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The suit filed in Harrison County alleged that Pfizer and Tris Pharma doctored quality-control tests for the drug Quillivant XR between 2012 and 2018 to hide that the medicine failed to dissolve like promised, and Pfizer then persuaded Texas' Medicaid program to add Quillivant to its list of preferred drugs.
“At no point did Defendants warn Texas Medicaid providers or decision-makers that Quillivant had known manufacturing issues affecting its efficacy, thereby depriving the Medicaid program of the crucial information it relies on,” the suit said.
“As a result, thousands of Texas children received an adulterated Schedule II Controlled Dangerous Substance,” it added.
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