{
  "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": "2026-08-05",
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          "manufacturer_d_city": "LAHAT PERAK",
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          "openfda": {
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      "date_changed": "20250729",
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      "patient": [
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      "event_key": "",
      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20080206",
      "manufacturer_contact_city": "",
      "mdr_report_key": "1003360",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20080212",
      "manufacturer_name": "",
      "report_source_code": "Distributor report",
      "remedial_action": [
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "17062212",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "ACCOUNT CLAIMS ONE FEMALE ASSISTANT HAD AN ALLERGIC REACTION TO THE LATEX EXAMINATION GLOVES. SHE DEVELOPED PIMPLE SORES AND WENT TO THE HOSP AND WAS PRESCRIBED PREDNISONE PILLS."
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      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": ""
    }
  ]
}