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| Digitek Recall By The FDA Announcement |
| submitted by astechno1 |
| The FDA has recently released a Class 1 Digitek recall for all strengths of Digitek tablets. The tablets, manufactured by Actavis Totowa, may possibly contain a double dose of the active ingredient in Digitek (digoxin). |
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| Topic: News |
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| Digitek recall tablets should not be consumed as they may cause severe side effects or death. This risk is increased for those who suffer from renal failure or who are currently taking a diuretic. |
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| Recalled Digitek tablets cause severe illness, digitalis toxicity, and may result in death. These side effects are serious, dangerous, and life altering. |
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