Dangerous Pharmaceuticals LitigationOrtho Evra • Vioxx • Bextra Nationwide Toll Free: 1-866-795-7500 The Law Offices of Carolyn St. Clair, R.N., J.D.represents clients nationwide in lawsuits and individual claims regarding use of dangerous drugs leading to injury or wrongful death. Carolyn St. Clair is a registered nurse with heart surgical experience who understands the technical and medical aspects of medical litigation. She is also an experienced product liability attorney of 20 years who has successfully tried many jury cases and negotiated substantial settlements on behalf of clients. Pharmaceutical manufacturers have a duty to provide safe, tested products to the patients who need them. If drug company hides or diminishes a drug's negative side effects in the pursuit of profits, the corporation can be held liable for damages by the patients harmed. Our firm has assembled a team of physicians, lawyers and scientists who can investigate claims of dangerous drugs and pursue compensation for patients and surviving family members. Based in Houston, Texas, we represent clients throughout Texas and across the United States. Contact us for claims involving the following prescription medications:  Ortho Evra
The FDA in November 2005 warned that women using the patch are exposed to higher levels of estrogen than most birth control pills and approved updated labeling for Ortho Evra contraceptive patches. Ortho Evra users are exposed to approximately 60 to 180 percent more estrogen than if taking a typical birth control pill. Increased estrogen leads to increased risk of serious life-threatening complications, including reported young women with: blood clots, heart attacks, strokes, hemorrhage, pulmonary embolisms and DVT (deep vein thrombosis). The FDA has not taken the birth control patch off the market and women are still using the Ortho Evra patch today. If you or a loved one has used Ortho Evra birth control patch, you may be eligible for damages. Read more about Ortho Evra...
DEPO-PROVERA INJECTIONS (synthetic progesterone ) manufactured by Pfizer Depo-Provera has been utilized for four decades as birth control by injections taken every 3 months. Long-term use may lead to serious and irreversible bone density loss leading to osteoporosis, fractures, brittle teeth, spine injuries and hip injuries. In November of 2004, Pfizer was ordered by the FDA to add a serious black box warning to the Depo-Provera label about these adverse effects. Women with osteoporosis risk factors should consider other methods of birth control. All adolescents are considered to be a high risk group. Depo-Provera may reduce an adolescent's peak bone mass and increase the risk of fractures later in life. Register your Depo-Provera Injection Complaint If you or a loved one has received Depo-Provera injections and suffered from osteoporosis, hip or spinal fractures or bone mineral density loss, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. FOSAMAX (Alendronate Sodium) manufactured by Merck Fosamax and other bisphosphonates, Aldonate, Aredia and Zometa, have been shown to reverse bone loss and are prescribed to treat osteoporosis and Paget's disease. All have been linked to Osteonecrosis of the Jaw (ONJ) or Dead Jaw. A Fosamax user can contract ONJ after a tooth extraction, an injury to the jaw, or a bone which fails to heal properly. ONJ can spread and lead to a degeneration of the bone structure requiring antibiotic therapy or surgery. In September 2004, both Merck and the US Food and Drug Administration (USDA) released warnings about these possible problems and adverse effects of Fosamax. Register your Fosamax Complaint If you or a loved one has suffered adverse effects while taking Fosamax you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. KETEK (telithromycin) manufactured by Sanofi-Aventis Ketek is an antibiotic that kills bacteria causing sinus infections, bronchitis and pneumonia. Adverse effects may include severe liver damage and failure, hepatitis, jaundice, drowsiness, dizziness, blurred or double vision, and death. On June 29, 2006, the FDA issued a safety alert concerning an association with serious liver injury, liver failure and reported deaths, then announced new safety information to be added to Ketek's label. The FDA rejected the drug in 2001 and 2003, then requested further safety information before the drug was approved in 2004. The FDA is now investigating that approval process. Register your Ketek Complaint If you or a loved one has suffered adverse effects while taking Ketek, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. RISPERDAL, SEROQUEL AND ZYPREXA Risperdal, Seroquel and Zyprexa are antipsychotic drugs that treat schizophrenia. Risperdal (risperidone), manufactured by Jannsen Pharmaceutica, is linked to deaths of many patients. Adverse effects include diabetes rates 50% higher than patients using other drugs, strokes, Neuroleptic Malignant Syndrome (NMS) leading to muscle rigidity and irregular blood pressure and Tardive Dyskinesia, a central nervous system syndrome which causes twitching and involuntary movement of the arms, legs, face, and tongue. Seroquel (quetiapine fumarate) manufactured by Astra Zeneca, is linked to a much higher incidence of diabetes in patients compared to older anti-psychotic drugs. Astra Zeneca is accused of unethical marketing tactics and reporting practices. Zyprexa (olanzapine) manufactured by Eli Lilly & Company, is linked to higher incidence of diabetes, ketosis, hyperglycemia, pancreatitis and other elevated blood sugar disorders which may lead to coma and death. In 2003, the FDA ordered Eli Lilly to warn patients of this serious complications. Symptoms include stomach pains, followed by nausea and vomiting. Eli Lilly & Company has set aside nearly $700 million dollars to settle legal claims of qualifying Zyprexa patients. Register your Risperdal, Seroquel and Zyprexa Complaint If you or a loved one has suffered adverse effects while taking Risperdal, Seroquel and Zyprexa you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. TEQUIN (Gatifloxacin) manufactured by Bristol-Myers Squibb Tequin is an antibiotic that treats lung, sinus or urinary tract infections and certain sexually transmitted diseases caused by bacteria. On April 27, 2006 Bristol-Myers Squibb Co. announced that it would stop selling Tequin due to an association with potentially fatal blood-sugar disorders, hyperglycemia (high blood sugar) and hypoglycemia (low blood sugar). Potential adverse effects of Tequin include nausea, vomiting, stomach pain, diarrhea, dizziness and headache. Serious adverse effects include allergic reaction, seizures, confusion, tremors, hallucinations, depression, or suicidal thoughts. Register your Tequin (Gatifloxacin) Complaint If you or a loved one has suffered adverse effects while taking Tequin, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. TRASYLOL (Aprotinin) marketed by Bayer HealthCare Trasylol is used to prevent bleeding during heart surgery. The adverse effects associated are kidney failure, stroke, heart attack, heart failure and death. On September 30, 2006 Bayer admitted to the FDA that it failed to reveal the risks of adverse of stroke and death to officials. Other agents are available to prevent bleeding other than Trasylol and should be used. Several members of the advisory committee stated they were shocked Bayer did not inform the FDA of the adverse results and Bayer should be investigated. Register your Trasylol Complaint If you or a loved one has suffered adverse effects from being administered Trasylol during heart surgery, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation or call 713-228-5000 or toll free 1-866-795-7500. PAXIL (Paroxetine HCI) manufactured by GlaxoSmithKline Paxil and Paxil CR (controlled release) are antidepressants prescribed for depression, anxiety and stress. Paxil CR is indicated also for premenstrual dysphoria and panic disorders. Paxil is sold as Seroxat outside of the United States. On December 8, 2005, the FDA stated that exposure to Paxil in the first trimester of pregnancy may increase the risk for congenital and cardiac malformations. The FDA also indicated that physicians should encourage discontinuation of Paxil in pregnant patients. Additionally, Paxil has been associated with the adverse effects of suicide, aggressive violent behavior and withdrawal, particularly in children. Other adverse effects reported are pain, itching, hypertension, vertigo and nausea. Patients choosing to discontinue treatment should talk to their physician and taper the drug over time. The FDA warning recommends patients treated with antidepressants be observed closely for suicide. Register your Paxil Complaint If you or a loved one has suffered adverse effects while taking Paxil, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. RENU Moisturloc solution manufactured by Bausch & Lomb On May 15th, 2006, Bausch & Lomb announced that they would permanently withdraw ReNu with MoistureLoc. Bausch & Lomb Inc. delayed revealing that numerous blinding eye infections due to fungus were linked to the recalled ReNu with MoistureLoc contact lens cleaner, the Food and Drug Administration said. Bausch and Lomb did not previously report the number of fungal eye infections used with ReNu. Register your ReNu Complaint If you or a loved one has suffered adverse effects while using ReNu, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. VIAGRA, CIALIS, LEVITRA Viagra, Cialias, Levitra are drugs used to temporarily treat erectile dysfunction, but may contribute to sudden blindness. When the blood flow to the optic nerve is substantially blocked, a condition known as Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION) can cause permanent partial or total vision loss in one or both eyes. There are medical reports of vision loss occurring within 36 hours of a Viagra dose. Prior to the vision loss, short-term color changes or hues of green or blue have been reported. The FDA has numerous reports of blindness and Cialis has now included a warning on their drug inserts. Drug representatives and the FDA are discussing the risk of blindness. Over 30 million men around the world have taken Viagra. Register your Viagra, Cialis or Levitra Complaint If you or a loved one has suffered adverse effects while taking Viagra, Cialis, Levitra, you may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. TAINTED TISSUE TRANSPLANTS Transplanted tissue and bone patients, and their spouse or partner, risk exposure to serious diseases when receiving the tissue or bone taken from diseased cadavers. These risks include contracting certain infectious diseases such as HIV or Hepatitis C. Symptoms of these potentially fatal diseases include flu-like symptoms leading to abnormal liver enzymes and liver failure. The FDA has provided information on its investigation into human tissue transplantation and recalls have been issued by tissue processing firms, including; Blood and Tissue Center of Central Texas, Austin, Texas; LifeCell Corporation of Branchburg, New Jersey; Lost Mountain Tissue Bank of Kennesaw, Georgia; Tutogen Medical, Inc. and Regeneration Technologies, Inc., both of Alachua, Florida. Register your Transplant Complaint If you or a loved one has received a transplant of bone or tissue in 2004 or 2005, you may be at risk and may qualify for damages or remedies that may be awarded in a possible class action or lawsuit. Please click the link carolynstclair@att.net to submit your complaint for a free case evaluation, or call 713-228-5000 or toll free 1-866-795-7500. Vioxx (Rofecoxib)
In September 2004, drug manufacturer Merck withdrew Vioxx (chemical name rofecoxib) from the market due to a clinical trial resulting in increased risks of heart attack and stroke for long term Vioxx users. Vioxx is an anti-inflammatory drug (NSAID ) which the FDA approved in 1999 to reduce pain and inflammation caused by osteoarthritis, treat menstrual pain and rheumatoid arthritis. If you or a loved one has taken Vioxx, you may be eligible for compensation.  Bextra (Valdecoxib)
In April 2005, the FDA requested the drug manufacturer, Pfizer, to suspend sales of Bextra (also known as Valdecoxib) based upon a scientific study of 5,930 people that found patients taking Bextra were more than twice as likely to suffer heart attacks or stroke. Bextra was prescribed for the treatment of pain, tenderness and swelling caused by osteoarthritis and adult rheumatoid arthritis. Additionally, Pfizer sent a letter to doctors warning that Bextra users could develop a skin reaction known as Stevens Johnson syndrome that can be fatal. Stevens Johnson syndrome occurs when the immune systems turns on itself to excrete a drug, resulting in severe, painful blistering of the mucous membranes and skin as the patient is burned from the inside out. If you or a loved one has taken Bextra, you may be eligible for compensation. See more information on our Pharmaceuticals Links.
The law limits the time to file a claim, which varies in each state. We understand the medical legal issues you may be facing. If you or a loved one has suffered an injury or death from a dangerous drug, please contact Carolyn St. Clair, R.N., J.D. immediately for a free case evaluation at carolynstclair@att.net or 1-866-795-7500 or 713-228-5000. Law Offices of Carolyn St. Clair, R.N., J.D.
440 Louisiana, 9th Floor Lyric Centre,
Houston, TX 77002
713-228-5000 Toll Free Nationwide: 1-866-795-7500 Carolyn St. Clair is a registered nurse and an attorney, practicing in litigation involving medical devices, dangerous pharmaceuticals, birthing trauma, cerebral palsy, auto construction, railroad, refinery, truck accidents involving personal injury and wrongful death and sexual harassment cases. Her law firm also provides focus groups and trial consulting for law firms. Based in Houston, Texas, she represents clients in El Paso, Dallas, Fort Worth, San Antonio, Austin, Lubbock, Waco and statewide, as well as plaintiffs throughout the United States. Printer Friendly View
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