If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact Zostavax lawyer Timothy L. Miles today
Zostavax is a vaccine approved by the Food and Drug Administration (FDA) in 2016 as a way to reduce the risk of shingles and its complications in adults aged 60 and older. However, soon after Zostavax was released to the public, there were numerous reports of Zostavax side effects that appeared to be directly linked to its use. Now, several Zostavax lawsuits have been filed against the manufacturer. If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact Zostavax lawyer Timothy L. Miles today to see if you are eligible for a Zostavax lawsuit and possibly entitled to substantial compensation.
What is Zostavax?
Zostavax became the first shingles vaccine to be approved by the U.S. Food and Drug Administration (FDA) in 2006. FDA. Zostavax is administered as a shot to the upper and works using a live, but weakened form, of the varicella-zoster virus to decrease the risk of shingles. The varicella-zoster virus also causes chickenpox in children.
It was thought to be highly effective at the time and Zostavax seemed to be an important breakthrough in the containment of the disease. Zostavax would help Merck earn nearly $750 million in profits over the next 12 years. Who Can File a Zostavax Lawsuit?
Individuals of all ages who have experienced severe or debilitating Zostavax side effects as a result of receiving Zostavax may be eligible to file a Zostavax lawsuit and receive compensation for damages related to the vaccine. Zostavax is approved for people who are at least 50 years of age, but some people in their 40s have also been prescribed it. When deciding whether to apply for the vaccine, it is important to weigh the benefits against the potential side effects and risks. Not everyone who is at risk is a good candidate for the vaccine. Because Zostavax is a live vaccine, it is not appropriate for people who are immunocompromised or pregnant. Most of the Zostavax lawsuits focus on individuals who have experienced serious Zostavax side effects.
If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact us today. (855) Tim-M-Law (855-846-6529). Product Liability and Defects in Manufacturing
Zostavax lawsuits often highlight the fact that the FDA’s warning label for the vaccine reads that “Zostavax has not been proven to prevent shingles in people 50 years of age or older,” meaning that the vaccine’s manufacturer cannot guarantee that it will prevent shingles in any age group. In addition, some Zostavax lawsuits point to the vaccine’s problematic manufacturing process as an indication of product liability.
This manufacturing process may have included the use of human fetal cells, which is a known source of contamination linked to the development of infectious diseases. While the FDA did approve Zostavax in 2016, it is important to note that they did so with the recommendation that the manufacturer conducts more research on the vaccine’s effectiveness in adults 50 years of age and older. Whether or not the manufacturer failed to conduct this follow-up research, the FDA failed to hold them accountable for it, or both remains unclear as the zostavax lawsuit proceeds. Negligence and Failure to Warn
Some Zostavax lawsuits include claims of negligence on the part of the manufacturer, suggesting that the company failed to inform patients about the true risks of the vaccine or failed to provide adequate warning about its side effects. In addition to these allegations of negligence, some lawsuits also include allegations of failure to warn, which suggest that the manufacturer knew of the vaccine’s side effects but failed to warn patients about them. While some vaccine injury lawsuits are filed on behalf of individuals who were injured or contracted an illness related to the vaccine, others are filed on behalf of individuals who experienced no negative side effects but want to raise awareness about the potential risks associated with the vaccine.
Conclusion
If you or a loved one suffered serious Zostavax side effects including shingles, blindness or even death, contact Zostavax lawyer Timothy L. Miles today to see if you meet the requirements for a Zostavax lawsuit and possibly may be entitled to substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today. (855) Tim-M-Law (855-846-6529).
Timothy L. Miles, Esq.Timothy L. Miles is a nationally recognized shareholder rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2022 Top Ranked Lawyer, 2022 Top Rated Litigator. and a 2022 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, and more. Please visit our website.
More than 7,000 people have filed a Byetta lawsuit against the makers of the drug Byetta since its release in 2003. The most common Byetta lawsuits stem from the drug’s dangerous side effects, which can include hepatitis and pancreatic cancer, as well as claims that Pfizer and AstraZeneca withheld information about the drug’s risks and potential side effects. If you or someone you know took Byetta and were diagnosed with pancreatic cancer, contact Byetta lawsuit lawyer Timothy L. Miles to see if you are eligible for a Byetta lawsuit.
If you or a loved one took Byetta and were diagnosed with pancreatic cancer, Contact Byetta lawsuit lawyer Timothy L. Miles today
Byetta Background
The drug Byetta was developed and released in 2003. It contains the ingredients Exenatide and human insulin, and it comes in the form of a once-daily injection. While the drug was approved for the treatment of Type 2 diabetes, it is also used for obesity. According to the FDA, Byetta is indicated as an “adjunct to diet and exercise for the treatment of type 2 diabetes mellitus in patients inadequately controlled on diet and exercise.” The drug is also indicated for “combination therapy in patients with type 2 diabetes mellitus who require initial combination therapy. It is also indicated for “adjunctive therapy to diet and exercise for the prevention of diabetic complications.” Byetta is manufactured and distributed by Pfizer and AstraZeneca.
Byetta Side Effects
Byetta side effects include, among others:
Pfizer and Byetta Lawsuits
Pfizer and AstraZeneca are being sued by people who suffered serious side effects as a result of using Byetta. The side effects include pancreatitis, pancreatic cancer, and other serious injuries. In March and April 2019, two federal class action lawsuits were filed against Pfizer and AstraZeneca regarding Byetta. The lawsuits were filed in the U.S. District Court for the Southern District of New York by litigants on behalf of all individuals who were harmed by the drug. The lawsuits allege that Pfizer and AstraZeneca engaged in deceptive marketing when they aggressively marketed Byetta to doctors and patients. The lawsuits also allege that Pfizer and AstraZeneca failed to inform doctors of the risks associated with the drug.
AstraZeneca and Byetta Lawsuits
In addition to being sued, AstraZeneca has been named in many Byetta lawsuits as a co-defendant. The lawsuits allege that the company failed to provide adequate warnings about the risks and side effects of the drug. They also claim that the company failed to monitor the use and adverse events associated with the drug. The first Byetta lawsuit against AstraZeneca was filed in November 2018. The lawsuit was filed by a man who used Byetta and allegedly suffered a heart attack as a result of the drug. The lawsuit claimed that the drug’s warning label was inadequate and failed to disclose the risk associated with the use of the drug.
Dangerous Ingredients in Byetta
Some of the ingredients in Byetta have been linked to serious side effects. These include Exenatide and human insulin. Exenatide - Exenatide, one of the ingredients in Byetta, is associated with an increased risk of pancreatitis, a serious condition that can result in hospitalization and death. - Exenatide, one of the ingredients in Byetta, is associated with an increased risk of pancreatitis, a serious condition that can result in hospitalization and death. Human insulin - The insulin that makes up another part of Byetta has been associated with hypersensitivity and allergic reactions, including anaphylaxis.
Conclusion
The drug Byetta has been linked to a wide range of serious side effects. It has also been linked to an increased risk of cancer in some patients. If you or a loved one took Byetta and were diagnosed with pancreatic cancer, you may be eligible for a Byetta lawsuit. Contact Byetta lawsuit lawyer Timothy L. Miles today and see if you meet the requirements for a Byetta lawsuit and could be eligible for substantial compensation. While there is still time to file a lawsuit, be mindful that these cases are time sensitive, and give us a call today.
Timothy L MilesTimothy L. Miles is a nationally recognized shareholder rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2022 Top Ranked Lawyer, 2022 Top Rated Litigator. and a 2022 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, and more. Please visit our website Statutes of limitations are laws that limit the amount of time you have to file a lawsuit following an injury or wrongful action. If you fail to file your lawsuit within the allotted time, you can no longer file a lawsuit. It is important to understand how statutes of limitations work because they might limit your right to take legal action following an accident and recover compensation. Every state has different statutes of limitations when it comes to bringing a personal injury claim against another individual or company. Understanding the statute of limitations in your state and analyzing when yours will expire is vital before making a final decision on whether or not to proceed with a personal injury claim. What is a Statute of Limitations?A statute of limitations is a law that sets a strict time limit for filing a lawsuit for a particular cause of action. Each state has its own statutes of limitations that vary depending on the type of lawsuit. For example, if you were hit by a car and suffered an injury, you might decide to file a personal injury lawsuit against the other driver for your losses. The statute of limitations for bringing a personal injury claim varies from state to state, but in most states, it is two to three years from the date of injury. If the driver hit you on June 5, 2016, your state’s statute of limitations would expire on June 5, 2018, and you would be barred from filing a lawsuit after that date. There are several important reasons why statutes of limitations exist. First, to ensure that disputes are resolved quickly and fairly, while also giving people the necessary time to file a claim. Second, they are meant to prevent stale and fraudulent lawsuits. These laws help determine what type of evidence may be allowed during your trial and what type of evidence is considered legitimate. When Are Statutes of Limitations Applied?Each state has a different statute of limitations that determines how long you have to file a lawsuit. Some events, such as the death of a loved one, may be outside the statute of limitations. This means that you do not have a legal right to bring a lawsuit in these situations because the limitations period has expired for taking action. However, there are a few exceptions to this rule. For example, minors and disabled people may have longer to file a lawsuit than an adult would, depending on the situation. A minor's statute of limitations may not start running until they reach the age of consent. Important Points to Remember About Statutes of LimitationsDeadlines matter. You will need to look up the statute of limitations in your state or jurisdiction to see the time frame you have to file a lawsuit. Statutes are not a “rule” but rather a “guideline.” Judges can extend this time frame if they see that it is justifiable to do so under the circumstances. 2 Common Misconceptions About Statutes of LimitationsOne misconception people have is that the statute of limitations does not apply to minors or children. This is not true. The same time limit applies, but in most cases the statute of limitations does not begin to run until the victim’s 18th birthday. Another misconception is that you only have one chance to file a claim and that if you miss the deadline, you cannot sue the person or company at all. This is not true, because judges can extend the time frame if they see it is justifiable to do so. 2 More Things You Should Know About Statutes of LimitationsYour state’s statute of limitations might apply to different types of lawsuits. For example, in most states, you have two years to file a personal injury lawsuit, but you have three years to file a medical malpractice suit. The type of lawsuit you file will determine how long you have to file your claim. There are other time frames that can affect your ability to file a lawsuit. You might have to file a lawsuit within a certain time frame if the defendant was a minor at the time of the incident or if the defendant is a government agency. ConclusionStatutes of limitations are laws that set specific time frames during which you have to file a lawsuit. If you do noy file your lawsuit within the allotted time, except in limited circumstances, you cannot proceed with your case. Understanding statutes of limitations can help you protect your rights and avoid falling victim to another person’s wrongful actions. For more information, or if you have any questions, contact Nashville attorney Timothy L. Miles today. Timothy L. MilesTimothy L. Miles is a nationally recognized shareholder rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2022 Top Ranked Lawyer, 2022 Top Rated Litigator. and a 2022 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, and more. Please visit our website
Contact Paragard IUD removal lawyer Timothy L. Miles today about a Paragard IUD removal side effects lawsuit.
Some people who have used the ParaGard IUD birth control have complained that they suffered significant and unexpected complications when attempting to have the birth control device -removed. Some of the ParaGard removal side effects they have reportedly suffered include:
This is not all the Paragard removal side effects, or other Paragard removal complications, just the most common that have been reported. If you suffered Paragard removal symptoms or any other Paragard IUD removal complications, contact Paragard IUD removal lawyer Timothy L. Miles today about a Paragard IUD removal side effects lawsuit. What is the Paragard IUD?
The Paragard IUD is manufactured by Teva Pharmaceuticals and has been around since the late 1980s. An intrauterine device (IUD) is a small plastic T-shaped device used for birth control. It is inserted into the uterus where it stays to prevent pregnancy. It is a small piece of flexible plastic shaped like a T. Sometimes it is called an IUC — intrauterine contraception. The Paragard IUD device has a specially designed copper coil connected to a plastic base. The device is implanted in a women's uterine cavity.
How Does the Paragard IUD Work?
Paragard works using just 1 simple active ingredient which is copper. Paragard works by preventing the sperm from reaching and fertilizing the egg and may also prevent implantation. However, because Paragard is hormone free, it will not prevent your natural menstrual cycle or stop you from ovulating each month. At first, periods may become heavier and longer with spotting in between as a result of the IUD.
What Are the Benefits of a Paragard IUD?
Paragard Is an effective long-term contraception which can be used by premenopausal women of all ages, including teenagers. Some on the benefits of the Paragard IUD include that it:
What Are the Risks in Using the Paragard?
If you do conceive while using the Paragard IUD you are at high risk of having an ectopic pregnancy (a condition where the fertilized egg implants outside the uterus, usually in a fallopian tube.). However, as noted by the Mayo Clinic less than 1% of women who use the Paragard IUD become pregnant and the risks remain very low over time. As a result, because the rate of pregnancy is so low for those who use the Paragard IUD, their rate of getting ectopic pregnancy is low than women who are sexually active but do not use contraception.
Additionally, the Paragard IUD does not protect against sexually transmitted diseases, including HIV. Finally, as discussed below, there are the risks of experiencing Paragard removal side effects or other Paragard removal symptoms when you decide to have the device removed. Who Should Not Use the Paragard IUD?
Paragard is not an appropriate alternative for everyone, and your doctor may discourage you from the Paragard IUD and urge to use another alternative if you have any of the following:
What Is the Problem with the Paragard IUD?
Serious production defects have led to broken IUDs, with the breakage occurring either during the implantation process or during removal along with other Paragard removal symptoms. According to ongoing ParaGard IUD lawsuits, Teva was aware of the potential of Paragard removal side effect since 89.
What are the Paragard Removal Side Effects?
ParaGard IUDs are removed by a healthcare provider. IUDs should be removed when they expire (they typically last from 3 to 10 years), when the user wants to get pregnant, or after experiencing ParaGard side effects. Some typical ParaGard removal side effects include: light bleeding between periods, cramping, pain, and heavy bleeding during periods. Several ParaGard IUD users have reported that the device can also reportedly break during removal, leaving part of the device embedded in the uterus, according to a report published in the Open Journal of Clinical & Medical Case Reports.
Some of the complications caused by a broken or fractured IUD, or other ParaGard removal side effects, include:
If the fragmented arms of the device break off inside the woman's body, they can cause various internal injuries. Furthermore, if breakage occurs, it may require that the device be removed with serious invasive treatments such as surgery to remove any leftover pieces and total hysterectomy, which may result in infertility issues for those affected. Note there may be other Paragard removal symptoms not listed here, you should check with a medical professional. What Should I do if I Suffered Paragard IUD Removal Complications?
ParaGard IUD removal complications can be debilitating and interfere with a person’s quality of life.
ParaGard IUD removal complications may cause those affected to be hit with large medical bills, pain and suffering, emotional distress, lost wages and other damages from having to take off from work to recover from their injuries. A growing number of people are coming forward with allegations of serious ParaGard removal side effects and other Paragard removal symptoms and filing Paragard lawsuits. Those who have suffered from ParaGard IUD removal complications should consider filing a ParaGard IUD removal side effects Lawsuit to seek compensation for their injuries, as well as compensation for other ParaGard users who suffered Paragard IUD removal complications or other Paragard removal symptoms. A ParaGard lawsuit is one way to hold Teva accountable for the safety of its intrauterine copper contraceptive and the pain and suffering you experienced from Paragard IUD removal complications. So, if you suffered ParaGard removal side effects, call Paragard IUD Removal Lawyer Timothy L. Miles about a ParaGard IUD removal side effects lawsuit today who can explain the process and who will fight for the compensation you deserve. (855) Tim-M-Law (855-846-6529). What Can I Get in a Paragard IUD Lawsuit?
If you meet the Paragard lawsuit criteria, a successful plaintiff is entitled to compensatory damages which would include compensation for things such as:
If your case proceeds to trial it is also possible the court could impose punitive damages, intended to punish the defendant for their actions. Call a l ParaGard Lawyer about a ParaGard Lawsuit if You Suffered ParaGard Removal Side Effects
If you or a loved one experienced serious ParaGard removal side effects, or other Paragard IUD removal complications contact Paragard lawyer Timothy L. Miles today at 855/846-6529, or by submitting the form below, as you may be entitled to substantial damages if you meet the Paragard lawsuit criteria.
Give us a call, it is free, and see what a Paragard Lawyer can do for you and if your eligible for a ParaGard IUD removal side effects lawsuit. (855) Tim-M-Law (855-846-6529) Timothy L. Miles, Esq.Timothy L. Miles is a nationally recognized shareholder rights attorney raised in Nashville, Tennessee. Mr. Miles was recently selected by Martindale-Hubbell® and ALM as a 2022 Top Ranked Lawyer, 2022 Top Rated Litigator. and a 2022 Elite Lawyer of the South. Mr. Miles also maintains the AV Preeminent Rating by Martindale-Hubbell®, their highest rating for both legal ability and ethics. Mr. Miles is a member of the prestigious Top 100 Civil Plaintiff Trial Lawyers: The National Trial Lawyers Association, a superb rated attorney by Avvo, a recipient of the Lifetime Achievement Award by Premier Lawyers of America (2019) and recognized as a Distinguished Lawyer, Recognizing Excellence in Securities Law, by Lawyers of Distinction (2019). Mr. Miles has published over sixty articles on various issues of the law, including class actions, whistleblower cases, products liability, and more. Please visit our website.
If you have taken singulair and experienced suicidal ideation or other adverse Singulair mental health symptoms, contact a Singulair lawyer today
Singulair (montelukast) is a drug prescribed to patients suffering from asthma or severe allergies that can provide symptom relief and help them manage their condition. It is a very successful drug for its manufacturer, Merck & Co. (Merck). Singulair received the U.S. Food & Drug Administration’s (FDA) marketing approval in 1998; by 2004, Singulair was doing $2.62 billion in sales.
But by 2009, there were concerns that Singulair may have an adverse effect on its users’ mental health. That year, the FDA updated its potential side effect warning about Singulair to include the potential for “neuropsychiatric events.” The FDA warned that the potential adverse mental health symptoms could include: ”postmarket cases of agitation, aggression, anxiousness, dream abnormalities and hallucinations, depression, insomnia, irritability, restlessness, suicidal thinking and behavior (including suicide), and tremor.” These concerns have only grown over time — in March 2020, the FDA began requiring a “black box” warning label (the FDA’s highest danger advisory) on every unit of Singulair, warning of the potential for severe mental health symptoms, including suicidal ideation and attempted suicide. In light of these mounting concerns, the FDA now advises against the use of Singulair to treat seasonal or chronic allergies, except in cases where no other medication works for that specific patient. Merck & Co. is now facing Singulair mental health lawsuits from Singulair users who allege that the medication caused them to experience adverse mental health symptoms, including suicidal ideation. If you or a loved one have taken singulair and experienced suicidal ideation or other adverse Singulair mental health symptoms, you may be eligible for compensation. Contact a Singulair Lawyer today. How Were the Singulair Mental Health Symptoms Discovered?
The FDA based their new warnings and recommendations on Singulair-associated neuropsychiatric incidents that were reported to the FDA’s Sentinel Initiative, as well as animal studies and reports of suicides. The FDA identified 82 cases where a suicide was linked to montelukast. Forty-five cases involved a patient older than 17, 19 involved one younger than 17, and 18 case reports did not indicate the patient’s age. A study of montelukast in mice found the drug molecule inside the brain, indicating that the drug can cross the blood-brain barrier. This would suggest that montelukast/Singulair could enter and harm the brain as well. The combination of all this information caused the FDA to update their assessment of the possible mental health risks posed by the Singulair mental health symptoms.
What Are the Singulair-Associated Neuropsychiatric Incidents ?
The Singulair mental health symptoms include a wide range of Singulair-associated neuropsychiatric incidents that have reportedly been experienced by Singulair users. These include Suicidal thoughts, potentially escalating to suicidal ideation and attempted suicide as well as:
If you or a loved one has experienced any of these Singulair-associated neuropsychiatric incidents or any other Singulair mental health symptoms, you may have grounds for a Singulair lawsuit against the drug manufacturer if you meet the Singular Lawsuit Criteria. Contact Singulair Lawyer Timothy L. Miles today for a free case evaluation who can answer any question you have as well as let you know if you do meet the Singulair lawsuit criteria and may be eligible for a Singulair mental health lawsuit and possibly entitled to substantial compensation. Should I Stop Taking Singulair?
You should talk to your doctor about your options before making any changes. The FDA has expressed concerns that not all doctors and healthcare providers are currently aware of the updated understanding of Singulair’s risk profile, so make sure that your doctor knows about the March 2020 FDA update and if you are experiencing Singulair mental health symptoms.
Should I Report any Singulair Mental Health Symptoms?
Yes, the FDA is encouraging people who had a problem related to prescription medications to report the problem through the MedWatch Voluntary Reporting Form or call 1-800-332-1088 for more information. Make sure to provide all information including dosage, how long you have been taking Singulair, and which Singulair mental health symptoms you suffered including any Singulair-associated neuropsychiatric incidents.
What Is a Singulair Lawsuit?
A Singulair Lawsuit is a demand from the defendant for monetary compensation by patients who took Singulair and subsequently suffered adverse Singulair mental health symptoms, or experienced Singulair-associated neuropsychiatric incidents. The lawsuits allege the defendants made a defective drug and failed to warn physicians about its carcinogenic properties. If eligible you may participate in a Singulair lawsuit and possibly be entitled to substantial compensation. A Singulair Lawyer can answer these questions and is available anytime just give us a call or submit the form below for a free case evaluation.
Do I Meet the Singulair Lawsuit Criteria?
If you or a loved one took Singulair and has since experienced any of the above adverse Singulair mental health symptoms, you most likely meet the Singulair Lawsuit Criteria. If successful, you could win compensation for any financial losses incurred as a result your Singulair mental health symptoms, including medical costs, as well as damages for pain and suffering. If you have more questions on the Singulair Lawsuit Criteria, call Singulair Lawyer Timothy L. Miles today for a free and confidential case evaluation who can listen to you case and let you know if you may meet the Singulair lawsuit criteria.
What Can I Get Out of a Singulair Lawsuit?
If you meet the Singulair lawsuit criteria you could be eligible for substantial compensation as a result of having suffered Singulair mental health symptoms. A successful plaintiff is entitled to compensatory damages which would include compensation for things such as:
If your case proceeds to trial it is also possible the court could impose punitive damages, intended to punish the defendant for their actions. For more information, contact Singulair Lawyer Timothy L. Miles today. How Much Does It Cost to Hire a Singulair Lawyer?
It does not cost anything to hire a Singulair lawyer. We take all cases on a contingency basis which means we do not get paid unless we win your case. A Singulair Lawyer can listen to your story and look at all the facts and determine if you meet the Singulair lawsuit criteria, and if so, will explain the process and answer any questions you may have. Call Singulair Lawyer Timothy L. Miles today for a free case evaluation.
Call a Singulair Lawyer today about a Singulair Lawsuit |