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Early and Periodic Screening, Diagnostic and Treatment (EPSDT) is the child health component of Medicaid.Federal statutes and regulations state that children under age 21 who are enrolled in Medicaid are entitled to EPSDT benefits and that States must cover a broad array of preventive and treatment services.
These services include enrollment in Medicaid, the Kentucky Children’s Health Insurance Program (KCHIP) and the Kentucky Integrated Health Insurance Premium Payment program. In addition, qualified families can now also access SNAP food assistance benefits along with other family and childcare assistance programs. [10]
The Medicaid Drug Rebate Program is a program in the United States that was created by the Omnibus Budget Reconciliation Act of 1990 (OBRA'90). The program establishes mandatory rebates that drug manufacturers must pay state Medicaid agencies related to the dispensing of outpatient prescription drugs covered by Medicaid.
Under the bill introduced this week, out-of-state residents who came to Kentucky for treatment but failed to establish residency would be fined and required to reimburse Kentucky Medicaid for any ...
The Centers for Medicare & Medicaid Services confirmed to lawmakers that the drug company that makes EpiPen, has been overcharging the government. CONFIRMED: The maker of EpiPen overcharged the ...
“We know that when people cannot see or hear well, or have poor oral health, it hinders their ability to seek and maintain a job,” Gov. Beshear said of the expansion for 900,000 Kentuckians.
A Katie Beckett waiver or TEFRA waiver is a Medicaid waiver concerning the income eligibility for home-based Medicaid services for children under the age of nineteen. Prior to the Katie Beckett waiver, if a child with significant medical needs received treatment at home, the child's income would be deemed to include the parents' entire ...
The EpiPen had 89% of the market for epinephrine autoinjectors in 2015; [57] in the first half of the year it had about 85% share and Auvi-Q had about 10% share. [29] In March 2016, Teva's ANDA for a generic EpiPen, which had already faced several delays, was rejected by the FDA. [77]
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