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Prescribed Drugs Provider Manual - Iowa Department of Human ...

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<strong>Iowa</strong><strong>Department</strong><strong>of</strong> <strong>Human</strong>Services<strong>Provider</strong> and Chapter<strong>Prescribed</strong> <strong>Drugs</strong>Chapter III. <strong>Provider</strong>-Specific PoliciesPage83DateAugust 1, 2013For prior authorization to be considered, the prescriber must submit acompleted Selected Brand Name <strong>Drugs</strong> PA form and <strong>Iowa</strong> Medicaid MedWatchform with:♦ Documentation <strong>of</strong> trials and therapy failures with two different genericmanufacturers <strong>of</strong> the same chemical entity. If an allergy to an inactivecomponent is suspected, the second trial must be with a generic productthat does not contain the allergen, if available.♦ Documentation <strong>of</strong> the failure must include the specific adverse reaction asdefined by the FDA. (See Section B <strong>of</strong> the MedWatch form).Intolerances, such as nausea and vomiting, to the generic drugs will notbe considered as a basis for approval.Trials may be overridden when evidence is provided that use <strong>of</strong> the genericproduct would be medically contraindicated.Use forms 470-5039 and 470-4119, Request for Prior Authorization:Selected Brand Name <strong>Drugs</strong>, to request prior authorization. Click here to seea sample <strong>of</strong> form 470-5039. Click here to see a sample <strong>of</strong> form 470-4119.66. Serotonin 5-HT1 Receptor AgonistsPrior authorization is required for serotonin 5-HT1 receptor agonists forquantities exceeding 12 unit doses <strong>of</strong> tablets, syringes, or sprays per 30days. Payment for serotonin 5-HT1 receptor agonists beyond this limit will beconsidered on an individual basis after review <strong>of</strong> submitted documentation.Prior authorization is required for all nonpreferred serotonin 5-HT1 receptoragonists beginning the first day <strong>of</strong> therapy. Payment for nonpreferredserotonin 5-HT1 receptor agonists will be authorized only for cases in whichthere is documentation <strong>of</strong> previous trials and therapy failures with twopreferred agents.Requests for nonpreferred combination products may be considered onlyafter documented separate trials and therapy failures with the individualingredients.For consideration, the following information must be supplied:♦ The diagnosis requiring therapy.♦ Documentation <strong>of</strong> current prophylactic therapy or documentation <strong>of</strong>previous trials and therapy failures with two different prophylacticmedications.

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