Digitek (Digoxin Tablets) Recall

Digoxin is used to treat congestive heart failure and atrial fibrillation/atrial flutter (types of fast heartbeats). Digoxin is available via prescription under various brand names, including Digitek.

DIGITEK WAS SUBJECT TO A NATIONWIDE
RECALL ON APRIL 25, 2008

The recall applied to all oral strength tablets of Digitek. The recall was due to Digitek tablets containing twice the approved level of active ingredient. The Recall - Firm Press Release can be seen at:

http://www.fda.gov/oc/po/firmrecalls/actavis04_08.html

Robert J. DeBry & Associates, is representing victims of Digitek overdose or Digitek toxicity due to pills containing twice the normal dose of active ingredient.

Recalled medications Include:

• Digitek
• Digoxin
• Cardoxin
• Lanoxin
• Lanoxicaps

Digitek Overdose

If you took Digitek, Cardoxin, Lanoxin or Lanoxicaps and suffered from overdose, it could be due to taking defective tablets containing twice the active ingredient as approved. Symptoms of Digoxin overdose may include any of the following: nausea, vomiting, decreased appetite, diarrhea, confusion, seizures, hallucinations, light “halos” around objects, green or yellow vision, fatigue, irregular heartbeats, and abnormally fast or slow heartbeats.

If you experienced a life threatening adverse reaction from Digitek or your loved one has died as a result of this medication – the time is right to contact Robert J. DeBry & Associates.

CALL US NOW for a free consultation.

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