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    Category Archives: Personal Injury Blog

    Product Liability Lawyer Weaver & Associates

    Your Local Product Liability Lawyers – Call Our Offices for Quick, Local Legal Help

    Whether we’re talking about defective drugs, defective appliances. Other medications, car parts, baby products, tools from your trade, or dangerous baby toys for your child. Many of the products that families use daily can also end up harming them. If a product that you purchased is defectively designed or produced, sometimes dangerous and serious injuries can result in huge life-altering events with major consequences.

    The Injury Lawsuit liability attorneys of Weaver & Associates represent victims all throughout the state of Texas, but also all over the country. If you have been injured by a dangerous products, trust the law offices of our firm to quickly and conscientiously help you with your legal claim. Our attorneys have recovered many millions for our valued clients. If you would like to talk with us about your case, call our local Texas attorneys and national hotline at  (800) 403-6902.

    Call Now (800) 403-6902 or simply fill out the form to the right and receive a fast response from one of our trained legal professionals or lawyers regarding your situation.

    Does Product Liability Include Just Consumer Products?

    Product liability is a branch of law which holds producers, as well as designers and retailers of defective and dangerous products accountable for any injuries which have been linked with their products.

    Product liability encompasses a legal doctrine called negligence, as well as the doctrine strict liability. It also is affected under the legal principles covering a breach of a warranty.

    If there has been a case of negligence, the producers who created and/or distributed the product hold what is called a duty of care toward the end user or buyer of the product. They owe the duty of preventing injury which is reasonably foreseeable. Additionally, if a product has been carelessly built or designed and ends up injuring an end user, the producer is accountable for the cost of handling injury and other incidental costs from the product’s injuries.

    Another legal doctrine called strict liability also holds sway in these type of cases. If a product with a defective condition has been sold which is deemed unreasonably harmful or dangerous to the typical type of user, any defect causing these kinds of injuries can be linked with how it’s built, designed, and also with how it is packaged. The liability also includes instructions regarding the assembly or use of the product including failure on the part of the manufacturer to warn its users properly of a product’s dangers. Under strict liability legal theory, a user must not prove carelessness or negligence on the part of the manufacturer. Simply by nature of producing a product that ends up injuring or harming a user, the legal theory applies.

    What Kinds Of Consumer and Other Products Bring About Product Liability Lawsuits?

    Product liability encompasses almost any type of item you could imagine – whether its a consumer product, a construction tool, or a prescription drug. This is a list of many common household products which have been involved with product liability suits:

    • Appliances for the home like space heaters, toasters, dryers, ovens, washers & dryers.
    • Auto parts, such as brake pads, brakes, steering wheels, airbags, seats, and seatbelts
    • Prescription and over the counter medicines like diabetese medications, birth control, and antidepressants
    • Other medical products like diet pills and hip implants, vaginal mesh, and more
    • Baby and pregnancy items like cribs, baby carriers, strollers, car seats and toys
    • Toys which specifically pose risks for choking, causing strangulation or which have included harmful lead paint
    • Tools, such as for welding, other power tools, riding and push lawnmowers as well as garage doors and their associated openers

    There is a statutory length of time under which a person may file their product liability claim or bring a lawsuit following a product liability injury. Time has been limited in the different states based on local state laws. For example, Texas holds a 2 year statute of limitation but Florida holds a 4 year statute of limitations. See a list of statutes of limitations by states.

    GET HELP NOW! If you or a loved one has been injured from defective products, call the product liability attorneys of Weaver & Associates today. Receive a free legal consultation.

    Call Now (877) 734-0251 or fill out the form to the right.

    Zoloft Lawsuit

    Zoloft Lawsuit? Call Our Zoloft Attorneys Now

    Zoloft which is also known as the chemical name sertraline chloride functions as an antidepressant and has been developed, produced and marketed by Pfizer during the 1990′s. After being originally developed for the market in the U.K., it was released with the name Lustral. Pfizer created and marketed the drug Zoloft as under the banner as a safer drug with less side effects as well as less severe withdrawal symptoms as compared to competitor pharma like Prozac.

    9 years following its U.K. release, the FDA approved Zoloft in the US. Zoloft becamse the most widely prescribed drug for treatment of depression by 2005 in the U.S., having almost 30 million Zolof prescriptions written.

    If you have used Zoloft and been injured, call our law offices to discuss your options.

    Uses for the Drug Zoloft

    Zoloft has mainly been prescribed as treatment for MDD (major depressive disorders). Yet, physicians also write Zoloft prescriptions for PTSD, premenstrual dysphoric disorder, OCD, as well as additional panic and social anxiety disorders.

    Common Side Effects for the Drug Zoloft

    Zoloft  generally holds in a well-tolerated way by the majority of patients. If you or a loved one has been injured while taking Zoloft or your baby was born with birth defects. Call our law offices at the number above or fill out the associated form and we’ll reach out to you to discuss your potential for receiving a financial settlement or award.

    Avandia Drug Lawyer

    Avandia Lawsuit

    Serious cardiovascular adverse reactions along with potentially fatal drug complications due to use of the drug Avandia led scores of thousands of Avandia patients in the US to sue its maker, GlaxoSmithKline. GSK’s liabilities in the lawsuits could top 6 billion when all is said and done.

    Clinical research show Avandia to elevate risk for heart attack by levels of over 43% and twice the chance for heart failure following a single year of Avandia use.

    During research trials in a clinical environment, more patients died from cardiovascular problems while taking Avandia than patients on placebo. Yet Avandia’s stark black-box warning made no mention of this elevated risk for death linked to Avandia causing cardiovascular events. The FDA released a warning regarding Avandia’s cardiovascular death risks in the year 2007 at which point the warning was added to the black box label.

    A 2-year Senate investigation discovered that GlaxoSmithKline attempted to stifle health concerns which were duly noted by several of its own physicians as well as outside doctors who complained about the medication. A large number of Avandia patients hold GlaxoSmithKline responsible for not making doctors as well as especially its own patient consumers aware regarding risks for death linked to use of Avandia.

    Ongoing Avandia Drug Lawsuits

    Over 50,000 Avandia drug lawsuits have already been filed in federal and state courts in the US, which name GlaxoSmithKline’s intentional failure to notify patients regarding potentially serious and life-threatening cardiovascular risks and health symptoms, such as stroke from Avandia, Avandia induced heart failure, heart attack caused by use of Avandia, loss of vision and even death.

    Avandia has become a class action suit. If you or a family member has been injured due to the use of Avandia, call our law offices today or fill out the form to the right and we’ll contact you right away regarding your legal options and potential for obtaining financial compensation for your injuries or for a wrongful death of a loved one.

    Actos Quick Facts

    Quick Facts Regarding Actos

    Actos Drug Guide

    Actos Generic Pharmaceutical Drug Name
    Pioglitazone hydrochloride

    Date Actos was FDA Approved
    July 15, 1999

    Other Types of Actos
    Actosplus Met XR
    Actosplus Met
    Duetact
    Metformin Hydrochloride as well as Pioglitazone Hydrochloride Chloride
    Pioglitazone

    Actos Manufacturer
    Eli Lilly

    Current Status of Actos
    Actos is currently being marketed for approved drug uses for Diabetes

    Serious and Dangerous Actos Side Effects
    Heart Attacks
    Bladder Cancer
    Cardiovascular Conditions
    Pitting Edema and Standard Edema
    Congestive heart disease
    Feet swelling
    Hepatitis (Inflammation of the liver)

    Many patients who have used Actos in the past do not realize many of just the most basic facts regarding Actos. There are certainly millions of patients who have used the drug. For this reason, since the drug was so widely prescribed, there are literally tens of thousands of people who have had severe negative side effects from the drug. Consider the quick facts regarding Actos above when deciding whether the drug Actos is the right choice for you. Consult with your physician before making any determinations.

    Additionally, if you or a loved one in your family or a close friend has been negatively affected by the drug you should call our offices immediately or fill out the form to the right so that we can help you to make a determination regarding your legal recourse for financial damages to cover the cost of your injuries and other incidental costs such as pain and suffering. In severe cases and the unfortunate cases of wrongful death, you may be entitled to compensation. So call our offices today before the statute of limitations runs out for your Actos drug lawsuit claims.

    Actos Lawyers and Actos Drug Lawsuits Weaver & Assoc.

    Actos Drug Lawsuits from Bladder Cancer

    Actos (which is the drug called Pioglitazone Hydrochloride) Has Associated Dangerous Side Effects Which Can Include the Following Heart Attacks, Especially Bladder Cancer, Other forms of Cardiovascular Disease and other Heart Risks | This FDA Warning Was Issued: Actos may Increase Risk of Bladder Cancer | Actos Associated With Severe Health Conditions (Click Here for an Actos Quick Fact Guide)

    Actos Image Bladder Cancer

    Actos Lawsuits Related to Bladder Cancer, Research Study into Actos Side Effects

    According to leading medical clinical studies conducted in August of 2011 reviewing the Actos side effects from using they determined that the link between Actos and the risk of bladder cancer are intense and serious. According to this report, thousands of people in the study (22,512) acknowledged having negative Actos side effects during or following having taken Actos. Among these side effects a FIFTH of a PERCENT were diagnosed with bladder cancer. Among bladder cancer patients, the largest subset (around 43% of bladder cancer patients) had used Actos from 2-5 yrs prior to developing Bladder Cancer. The following highest concentration (around 29% of bladder cancer patients) had used Actos for a period of ONE to SIX months.

    Liver Cancer WARNING for Actos

    The Actos Attorneys of Weaver & Associates and several other drug lawsuit attorney offices are investigating different, additional cancers which may be linked to the use of Actos, that also includes the condition of liver cancer. For those people who have developed any kind of liver cancer or if a loved one has contracted liver cancer after taking Actos, our dangerous drugs side effect attorneys are prepared to hear from you now. Our law offices offer free legal evaluations for any type II diabetic patients which have used Actos with a subsequent liver cancer diagnosis.

    Prostate Cancer WARNING for Actos

    The Actos attorneys of Weaver & Associates are in process of investigating additional potential associations linking Actos with cancer of the prostate. If you are a male and used Actos for your type II diabetes, with a subsequent diagnosis of prostate cancer, you’re urged to call our Actos attorneys today and we’ll provide you a free evaluation of your legal rights to financial compensation.

    Kidney Cancer WARNING for Actos

    The Actos attorneys of Weaver & Associates have started an investigation into possible links into Actos treatments that are connected to kidney cancer. Our attorneys want to talk with type II diabetics that have kidney cancer or who had it previously after or during Actos treatment for type 2 diabetes.

    List of Actos Drugs

    • ACTOPLUS MET. Main active Ingredients which include METFORMIN HYDROCHLORIDE as well as PIOGLITAZONE HYDROCHLORIDE.
    • PIOGLITAZONE HYDROCHLORIDE as well as METFORMIN HYDROCHLORIDE. Main active ingredients includ METFORMIN HYDROCHLORIDE as well as PIOGLITAZONE HYDROCHLORIDE.
    • ACTOPLUS MET XR. The main active ingredients include METFORMIN HYDROCHLORIDE as well as PIOGLITAZONE HYDROCHLORIDE.
    • ACTOS. The main active Ingrediaet is singly PIOGLITAZONE HYDROCHLORIDE.
    • PIOGLITAZONE. The main and singly active ingredient is PIOGLITAZONE HYDROCHLORIDE.
    • DUETACT. The main active ingredients are GLIMEPIRIDE as well as PIOGLITAZONE HYDROCHLORIDE.

    Are you a type II diabetic who has used Actos with a subsequent bladder cancer diagnosis? The defective pharmaceutical lawyers of Weaver & Associates will provide you a free legal evaluations regarding your injury lawsuit claims for financial compensation.

    The Actos attorneys of Weaver & Associates are furthermore investigating other potential cancer links possibly linked to the use of Actos. If your loved one or you used Actos with a subsequent cancer diagnosis of any type of cancer. These other cancers could include prostate cancer, liver cancer, or cancer of the kidney, our attorneys want to talk with you. Do not hesitate or worry about contacting our Actos attorneys today. Call us today or fill out the online form here on the page.

    Actos’s Dangerous Side Effects, Bladder Cancer Risk

    Actos Abdominal Pain Risks and Side Effects Bladder Cancer

    What Are Actos’ Side Effects?

    In 2011, Type II Diabetes treatment by the name of Actos (drug name piogliatazone) had sales halted by France’s as well as Germany’s medical regulators due to possible links to bladder. These decisions in Europe to place drug bans on Actos followed a study which was commissioned by the FMA (French Medicines Agency) and which concluded that patients who took Actos had higher likelihood of developing cancer of the bladder, which is an unfortunate and dangerous aggressive type of cancer.

    Also in mid 2011, US Food and Drug Administration (FDA) released an announcement that it was looking into Actos due to a potential potential bladder cancer elevated risk as of late 2010. The FDA said that early research coming from a ten year clinical trial which was submitted by Actos’ manufacturer Takeda indicated significant links with exposure between Actos with bladder cancer. Yet, some clinical evidence indicated that Actos patients who were on the drug a minimum of 2 years held higher risks for being diagnosed with bladder cancer.

    Early 2011, another clinical Actos study, reviewing Actos’ Adverse Event data reported to the Food & Drug Administration from the years 2004 to 2009, indicated patients of Actos had “disproportionate risk[s]” for suffering bladder cancer.

    New Actos Research Could Indicate Elevated Risk of Cardiovascular Side Effects

    Actos Causes Cardiovascular Injuries and Heart DiseaseLink between Actos and Cardiovascular Diseases among Actos Patients.

    New Actos clinical research has piled onto the mounting pile of clinical evidence which links Actos and Avandia with elevated serious negative health risks. While Avandia long was surrounded and mired in the negative health debate regarding cardiovascular conditions, Actos is a newcomer to this debate. Actos was formerly held to be a less dangerous type 2 diabetes medication alternative that caused its sales to go through the roof and major declines for Avandia.

    Another Actos Research Study Could Indicate Elevated Risk For Bone Fractures

    Actos Risk of Bone Fracture InjuriesMany older Americans could be at elevated risk of having bone fractures.

    Weaver & Associates had formerly noted a different study associated with Avandia as well as Actos and elevated bone fracture levels. The study from the Journal of Clinical Endocrinology & Metabolism determined that Actos and Avandia raised risks for fractures among older postmenopausal females who have Type II diabetes. With men who have Avandia or Actos loop diuretics the same caution holds true for bone fracture elevated risks.

    Females over the age of 50 with broken bones had 71% greater likelihood to have a thiazolidinedione prescription. Among men, the elevated risk was at a triple rate over those patients who took a thiazolidinedione at the same time as a loop diuretic, such as Lasix.

    FDA Requires Black Box Warning for Actos

    Actos Blackbox Warning Required by FDA

    Following intense debate regarding the lack of safety of Actos–the type II Diabetes drug, FDA officials stated that risk for Actos would receive the black box warning which equates to a large black outline due to severe risks of having adverse heart and other cardiovascular conditions, such as heart failure, heart attack, as well as other cardiovascular deaths. The infamous drug black box warning holds the most severe FDA-ordered label change. The only thing more strongly ordered by the FDA is a mandatory drug recall.

    Actos Victims – Legal Help for Actos

    Did you take Actos and get bladder cancer or other dangerous side effects? Did someone you love take Actos and get bladder cancer, liver cancer, kidney cancer or side effects of a different nature that were severe? Please don’t hesitate in calling us or filling out the legal case evaluation form here on the web page to get a free injury case evaluation from a competent defective drug attorney in our offices. You may also call us at the number at the top of this page.

    Important New References for Actos:

    http://www.taf.org/whyfca.htm

    http://www.fda.gov/drugs/drugsafety/postmarketdrugsafetyinformationforpatientsandproviders/ucm109136.htm

    http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/000285/human_med_000624.j

    GERMANY HALTS DIABETES PHARMACEUTICAL DRUG ACTOS DUE TO LINK WITH BLADDER CANCER

    Tags: Actos Lawsuits  Thizolidinediones  Drug Side Effect Lawsuits Heart Disease  from Actos  Heart Failure from Actos

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    Fosamax Lawyer for Fosamax Litigation & Lawsuit Attorney

    Fosamax Lawyer for Litigation Were you taking Fosamax and experienced bone breaks? If you had bone fractures while on Fosamax, you could be eligible to receive compensation from a Fosamax settlement or lawsuit. Call Weaver & Associates 800-403-6902 ...

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    Information about Yaz, Yasmin, and Ocella – Financial Awards for Personal Injuries

    Information about Yaz, Yasmin, Ocella, and Zarah Financial Awards for Personal Injuries

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    Legal Help
    Published on 08-10-2012 06:50 PM
    What Is the Drug Yaz and What is It Intended to Treat?

    Yaz is a contraceptive pill claiming 99.9% effectiveness when a patient takes the Yaz birth control pill within the same 4 hour window each day. Yaz is also known by the scientific name drospirenone and is manufactured by Bayer HealthCare.What Is the Drug Yasmin?

    Yasmin is also manufactured by Bayer HealthCare Pharmaceuticals but comes in a form containing the exact same doses for drospirenone as its counterpart Yaz, but containing lower amounts of ethinyl estradiol which is a bioactive type of estrogen contained in the majority of birth control pills.What Kinds Of Health Issues and Dangerous Health Problems Does Yaz Cause as Side Effects?

    Many Yaz lawsuits have been and continue to be filed due to alleged drug side effects coming from contraceptive pills. Many of these risks included higher risks for heart attacks, DVT or deep vein thrombosis, strokes, pulmonary embolisms, disease of the gallbladder, and even death. Additional serious medical injuries have also been sustained by Yaz or Yasmin patients. Lawsuits have also been filed for use of generic versions of Yasmin such as Ocella as well as Zarah. Lawsuits regarding generic Yaz have also been filed against makers of Gianvi.

    What Kinds Of Side Effects May I Sue For as a Result of Taking Yaz, or Yaz Generics, or Yasmin, or Yasmin Generics?

    Some women suffered heart attacks, stroke, and other serious side effects. These patients who suffered heart attacks certainly have a claim under which they may sue. Other women who suffered strokes and/or heart attacks as well as those who suffered deep vein thrombosis, Pulmonary Embolisms or Gallbladder Disease have the right to sue for financial and other damages due to these conditions or injuries. If you or a loved one, or someone that you know has died suddenly, you could have a claim for a valid lawsuit regarding Yaz or Yasmin or Yaz/Yasmin generics and against their manufacturer.

    Why Have Yaz or its Counterpart Yasmin Been Causing Health Problems, Health Hazards, and Making People Sick?

    Initial reports indicate the reasons for illness are linked to the drospirenon in Yas, Yazmin, and the generic versions of those drugs. Drospirenon may raise levels for potassium in your blood which causes hyperkalemia. These elevated levels for blood potassium can further lead to elevated risks for heart attacks, strokes and other dangerous health hazards from taking Yaz and Yasmin.

    Are Blood Clots Caused by Yaz or Yasmin or Generic Versions of Yaz/Yasmin like Ocella and Zarah

    Some of the more recent research has been released in Britain’s Medical Journal which published a research study based on women taking Yaz or Yasmin. These women who took Yaz, Yasmin, Ocella, or Zarah were at a risk for suffering a blood clot at a rate of 6.3 times more than other women not taking birth control. When compared with other types and forms of contraceptive pills that indicated a risk of only 4 times more likelihood of suffering from dangerous blood clots.

    Should I Talk to an Attorney about Yaz or Yasmin? And if so, What type Of Attorney Should I Consult With?

    If you have been affected by taking Yaz, Yasmin, Ocella, or Zarah and are thinking that you could have been affected from taking Yaz and Yasmin, then you should talk to an experienced personal injury attorney immediately. It’s important not to delay because consulting an experienced medical malpractice, defective product attorney, or personal injury attorney with expertise in pharmaceuticals and/or specifically with Yaz will ensure that you do not miss important timelines for filing your claim and receiving financial compensation for having been injured by taking Yaz, Yasmin, Ocella, or Zarah. The specialization required in handling these types of lawsuits is very important because an experienced attorney skilled with this kind of law will be able to better handle your case and get you financial rewards for your injuries.

    What Kind of Financial Damages May I Recover For Yaz Injuries? What Type of Financial Damages May I collect For Yasmin Injuries? What Kind of Financial Damages Can I Collect for Taking Ocella or Zarah?

    There are several kinds of financial compensation that you may receive from your injuries and damages you suffered. The list can include outstanding medical costs and medical bills, costs from ongoing medical treatment, as well as damages from additional health issues you suffered as a result of your injuries. You can also successfully sue for pain and suffering damages as well as for costs associated with past and future lost wages resulting from your Yaz injuries.

    What are Some Additional Differences between Yaz and Yasmin?

    Some people aren’t aware that there are major differences between Yaz and Yasmin. They simply think of them as the same thing. These two contraceptive pills are quite similar in some ways, but they have some additional minor differences that have quite an impact in how the drug is prescribed, taken, and how it affects the body before, leading up to, and during a period.

    Yaz which is also called drospirenone with ethinyl estradiol as well as Yasmin which is also drospirenone with ethinyl estradiol both use oral birth control that contain estrogen as well as progestin. Yaz and Yasmin both work in preventing pregnancy through preventing or stopping ovulation which is defined as the maturation as well as eggs being released out of the ovaries. The birth control medications Yaz and Yasmin alter cervical mucus as well as uterus lining.

    These two medications Yasmin, Yaz, as well as their generic versions Ocella, Zarah, and others differ from standard birth control methods and other contraceptive pills in important aspects. Progesterone used in Yaz, Yasmin, Ocella, and Zarah is called drospirenone and has been closely associated with spironolactone which is a drug used for diuretics. Commonly known as a water pill, this spironolactone is similar to the drospirenone used in Yaz and Yasmin and has anti-androgenic specific activities, meaning that these work against male testosterone as well as other male hormones. Women having small amounts of the hormones and are generally referred to as “male hormones.” These hormones lead to incidentals like acne and other skin issues.

    How does Yaz/Yasmin and its Generics Ocella/Zarah Differ in Daily Use from Other Birth Control Pills?

    The main difference between the medications Yaz and Yasmin is that 24 pills that are active come with Yaz along with 4 pills that are inactive. The majority of contraceptive pills which also includes the form called Yasmin come with 21 pills that are active along with 7 pills that are inactive. This difference in having fewer pills that are inactive appears to decrease a handful of the annoying and bothersome symptoms occurring just prior as well as during a woman’s period.

    How to File a Mesothelioma Claim for Asbestos Litigation

    How to File a Mesothelioma Claim for Asbestos Litigation

    Because of the passage of legal statutes allowing mesothelioma victims the legal right to sue asbestos companies for damages more than 600,000 such mesothelioma cases for compensation have already been filed. Asbestos attorneys which have experience can help you obtain your claim money through their well-operated law offices when taking on big asbestos companies. The asbestos companies and trusts employ a whole cadre of powerful attorneys and so it is important to have a good lawyer on your side.

    Because the required burden for proving a mesothelioma claim lies with the victim, it’s important to understand the rights as well as the processes that are involved with filing an asbestos claim. These claims involve victims who are alive and suffering or incapacitated and even victims who are now deceased.

    First, where should I file my asbestos claim? The place where a mesothelioma claim is filed can affect how long it will take to finish your claims process. Your lawyer will generally work very closely with you and help you determine the best court to file your meso case. It’s common for someone to file in a state where they don’t live currently due to a more appropriate or more favorable jurisdiction. This doesn’t necessarily involve being required to travel to this other state, however, as your mesothelioma lawyer will typically handle everything and they’ll do all the necessary traveling and come to you if it’s needed.

    What documents, or other information is needed to file a mesothelioma claim? You will need to file a legal document called a complaint, which in the legal world is also known as a legal petition. This begins your asbestos lawsuit. The asbestos attorney which represents you will draw up this complaint and then file this document on behalf of you as the victim. Your lawyer will generally send this complaint both to the companies which you’re suing for damages, as well as to the courts.

    The companies which you’re suing are known as the defendant or defendants and they have a specific amount of time with which they’re required to answer your claim. Many situations will involve an offer from the defendant in which they ask you if you would like to settlement your claim immediately. These cases typically involve the defendant denying any responsibility of liability for your injuries and in the case where your complaint doesn’t state your claim clearly or satisfy the legal rules and procedures, the asbestos company defendant will attempt to convince the court to agree to dismiss the claim entirely. When working with an experienced asbestos lawyer, this is not likely to happen.

    Lawsuits Against Fresenius’ for Failure to Warn

    GranuFlo & NaturaLyte Recalled

    Fresenius Recall Lawsuit

    Our Legal Injury Lawsuit team is aggressively moving forward with injury lawsuits for people experiencing injury or cardiovascular issues, cardiovascular disease, death, sudden cardiac death, cardiopulmonary attack, or any other type of cardiovascular event, of a serious nature with regards to cardiovascular injury after receiving GranuFlo as well as NaturaLyte during dialysis.

    Naturalyte and Granuflo come from Concentrate. They’re utilized in treatment of acute and chronic renal problems during hemodialysis. This acid concentrate is formulated as a three-stream machine use in hemodialysis. Three-stream equipment in hemodialysis is calibrated for use with acid/base concentrates.

    Lawsuits Against Fresenius’ for Failure to Warn

    In 2011, Fresenius sent internal memos directed toward physicians that practiced internally in the Fresenius dialysis facilities. This memo warned the doctors regarding failure on the part of medical personal in prescribing GranuFlo properly. The memo discussed the appearance of  a sharp rise in patient death risk via cardiac arrest. The internal Fresenius memo additionally was quoted as saying that doctors should take intense corrective action in view of the troubling and dangerous findings.

    Although the risks were stated clearly to be high and extremely solemn, Fresenius failed to make any outside warning of any kind toward its patients, customer clinics, or any other groups such as the FDA until March of 2012. Fresenius only alerted these groups once the FDA had been delivered a memo regarding Fresenius’ internal memo anonymously. Only after the FDA contacted Fresenius, and following this communication, Fresenius contacted customers.

    GranuFlo & NaturaLyte are some of the most widely used prescription dry acid medical products in the kidney dialysis branch of medicine. Fresenius uses GranuFlo as well as NaturaLyte at its own dialysis centers, and other hemodialysis locations which purchase dialysis supplies directly from Fresenius. About 125,000 people are treated using GranuFlo, not including Fresenius’ own centers.

    Obtain a Free GranuFlo Dialysis Consultation.

    Obtain a Free NaturaLyte Dialysis Consultation

    Obtain a Free Metabolic Alkalosis Consultation

    Obtain a Free Lawsuit Consultation Regarding Cardiac Side Effects From GranuFlo and NaturaLyte

    If it is the case that you or someone you love has been injured in a serious way from GranuFlo or has been injured seriously from NaturaLyte. Or if you or a loved one has suffered additional losses from GranuFlo and/or NaturaLyte or have suffered metabolic alkalosis, then you could be deserving of financial compensation from Fresenius.

    Fill out the form to the right to obtain your Free GranuFlo – NaturaLyte Injury Lawsuit Consultation.

    GranuFlo Lawsuit Information -NaturaLyte Lawsuit Information

    GranuFlo Attorneys for Compensation

    Granuflo & NaturaLyte Acid Concentrate for Dialysis Treatment Recalled

    Fresenius Medical Recall Lawsuit

    Our Law offices are currently pursuing lawsuits with regards to individuals who have experienced some form of injury or other loss as a result of cardiovascular problems, cardiovascular death, sudden heart attack death, cardiopulmonary arrest, any kind of heart attack, and/or other serious cardiovascular injuries following having been administered GranuFlo and/or NaturaLyte while undergoing recent dialysis.

    Naturalyte along with Granuflo Dry Acid come from Concentrate and are utilized for treatment for acute as well as chronic kidney failure while undergoing hemodialysis. The acid concentrate is generally formulated for use with a 3-stream hemodialysis equipment. Three-stream machines for hemodialysis are calibrated to be used with acid & its converse bicarbonate concentrates.

    The maker of GranuFlo and NaturaLyte is Fresenius Medical Care.  Fresenius is currently the subject of investigation from the FDA regarding heart attacks, cardiac death, as well as additional cardiac events which have been linked to GranuFlo.

    Obtain a Cost Free Consultation Regarding GranuFlo Dialysis

    Obtain a Consultation Free Regarding NaturaLyte Dialysis

    Obtain a Consultation Regarding Free Metabolic Alkalosis

    Free GranuFlo and NaturaLyte Consultation Regarding Cardiac Side Effects

    The procedure used to clean out and filter toxic waste out of the blood is called dialysis and is used for patients with kidney failure of various levels of renal failure. In the process of dialysis, bicarbonate gets introduced into the blood to neutralize acid that congregates in the blood at high levels.

    Because Fresenius’ product, GranuFlo, also contains a component which has been shown to be converted into bicarbonate at greater levels than products sold by competitors. Because of these high levels of bicarbonate in Fresenius patients, the investigation was triggered.

    What is the Medical Problem?

    See the following page for information on Fresenius Failure to Warn Lawsuits.

    Fresenius makes two products which are utilized in kidney dialysis, namely GranuFlo and also NaturaLyte. These dialysis medications are now being linked with a condition called alkalosis. This condition is linked to increased cardiovascular death and other dangerous cardiac events.

    The Food and Drug Administration has received multiple complaints which describe errors in alkali dosing during hemodialysis where dialysate is used as concentrate and which contain acetic acid. When these medications are metabolized, they become sources for alkali that contribute and cause higher levels of bicarbonate in patients.

    The following risk factors are linked with this elevated rate of metabolic alkalosis:

    • Cardiopulmonary arrest from hemodialysis
    • Sudden heart attack
    • Cardiopulmonary arrest
    • Low blood pressure
    • Cardiac arrhythmia
    • Stroke
    One major research study has been conducted in 2010 which showed that patients having pre-dialysis levels of bicarbonate of more than 28mEq/L had more than 4.7 greater chances of experiencing cardiac arrest. The research also showed that hemodialysis patients having pre-dialysis levels of potassium under 4 mEq/L were 6.3 x more likely to suffer heart attack.

    In 2012 the Food and Drug Administration contacted medical providers in order to look into whether the presence of acetate, as well as the concentration of citrate and acetic acid when used in dialysate are used in determining prescription levels for these medications.

    Class 1 Recall of GranuFlo. Class 1 Recall of NaturaLyte. GranuFlo and NaturaLyte Class 1 Recall.

    Last month, Fresenius Medical Care issued a class 1 medical recall in North America, which is the region where they cited reasons for the recall to be the following points.

    • Clinicians are cautioned regarding acetate concentration.
    • Clinicians are cautioned regarding concentrations of sodium diacetate (also called acetic acid + acetate).
    • Clinicians are cautioned specifically regarding Fresenius’ Naturalyte and Granuflo Dry Concentrate.
    • Clinicians are cautioned regarding inappropriate prescription levels which lead to high sodium bicarbonate levels .
    • Clinicians are cautioned regarding metabolic alkalosis (a major risk factor linked to low blood pressure, hypoxemia, hypercapnia, hypokalemia and cardiac arrhythmia.
    • Clinicians are cautioned that if these incorrect levels are not properly treated, cardiopulmonary arrest could occur.
    • Clinicians are cautioned that GranuFlo and NaturaLyte may cause death or other major negative health outcomes.

    The FDA has issued communication regarding the danger linked with inappropriate levels of prescription and the resulting alkalosis from dosage errors when used in dialysate hemodialysis.

    The Fresenius Serial numbers and GranuFlo and NaturaLyte serial numbers for recalled Acid Concentrate fall within the following ranges:

    GranuFlo and NaturaLyte serial number 08-0231-4
    GranuFlo and NaturaLyte serial number  08-3251-9
    GranuFlo and NaturaLyte serial number 08-4231-0
     GranuFlo and NaturaLyte serial number 08-1231-3
     GranuFlo and NaturaLyte serial number 08-4223-7
     GranuFlo and NaturaLyte serial number 08-4323-5
     GranuFlo and NaturaLyte serial number 08-2201-5
      GranuFlo and NaturaLyte serial number 13-1251-1
      GranuFlo and NaturaLyte serial number 13-2251-0
      GranuFlo and NaturaLyte serial number 08-2301-3
      GranuFlo and NaturaLyte serial number 13-4123-1
      GranuFlo and NaturaLyte serial number 08-3231-1
      GranuFlo and NaturaLyte serial number 13-4325-1
      GranuFlo and NaturaLyte serial number 08-4325-1
      GranuFlo and NaturaLyte serial number 08-4123-1
      GranuFlo and NaturaLyte serial number 13-2231-2
      GranuFlo and NaturaLyte serial number 13-3251-9
      GranuFlo and NaturaLyte serial number 08-4230- 2
      GranuFlo and NaturaLyte serial number 13-4225-1
     GranuFlo and NaturaLyte serial number  08-3201-4
      GranuFlo and NaturaLyte serial number 13-3231-1
     GranuFlo and NaturaLyte serial number  08-1001-0
     GranuFlo and NaturaLyte serial number  08-1201-8
     GranuFlo and NaturaLyte serial number  08-1251-1
     GranuFlo and NaturaLyte serial number  08-1301-4
     GranuFlo and NaturaLyte serial number  08-2231-2
     GranuFlo and NaturaLyte serial number  08-2251-0
     GranuFlo and NaturaLyte serial number  13-4220-1
     GranuFlo and NaturaLyte serial number  08-4225-1
     GranuFlo and NaturaLyte serial number 08-2351-8
     GranuFlo and NaturaLyte serial number  08-3301-2
     GranuFlo and NaturaLyte serial number  13-2201-5

    NaturaLyte Recall Serial numbers (powder) Concentrate fall within the following ranges:

    GranuFlo and NaturaLyte serial number OFD1201-3B
    GranuFlo and NaturaLyte serial number  OFD1251-3B
    GranuFlo and NaturaLyte serial number OFD2123-3B
     GranuFlo and NaturaLyte serial number OFD2201-38
     GranuFlo and NaturaLyte serial number OFD2223-3B
     GranuFlo and NaturaLyte serial number OFD2220-3B
     GranuFlo and NaturaLyte serial number OFD2251-3B
      GranuFlo and NaturaLyte serial number OFD2301-3B
      GranuFlo and NaturaLyte serial number OFD2323-3 B
      GranuFlo and NaturaLyte serial number OFD3201-3B
      GranuFlo and NaturaLyte serial number OFD2325-3B
      GranuFlo and NaturaLyte serial number OFD3231-3B
      GranuFlo and NaturaLyte serial number OFD2231-3 B
      GranuFlo and NaturaLyte serial number OFD3251-3B
      GranuFlo and NaturaLyte serial number OFD3301-3B
      GranuFlo and NaturaLyte serial number OFD2225-3B
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