Nuvaring Lawsuit 2010 News

Nuvaring side effects involving a pulmonary embolism pose dangerous health risks for some women, regardless of whether they have experienced blood clot problems in the past. The condition is usually caused when blood clots within the deep veins of the legs break away and travel to the heart. They migrate into one of the pulmonary arteries and eventually become lodged. If the clot prevents blood from reaching your lung tissue, that portion of your lung will sustain damage. Depending on the extent of this damage, you may suffer one or more long-term Nuvaring problems. Please contact us for the latest Nuvaring lawsuit 2010 news.

Long-Term Problems Caused By PE

A small pulmonary embolism may exist without presenting noticeable symptoms. Lacking obvious signs of a lung blockage, many people fail to realize they are suffering a PE. This is dangerous. If an obstruction is allowed to remain in one of the lung arteries, it can lead to progressive lung damage, heart damage, and other serious complications.

For example, small blood clots can become caught in a pulmonary artery and create a partial – rather than full – obstruction. Blood may be able to pass through the restricted opening to reach the lung tissue, but requires more pressure in order to do so. This cause a condition known as pulmonary hypertension. Over time, blood pressure within the arteries continues to build, forcing the right side of your heart to work harder. Right-sided heart failure often follows.

A large obstruction that is left untreated can cause a portion of your lung tissue to die. This is known as pulmonary infarction. The affected lung will become less capable of oxygenating blood for the rest of your body. If the lung tissue death is extensive, your other organs that depend on oxygen-rich blood may also sustain damage.

Nuvaring side effects causing a pulmonary embolism can also result in an arrhythmia. Most are minor, but they can occasionally disrupt the heart’s electrical signals. This can lead to clotting within the chambers. If clots form within the heart’s left atria or ventricle, they can break away, migrate to the brain, and cause a stroke.

Blood Thinners And Dietary Changes

Following a PE, your doctor will prescribe anticoagulant medications. The purpose of these drugs is to reduce the likelihood of further clotting, both in your leg veins and your heart. Therapy can range from a few weeks to twelve months, depending on whether you suffer from deep vein thrombosis (DVT). If your doctor suspects there is a high chance of clots causing a subsequent PE, he or she may recommend blood thinners indefinitely.

Long-term anticoagulant therapy is delivered with warfarin, which comes in pill form. The effects of this medication are influenced by the level of vitamin K in your body. For this reason, you’ll need to regulate the amount of vitamin K contained in foods you consume. Consistency is key. A dramatic increase or reduction requires a change in the dosage of warfarin.

Graduated Compression Stockings

Because DVT is one of the most common catalysts for pulmonary embolism, your doctor will recommend measures to encourage circulation in your legs. One method is to wear fitted compression stockings around calves. They are tighter near the ankle and become slightly looser as they rise toward the knee. These stockings promote blood flow and prevent pooling within the leg veins. While they can be effective, they are often uncomfortable.

Nuvaring Lawsuit 2010

The risk of a pulmonary embolism problems pose an ongoing risk for some women using the birth control ring. If you or someone you know has suffered DVT, PE, or other Nuvaring side effects, explore your legal rights. Contact a Nuvaring settlement lawyer to discuss your options.

Accutane Lawsuit 2010 Update

Accutane is a medication derived from vitamin A that is used to treat severe cystic acne. The medication is supposed to be prescribed for dermatology patients with severe acne, but it can also have some serious side effects. Accutane side effects over the short term include dry skin, fatigue, and muscle pain. Accutane long term side effects are more serious, and may include severe depression, birth defects in the children of women who are taking the medication, and the development of serious gastrointestinal problems like Crohn’s Disease.

Accutane lawsuits are becoming quite common, even after the medication was discontinued in June 2009. Now, it still lives on in some generic forms, including Claravis and Sotret, though Roche Pharmaceuticals, the manufacturer of the name brand drug, has stopped making it.

The lawsuits against Accutane are one of the main reasons Roche cited for discontinuing the medication. Having paid out about millions of dollars in actual lawsuits, as well as amounts in settlements as of 2010, Roche decided they no longer wanted to manufacture the medication that millions of people worldwide were using.

Accutane Lawsuit 2010
The Accutane Crohn’s lawsuit is one of the most common ways that people have looked for compensation from Roche for their Accutane side effects. Unfortunately for many users of this medication, Accutane side effects years later can even years after they cease taking it. Sometimes, the side effects start while a patient is on the medication, but then persist for a long period of time after use has ceased.

Crohn’s Disease is a form of Irritable Bowel Disease in which certain parts of the gastrointestinal track become inflamed. When this happens, bleeding, pain, and cramps can occur. Also, many people with Crohn’s Disease struggle with malnutrition and unintentional weight loss, as nutrients are poorly absorbed through the walls of an irritated bowel.

Recently, one man who had been on Accutane for years succeeded in an Accutane lawsuit for several million dollars because he had developed Irritable Bowel Syndrome and Crohn’s disease. This most recent case ended in early 2010, but Roche plans to appeal the decision to award the plaintiff with over ten million dollars for his long-term suffering.

When dealing with a disease like Crohn’s or IBS, your medical expenses can increase over time. These problems take special dietary precautions, lifestyle changes, and medications over the long-term. Plus, this doesn’t account for of all of the pain and suffering caused by the side effects of Accutane.

If you have taken Accutane in the past and have noticed symptoms like unexplained weight loss, abdominal discomfort or pain, chronic diarrhea, or a host of others related to IBS or Crohn’s Disease, you may need be eligible to file a claim. An attorney can help explain your legal options including the latest Accutane lawsuit 2010 news.

Paxil And Pregnancy Lawsuits

Paxil is a well-known and popular treatment for several different anxiety and depression disorders. It is among one of the first selective serotonin reuptake inhibitors to be introduced on the market. There have been thousands of lawsuits filed in relation to this drug; many of them have to do with Paxil birth defect incidences. Paxil and birth defects are established to be connected and there are specific disorders that are linked to this drug. The number of Paxil and pregnancy lawsuits continue to increase as more families become aware of the connection between Paxil and birth defects.

Paxil PPHN

PPHN is a birth defect that affects the baby’s heart and lungs. The acronym stands for Persistent Pulmonary Hypertension in the Newborn. It is very serious, sometimes fatal and oftentimes has long-lasting effects. Primarily, it starves the blood of oxygen and can cause damage to organs including the kidneys and the eyes.

Paxil is also associated with other malformations of the heart and skull. Paxil birth defects of this type are just as serious. The FDA specifically recommends that this particular drug not be used for the treatment of pregnant women. If you weren’t’ warned about this, you may well be able to file a Paxil lawsuit.

Other Paxil Side Effects

This drug has a host of other side effects, as well, some of them very serious. In younger people—specifically under the age of 24—it is strongly implicated in their idealizing suicide and, in some cases, in suicidal tendencies. It has also been associated with feelings of electricity rushing through the nerves, nightmares, dizziness, sexual dysfunction and weight gain. This drug is not recommended for use in those under 24 years of age unless, after exacting examination, it has been determined that the potential rewards outweigh the potential risks of continuing treatment with this drug.

Paxil Lawsuit 2010

There are lawyers who specialize in these types of cases. Chances are, you’re not the only one who needs a wrong done to them redressed. These lawyers can help explain your legal rights and discuss the latest news regarding Paxil birth defect settlements.

Hernia Patch Recall

Hernia mesh complications have required the manufacturer of some of the most widely used hernia repair patches, Davol, Inc., to recall several lots of their products. The hernia patch recall has been one of a series of manufacturer recalls that have taken place since the end of 2005. These recalls affect several other products made by the same manufacturer, as well, and were brought about by significant complaints about the safety of these products.

Understanding the Hernia Mesh Recall Actions

The Kugel mesh was recalled due to numerous different issues. Some of the Kugel mesh complications, and the problems with other devices by this manufacturer, had to do with patients having reactions to the materials from which the patches were made. Other cases involved parts of the device breaking, such as the ring that constitutes a major part of its structure. Ring breakage has caused several injuries to patients, including perforated bowels and bowel obstructions, which have both been significant reasons that hernia mesh recall actions have been taken.

How Hernia Mesh Problems Arise

The most common type of hernia is an abdominal hernia. These conditions constitute weakening of the abdominal and pelvic walls and are associated with exertion and age. The Kugel mesh complications that have led to so many recalls have to do with the way these devices do their job. At the simplest level, a Kugel mesh patch is a ring with a polypropylene mesh attached to it. It is named for the doctor who designed it and it provides support to weakened areas of the anatomy by reinforcing weakened and torn tissues.

The hernia mesh complications that affect most patients arise when the metal ring that provides the frame for the mesh breaks. This results in the sharp edge of the ring being exposed. This can lead to complications including bowel perforations, hernia mesh infection and others that are very serious and which require medical intervention.

There are several different patches that have been recalled since 2005. They include the extra large patches. Hernia repair mesh recall actions have also been taken for Bard, Composix and Kugel brand-name products. If you have such a device, you were likely notified by mail of the hazards associated with your product. The company sent notifications via FedEx on the occasions when the hernia mesh recall had to be undertaken.

Who Is Affected by the Hernia Mesh Patch Recall?

There are over 600,000 hernia operations performed annually. There are few other treatments for this condition and, because of that, the patients have little recourse but to hope for the best from this radical intervention. If you have a hernia patch, you may be at risk for hernia mesh complications.

If you’ve received notice that the hernia mesh patch recall affects you, you can contact a lawyer. You may have a case to file a hernia mesh lawsuit due to your injuries. If you have one of these patches and are concerned, consult with your doctor and then, if needed, with an attorney who can explain your legal rights and discuss the latest information regarding Kugel mesh settlement amounts.

Reglan Lawsuit News

Reglan, also referred to by the generic name metoclopramide, is used as a short-term treatment of certain conditions such as gastroesophageal reflux disease (commonly referred to as GERD, acid reflux disease or persistent heartburn) and gastroparisis (a disorder seen in diabetic patients where the stomach takes too long to empty). Metoclopramide belongs to a class of drugs known as dopamine receptor blockers. This medication works by increasing stomach emptying and movement in the upper intestines. Over 2 million Americans have been prescribed the Reglan drug. If you or a family member suffer from tardive dyskinesia please contact us for the latest Reglan lawsuit news.

Metoclopramide is available in several forms including:
• Reglan Tablets
• Reglan Oral Disintegrating Tablets
• Metoclopramide Oral Solution
• Reglan Injection

Reglan acts in the upper end of the digestive system and works by speeding up the movement of the stomach muscles, thus increasing the rate at which the stomach empties into the intestines. It is used as a short-term treatment of gastroesophageal reflux disease in patients who have not responded to other therapies, and to treat diabetic gastroparesis (slowed emptying of the stomach’s contents into the intestines). It is recommended that treatment not exceed twelve weeks, however it is estimated that around thirty percent of patients who are prescribed products containing metoclopramide take the medication for a much longer period of time. Chronic, long-term and/or high dose use of metoclopramide has been linked to serious drug induced movement disorders such as tardive dyskinesia.

Tardive dyskinesia (TD) is a drug-induced movement disorder caused by the long-term use of neuroleptic drugs. Tardive means “delayed” and dyskinesia means “abnormal movement.” This serious neurological syndrome is often irreversible and may become permanent. Since the 1950’s a family of drugs referred to as dopamine receptor blocking drugs (DRB) have been prescribed for certain mental health conditions and are now also commonly prescribed for the treatment of GERD and nausea.

Tardive dyskinesia (TD) is a drug-induced movement disorder caused by the long-term use of neuroleptic drugs. Tardive means “delayed” and dyskinesia means “abnormal movement.” This serious neurological syndrome is often irreversible and may become permanent. Since the 1950’s a family of drugs referred to as dopamine receptor blocking drugs (DRB) have been prescribed for certain mental health conditions and are now also commonly prescribed for the treatment of GERD and nausea. Metoclopramide / Reglan is a dopamine receptor blocking drug. If you have suffered from involuntary movement problems please contact us, we have a Reglan lawyer ready to answer your questions and help explain your legal options.

Treatment of tardive dyskinesia includes stopping or reducing the use of Reglan (metoclopramide). However, the symptoms of tardive dyskinesia may continue long after discontinuation of Reglan (metoclopramide) and there is no known treatment. In some patients, symptoms may lessen or disappear after Reglan (metoclopramide) treatment has stopped. The majority of patients who have developed tardive dyskinesia have been treated with Reglan (metoclopramide) for more than three months.

The U.S. Food and Drug Administration (FDA) announced in February 2009 that manufacturers of Reglan drugs including metoclopramide are required to add a black box warning to their labeling regaridng the risk of the involuntary movement disorder tardive dyskinesia associated with its long-term and/or high-dose use. In addition to the black box warning, the FDA is requiring manufacturers to implement a risk evaluation and mitigation strategy so that patients are provided with a medication guide that explains the risk of tardive dyskinesia with chronic metoclopramide treatment. Please contact us for the latest information regarding Reglan lawsuit awards.

Medtronic Lead Lawsuit

For many people, an implanted defibrillator is a life-saving device. They allow a patient with an abnormality in their heart rhythm to live a normal life without the constant threat of having a heart attack. However, in October of 2007, there was a Medtronic lead recall that affected literally hundreds of thousands of people. While this is distressing enough, the potential of suffering from a Medtronic lead fracture rather puts those who have one of these leads in a very difficult place.

What They Are

The Medtronic recall affected one of the most vital parts of an implanted defibrillator. When the heart in a patient who has one of these devices takes on an irregular rhythm, the automatic device sends a jolt of electricity into the heart that restores it to a normal beat. These leads need to be reliable, of course, and there is no room for error.

Unfortunately, there was a danger of fracture in these leads that could cause problems. The Sprint Fidelis lead fracture causes the device to send signals at inappropriate times and, potentially, to fail to perform its function when it matters the most. This led to the recall that affected so many patients.

The Consequences of the Sprint Fidelis Lead Recall

Those patients who have these devices installed face a serious dilemma. According to the manufacturer, the patients may face a higher risk from a procedure to remove the device than they do from the device itself. Either way, of course, there is risk, which is why there was a Medtronic lead recall in the first place. This risk was discovered largely due to patient suffering from problems caused by lead failures.

A Medtronic lead failure sometimes results in the patient with the device getting jolts at times where there is no reason for it. This was reported to doctors and the origin of the problem was traced to the Sprint Fidelis lead fracture problems. Sometimes, you may experience these instances as dizziness and lightheadedness. Get to your doctor if you have been experiencing these symptoms.

The Medtronic Lead Lawsuit

Because there were individuals who were affected by the Medtronic lead failure issues all over the nation—there were well over 100,000 patients with leads implanted, in fact—the case was moved to the home city of the company itself, Minneapolis, MN.
You should contact a doctor, and then a lawyer, if you have any of the following products implanted:

• Sprint Fidelis 6930
• Sprint Fidelis 6931
• Sprint Fidelis 6948
• Sprint Fidelis 6949

These models are all part of the Medtronic lead recall and are known to be at risk for lead fracture. Contact your doctor immediately if you have one of these implanted and if you weren’t notified about the recall already. Please contact us for the latest Medtronic recall 2010 news.

Nuvaring Side Effects

NuvaRing side effects including blood clots, stroke and pulmonary embolism have been linked to women using this third-generation form of birth control. Many women reported no previous health issues related to blood clots and did not have any serious risk factors. Some studies suggest that side effects of NuvaRing are associated with the hormone desogestrel which can cause changes in the blood clotting system allowing blood clots to form more easily. NuvaRing birth control was approved by the Federal Drug Administration (FDA) on October 3, 2001 and first marketed in the United States in July 2002. NuvaRing is used by approximately 1.5 million women worldwide.

NuvaRing is a small flexible ring around 2 inches in diameter. NuvaRing is a relatively new type of combination hormonal contraceptive. It contains a combination of the hormones estrogen and etonogestrel which is a synthetic form of the progestin desogestrel. NuvaRing uses a different form of progestin compared to older contraceptives. Third generation contraceptives containing desogestrel have recently come under scrutiny due to the increased risk of blood clots (venous thrombosis). The newer progestins (desogestrel) in third generation contraceptives were intended to lessen the adverse effects caused by older contraceptives such as hirsutism, weight gain, and acne.

Combination hormonal contraceptives contain both estrogen and progestins. NuvaRing contains the progestin desogestrel which, according to studies going back to 1995, doubles the risk of blood clots compared to second generation oral contraceptives. Please contact us for the latest Nuvaring litigation news and information.

If a blood clot is suspected there are several possible test that a doctor may recommend. The initial test is usually an ultrasound. Additional tests may be used when ultrasound results are unclear. These tests may help diagnose or exclude a blood clot but are not frequently needed:

1. CT or MRI scans. Both computerized tomography (CT) and magnetic resonance imaging (MRI) can provide visual images of your veins and may show if a clot is present. Sometimes a venous thrombosis is found when these scans are performed for other reasons.
2. Blood test. Almost all people who develop severe deep vein thrombosis have an elevated blood level of a clot-dissolving substance called D-dimer. However, D-dimer is elevated in other conditions, too. Thus, a test for D-dimer is not very conclusive. It is most useful for ruling out DVT or identifying people at risk of recurrence.
3. Venography. A dye is injected into a large vein in your foot or ankle. An X-ray procedure creates an image of the veins in your legs and feet to look for clots. This test is used less frequently today because less invasive studies can usually confirm the diagnosis.

If you have suffered from problems after using the birth control ring please contact us for the latest Nuvaring lawsuit settlements news.

Yaz Gallbladder Removal

For some women, Yaz gallbladder side effects have caused health problems that required hospitalization, medications, and in some cases, even Yaz gallbladder removal surgery. The connection between this oral contraceptive and gallstones is often unclear. Some people believe the hormones contained in Yaz, while effective for reducing the likelihood of pregnancy, cause a number of unintended side effects, including stones.

Estrogen and an artificial progestin called drospirenone are thought to cause two outcomes that affect the gallbladder. First, these two hormones increase cholesterol output from the liver. This cholesterol is secreted into bile fluid, which flows into the gall bladder. Second, they reduce the gallbladder’s contraction activity – both frequency and force. This allows cholesterol-heavy bile fluid to remain within the organ. These factors set the stage for the formation of biliary sludge and stones.

Biliary Sludge Explained

Reduced gall bladder motility allows bile, calcium salts, bilirubin, and excess cholesterol secreted by your liver, to accumulate. These compounds collect and form a thick substance called biliary sludge. The composition of this material can vary depending on the availability of each compound, but the end results are usually the same.

Three circumstances can develop. First, the sludge may resolve on its own, causing few to no symptoms. Second, the material can evolve into gallstones. Third, the sludge may exit the gallbladder when the organ contracts, thereby moving into the cystic and common bile ducts. If you have suffered from problems after using this birth control pill, please contact us for the latest Yaz gallbladder settlement news.

This last circumstance can produce side effects similar to those caused by stones. The biliary sludge can form an obstruction in the duct, preventing bile from flowing past. If bile backs up to the gall bladder, it can trigger inflammation within the inner lining of the organ. This is characteristic of Yaz gallbladder disease.

The sludge may also flow past the juncture where the common bile duct merges with the pancreatic duct. If it forms a blockage in this area, pancreatic secretions will be prevented from flowing into the duodenum. This causes the pancreas to become inflamed, a serious condition known as pancreatitis.

Excess Cholesterol Contributes To Yaz And Gallstones

Gallstones are comprised of cholesterol, which is nearly insoluble. Once the compound has been secreted by the liver, it is transported to the gallbladder while contained in bile salts.

At normal levels, the cholesterol can be absorbed into the lining of the gall bladder, which prevents it from accumulating and crystallizing into hard particles. When excess levels of the compound are secreted, however, the organ cannot sufficiently absorb all of it. The cholesterol precipitates within the bile salts, partly aided by the lack of proper emptying due to decreased motility. Eventually, gallstones form.

Dangerous Side Effects Of Gallstones

Most stones are asymptomatic, and thus present no noticeable symptoms. However, abdominal pain may erupt quickly if the gall bladder suddenly becomes inflamed. The pain can last for hours, which is sufficient for most people to seek medical attention. During the event, you may also experience chills, nausea, and periodic bouts of vomiting.

The above symptoms are immediate indications of Yaz gallbladder disease. While they are physically taxing, the condition can cause side effects that are much more serious. For example, inflammation within the lining of the organ can cause bacteria to grow, leading to infection. In severe cases, this might cause a perforation to develop in the gall bladder, an event that is potentially life-threatening.

Infection can also spread throughout the common bile duct if stones migrate into the duct and form a blockage. If antibiotics are unsuccessful in controlling the infection, it will climb toward your liver, potentially causing damage to the organ.

Stones that migrate closer to the sphincter of Oddi can, like biliary sludge, block fluids secreted by the pancreas. As described above, this leads to pancreatitis.

Gallstones and gall bladder problems are among the more serious Yaz side effects that otherwise healthy women have experienced. If you or someone you know has suffered stones or gallbladder disease after using this birth control pill, contact an experienced birth control lawyer. Find out whether you should file a Yaz lawsuit gallbladder claim against the manufacturer.

Kugel Mesh Settlement News

If you have a painful protrusion in your abdominal area that seems to expand when you cough or strain to lift a weight, you may have an abdominal hernia. In the last several years there has been a hernia mesh recall of certain types of hernia patch repairs. Attorneys are currently looking at a Kugel mesh settlement for their clients and claims are being filed individually rather than in a national hernia mesh class action.

A hernia occurs when an organ pushes through a weak muscle wall or area of tissue. In the case of abdominal hernias, part of the intestine can push through the stomach wall, creating a bulge.

For most people, the hernia is caused by an inherent weakness in the muscle, coupled with something that puts stress on that area. Obesity, pregnancy, heavy weightlifting, excessive coughing and straining during bowel movements can provide enough force that a hernia develops in a vulnerable area. Hernias may also develop at incision sites from previous surgeries.

Hernias may exist without being noticed, and they may not cause any problems, but for many people, hernias can cause pain. When this happens, a doctor may recommend surgery to repair the weak area.

In this surgery, called a hernioplasty, doctors may insert a patch of material over the weakened area. This mesh material can remain in the body and bolsters up the muscle or tissue to keep the organ from bulging through.

An untreated hernia can lead to complications. If an organ, like the intestine, pushes through the stomach wall, it can become trapped there and its blood supply can be cut off. Without oxygen and blood, that organ will develop tissue damage. In extreme cases, gangrene may occur, and the gangrenous area would have to be removed.

Although treating a hernia through surgery is standard practice, even this relatively simple procedure can have risks.

In recent years, some patients have had hernia mesh problems due to a malfunction in a part of the Bard Composix Kugel Hernia Patch. With the Kugel patch, a plastic ring that connected the two pieces of mesh would sometimes break, and the sharp edges from the ring could puncture internal organs, causing serious complications.

One complication is a perforated bowel, in which the ring creates a hole in the stomach or intestine and food from one of those organs leaks into the abdominal cavity, causing a potentially life-threatening infection. Another complication is a fistula, which is an abnormal connection or passageway between two parts of the intestine. This can cause both pain and infection. Over 80 injuries and problems have been reported as a result of broken rings, including several fatalities.

Although the Kugel patch has been recalled and revised patches have been developed, patients are advised to leave functioning patches in place until or unless a problem arises.

If you or someone you know is affected by the Kugel hernia mesh recall, you may have important legal rights. Perhaps you have had hernia surgery, but are unsure of whether or not you received the Kugel patch. There is a limited time to file a hernia patch lawsuit.

Yaz Lawsuit 2010 News

Yaz problems involving a stroke occur when a portion of the brain becomes injured. This happens when a blood vessel bursts and floods the surrounding tissue, or becomes blocked so blood is prevented from reaching the brain. Functions controlled by the affected area become impaired. You might lose the ability to move one side of your body, see clearly, speak, or comprehend what others are saying. Please contact us for the latest Yaz lawsuit 2010 news and information.

It’s possible to regain much of the function lost as the result of a stroke. This is accomplished with the help of physical, speech, and occupational therapists. However, it’s worth noting that a Yaz stroke is potentially fatal. The following circumstances, though rare, can lead to severe impairments, and in some cases, death.

Yaz And Blood Clots In The Basilar Artery

Most strokes occur in the cerebrum, a part of your brain that influences abilities related to speech, movement, cognition, memory, and emotions (among other functions). They can also affect the cerebellum, the area that controls your coordination, balance, and muscle activity. While impaired function is common in both cases, they seldom lead to death.

On rare occasions, a stroke can impact the brainstem. This is the area of your brain that influences critical functions, such as your heart rate, breathing, body temperature, and blood pressure. It is supplied with oxygen-rich blood by the basilar artery. Blood clots that migrate into this artery can create a blockage that prevents blood from reaching the brainstem. Death is common with this type of stroke.

Ischemia In “Watershed” Areas Of The Brain

Certain areas of your brain are referred to as “watershed” areas. They are located at the farthest reaches of arterial perfusion and thus, are especially susceptible to drops in blood pressure. Insufficient blood pressure causes ischemia, which quickly results in the death of the brain tissue. Claims for side effects caused by Yaz are being brought individually and currently there is no national Yaz class action lawsuit.

Watershed areas control functions related to large groups of muscles located throughout your body. As such, a stroke that affects these areas, while rarely deadly, can result in severe paralysis.

Bleeding In The Brain

Hemorrhagic strokes are caused by different factors than those which cause ischemia, or insufficient blood flow. These factors include aneurysms, trauma to the head, and elevated blood pressure in the arteries supplying the brain tissue. When a blood vessel ruptures, the area is flooded, which causes nearby tissue to be pressed against the skull. This increases the pressure placed upon the tissue and eventually causes the affected portion of the brain to stop functioning.

This type of stroke must be treated immediately and aggressively. Otherwise, even small ruptures can cause extensive brain damage and death.

Large Ischemic Strokes

Most ichemic strokes are caused by blood clots that form within one of the arteries of the brain or elsewhere in the body. In the latter case, the clot breaks free from its venous mooring and migrates to the brain. It travels down a blood vessel until the passage narrows to the point where it can migrate no further. The clot forms a blockage and prevents blood from flowing to the underlying tissue.

This usually occurs in smaller blood vessels that supply oxygen and blood to small portions of the brain. As such, the accompanying impairments are also small. Large embolic strokes, however, can clog large arteries that supply a significant portion of the brain. Impairments are often severe in such cases and can occasionally be fatal if left untreated.

Fortunately, most stroke problems caused by Yaz side effects are limited in nature. Impairments of functions controlled by the affected areas of the brain can be addressed successfully through patient rehabilitation. On rare occasions, though, the event can cause extensive brain injury and death.

If you have suffered blood clots, stroke, or other dangerous Yaz side effects, you may be able to file a claim for compensation for your injuries. Contact a Yaz lawsuit attorney to discuss your case.