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Digoxin Recall

By Oguz Ozdemir

Two drug repackaging companies are responsible for the recall of the drug Digoxin made by Caraco. On May 12, 2009, AS Medication Solutions, LLC announced that the drug, which is used for patients suffering from heart failure or abnormal heart rhythms, showed up in different sizes which had a bearing on the dose. The variations in the sizes of the medications could create problems in either too little a dose or too much.

The Digoxin that was packaged by AS Medication Solutions includes all tablets that are USP 0.25 mg and have been distributed before March 31, 2009 with an expiration date up to and including August of 2011. The product was manufactured by Caraco Pharmaceutical Labs and the scored white tablets are imprinted with the number 441 and an NDC number 54569-5758-0.

If a patient takes a Digoxin that has a higher dose than expected it could result in digoxic toxicity in patients who have kidney problems. Side effects of digoxin toxicity include low blood pressure, cardiac instability, bradycardia, and vomiting. This condition is very serious and can result in death.

A too low dosage will not deliver the appropriate medication level that the patient assumes they are getting by taking the Digoxin. If a patient receives too low of a dose of Digoxin it could result in an unstable cardiac situation which includes heart failure and abnormal heart rhythms.

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:
Digoxin Tablets, USP, 0.25 mg
54569-5758-0 (30-count)

If you have taken or are still taking Digoxin as a treatment for heart problems, check your packaging against the recalled products listed above. Because the expiration dates are not until August of 2011 you could very well have recalled medications in your possession. If you do, the FDA warns that you not take this product and either return it to the company for reimbursement or speak with your physician about an alternative form of medication.

If you have taken Digoxin and have experienced any side effects from receiving too high a dose or too low of a dose you should consult your physician regarding alternative medications. You may also wish to speak with an attorney regarding your rights with regards to receiving an incorrect dose of medication due to the negligence of packaging companies.

The legal team at the Napoli Bern Ripka Law Firm has extensive experience in dealing with physicians and the negligence associated with FDA drugs. You can input your information on the company's website in the Quick Contact section.

If you would rather speak with an attorney in person, call our office at 1-888-LAW IN NY . Our office is located in the Empire State building and your initial consultation is no charge. We would love the opportunity of helping you receive the compensation that you deserve as a victim of using any of the above mentioned medications without the proper knowledge of the risks and side effects that are involved with their use. Call today for your complimentary consultation.

Originally posted at InjuryBoard by Oguz Ozdemir

Full post as published by New York City Personal Injury Lawyer on July 28, 2009 (boomark / email).