Since the inception of the Food and Drug Administration (FDA), people like you have trusted that the pharmaceutical products they purchase or have been prescribed were stringently tested and been found safe for consumption. Unfortunately, that is not necessarily the case.
Taking full advantage of the public’s need for new medicines and driven by profits, the pharmaceutical companies are pushing harder than ever before for quick FDA approval. They encouraged the passage of the Prescription Drug User Fee Act, which provides fast-tracking drug approval provisions that have resulted in a flood of new drugs available to the consumers since 2000.
This fast-track, minimal quality check approach has allowed pharmaceutical companies to enjoy some of the largest profits in the world, all while many people who use their products are suffering from serious injuries or dying due to inadequate drug testing.
A Firm With The Resources And Dedicated Attorneys You Need Fighting For You
Harrison Davis law firm has a national reputation, the skilled legal professionals and the financial resources to fight the big pharmaceutical companies and bring them to justice. We have successfully handled numerous large-scale pharmaceutical litigation cases — where dangerous drugs have caused serious injuries, disability, or the loss of a loved one — throughout the United States. Due to the significant portion of medical device and pharmaceutical litigation we handle, we staff a legal nurse consultant who works with the clients and attorneys to prepare the cases.
Our Current Pharmaceutical Cases
We handle all types of pharmaceutical litigation, and are currently investigating or pursuing claims involving:
- Actos ®
- Axiron and other low testosterone drugs
Our lawyers have years of experience and understanding of technological advances needed to investigate and handle large numbers of cases involving these drugs and other products manufactured by the pharmaceutical companies.
Past Pharmaceutical Litigation
Past pharmaceutical litigation cases we have handled have involved drugs and conditions such as:
Methadone Deaths Lawsuit
Methadone misinformation, physician errors and pharmacy negligence have caused Methadone deaths nationwide. Harrison Davis Trial Lawyers represent families of Methadone victims from California to Maine, and had the first Methadone litigation team in the country.
Experienced National Methadone Litigation Attorneys
The law firm of Harrison Davis has filed suit against both manufacturers of Methadone. We have traveled to all corners of the country to fight for our clients.
Some of our clients are founding members of Methadone organizations such as MothersAgainstMedicalAbuse.org and HARMD.org. We are committed to aggressively pursuing those who have caused Methadone deaths throughout the United States. Our staff includes a legal assistant who was a licensed nurse, and helps in review medical records as well as a licensed private investigator who assists in researching drug manufacturers, pharmacies and other health care providers involved in our cases.
Paxil is an antidepressant drug manufactured by GlaxoSmithKline (Glaxo or GSK). Paxil is used to treat anxiety, depression and obsessive-compulsive disorders. This drug has been scientifically linked to these unfortunate injuries in newborns.
Experienced Texas Pharmaceutical Litigation Attorney
Harrison Davis Trial Lawyers are dedicated to assisting injured victims and their families in pharmaceutical litigation, including injuries or wrongful death resulting from Paxil, especially pregnant woman who used this dangerous drug and had a child born with a defective heart or lung damage, or a child who died shortly after birth.
Paxil may cause newborn babies to suffer seizures, which may be deadly to the infant. The likelihood of this type of seizure may increase for infants whose mothers took Paxil during the last trimester of their pregnancy.
If you took Paxil during your pregnancy and you lost a child, or your baby was born unhealthy, you should consult an experienced Paxil lawsuit attorney.
Trasylol ® Lawsuit
Trasylol ® is a drug used to reduce blood loss and the need for blood transfusions in patients undergoing heart bypass and related surgeries. Studies have linked Trasylol ® to an increased risk of serious kidney damage, heart attacks, and strokes. The FDA issued an alert based on studies performed on Trasylol ® which showed an increased risk for these injuries.
Experienced Texas Pharmaceutical Litigation Lawyer
Whether you are seeking to bring a claim from serious liver damage or other injuries from Trasylol ® or a lawsuit for wrongful death, we have the resources and experience to provide you with aggressive representation designed to get results. In order to assist you and keep open the lines of communication with you, Harrison Davis staffs a legal nurse consultant who will work with you and our pharmaceutical litigation attorneys to prepare the cases.
Vioxx is a nonsteroidal, anti-inflammatory drug used in the treatment of arthritis, osteoarthritis, acute adult pain, and other disorders. This drug has been associated with an increased risk of serious side effects such as strokes, heart attacks, and cardiovascular problems.
Vioxx was pulled off the shelves by Merck, its maker, on September 30, 2004. Since that time, there have been numerous lawsuits filed across the country.
We reviewed approximately 700 cases and are honored that so many sought our advice. We are proud of our efforts on behalf of our clients and gratified by the potential financial recoveries and personal satisfaction we believe we have achieved for them. Of course, not every case is successful and past successes do not guarantee the outcome in future cases. The results in each case are dependent on the facts in each circumstance.
Hydroxycut is a supplement that is advertised to aid weight loss, increase energy and enhance metabolism. Unfortunately, Hydroxycut has been linked to liver damage and other health problems. If you have taken Hydroxycut and have suffered from liver damage or liver failure contact
On May 1, 2009, the U.S. Food and Drug Administration (FDA) warned consumers to immediately stop using Hydroxycut, manufactured by Iovate Health Sciences, Inc., of Oakville, Ontario and distributed by Iovate Health Sciences USA Inc. of Blasdell, New York. Iovate has agreed to recall Hydroxycut from the market.
Hydroxycut Can Cause Serious Health Issues
The FDA has already received 23 reports of serious health problems ranging from jaundice and elevated liver enzymes, an indicator of potential liver injury, to liver damage requiring liver transplant. There has been one death due to liver failure caused by Hydroxycut has been reported by the FDA. Other health issues include seizures, cardiovascular disorders, and rhabdomyolysis, a type of muscle damage that can lead to other serious health problems such as kidney failure.
Symptoms of liver injury include nausea, vomiting, light-colored stools, excessive fatigue, weakness, stomach or abdominal pain, itching and loss of appetite.
If you have taken any of the following products and has suffered liver damage, seizures, cardiovascular disorders or rhabdomyolysis, call today:
- Hydroxycut Regular Rapid Release Caplets
- Hydroxycut Caffeine-Free Rapid Release Caplets
- Hydroxycut Hardcore Liquid Caplets
- Hydroxycut Max Liquid Caplets
- Hydroxycut Regular Drink Packets
- Hydroxycut Caffeine-Free Drink Packets
- Hydroxycut Hardcore Drink Packets (Ignition Stix)
- Hydroxycut Max Drink Packets
- Hydroxycut Liquid Shots
- Hydroxycut Hardcore RTDs (Ready-to-Drink)
- Hydroxycut Max Aqua Shed
- Hydroxycut 24
- Hydroxycut Carb Control
- Hydroxycut Natural
Pharmaceutical Companies Motivated by Profits, Not Safety
Taking full advantage of the public’s need for new medicines and driven by profits, the pharmaceutical companies are pushing harder than ever before to get their drugs and supplements on the market. The manufacturer of Hydroxycut sells over 1,000,000 bottles annually. Even though many people are suffering from serious injuries or dying due to inadequate drug testing, the pharmaceutical companies now enjoy some of the largest profits in the world.
Byetta® is a drug taken by diabetic patients that has been linked to severe pancreatic problems. If you have taken Byetta® and have suffered acute pancreatitis, a swelling of the pancreas that may cause nausea, vomiting and abdominal pain, contact our Byetta®lawyers today at 866-539-2648 for a free case evaluation. In October 2007, the Food and Drug Administration (FDA)issued a public health alert after receiving reports that as many as 30 patients had developed significant pancreatic problems after using Byetta®. These problems included acute pancreatitis, which if not treated could be fatal. However, even if caught and treated, the patient could face life-long medical treatment. FDA Focuses on Byetta® Deaths Recently, the FDA reported six additional cases of patients who took Byetta®and suffered hemorrhagic or necrotizing pancreatitis. Of the six new cases, two patients died. We have asserted on behalf of our clients that the manufacturers’ warnings were deficient. The FDA is now working with the manufacturers of Byetta to strengthen the warnings on the label. Since the inception of the FDA, people like you have trusted that the pharmaceutical products that they purchase or that have been prescribed were stringently tested and been found safe for consumption. Unfortunately, that is not necessarily the case for the consumer ingesting some pharmaceutical drugs or the doctors prescribing them. Pharmaceutical Companies Motivated by Profits, not Safety Taking full advantage of the public’s need for new medicines and driven by profits, the pharmaceutical companies are pushing harder than ever before for quick FDA approval. The manufacturer of Byetta®had sales of over $600 million last year alone. Even though many people are suffering from serious injuries, the pharmaceutical companies now enjoy some of the largest profits in the world.
We’re Here to Help.
Harrison Davis Steakley Morrison Jones, P.C., a Texas law firm with a national reputation, has the expertise and the financial resources to fight the big pharmaceutical companies and bring them to justice. We have successfully handled numerous personal injury and product liability claims in Texas and throughout the United States, including cases dealing with drug companies and pharmaceutical litigation. Our Byetta® lawyers are available to answer your questions and pursue any claim you might have.
For a long time, women had been advised by the medical community that hormone therapy after menopause could reduce their chances of heart disease – and even keep certain effects of aging at bay.
It was all good news, until studies proved otherwise, linking combined estrogen-progestin drugs – like PremproTM, from Wyeth Pharmaceuticals – to an increased risk of breast cancer, stroke, heart attack, blood clots in legs and lungs, and ovarian and endometrial cancer.
As a result, many medical organizations have issued warnings urging women to avoid using combined estrogen-progestin drugs, or to use them in the lowest possible doses for the shortest possible time.
After some early false starts, litigation involving Prempro is now gaining steam, and HDSMJ Trial Lawyers represent women who have taken the drug and suffered devastating consequences. Our work has given us insight and experience into these troubling cases – and put us in position to help.
For additional information about Prempro, or to discuss the wrongful death of a loved one due to Prempro, please call an experienced personal injury attorney who is familiar with handling pharmaceutical lawsuits at 866-539-2648 (toll free) or 254-633-2813. If you prefer, you can fill out our intake form and we will contact you.
Contact An Experienced Pharmaceutical Litigation Lawyer
Call the lawyers at Harrison Davis at 254-761-3300 (Waco area) or 409-753-0000 (Beaumont area) to arrange a consultation about your dangerous drug case. We serve clients in Texas and across the nation.