Are you over 18 and want to see adult content?
More Annotations
A complete backup of bryhercampsite.co.uk
Are you over 18 and want to see adult content?
A complete backup of fabricegueroux.com
Are you over 18 and want to see adult content?
A complete backup of brunata-metrona.de
Are you over 18 and want to see adult content?
A complete backup of biologiadinamiica.blogspot.com
Are you over 18 and want to see adult content?
Favourite Annotations
A complete backup of www.coedcherry.com
Are you over 18 and want to see adult content?
A complete backup of travestismexico.com
Are you over 18 and want to see adult content?
A complete backup of www.artofzoo.com
Are you over 18 and want to see adult content?
A complete backup of www.topboard.org
Are you over 18 and want to see adult content?
A complete backup of www.thecandidforum.com
Are you over 18 and want to see adult content?
A complete backup of www.www.streamray.com
Are you over 18 and want to see adult content?
A complete backup of www.www.zenra.net
Are you over 18 and want to see adult content?
Text
(888) 994-5118
* News
* Lawsuits
*
* Actemra Lawsuit
* 3M Combat Arms Earplugs Lawsuit * Hernia Mesh Lawsuit * Hip Replacement Lawsuits * IVC Filter Lawsuit* Invokana Lawsuit
* Monsanto Roundup Lawsuit* Nexium Lawsuit
* Onglyza Lawsuit
* Risperdal Lawsuit
* Valsartan Lawsuit
* Zantac Lawsuit
*
Free Case Review
If you or a loved one has been injured as a result of a prescription medication or defective medical device, you may be entitled to faircompensation.
(888) 994-5118
* Recalls
*
* ConforMIS Knee Recall * Cook Medical Beacon Tip Catheter Recall * MicroPort Profemur Modular-Neck Hip Recall * OMNI Apex K2 Hip Implant Recall * Stryker Hip Replacement Recall * Transvaginal Mesh Recall* Valsartan Recall
*
Free Case Review
If you or a loved one has been injured as a result of a prescription medication or defective medical device, you may be entitled to faircompensation.
(888) 994-5118
* Drugs & Devices
* Manufacturers
* Health Info
*
* Drug Interactions
* Drug Side Effects
* Food and Drug Administration * Men: Health Information * Women: Health Information * Seniors: Health Information * Thrombotic Thrtombocytopenic Purpura*
Free Case Review
If you or a loved one has been injured as a result of a prescription medication or defective medical device, you may be entitled to faircompensation.
(888) 994-5118
* Legal Library
Dangerous Drugs And Medical Devices * RX Injury Help provides you with the latest information and news on dangerous drugs and medical devices. * Our team can assist you in making sense of the complications you are experiencing and help you find an attorney. Harmed by a Prescription Drug or Medical Device? Private Case Review - _(888) 994-5118_ Private Case Review_Were you or a loved one harmed by a prescription drug or medical device? Get a free case review._Connect with:
* Full name*
* Telephone*
* Email*
* Tell us about your case...*
*
*
*
*
*
*
*
* Phone
This field is for validation purposes and should be left unchanged. I agree to the Privacy Policy and Terms of Servicesand to receive
future email communications. DEFECTIVE DRUGS AND MEDICAL DEVICES ON THE U.S. MARKET Every year, billions of Americans are prescribed drugs and medicaldevices , all of
which are intended to make their lives better. While that’s exactly what these products do for most people, thousands of patients are injured every year as a result of dangerous drugs and devices. Unfortunately, most medications, surgical tools, and medical implants are not subjected to enough pre-market scrutiny to completely ensure their safety. And all too often, the dangerous side effects associated with particular drug or medical device are not revealed until the product has been used in thousands of patients. Ongoing Pharmaceutical Warnings & Litigation * Monsanto Roundup Lawsuit Monsanto is facing thousands of Roundup lawsuits, all of which were filed on behalf of individuals diagnosed with non-Hodgkin’s lymphoma and related... Read More* Zantac Lawsuit
Federal health regulators recently warned that prescription and over-the-counter versions of Zantac (ranitidine) had tested positive for the presence ... Read More * Firefighter Foam Lawsuit A growing number of firefighter foam lawsuit filings claim the 3M Company and other manufacturers failed to warn that exposure to PFAS (PFOA and PFOS)... Read More * 3M Combat Arms Earplugs Lawsuit A 3M Combat Arms Earplugs lawsuit may be an option for military veterans who suffered hearing loss or tinnitus (ringing in the ears) because of defect... Read More * Hernia Mesh Lawsuit Filing a hernia mesh lawsuit may be an option for patients who experienced severe complications, including hernia recurrence and the need for revision... Read More * Hip Replacement Lawsuits Patients who are recommended artificial hip replacement surgery are generally hoping to experience increased mobility and less pain. Unfortunately for... Read More* Onglyza Lawsuit
Potentially hundreds of Type 2 diabetes patients could opt to file an Onglyza lawsuit, following the release of a clinical trial that tied saxagliptin... Read More* Nexium Lawsuit
Nexium, a proton pump inhibitor (PPI) used to treat GERD and other gastrointestinal issues, has been linked with a number of serious complications, ... Read More* Prilosec Lawsuit
Prilosec lawsuits are being investigated over kidney disease, heart attacks and other complications that might re associated with use of the popular... Read More* PrevAcid Lawsuit
Filing a PrevAcid lawsuit could be an option for individuals who suffered complications allegedly related to use of the Proton Pump Inhibitor (PPI).... Read More * IVC Filter Lawsuit Scores of people have filed IVC Filter lawsuits against C.R. Bard Inc. and other companies that manufacture and market retrievable inferior vena cava ... Read More* Risperdal Lawsuit
Following a growing body of evidence that ties a popular Johnson & Johnson medication to gynecomastia, a condition referring to male breast growth... Read MoreDANGEROUS DRUGS
The U.S. Food & Drug Administration (FDA) requires pharmaceutical companies to take extensive steps to ensure their medications do not place patients at risk for serious adverse events. Prior to FDA approval, all prescription drugs must endure a clinical trial process meant to establish a product’s safety, toxicity, side effects and efficacy. Once on the market, drug makers are required to disclose any serious adverse events associated with a particular drug to theagency.
Unfortunately, this system isn’t fool proof, and latent side effects can reveal themselves in the years after a medication is brought to market. When this occurs, the FDA can order drug manufacturers to add new information to their product labels to inform doctors and patients about associated risks. The FDA’s most serious type of label warning is known as a “Black Box.” Black Box warnings are usually added to a medication’s label when it has the potential to cause serious, life-threatening side effects, or when the frequency or severity of such side effects can be reduced through proper use of the medication. In the most serious situations involving a defective drug, the FDA can ask a manufacturer to pull a product from the market. Drug recalls can be issued for a number of reasons, including the emergence of dangerous side effects, or manufacturing defects that pose a risk ofharm to patients.
DEFECTIVE MEDICAL DEVICES In recent years, dangerous medical devices, including transvaginal mesh, metal hip implants, stents and cardiac defibrillators, have caused harm to thousands of patients. Shockingly, many of these devices were never subjected to human clinical trials prior to coming to market. As a result, design defects, manufacturing issues, and other problems that put the public at risk were not realized until they had been used in thousands of patients. Certain new medical devices can be cleared for sale through the FDA’s 510(k) program which allows a product to avoid human clinical trials if a manufacturer can demonstrate that it is “substantially equivalent” to a product already on the market. In 2011, an analysis conducted by the Institute of Medicine concluded that the 510(k) process was “flawed” and could not ensure public safety. The authors of the report suggested the FDA develop an “integrated premarket and postmarket regulatory framework” to better improve its oversight of new medical devices. FDA DRUG AND DEVICE RECALLS Recent data indicates that FDA recalls are surging. According to the agency, 2012 saw nearly 500 pharmaceutical product recalls . In 2013, the number spiked to over 1,200. By mid-2014, more than 800 drug and device recalls had already been recorded by the FDA. The FDA classifies drug and medical device recalls according to theirseriousness:
* Class I Recall – A reasonable probability exists that the use of a drug or device will cause serious adverse health consequences ordeath.
* Class II Recall – The medical product in question will cause temporary or medically reversible adverse health consequences, or the probability of serious adverse health consequences is remote. * Class III Recall – The drug or devices is not likely to cause adverse health consequences. DRUG AND DEVICE LAWSUITS When a drug or medical device causes harm to consumers, those affected may be able to obtain compensation for their injury-related damages by filing a product liability lawsuit against the product’s manufacturers, distributors and marketers. In cases where consumers have suffered very similar injuries, a class action lawsuit may provide an adequate legal avenue for obtaining such compensation. But in most cases involving dangerous drugs and medical devices, the harm done is significant and varies from plaintiff to plaintiff. In these instances, filing an individual lawsuit will best serve the interests of someone who was hurt by a defective drug or device. Sometimes, a dangerous medical product can become the subject of hundreds – if not thousands – of legal claims. When this occurs, state and federal courts can create consolidated litigations to aid in the efficient prosecution of these lawsuits. On the federal court level, such proceedings are known as multidistrict litigations. State courts use a number of names, including multicounty litigations and mass tort proceedings. Any of these consolidated litigations allow lawsuits involving the same product and similar allegations of fact to go through coordinated pretrial proceedings, including discovery and motions practice. The aim of such a proceeding is to preserve the resources of the courts, parties and witnesses. Despite the consolidation of the cases, each lawsuit on the docket continues to maintain its own identity and will be judged according to its own merits.Page Sources
* FDA. (August 2014) “Drug Safety and Availability” http://www.fda.gov/drugs/DrugSafety/default.htm * FDA. (June 2014) “510 K Clearances” http://www.fda.gov/medicaldevices/productsandmedicalprocedures/deviceapprovalsandclearances/510kclearances/default.htm * Institute of Medicine. (July 2011) “Medical Devices and the Public Health: The FDA 510(k) Clearance Process at 35 Years. Instituteof Medicine”
http://www.iom.edu/Reports/2011/Medical-Devices-and-the-Publics-Health-The-FDA-510k-Clearance-Process-at-35-Years.aspx * Regulatory Focus. (August 2014) “Number of Drug Recalls Surges at FDA, Led by Mid-Level Concerns” http://www.raps.org/Regulatory-Focus/News/2014/08/11/20005/Number-of-Drug-Recalls-Surges-at-FDA-Led-by-Mid-Level-Concerns/ * FDA. (May 2010) “FDA 101 – Product Recalls” http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm049070.htm About RX Injury Help Our goal at RX Injury Help is to connect our readers with the tools to protect themselves against defective drugs and medical devices on the market today. To do that, the online resource guide provided by the attorneys at Bernstein Liebhard LLP offers routinely updated medical information on these dangerous products, as well as relevant updates in the growing litigation of lawsuits that have been filed against their manufacturers. If you or someone you love has been injured as a result of a defective medical device or medication on the market today, our Firm can help you seek compensation for damages these products may have caused you.*
*
*
Recent News
*
Firefighter Foam Lawsuits Mount, as Filings Exceed 800 in Federal Multidistrict LitigationNovember
19, 2020
*
FDA Announces Campaign to Publicize Allergan Breast Implant RecallJune
2, 2020
*
Zantac Lawsuits Move Forward, as Federal Litigation Convenes InitialConference
June
2, 2020
*
California Appeals Court Set to Hear Oral Arguments in First MonsantoRoundup Verdict
June
1, 2020
*
FDA Seeks Metformin Recalls after Tests Confirm NDMA ContaminationJune
1, 2020
* News
* Drugs & Devices
* Lawsuits
* Recalls
* About Us
* Sitemap
Private Case Review_Were you or a loved one harmed by a prescription drug or medical device? Get a free case review._* Full Name*
* Telephone*
* Email*
* Tell me about your case...*
*
*
*
*
*
*
*
* Phone
This field is for validation purposes and should be left unchanged.Follow Us:
BERNSTEIN LIEBHARD LLP10 East 40th Street
New York, NY 10016
Phone: (888) 994-5118 Attorney Advertising: Prior outcomes do not guarantee similar results. Your use of our Web site or its facilities constitutes your acceptance of the Terms of Use and Privacy Policy.
2020 RXInjuryHelp.com. All Rights Reserved. ShareThis Copy and PasteDetails
Copyright © 2024 ArchiveBay.com. All rights reserved. Terms of Use | Privacy Policy | DMCA | 2021 | Feedback | Advertising | RSS 2.0