{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-28"
  },
  "results": [
    {
      "term": "NO ADVERSE EVENT",
      "count": 5
    },
    {
      "term": "NEEDLE ISSUE",
      "count": 4
    },
    {
      "term": "PRODUCT ADMINISTRATION INTERRUPTED",
      "count": 4
    },
    {
      "term": "PRODUCT USE COMPLAINT",
      "count": 4
    },
    {
      "term": "ANGIOEDEMA",
      "count": 1
    },
    {
      "term": "HEADACHE",
      "count": 1
    },
    {
      "term": "HYPERSENSITIVITY VASCULITIS",
      "count": 1
    },
    {
      "term": "INJECTION SITE PAIN",
      "count": 1
    },
    {
      "term": "LUNG DISORDER",
      "count": 1
    },
    {
      "term": "LYMPHADENOPATHY",
      "count": 1
    },
    {
      "term": "MEDICATION ERROR",
      "count": 1
    },
    {
      "term": "PRODUCT PHYSICAL CONSISTENCY ISSUE",
      "count": 1
    },
    {
      "term": "PRODUCT SUBSTITUTION ISSUE",
      "count": 1
    }
  ]
}