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Benicar Gastrointestinal Injury Attorneys

Written by lisaspitzer on . Posted in Benicar Villous Atrophy Attorneys, Drug Lawsuits, Drug Warnings, Drugs and Devices lawsuit attorneys

Benicar Gastrointestinal Injury  Lawyers

Filing Benicar Intestinal Injury Lawsuits

What Is Benicar?

Benicar is a  high blood pressure medication.   Benicor has been  linked to severe intestinal injury, intestinal damage, chronic diarrhea, malnourishment and severe weight loss. Seniors are the largest population receiving prescriptions for Benicar and are the most vulnerable to sever injury from Benicar.

FDA Benicar Warnings

The FDA   has warned patients and doctors that Benicar (olmesartan medoxomil) may cause a severe gastrointestinal (GI) problem called Villous Atrophy. Benicar causes the intestines to lose the texture and makes it difficult to absorb nutrients. This leads to malnutrition which and other digestive problems. This is very dangerous for seniors and can lead to death or hospitalization because of dehydration, chronic diarrhea and malnutrition. Villous Atrophy can result in limiting  the ability of the small intestines to absorb nutrients from food. At the most serious stages,  villous atrophy  causes  damage to the intestinal crypts, which is the intestinal lining that surround the villi.

Benicar Villous Atrophy Lawyers Filing Benicar Lawsuits

Benicar has been used by millions of people. Benicar warnings did not adequately disclose  how serious the side effects form this medication is. The Benicar lawyers at Class Action Lawyer Network are  filing claims for individuals who have experienced chronic diarrhea, sprue-like enteropathy or villous atrophy after using Benicar.  

Resperdal Class Action Lawyers, Resperdal Lawsuit Helpline

Written by lisaspitzer on . Posted in Alabama Multidistrict Litigation Lawyers, Arizona Multidistrict Litigation Lawyers, Arkansas Multidistrict Litigation Lawyers, California Multidistrict Litigation Lawyers, Colorado Multidistrict Litigation Lawyers, Delaware Multidistrict Litigation Lawyers, Drug Lawsuits, Florida Multidistrict Litigation Lawyers, Georgia Multidistrict Litigation Lawyers, Indiana Multidistrict Litigation Lawyers, Kansas Multidistrict Litigation Lawyers, Massachusetts Multidistrict Litigation Lawyers, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Missouri Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, New Jersey Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, New York Multidistrict Litigation Lawyers, Ohio Multidistrict Litigation Lawyers, Resperdal lawsuits

Risperdal Lawyers Filing Gynecomastia Lawsuits

If you or a loved one was prescribed Risperdal as a teenage boy and now have enlarged breasts, developed female type breasts and /or been diagnosed with Gynecomastia,  contact Class Action Lawyer Network  Risperdal Injury Lawyers today to discuss your options in a Risperdal lawsuit.

Our Resperdal lawyers are reviewing cases for young  boys diagnosed with gynecomastia or male breasts after using Risperdal. Problems may result in:

  •     Breast Growth Among Boys
  •     Puffy Nipples or Enlarged Nipples
  •     Galactorrhea (production of milk from breasts)
  •     Painful Breasts or Nipple Discharge
  •     Mastectomy or Gynecomastia Surgery to Remove Male Breasts
  •     Gynecomastia (growth of male breasts, which may be painful or tender)

If your son has been diagnosed with Gynacomastia call our Resperdal helpline and speak to our trained medical social worker today.

Rispedral Side Effects In Male Children

Risperdal (risperidone) is an antipsychotic manufactured by Johnson & Johnson. It  was originally approved by the FDA for use for adults with schizophrenia.  Risperdal has also been widely used by children for bi-polar disorders, autism, irritability, aggression and behavior disorders.

Speak To A Risperdal Lawyer

The Riserdal  lawyers are reviewing cases for Risperdal breast growth among boys.

Children Are Being Injured By Risperdal

Lawsuits are being filed  for  abnormal development of large mammary glands among boys and adolescents, resulting in breast development.  Surgery has been  necessary to remove the breasts caused by the Risperdal gynecomastia.  This has caused emotional trauma for boys and young adult males and some incidents of suicide. Parents throughout the United States are pursuing a Rispedal lawsuit on behalf of kchildren  who developed breasts on Risperdal.

Lawsuits allege that Johnson & Johnson failed to adequately research the effects of their medication or warn about the connection between Risperdal and breast growth.

Risperdal Lawsuit Update

Although Resperdal is not currently an MDL, settlements for Risperdal breast growth have been reached by Johnson & Johnson in lawsuits bellwether trials where a number of cases are presented to juries to test the potential settlements and outcomes. Do not delay. Call no to discuss a Resperdal lawsuit.
 

 

 

Tylenol Lawsuits For Liver Damage Multi District Litigation Consolidation

Written by lisaspitzer on . Posted in Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuit News

Class Action Lawyer Network Tylenol liver damage lawyers report that tylenol liver failure  lawsuits will be centralized in a multidistrict litigation in Pennsylvania  Federal Court,

Tylenol Lawsuit Consolidated In Pennsylvania

All Tylenol liver damage  lawsuits filed against McNeil-PPC, Perrigo, Novartis and others have  been consolidated under multidistrict litigation in the Eastern District of Pennsylvania to facilitate the pretrial proceedings for  these cases

The U.S. Judicial Panel on Multidistrict Litigation (MDL) has ruled that 27 Tylenol liver damage lawsuits filed against  the manufacturers of tylenol related products will be consolidated under Tylenol Lawsuit MDL 2436 in the Eastern District of Pennsylvania.
All of the cases conslidated in MDL 2436 involve liver damge related injury or wrongful death. These  claims alledged that use of over-the-counter (OTC) Tylenol (generically acetaminophen) caused the victims to suffer from serious liver damage or  liver failure.

Call Class Action Lawyer Network's Tylenol Liver Damage Lawsuit Department Today.

The MDL  Judicial Panel feel that the  allegations of liver injury associated with the use of OTC Tylenol, the cases share factual issues regarding the design, manufacture, labeling, marketing and sale of Tylenol. Consequently, the centralization of these cases in the Eastern District of Pennsylvania would eliminate duplicative discovery facilitate the proceedings.

Class Action Lawyer Nwtwork  attorneys  have decades of collective dangerous drig  and device lawsuit experience,

If you or a loved one has suffered liver damage or liver failure while taking Tylenol call us to discuss a Tylenol liver damage lawsuit or Tylenol liver failure lawsuit.

Tylenol Liver Damage Lawsuit Criteria

Have you or a loved one been diagnosed with Liver Failure, liver damage from taking Tylenol? Do you have a clean medical history of any liver problems such as: Liver cancer, liver mass, Autoimmune Hepatitis, Alcoholic Cirrhosis,Primary Sclerosing Colangitis, Wilson’s disease, or Budd Chiari Syndrome  and yet,  now have liver damage after taking Tylenol?
Our Tylenol liver damage lawyers are accepting Tylenol liver failure cases  if  the liver failure results in hospitalization, liver transplant, or liver transplant waiting list or death. If you meet this criteria we would like to speak to you regarding filing a Tylenol liver damage or liver failure case.

Class Action Lawyer Network  accepting Tylenol liver damage lawsuts  or liver failure  lawsuits for individuals who experienced  any of the following within a week after taking  an acetaminophen medication such as Tylenol:

  •     Hospitalization Due to Severe Liver Injury or Liver Problems
  •     Diagnosed with Liver Failure
  •     Liver Transplant or Placed on Waiting List for Liver Transplant
  •     Death from Liver Failure

Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuits

Written by lisaspitzer on . Posted in Class MDL Class Action News, Drug Lawsuits, Drug Warnings, Florida Multidistrict Litigation Lawyers, Tylenol Liver Damage Lawsuits, Tylenol Liver Damage Lawyers, Tylenol Liver Failure Lawsuit News

Tylenol Liver Damage Lawyers of Class Action Lawyer Network Are Filing  Nationwide Tylenol Liver Failure  Lawsuits

The Tylenol liver damage lawyers of Class Action Lawyer Network are accepting nationwide lawsuits for you , your loved one or child who has suffered liver damage from Tylenol. Our Tylenol Liver Damage Helpline is helping victims of liver damage from Tylenol.

The Tylenol Liver Damage Facts

It is now known that Tylenol can result in acute liver failure and death. Statistics have shown taht  Tylenol is the leading cause of acute liver failure in the United States; nearly half of U.S. incidents of acute liver failure are caused by  taking too much acetaminophen. Acetaminophen is anactive ingredient in Tylenool.  Call our Tylenol liver failure  helpline to speak to lawyers help who are filing liver damage lawsuits for victims  of Tylenol who have been diagnosed with Tylenol liver damage or failure.

Symptoms Of Liver Damage

  •     Discolored skin and eyes that appear yellowish
  •     Abdominal pain and swelling
  •     Itchy skin that doesn't seem to go away
  •     Dark urine color
  •     Pale stool color
  •     Bloody or tar-colored stool
  •     Chronic fatigue
  •     Nausea
  •     Loss of appetite
     

Class Action lawyers For Tylenol Liver Failure

  • Tylenol's manufacturer lowered the safe maximum dosage from 4000 mg to 3000 mg per day.
  • Tylenol liver Failure Helpline lawyers are fighting for justice for victims of tylenol Llver damage and liver failure
  • If you or a family member has  been diagnosed with  severe liver damage or acute liver failure from excessive use of Tylenol or other over the counter medications that contain acetaminophen the Tylenol liver damage helpline is here for you.
  • People who have experienced acute liver failure or serious liver damage related to Tylenol use may file a Tylenol liver damage lawsuit  lawsuit

Tylenol Lawsuit Multi District Litigation Has Formed

The  Tylenol injury lawsuits have now been centralized as part of multidistrict litigation in federal district court in Pennsylvania.

The lawsuits filed alledge a strong link between acetaminophen and liver failure. Lawsuits are  alleging that acetaminophen in various Tylenol products was responsible for users’ severe liver damage.

Tylenol Liver Damage Lawsuit Criteria

Have you or a loved one been diagnosed with liver Failure, liver damage or a severe liver injury from taking Tylenol?

Our Tylenol liver damage lawyers are accepting Tylenol liver failure if  the liver failure results in hospitalization, liver transplant, liver transplant waiting list or death. If you meet this criteria we would like to speak to you regarding filing a Tylenol liver damage lawsuit where there is no prior medical history of liver damage or any liver damage related medical conditions.
 

Call our Tylenol Liver Damage Helpline to file your liver damge lawsuit.

DePuy Hip Replacement Lawsuit News, Hip Replacement Lawyers Filing Lawsuits

Written by lisaspitzer on . Posted in Class MDL Class Action News

DePuy Hip Replacement Lawsuit Update

DePuy ASR lawsuit claims stemming from the 2010 DePuy hip recall continue to move forward in courts throughout the country . According to documents filed in California’s San Francisco Superior Court on April 25th, a Plaintiff who had been seeking an expedited trial of her DePuy hip lawsuit is voluntarily seeking dismissal of the case. (Tilman v. DePuy Orthopaedics, Inc., et al., No. CGC11508806; Calif. Super. Ct., San Francisco).

This news is particularly interesting as when a case is voluntarily dismissed it is often an indication that the parties have come to an agreement. 

DePuy ASR Hip Lawsuits Lawyers Filing DePuy Lawsuits

Court records indicate that there are more than 10,000 DePuy ASR hip lawsuits currently pending in courts throughout the U.S. The DePuy hip recall was announced after the metal-on-metal hip implants were found to be failing in an unacceptably high number of patients. The U.S. Food & Drug Administration (FDA) is now reviewing the safety of all metal hip implants, over fears that the devices can shed dangerous amounts of metal debris into patient’s bodies, leading to premature failure of the hips and other serious complications. In January, the agency proposed a new regulation that would make such devices ineligible for the agency’s 510(k) clearance process, which allowed all-metal hips like the ASR hip to gain FDA approval without first undergoing human clinical trials. The FDA also advised doctors to test metal hip implant patients for elevated metal ion levels if they present with symptoms of a failing hip implant.*

The majority of DePuy hip lawsuits have been filed in a multidistrict litigation now underway in U.S. District Court, Northern District of Ohio. Court records indicate that the first trials in that litigation will begin this September. (In re: DePuy Orthopaedics, Inc. ASR Hip Implant Products Liability Litigation – MDL 2197) Two lawsuits have already gone to trial at the state level, one of which ended with a California Superior Court jury awarding the Plaintiff more than $8 million in damages. (Kransky v. DePuy, BC456086, California Superior Court, Los Angeles County) However, the jury hearing a second trial in Illinois state court found for DePuy. (Strum v. DePuy, 2011-L-9352, Circuit Court of Cook County) According to an April 16th report from The New York Times, documents submitted as evidence in both of those trials indicated that Johnson & Johnson and its DePuy Orthopaedics unit knew that the ASR was flawed years before the recall was announced, but did not disclose this information to the public or the medical community.**

Earlier this month, DePuy Orthopaedics announced it would end sales of metal-on-metal hip implants, citing recent FDA actions and decreased demand for the products, according to the New York Times. The sales suspension includes a metal-on-metal version of the company’s DePuy Pinnacle hip replacement system, which is also the subject of lawsuits.

If you have a faulty DePuy and have had revision surgery or have been told you need revision surgery call and speak to a hip replacement lawyer today.

Yaz Injury Lawsuit Alert, Yaz Lawyers Accepting Blood Clot Yaz Lawsuits

Written by lisaspitzer on . Posted in Drug Lawsuits, Drug Warnings

The Yaz warning date has been established as July of 2012 meaning that if you or a loved one has been injured by Yaz Birth control pills you may still be able to file your Yaz lawsuit.

Class Action Lawyers For Yaz Injury are accepting Yaz lawsuits for:

  • Blood Clots
  • Stroke
  • Pulmonary embolism
  • Deep vein thrombosis
  • Death

Class Action Lawyer Network Yaz lawyers are not accepting Yaz Gallbladder injury cases. If you or someone you love has been harmed as a result of using Yaz, you need to contact our Yaz lawyers today. You need sound answers regarding your Yaz lawsuit in order to proceed properly, so contact our Yaz Lawsuit injury team today.

Yaz Injury Lawsuit Alert

There are approximately 1,100 YAZ lawsuits pending in federal court . Bayer's settlement payouts to settle Yaz and Yasmin claims who developed blood clots and other serious side effects from these birth control pills has now exceeded $1 billion. Do not be left out. File your Yaz lawsuit today.

Transvaginal Mesh Lawyers, Transvaginal Mesh Lawsuits

Written by lisaspitzer on . Posted in Medical Device Lawsuits

Transvaginal mesh lawyers of Class Action Lawyer Network are filing trnasvaginal mesh lawsuits for women nationwide. For Complications such as:

  •  
  •     Pain while urinating
  •     Prolapsed organs
  •     Urinary tract infections
  •     Bowel and Bladder problems
  •     Digestive problems
  •     Urination problems
  •     Painful sexual relations
  •     Urinary retention
  •     Relentless Infections
  •     Mesh erosion into the vagina, bladder, uterus, or intestines
  •     Lower back pain
  •     Severe relentless pain and suffering
  •     Mesh  erosion thru the vaginal wall

If you have experienced any of these side complications   being implanted with a transvaginal mesh call to be included in the nationwide mesh lawsuits. Do not wait. Time is running out.

Pelvic Mesh Lawyer, Pelvic Mesh Lawsuit

Written by lisaspitzer on . Posted in Class MDL Class Action News

Pelvic Mesh Lawyers of Class Action Lawyer Network are filing Pelvic Mesh Lawsuits as a part of the Vaginal mesh class action, multi district litigation. We are accepting most states nationwide.

Thousands of Women Are Suffering From the Failed Pelvic Mesh

Class Action Pelvic Mesh Lawyers are filing lawsuits for  women, nationwide hjat have a pelvice mesh, transvaginal mesh (TVT) ,vaginal mesh, bladder slings or transvaginal mesh patches

Pelvic Mesh Complications Are Horrific and Include:

  • Hemorrhage 
  • Urinary tract Infection
  • Chronic Pain 
  • Urinary problems
  • Digestive disconmfort
  • Bowel problems
  • Pelvic pain 
  • Bleeding
  • Recurrence of prolapse
  • incontinence 
  • Intense relentless pain
  • Lower back pain
  • Mesh erosion into vagina, bladder, intestines and uterus 
  • Perforations  of the bowel, bladder or blood vessels
  • Inability to have intimate relations
  • Decrease in quality of life due to discomfort and pain.

To file your pelvic mesh lawsuit call us today.

Dow Corning Breast Implant Removal Benefits Program Launched

Written by lisaspitzer on . Posted in Class MDL Class Action News

Dow Corning Settlement Trust as has announced a breast implant explant ( removal ) program for women as a part of the Dow Corning Class Action:

If you have filed and registered with Dow Corning regarding your Breast Implant Settlement Claim and need help with the new Breast Implant Explant Program, Dow Corning breast Implant explant lawyers are here to help women with Dow Corning claims.

Dow Corning Breast Implant Explant Letter

The following notice is being sent to all claimants who may be eligible for an Explant ( removal ) claim at the Settlement Facility Dow Corning Trust.

If you have received this letter you should contact Class Action Lawyer Network and speak to one of our Dow Corning Breast Implant Class Action lawyers today. You do not want to do this on your own. Our lawyers can help you with the process and make sure the claim is filed correctly at no cost to you.

If you choose to participate in the Explant Assistance Program, please note that these claims may take upto 60 days to process.
We recommend that you contact the Settlement Facility regarding your status before you schedule your surgery.
The Dow Corning Plan of Reorganization set June 2, 2014 as the deadline for eligible claimants to file a
claim for Explant Benefits.

Eligibility for compensation in Class 5 or 6 for Explant benefits is as follows:
1.Submission of the Proof of Manufacture form and written proof that you were implanted with a DowCorning breast implant
2.Submission of the Explant Claim form and written proof that your Dow Corning implants were removed by June 2, 2014. The Settlement Plan only offers the Explant benefit for the removal of Dow Corning breast implants. No other brands of implants are eligible for this payment.
3.Written proof that you did notreceive a silicone gel breast implant as a replacement after your Dow Corning breast implant was removed. If your Dow Corning breast implants are removed and replaced with a silicone gel implant, you will no longer qualify for payment. You may receive a replacement saline implant or other reconstruction. The Explant Assistance Program (EAP) is an option available to claimants who need financial help to have their implants removed. This program is designed for direct payment to the doctor and/or hospital that provides your explant service. This process may take several months to complete, so it is important to start this process well in advance of the June 2, 2014 deadline. If you wait until the filing deadline, your claim may be denied.
Eligible Claimants are responsible to keep the SF – DCT updated on any change in address and other contact information. Claimants whose contact information is not current may not receive payments for which they are eligible. For copies of the Claim Forms
 further information about the Explant program, EAP, or the deadline contact:
Claims Assistance www.sfdct.com Telephone: 866-874-6099,Email: info@sfdct.comFor additional assistance

The Claimants Advisory Committee:
http://www.tortcomm.org
NOTE: Your claim must meet the definition of an Eligible claim as set forth in Article V of Annex A to the Plan of Reorganization in order to be eligible for payment

 Dow Corning Breast Implant lawyers are here to  to protect your rights under this new program. There is no cost to you for a breast implant explant lawyer.

Mirena IUD Lawsuit Updates, Mirena IUD Lawyers

Written by lisaspitzer on . Posted in Alabama Multidistrict Litigation Lawyers, Alaska Multidistrict Litigation Lawyers, Arizona Multidistrict Litigation Lawyers, Arkansas Multidistrict Litigation Lawyers, California Multidistrict Litigation Lawyers, Class MDL Class Action News, Colorado Multidistrict Litigation Lawyers, Connecticut Multidistrict Litigation Lawyers, Delaware Multidistrict Litigation Lawyers, Florida Multidistrict Litigation Lawyers, Georgia Multidistrict Litigation Lawyers, Hawaii Multidistrict Litigation Lawyers, Idaho Multidistrict Litigation Lawyers, Illinois Multidistrict Litigation Lawyers, Indiana Multidistrict Litigation Lawyers, Iowa Multidistrict Litigation Lawyers, Kansas Multidistrict Litigation Lawyers, Kentucky Multidistrict Litigation Lawyers, Louisiana Multidistrict Litigation Lawyers, Maine Multidistrict Litigation Lawyers, Maryland Multidistrict Litigation Lawyers, Massachusetts Multidistrict Litigation Lawyers, Medical Device Lawsuits, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Mirena IUD Lawsuit, Mirena IUD Lawyers, Mississippi Multidistrict Litigation Lawyers, Missouri Multidistrict Litigation Lawyers, Montana Multidistrict Litigation Lawyers, Nebraska Multidistrict Litigation Lawyers, Nevada Multidistrict Litigation Lawyers, New Hampshire Multidistrict Litigation Lawyers, New Jersey Multidistrict Litigation Lawyers, New Mexico Multidistrict Litigation Lawyers, New York Multidistrict Litigation Lawyers, North Carolina Multidistrict Litigation Lawyers, North Dakota Multidistrict Litigation Lawyers, Ohio Multidistrict Litigation Lawyers, Oklahoma Multidistrict Litigation Lawyers, Oregon Multidistrict Litigation Lawyers, Pennsylvania Multidistrict Litigation Lawyers, Rhode Island Multidistrict Litigation Lawyers, South Carolina Multidistrict Litigation Lawyers, South Dakota Multidistrict Litigation Lawyers, Tennessee Multidistrict Litigation Lawyers, Texas Multidistrict Litigation Lawyers, Utah Multidistrict Litigation Lawyers, Vermont Multidistrict Litigation Lawyers, Virginia Multidistrict Litigation Lawyers, Washington DC Multidistrict Litigation Lawyers, Washington Multidistrict Litigation Lawyers, West Virginia Multidistrict Litigation Lawyers, Wisconsin Multidistrict Litigation Lawyers, Wyoming Multidistrict Litigation Lawyers

Mirena IUD lawyers are reviewing Mirena IUD lawsuit cases for uterine, abdomen and organ perforation. The Mirena IUD lawsuits have been consolidated in a multi district litigation. Now is the time to file your Mirena IUD lawsuits. If you cannot feel your Mirena string you must see a doctor. If the IUD has moved, gravitated out of position and you have a uterine or abdomen perforation you need to have your case reviewed immediatley by a Mirena IUD lawyer.

On  April 8, 2013 an order was  issued by the United States Judicial Panel ("USJP") on Multidistrict Litigation, MDL 2434* consolidating federal lawsuits alleging device migration and similar injuries caused by the Mirena IUD, manufactured by Bayer Healthcare Pharmaceuticals, in the United States District Court for the Southern District of New York.The first case management order in the consolidated litigation is  setting May 17, 2013 at 10:30 a.m. as the date for an Initial Conference. In advance of this conference, the court is requiring that Position Statements be filed by counsel no later than May 11, 2013.

As Yiou can see the Mirena IUD lawsuits are moving along. The most serious Mirena injuries of perforation are the ones being considered for the lawsuits at this time.

Please see this checklist and advise
Do I Have A Mirena IUD Lawsuit?  Criteria That Must Be Met To File Your Mirena IUD Lawsuit.
The Mirena IUD causes many symptoms and complications however, in order to file a Mirena IUD lawsuit your Mirena IUD lawyer will be looking for the following:
1. Mirena  IUD must be the product implanted
2. You must have gone to  your 4-6 week follow up appointment  and  your doctor has confirmed that your Mirena IUD  was properly implanted.
3. The Mirena IUD has perforated your uterus or other organ. The Mirena must have moved out of position, gravitated and has become embedded  in your uterus or an organ and/or  there is a perforation injury.
 4. This usually means the Mirena , needs to be or will be Laparoscopic surgically removed.
A lot of Mirena women either don’t go to follow up appointment or by the time they go to follow up the Mirena has already moved. If that happens this becomes a med mal issue and not a products issue. The statute of limitations starts to run when you knew Mirena perforated an organ.
Of course, consult with your doctor if you are experiencing any of the symptoms listed above

Symptoms of Abdomen Perforation:

  • Abdominal pain – severe
  • Chills
  • Fever
  • Nausea
  • Vomiting

Symptoms of Uterine Perforation

 

  •     Rigidity, bloating and pain in the abdominal area
  •     Nausea
  •     Fever
  •     Chills
  •     Vomiting
  •     Rapid heartbeat
  •     Lower abdominal pain
  •     Heavy vaginal bleeding
  •     Inability to locate the Mirena IUD string

You must see a physician immediately if you cannot feel the string and you are experiencing any of these symptoms.

You must speak to a lawyers to participate in ther Mirena IUD lawsuits.