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  "documentTitle": "Harmony Biosciences (HRMY)",
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  "notes": "The slide presents a patient-reported adverse event (FAERS) to challenge the safety profile of a pharmaceutical product.",
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      "text": "We note that pitolisant is marketed as not having any withdrawal symptoms.",
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      "text": "53 year old male patient on 36mg, who stated he is a “heath professional” who has been a “clinical trials coordinator.” He experienced a 9 day gap in getting a refill due to a pharmacy error and “suffered continuous, severe, debilitating headaches” with “extreme nausea.” Symptoms improved within a day when Wakix was refilled. Patient stated that “It's important to note that according to all existing medical literature, to date, there are NO EXISTING REPORTS OF ADVERSE EFFECTS UPON SUDDEN DISCONTINUATION OF WAKIX. Because this is a newly released, novel medication, I thought it was important to report this finding directly to the FDA.” (all caps by patient) We note that pitolisant is marketed as not having any withdrawal symptoms.",
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      "text": "It's important to note that according to all existing medical literature, to date, there are NO EXISTING REPORTS OF ADVERSE EFFECTS UPON SUDDEN DISCONTINUATION OF WAKIX. Because this is a newly released, novel medication, I thought it was important to report this finding directly to the FDA. — Patient (Case ID: 18319093)",
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      "text": "Source: FDA FAERS – FOIA Case Report Information",
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