Digoxin
On May 12, 2009, AS Medication Solutions, LLC announced that certain batches of the drug, Digoxin, used to treat patients suffering from heart failure or abnormal heart rhythms, were being recalled due to manufacturing defects. The defective batches contained product that was inaccurately dosed. This could have the effect of a patient being administered too much or too little medication which could have dire consequences.
Recall Facts:
The recalled products are:
- Caraco Digoxin
- A-S Medication Solutions, Digoxin 0.25 mg is a scored round biconvex white tablet imprinted with “441”
- NDC Numbers:54569-5758-0 (30-count)
- Digoxin Tablets, USP, 0.25 mg
Potential Complications:
If a patient receives a greater dose than prescribed it could result in digoxic toxicity. Patients with impaired kidney function are especially at risk. Side effects of digoxin toxicity include low blood pressure, cardiac instability, bradycardia, and vomiting. Death may also result.
An under-dosage can result in heart failure or serious arrhythmias or death
Litigation:
Attorneys from across the nation are investigating cases against the manufacturer of Digoxin If you or a loved one have been injured as a result of taking Digoxin you must act quickly to preserve your right to file a claim.
If you or someone you know developed any of the complications described above they may be entitled to significant compensation. Contact us today to learn whether you can be compensated.
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