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Drug Alerts > December 2008 > For digoxin patients taking DIGITEK brand

For digoxin patients taking DIGITEK brand

12/5/2008
In April this year, the manufacturers of a brand of digoxin called Digitek recalled this product. They found it may have contained twice the amount of digoxin in each tablet. By taking the affected product consumers could have serious health problems or even die. There were two doses that were involved: 0.125 mg (yellow tablets imprinted with a “B” and “145”) and 0.25 mg (round white tablets imprinted with a “B” and “146”).

If you are using DIGOXIN tablets, check your bottle to make sure you don't have Digitek tablets that were recalled last spring. If you have not previously checked and if your tablets are made by Actavis, Mylan, Bertek or UDL, you should return them to your pharmacy to examine and possibly exchange. If you are not sure who has made your tablets, please take your bottle to your pharmacist for them to check as soon as possible.


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Other December Alerts:

      Dose changes for popular iron supplement for babies
      Warning. Do NOT swallow Benadryl Itch Stopping Gel!
      Hydromorphone 2 mg tablets drug recall
      Caution for patients using more than a single insulin product
      Babysitter gives pet medications to child
      Caution: Pharmacists and doctors have confused Depakote with Depakote ER (an extended release form)
      Help for detecting doctor mental slips on prescriptions
      Addressing Questions About Gardasil
      New FDA Warning on Seizure Medications
      Abbreviation of concern
      New Warning for Oral Sodium Phosphate Bowel Cleansing Products
      For digoxin patients taking DIGITEK brand
      Parents need to be involved to prevent vaccine errors
      Speed trap – speedy prescriptions might compromise safety
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