Mislabeling could lead to an overdose or an underdose.
the recall of one lot of Digoxin Tablets USP, 0.125mg, and one lot of Digoxin Tablets USP, 0.25mg.
The mix-up in labels can cause either overdosing or underdosing in patients who unknowingly take the wrong dose, the FDA said. Digoxin Tablets USP, 0.25mg are white to off-white, circular, beveled, uncoated tablets that are scored between “N” and “202″ on one side and plain on the other side.If patients accidentally overdose they can experience significant drug toxicity: mental disorientation, dizziness, blurred vision, memory loss and fainting.
According to Marlex Pharmaceuticals, no reports of adverse events related to this recall have been received.Digoxin 0.125mg Tablet – NDC 10135-0747-01, lot# E3810, expiration 2/2025The medication was distributed nationwide.
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