1\n- Human 1\n- Other 1\n\n## Top reported reactions (VEDDRA terms, top entries)\n- Abdominal pain 8\n- INEFFECTIVE, SEDATION 6\n- Recumbency 6\n- Bradycardia 4\n- Aggression 3\n- Anaphylaxis 3\n- Ataxia 3\n- Facial oedema 3\n- Hyperhidrosis 3\n- Anorexia 2\n\nSource JSON: `pdf-raw/ade/ade_active_ingredients_2026-07-22_b25.json` (openFDA animalandveterinary/event.json, pulled 2026-07-22).\n","sources":[],"tokens_estimated":235,"generated_at":null,"tip":"Use /api/v1/topics to discover more topics. /api/v1/nutrient for precise single-point queries. /api/v1/cross_compare for 2-3 standard comparisons."}