House Republicans will be launching an investigation into the Food and Drug Administration’s (FDA) decision that found a common decongestant in cold medicines was found ineffective. A House Oversight subcommittee sent a letter to FDA Commissioner Robert Califf on Sunday to ask him to brief the members on the decision to label the decongestant, known as phenylephrine, as ineffective in September. The subcommittee on Health Care and Financial Services is questioning how it took so long for the FDA to conclude that the drug was ineffective despite prior evidence over the years that said otherwise. “Due to these concerns, we ask that you provide a staff-level briefing to assist the Subc
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