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DRAFT PA CriteriaInitial Approval: April 10, 2019, Revised Dates: July 10, 2019, CRITERIA FOR PRIOR AUTHORIZATION Extended Release BILLING CODE Typer drug coverage and provider type information, see
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How to fill out extended release

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To fill out extended release, follow these steps:
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Read the instructions provided with the extended release medication.
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Take note of the recommended dosage and any specific instructions.
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Ensure that you have a supply of the extended release medication.
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Take the prescribed amount of medication at the recommended time.
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Swallow the extended release medication whole with a glass of water.
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Do not crush, chew, or break the medication as it may affect its extended release properties.
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If you have any questions or concerns, consult with your healthcare provider.

Who needs extended release?

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Extended release medications are typically prescribed to individuals who require a steady release of the medication over an extended period of time.
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Common examples include individuals with chronic conditions, such as hypertension, diabetes, or certain mental health disorders.
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Your healthcare provider will determine if extended release is suitable for your specific condition and needs.
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Extended release refers to a method of delivering a medication or substance in a way that prolongs its effect, allowing it to be released into the body gradually over time.
Entities that have specific financial reporting obligations or are involved in certain regulations that require them to report extended release information, often related to financial or tax filings.
To fill out an extended release, one must provide accurate financial data, comply with the specific form requirements, and ensure all necessary documentation is attached as per regulatory guidelines.
The purpose of extended release is to manage the timing and dosage of medication or information release to ensure prolonged effectiveness and compliance with regulations.
Information that must be reported may include financial data, compliance statements, and other relevant details as specified in regulatory requirements.
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