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Urine drug Testing & evolving genetic screening

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Clinical oversight for injured workers to prevent abuse

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Ancillary Benefits Management for Workers’ Compensation

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Mobile app for workers compensation

About Us

myMatrixx provides pharmacy and ancillary services for workers’ compensation programs. Our services control costs with proactive clinical oversight throughout the claims process. With one online tool also available in a mobile app, clients can manage claims with real time data and detailed reporting.

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Dyloject™ Approved by the U.S. Food and Drug Administration (FDA)

Posted by On January 05, 2015

The U.S Food and Drug Administration (FDA) has approved Dyloject™ (diclofenac sodium) injection by Hospira, Inc. Dyloject™ is a new formulation of diclofenac sodium, which is a proprietary non-steroidal anti-inflammatory drug (NSAID) indicated in adults for the management of mild to moderate pain and management of moderate to severe pain alone or in combination with […]

Kansas 2015 Fee Schedule Controls Pharmacy Spend

Posted by On December 23, 2014

The Kansas Department of Labor, Division of Workers’ Compensation 2015 Schedule of Medical Fees includes two important revisions related to pharmacy spend. For dates of service effective January 1, 2015, physicians must obtain prior approval for compounds and physician dispensed drugs. If the payer approves compound and/or physician dispensed medications, the reimbursement will be the […]

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Compound Oversight Transformation Coming to Texas?

Posted by On February 13, 2015

By Tammy Odierna, Regulatory Data Analyst  Concern over physicians referring patients to a compound pharmacy and sharing in profits is not a new issue in Texas. In an Interim Report authored by the House Committee on Public Health in December of last year, the concern that the Texas State Board of Pharmacy (TSBP) is impeded by […]

The Return of Embeda®

Posted by On January 23, 2015

By Alan Rook, PharmD, Clinical Pharmacist It’s Baaack…Embeda® Embeda® will be back in the marketplace on January 26, 2015, after the manufacturer voluntarily recalled the drug almost 4 years ago. On October 17, 2014, the FDA approved new labeling for Embeda® (morphine sulfate and naltrexone hydrochloride) extended-release capsules indicated for pain severe enough to require […]

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