{
  "docId": "019dd923-622c-750b-8b9a-21918ac10c17",
  "docSlug": "f3db2294dcf9",
  "documentTitle": "Harmony Biosciences (HRMY)",
  "authorId": "58_Scorpion_Capital",
  "authorName": "Scorpion Capital",
  "documentKindSlug": "research-note",
  "documentKindLabel": "Research note",
  "sourceTypeSlug": "short_seller",
  "sourceTypeLabel": "Short seller",
  "presentationDate": "2023-03-28 00:00:00",
  "orientation": "landscape",
  "aspectRatio": 1.3333334,
  "pageNumber": 188,
  "pageCount": 366,
  "prevPage": 187,
  "nextPage": 189,
  "slideType": "other",
  "function": "other",
  "density": "dense",
  "nDataPoints": 0,
  "notes": "This is a raw FDA FAERS FOIA case report document.",
  "elementsJson": [
    "paragraph",
    "screenshot",
    "footnote"
  ],
  "metadataConfidence": 1,
  "imagePath": null,
  "slideHref": "/slides/019dd923-622c-750b-8b9a-21918ac10c17/188",
  "deckHref": "/decks/019dd923-622c-750b-8b9a-21918ac10c17",
  "deckJsonHref": "/decks/019dd923-622c-750b-8b9a-21918ac10c17.json",
  "deckAnchorHref": "/decks/019dd923-622c-750b-8b9a-21918ac10c17#slide-188",
  "components": [
    {
      "bbox": {
        "h": 0.06,
        "w": 0.9,
        "x": 0.07,
        "y": 0.18
      },
      "kind": "callout",
      "text": "Limited details regarding medical history, concomitant medications and clinical course were provided; however, due to the temporal relationship, a causal role of WAKIX cannot be ruled out.",
      "attrs": null,
      "subkind": "primary",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "a24018cf-9b55-472c-bca5-b08c2ed1d280",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.05,
        "w": 0.1,
        "x": 0.12,
        "y": 0.61
      },
      "kind": "image",
      "text": "FDA",
      "attrs": null,
      "subkind": "logo",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "1e626fe1-54c2-44bb-9a4d-618bc9b30f18",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.08,
        "w": 0.9,
        "x": 0.07,
        "y": 0.1
      },
      "kind": "paragraph",
      "text": "A 42-year old female was hospitalized for acute kidney failure secondary to acute urinary retention, 37 days after starting pitolisant (18mg). Pitolisant was discontinued the same day and the patient recovered on an unspecified date.",
      "attrs": null,
      "subkind": "paragraph",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "1546f2df-3a5d-4575-8a8e-2cab6e6f1c43",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.12,
        "w": 0.9,
        "x": 0.07,
        "y": 0.35
      },
      "kind": "paragraph",
      "text": "Event/Problem Narrative: On 06-May-2022, information was received from a physician in France, via Bioprojet, describing a 42-year-old female patient who was being treated with WAKIX (pitolisant)...",
      "attrs": null,
      "subkind": "paragraph",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "2cf95228-47e7-422e-bf71-0c425f00b14b",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.08,
        "w": 0.9,
        "x": 0.07,
        "y": 0.74
      },
      "kind": "paragraph",
      "text": "Case ID: 20840813. This report describes a 42-year-old female who experienced acute renal failure secondary to acute urinary retention 37 days after initiating WAKIX...",
      "attrs": null,
      "subkind": "paragraph",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "64b44f02-3ea8-45e2-87fb-1d8e6dcdfd87",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": null,
      "kind": "quote",
      "text": "Limited details regarding medical history, concomitant medications and clinical course were provided; however, due to the temporal relationship, a causal role of WAKIX cannot be ruled out. — FDA FAERS Case Report",
      "attrs": null,
      "subkind": null,
      "toolName": "Authority citation",
      "toolSlug": "authority-citation",
      "confidence": null,
      "componentId": "019dd953-64d0-7099-9cd8-985c26e82b2e",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.02,
        "w": 0.3,
        "x": 0.07,
        "y": 0.95
      },
      "kind": "source-note",
      "text": "Source: FDA FAERS – FOIA Case Report Information",
      "attrs": null,
      "subkind": null,
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "c1417eff-0d65-4c33-a98d-26a40ea45317",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.03,
        "w": 0.5,
        "x": 0.07,
        "y": 0.07
      },
      "kind": "title",
      "text": "Case ID: 20840813, Event date: Jan 20, 2022",
      "attrs": null,
      "subkind": "headline",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "e0d49c32-0dd6-42ee-a404-c814cddad861",
      "frameworkName": null,
      "frameworkSlug": null
    },
    {
      "bbox": {
        "h": 0.04,
        "w": 0.3,
        "x": 0.36,
        "y": 0.61
      },
      "kind": "title",
      "text": "FDA - Adverse Event Reporting System (FAERS) FOIA Case Report Information",
      "attrs": null,
      "subkind": "subtitle",
      "toolName": null,
      "toolSlug": null,
      "confidence": null,
      "componentId": "fe28ef8e-7be0-4178-8793-3f473d048473",
      "frameworkName": null,
      "frameworkSlug": null
    }
  ],
  "metrics": [],
  "tools": [],
  "frameworks": [],
  "arcBeats": [],
  "loops": [],
  "imagePathAlt": null,
  "thumbSrc": null,
  "thumbSrcAlt": null,
  "locked": true
}