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.

Levaquin Tendon Rupture Warning From FDA

Levaquin is a popular antibiotic which is used to treat serious bacterial infections. Levaquin levofloxacin is a fluoroquinolone medication - a group of medication which has received a great amount of attention by the FDA recently. Fluoroquinolones are oral antibiotics used to treat infections, but have considerably serious side effects.

Levaquin has been linked to causing tendon ruptures, tendinitis, and other tendon disorders in patients; sometimes these injuries are so serious they require extensive surgery to repair. Levaquin also has a number of other serious side effects including seizures, hallucinations, and jaundice as well as a number of other side effects.

Levaquin (levofloxacin) has also been linked to very serious side effects in patients with the following conditions:

• Diabetes
• Spinal injuries
• Brain cord conditions
• Those with kidney disease

Patients suffering from these conditions may experience uncontrollable seizures, blood level irregularities, and slow absorption while taking Levaquin.

Levaquin injuries may occur at any time - 2 weeks into taking the medication or months after. The most common tendon disorder Levaquin has caused is injuries to the Achilles tendon and shoulder.

If you or a loved one has suffered from a tendon rupture, disorder, or other serious side effect after taking Levaquin contact McEwen Law Firm today. We offer free, no obligation, consultations to help you decide what the next step should be regarding your injury.

McEwen attorneys are available by phone at (800) 732-3070 or through our free contact form.

Shoulder Pain Pump Lawsuit

Shoulder pain pumps are frequently used after arthroscopic shoulder surgery. After surgery has been preformed, the pain pumps are attached to the shoulder using a catheter and medication is provided to the shoulder area continuously for a select amount of time. Normally, shoulder pain pumps stay in place for 2 to 3 days after surgery.

While the shoulder surgery and application of the pain pump may seem simple and nonevasive, the side effects caused by the pain pump are life altering.

Pain pumps have frequently been used in other surgeries; however, the painful side effects have not presented themselves to the extent they have in shoulder pain pump patients.

Shoulder pain pumps have been put on a medical watch list by the FDA due to the shoulder condition, PAGCL, which they cause. PAGCL, Postarthroscopic Glenohumeral Chondrolysis, is a condition which involves the deterioration of cartilage in the shoulder. This condition is extremely painful, damaging, and currently has no cure.

If you or a loved one has been injured by a shoulder pain pump after a recent arthroscopic shoulder surgery call McEwen Law Firm today. Our attorneys are extremely knowledgable regarding shoulder pain pump lawsuits and are dedicated to providing you with the compensation you deserve after a shoulder pain pump injury.

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

Visit our Pain Pump Lawsuit Claim website for more information.

Duragesic Fentanyl Pain Patch Recall

Duragesic (fentanyl, transdermal) pain patches were recalled in February 2008 due to a manufacturer’s defect which allowed fentanyl, the active ingredient, to seep out through one side. Over abortion of fentanyl, whether in buccal or transdermal form, is extremely dangerous and can be fatal.

Duragesic (fentanyl) pain patches are manufactured by Johnson and Johnson and are sold by J&J’s PriCara unit, Sandoz, and Alza Corp.

Only Duragesic 25 microgram/hour patches were included in the February 2008 recall. However, other patch doses may be equally as dangerous and deadly if handled improperly.

This is the second Duragesic pain patch recall in recent years. In 2004 Duragesic pain patches were recalled for a similar defect which also allowed fentanyl to leak out at an uncontrolled rate. The 2004 Duragesic recall included all patch doses, and resulted in hundreds of deaths in the United States.

If you have lost the life of a loved one due to defective Duragesic patches, or have suffered serious side effects yourself contact McEwen Law Firm today. We offer free, no obligation, consultations to help provide you with the options necessary to procede with your case.

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

Duragesic Pain Patch Side Effects

Fentanyl is an opiate 80 times stronger than morphine which is used in popular pain patches, including Duragesic pain patches. When fentanyl is leaked onto the skin in a noncontrolled manor, as in the case of defective Duragesic patches, the patient becomes at risk of overdosing on fentanyl. Fentanyl overdoses result in serious side effects and may cause death.

Fentanyl may be found in either buccal form or gel form, as in the case of Duragesic transdermal patches. Duragesic patches come in a variety of dosages; however, only the 25 microgram/hour patches were recalled in 2008. It is also important to remember that the mishandling and/or mistreatment of properly manufactured Duragesic (fentanyl, transdermal) patches may also result in a fentanyl overdose.

Those suffering from a fentanyl overdose may experience:

• Difficulty breathing
• Shortness of breath
• Dizziness and/or confusion
• Faintness
• Extreme fatigue
• Small, pinpoint, pupils
• Difficulty talking, thinking, walking, etc.
• Coma
• Seizure
• Rash
• Chest pain

If you or a loved one are currently using Duragesic (fentanyl, transdermal) patches and experience any of the above symptoms you should seek medical help immediately.

The chance of a fentanyl overdose occurring while using Duragesic pain patches greatly increases when the patches are manufactured improperly. In the case of the 25 microgram/hour patches, a slit down one side allows fentanyl to leak out at a quick rate.

If you have experienced a fentanyl overdose as a result of defective Duragesic patches, or if you have lost a loved one due to a fentanyl overdose contact McEwen Law Firm today. We offer free, no obligation, consultations to provide you with the advice necessary to take the next step.

McEwen attorneys may be reached at (800) 732-3070 or through our contact form.

Shoulder Pain Pump PAGCL Attorney

Shoulder pain pumps have recently been linked to the condition PAGCL, or Postarthroscopic Glenohumeral Chondrolysis. PAGCL is a condition which is classified by the rapid deterioration of shoulder cartilage, and sometimes includes the deterioration of the bone itself.

PAGCL causes extreme discomfort in shoulder pain pump sufferers. As the cartilage wears down, the bones in the shoulder joint begin to rub against each other which decreases the range of motion and increasing pain levels (while at rest and in motion) in the shoulder.

PAGCL currently has no cure. Patients who develop PAGCL as a result of using a shoulder pain pump after surgery are faced with the disability for the rest of their lives.

Postarthroscopic Glenohumeral Chondrolysis may occur at any time after arthroscopic shoulder surgery has been preformed and a pain pump has been used. Typically, symptoms develop within a matter of months after the pain pump has been removed.

The attorneys at McEwen Law Firm are extremely knowledgeable regarding shoulder pain pump cases. The damage caused by these seemingly harmless pumps is life altering and unacceptable. Our attorneys realize this and will help you receive the compensation you deserve after suffering the painful side effects of a shoulder pain pump.

McEwen Law Firm offers free, no obligation, consultations if you are interested in more information about shoulder pain pumps or would like to get started on a lawsuit of your own. To reach a McEwen Law Firm Attorney call (800) 732-3070 or fill out our contact form.

Levaquin Side Effects Include Tendon Rupture

Levaquin has caused tendon ruptures, tendinitis, and other serious side effects in patients causing the FDA to issue a black box warning (as of July 2008).

Unlike other medications, the serious side effects Levaquin may cause do not always appear immediately. Levaquin related tendon ruptures, tendinitis, and other tendon disorders may appear six months or more after the antibiotic cycle has been completed.

This means that Levaquin side effects may strike at any time. Those who have used Levaquin in the past may believe they are completely healed when a sudden tendon injury strikes.

Depending on the severity of the injury, the sufferer may have to go extensive surgery to repair the tendon damage caused by Levaquin. This causes additional pain, suffering, and expense to the patient.

If you or a loved one have suffered a tendon injury due to Levaquin levoflaxacin contact McEwen Law Firm today. The suffering, pain, and damage caused by Levaquin is unacceptable, and our attorneys are dedicated to providing you with the legal support you need to receive compensation.

McEwen Law Firm offers free, no obligation, consultations to help set you on the right path regarding your Levaquin lawsuit. Contact us today at (800) 732-3070 or fill out our 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.

Shoulder Pain Pump Lawsuit Lawyers, Attorneys

The use of Shoulder Pain Pumps after arthroscopic shoulder surgeries has been linked to the development of an extremely uncomfortable shoulder condition called PAGCL. PAGCL (Postarthroscopic Glenohumeral Chondrolysis) is a condition which occurs when shoulder cartilidge begins to deteriorate.

Shoulder pain pumps cause cartlidge deterioration, and therefore cause PAGCL. While the use of pain pumps in other forms of surgery has been successful, the tight joint area of the shoulder and medication combination of the shoulder pain pump has proven ineffective and dangerous.

The damage caused by shoulder pain pumps may require surgery, or may not be repairable at all.

Patients who recieved shoulder pain pumps commonly suffer from:

Decreased range of motion
popping, clicking, grinding in the shoulder
shoulder stiffness and/or weakness
continous shoulder pain while in motion or at rest

Shoulder pain pump victims often must deal with the painful side effects of their pain pump for the rest of their lives, as no effective treatment has been developed to replace shoulder cartlidge.

If you have suffered severe side effects after your shoulder surgery and after recieving a shoulder pain pump contact McEwen Law Firm today. We understand the severe damage shoulder pain pumps cause and are determined to help you recieve the compensation you deserve for your injuries.

To contact a shoulder pain pump attorney today call (800) 732-3070 today.

Duragesic Pain Patch Recall Lawyers

Duragesic (fentanyl, transdermal) pain patches were recalled in February 2008 due to a manufacturer’s defect. Duragesic (fentanyl, transdermal) 25-microgram/hour patches were recalled due to a slit in the side which allows the active ingredient, fentanyl, to leak out.

All recalled Duragesic (fentanyl, transdermal) patches have an expiration date on or before December 2009. The 25 microgram/hour patches are commonly used in underweight patients and children. Children using Duragesic (fentanyl, transdermal) patches should be monitored extremely closly as they may not be able to communicate their side effects properly.

Over absorption of fentanyl results in serious side effects and death. Fentanyl is an opiate, and is 80 times stronger than the well known opiate Morphine.

Fentanyl pain patches have already affected hundreds of people across the United States. If you have lost a loved one due to defective fentanyl (transdermal, Duragesic) pain patches or have suffered serious side effects yourself, contact McEwen Law Firm today. Our fentanyl/Duragesic pain patch attorneys are dedicated to providing you with the compensation you deserve after suffering Duragesic/fentanyl injuries.

For a free, no obligation, consultation please call (800) 732-3070.

Next Page »