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Studies have found that they make certain birth control options, like the combined birth control pill, less effective [3]

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If the FDA ultimately moves toward broader acceptance, or even formal inclusion on the 503A bulks list, providers could see clearer pathways for incorporating these therapies into patient care plans

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While most patients reported no symptoms ( n = 107, 67%), it is worth noting that many ( n = 65, 43%) were lost to follow-up and that most subcutaneous injection exposures remained within a normal therapeutic dosing range (Table 3)