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Statement from FDA on continuing efforts to maintain its strong oversight of generic drugs
date:Feb 25, 2019
urprising. This type of discrepancy has been noted before in AE reporting, and likely represents health care professionals familiarity with and use of the brand name. This mismatch suggests the identification of the manufacturer in these reports is unreliable.

The differences in reporting among generic manufacturers are difficult to compare given the small numbers, known misclassification of product manufacturers in FAERS, and other biases. Additionally, reports typically involve more than one

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