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Study Number:ARQ151202NCT #:NCT03764475Official Title:A Phase 2, Multi center, OpenTable Extension Study of the Longer Safety of ARQ151 Cream 0.3% in Adult Subjects With Chronic Plaque Psoriasis Who
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01
Obtain the necessary information and forms for reporting long-term safety data of Arq-151.
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Record all relevant details about the patient, including medical history, adverse reactions, and treatment duration.
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Document any changes in the patient's condition or response to the medication over time.
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Follow-up with the patient regularly to monitor for any new side effects or complications.
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Submit the completed long-term safety report to the appropriate regulatory authorities.

Who needs long-term safety of arq-151?

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Patients who are prescribed Arq-151 for long-term use.
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Healthcare providers who are monitoring the safety and efficacy of Arq-151.
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Regulatory agencies that oversee the approval and monitoring of pharmaceutical drugs.
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The long-term safety of arq-151 refers to the ongoing monitoring and evaluation of the safety profile of the drug over an extended period of time.
The pharmaceutical company or sponsor who holds the marketing authorization for arq-151 is required to file the long-term safety report.
The long-term safety report for arq-151 should include data on adverse events, side effects, and any new safety information that has been identified since the initial approval.
The purpose of the long-term safety report is to ensure that any new safety concerns or issues with arq-151 are identified and addressed in a timely manner.
The long-term safety report should include information on serious adverse events, unexpected side effects, and any new safety findings related to the use of arq-151.
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