Digitek Recall

At the end of April, the pharmaceutical company Actavis Totowa announced a cross-country Digitek medication recall; the recall is a result of manufacturing defects which have caused a portion of the Digitek tablets to contain twice as much as the suggested amount of active ingredients. If ingested, the unsafe dosage could pose a serious risk and lead to a deadly illness called digitalis toxicity. It is particularly hazardous to patients with severe kidney problems.

Digitek, or digoxin, is a drug used to treat heart failure and irregular heartbeats. About 50 percent of the pill's nationwide supply is said to be affected by this production error. If you have a Digitek prescription, check your labels because the tablets of interest are under the "Bertek Digitek" and "UDL Digitek" names.

This digitek recall became official following numerous phone calls to Actavis regarding reports of digitalis toxicity complications. Based on some assessments, Actavis was first notified of the potential danger associated with the Digitek double dosage as far back as 2006.

Digitalis toxicity is a potentially lethal illness that is common among people with kidney troubles, especially those with renal failure. The sickness is triggered by the buildup of more digitalis than the body can tolerate. The following symptoms are linked to digitalis toxicity:

Nausea
Vomiting
Faintness
Low blood pressure
Cardiac instability
Bradycardia (low heart rate)

If you or someone you love has been taking a form of Digitek or experienced any of the symptoms related to digitalis toxicity, the product liability attorneys at Morgan & Morgan are on your side. If you have indeed been poisoned as a result of this mishap, we will work to get you the compensation you deserve. Contact us immediately with the details of your case.