Digitek Recall Lawyer

Digitek, a popular heart medication, was recently voluntarily recalled due to the high possibility of the production of tablets with twice the approved amount of active ingredient. The active ingredient in Digitek is Digoxin, a substance which is toxic if it is taken in large amounts.

Over consumption of Digoxin results in Digitalis, a condition which causes severe illness and death in patients. The risk of developing Digitalis increases if other medical conditions, such as kidney failure, are present.

Unfortunately, defective Digitek tablets may have fallen into the hands of the public. This has resulted in a number of unnecessary illnesses and wrongful death. Currently, there is a pending lawsuit against the makers of Digitek because of these side effects.

If you have suffered serious side effects as a result of consuming defective Digitek or lost a loved one, contact McEwen Law Firm today. Our attorneys are dedicated to defending the victims of Digitek as well as their families, and are determined to help victims receive the compensation they deserve.

To contact a McEwen Law Firm attorney today please call (800)732-3070 or fill out our online contact form.

Recalled Digitek Tablets Cause Death

Digitek (Digoxin) is made from a refined plant extract. It is a purified cardiac glycoside, and is used to treat heart failure and irregular heart beats.

Although the active ingredient in Digitek, digoxin, is natural the over consumption of Digitek can still make a person extremely ill.

Digoxon builds up in a person’s body when too much Digoxin is consumed. This results in Digitalis - a condition which can result in death or other serious side effects.

In 2008, all lots of Digitek were recalled due to the possibility of the creation of tablets with double the recommended dose. These tablets clearly pose a risk to the public, and were immediately recalled.

Unfortunately, recalled tablets still fell into the hands of the public and made many patients extremly ill or caused unnecessary death.

If you or a loved one were affected by recalled Digitek tablets contact McEwen Law Firm today. Our attorneys are dedicated to providing you with the inforamtion, support, and legal advice you need to win your Digitek case.

To contact a Digitek lawyer today call (800)732-3070 or fill out our online contact form.

Digitek Digoxin Digitalis Lawyer

Digitek (digoxin) is a medication given to patients suffering from heart problems. Typically, these patients suffer from heart failure or irregular heart beats.

The active ingredient in Digitek, digoxin, allows the heart to beat at a stronger, more normal, rate. When consumed in excess digoxin results in serious side effects including slowed heartbeat and low blood pressure, vision problems, irregular heartbeats, seizures, hallucinations, and more. Taking too much digoxin (Digitek) may also result in digitalis toxicity.

Digitalis toxicity is a condition which occurs when too much digoxin is built up in the body. Digitalis toxicity results in the patient feeling extremely ill and can be fatal.

Patients suffering from heart problems may also have other conditions, including kidney disorders. Kidney problems and other medications, such as diuretics, interact with digoxin and may result in digitalis toxicity at a quicker rate.

Recalled Digitek (digoxin) tablets contain a double dose of digoxin which may result in the above serious side effects and/or digitalis toxicity if consumed.

If you or a loved one has been a victim of recalled Digitek tablets contact McEwen Law Firm today. Our attorneys very knowledgable regarding the recent Digitek recall and are dedicated to providing you with the compensation you deserve.

McEwen Law Firm attorneys may be reached at (800) 732-3070 or through the online contact form. We offer free, no obligation, consultations to help provide you with options regarding your Digitek injuries.

Digitek Digoxin Recall Information

Digitek (digoxin) tablets were recalled on April 25, 2008 by the FDA due to a manufacturers defect which allowed tablets to be produced with twice the approved amount of the active ingredient (digoxin). Digoxin is a medication given to those suffering from heart failure or heart arrythmias, and allows the heart to beat at a stronger, more normal, rate.

Digitek (digoxin) tablets are manufactured b Actavis Totowa and distributed by Mylan Pharmaceuticals. Digitek (digoxin) tablets are also sold under the labels UDL or Bertek. Recalled Digitek (digoxin) tablets appear larger and thicker in size due to the double dose of digoxin found in them.

The double dose of digoxin found in Digitek tablets may result in digitalis toxicity. Digitalis toxicity occurs when digoxin accumulates in high levels in the body and may result in death.

If you have lost the life of a loved one due to recalled Digitek (digoxin) tablets or suffered serious side effects yourself, contact a McEwen Law Firm attorney today. We offer free, no obligation, consultations and work on a contingency so you won’t need to pay anything unless we win your case.

Our attorneys are dedicated to providing you with the best legal support possible after your Digitek injury, and are determined to help you win your Digitek Lawsuit case. To reach an Digitek Recall Lawyer today call (800) 732-3070 or fill out our online contact form.

Digitalis Toxicity Caused By Digitek Recalled Tablets

Digitek was recalled in 2008 due to the production of tablets with twice the approved amount of digoxin in them. Digoxin, the active ingredient in Digitek, is toxic when taken in large doses. The condition caused by over consumption of Digitek (digoxin) is called digitalis toxicity, and it can be fatal.

Digitalis toxicity occurs when digoxin accumulates in the body at a quick rate, and the body is unable to rid itself of the excess digoxin. Digitalis toxicity is also more likely to occur in patients who have an existing kidney disease or kidney failure, and in those taking diuretics.

Digitek is frequently prescribed to patients suffering from irregular heart beats or heart failure. Unfortunately, patients suffering from heart failure are also commonly prescribed diuretics. Diuretics typically cause potassium loss in patients, and low potassium levels increase the risk of developing digitalis toxicity.

Digitek (digoxin) recall tablets greatly increase the risk of developing digitalis toxicity. Digitalis toxicity symptoms include slowed heartbeat, vision problems, hallucinations, seizures, and many more serious symptoms. Digitalis toxicity can also result in death.

If you have taken recalled Digitek (digoxin) tablets and developed digitalis toxicity, or if you have lost a loved one due to digitalis toxicity contact McEwen Law Firm today. Our digitalis toxicity attorneys undertand the terrible side effects recalled Digitek tablets cause and are dedicated to helping provide you with legal compensation.

McEwen Law Firm provides free, no obligation, consultations. If you have any questions about the Digitek recall or would like to go forward with your case please contact us at (800) 732-3070 or use our online contact form.

Digitek Digoxin Recall Lawyer, Attorney

Digitek (digoxin, UDL, Bertek) was recently recalled due to the possibility of the production of double dose tablets. These double dose tablets contain twice as much active ingredient - digoxin - as safe tablets. The consumption of too much digoxin causes digitalis, a condition which may be fatal in some patients.

Digitek is commonly prescribed to patients suffering from heart failure or arrhythmias. Unfortunately, these patients are more likely to suffer from additional disorders causing Digitek (digoxin, UDL, Bertek) side effects to be extremely dangerous. Patients suffering from renal failure are at especially high risk due to the fact their bodies are unable to get rid of the digoxin at a quick enough pace, resulting in digitalis.

Symptoms of digitalis caused by defective Digitek (digoxin) include:

• Slow heartbeat and/or low blood pressure
• Irregular heartbeat (including extremely fast heartbeat)
• Dizziness
• Vision problems
• Nausea and/or vomiting
• Confusion
• Seziures
• Hallucinations
• Additional unusual symptoms

Digitalis can be fatal, and Digitek (digoxin) has already caused the deaths of many people across the United States.

If you have lost a loved one due to recalled Digitek (digoxin) or have suffered painful, debilitating, side effects yourself contact McEwen Law Firm today. We are extremely knowledgeable regarding the Digitek (digoxin) recall and have the experience necessary to help you recieve compensation for your injuries or loss.

To reach a Digitek (digoxin) attorney today call (800) 732-3070 for a free, no obligation, consultation.

Digoxin Recall Lawsuit - Digitek Risks and Side Effects

Actavis Totowa announced a nationwide Digitek recall due to manufacturing defects which caused the Digoxin tablets to have double the normal amount of dosage causing serious side effects. There is a large risk that the Digoxin overdose can lead to fatal illnesses. The illness is known as Digitalis Toxicity and is common among those with renal failure. Persons affected by the drug are urged to call the Digitek Recall Lawsuit lawyers at McEwen Law Firm at (800) 732-3070. All persons throughout the United States can call to receive consultation.

The Digitek recall came after Actavis Totowa and the FDA received numerous complaints of severe illness and the overdose illness known as Digitalis Toxicity. Since 2006, Actavis has receive such reports of Digitek side effects associated with the active ingredient in the drug tablets.

Digitalis Toxicity is linked to excessive amounts of digitalis in the body which cause serious Digitek Side Effects including: Nausea, Vomiting, Cardiac problems, Bradycardia, and confusion.

The Digitek Lawyers are McEwen Law Firm are currently investigating and gathering testimony from victims throughout the United States. Those who have taken the medication and have been affected by Digitalis Toxicity are urged to call for themselves, family, or friends to get involved in the Digitek lawsuit. Call today at (800) 732-3070.

Digitek Causes Toxicity and Death

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). Over ingestion of digoxin can result in severe side effects including digitalis toxicity, a condition which may result in death.

The recall of Digitek tablets are sold under the labels “UDL” and “Bertek” and are distributed by Mylan Pharmaceuticals.

Digitek is a medication prescribed to patients who suffer from heart failure or irregular heart beats. When taken properly Digitek (digoxin) allows the heart to beat at a regular, strong, pace. If taken in larger doses, as in the double strength recalled Digitek tablets, digitalis can build up in the body and digitalis toxicity may occur.

Recall of Digitek (digoxin, UDL, Bertek) drug tablets appear thicker and larger in size than safe Digitek tablets due to their increased strength. 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.

Actavis Group has decided to recall the heart drug because roughly 50% of all the tablets may be twice as thick and contain double the dosage of medication than it is supposed to. These stronger tables may cause toxicity in renal failure persons. Some patients have become very sick and many have died from the active ingredient which is fatal in large doses. All batch and lot numbers are subject to this recall and subject to recover compensation for injuries or medical costs.

Recalled Digitek tablets cause severe illness, digitalis toxicity, and may result in death. These side effects are serious, dangerous, and life altering. If you or a loved one has been affected by the Digitek recalls contact our law firm today. Our Digitek lawyers will provide you with the legal guidance, support, and help you need to receive compensation for your Digitek (Bertek, UDL, digoxin) injuries.

McEwen Law Firm provides free, no obligation, consultations. If you have any questions about the Digitek recall or would like to go forward with your case please contact us at (800) 732-3070 or use our online contact form.