Category: General

If you have been injured by using the birth control drug Yazmin, (Yaz, Ocella), you will need an experienced prescription drug lawyer who cares about you as a person and will be dedicated to fight for you to get fair and just compensation for your personal injury. Women taking this birth control drug deserve to know the side effects associated with Yazmin, (Yaz, Ocella).

Yazmin, Yaz, Ocella, (Drospirenone & Ethinyl Estradiol), is an oral medication prescribed for birth control, pre-menstrual symptoms, and moderate acne vulgaris in women at least 14 years of age.
The Yaz, Yasmin, Ocella is a group of birth control drugs that are oral contraceptives that contains progestin Drospirenone or DRSP.
The Yasmin birth control pill was originally developed by Berlex Laboratories, which has since been acquired by Bayer Pharmaceuticals.
Drospirenone is a diuretic drug and if the body is dehydrated it can lead to blood clotting, stroke, heart attack and disruptive heart rhythms.
Swiss media reported that more than 200 women have died while taking Yaz and Yasmin, Bayer’s blockbuster birth control contraceptives.
Yazmin is one of the best-selling oral contraception birth control pills in the U.S., with sales of $616 million in 2007.
Yaz is a combination birth control pill that also contains progestin and estrogen. Yaz is considered a low-dose pill that it contains .035 milligrams or less of estrogen.
Yasmin, Yaz, Ocella lawsuits also state that Bayer pharmaceuticals over promoted the benefits of Yazmin and Yaz, and advertised the drug for non-FDA approved uses.
Over 6,850 lawsuits have been filed since February 2012. These lawsuits claim that Yazmin birth control pills led to deadly blood clots, gall bladder damage and kidney failure.
The Yasmin birth control pill, manufactured and marketed by Bayer Pharmaceuticals has been linked to a number of serious, life-threatening side effects including sudden death.
All of the Yamin lawsuits involve allegations which state that Bayer knew, or should have known and failed to disclose about the health risks involved with its birth control pills and put the health of women at risk.

The DePuy Pinnacle Ultamet Hip Implant is a metal-on-metal artificial hip system designed to replace hip joints that require surgery. DePuy Pinnacle Ultamet Hip Implants have joint components that produce metal debris after continuos friction. Metal debris are small enough to enter into the blood stream and surrounding tissues, causing a multitude of health risks and have been linked to a high number of serious injuries.

The DePuy Pinnacle Ultamet Hip Implant is remarkably similar to the DePuy ASR Hip Replacement when used with the metal liner option, but only the DePuy ASR Hip was recalled from the market. Both Hip Implants caused similar health problems due to the metal content and have proved to be dangerous to hip replacement candidates. Both of these products were also approved to be sold on the market through an FDA loophole which required virtually no safety testing or clinical trials before being introduced to the public. Fortunately, the loophole has been closed to future metal-on-metal hip replacement devices.

The main issue with these designs is that they caused a degree of metal toxicity in the blood. One of the biggest risks involved with prolonged exposure to high levels of chromium and cobalt in the blood, is that they cause surrounding tissues to become necrotic. When the tissue surrounding a defective hip implant becomes necrotic, the patient will no longer be able to walk. Even if a defective hip is replaced with a better one, the damage to the tissue remains, as well as the inability to walk.

Common side effects and injuries associate with the DePuy Pinnacle Ultamet Hip Implant include:

Changes in Gait
Clicking Noises coming from the Hip
Death
Difficulty Standing
Difficulty Walking
Fractures
Groin Pain
Hip Pain
Hip Replacement Fracture, Degradation or Breakage
Infection
Inflammation
Instability
Joint Dislocation
Local Swelling
Loosening of the Joint
Metal Toxicity
Metallosis
Necrosis
Need for Revision Surgery
Nerve Damage
Numbness
Painful Complications
Tissue Damage to the Region
Wrongful Death
If you or a loved one was given a DePuy Pinnacle Ultamet Hip Implant and afterward experienced serious side effects or health issues, you may be entitled to compensation.

Contact us immediately for a FREE DePuy Pinnacle Ultamet Hip case evaluation. You may be entitled to financial compensation for your DuPuy Orthopaedics product-related injuries. Our team of Lawyers have experience in claims that involve defective medical devices, and they can help you today.

According to the Institute of Medicine, each year more than 97,000 annual deaths occur due to Medical Negligence.

In 2010 alone, 545 reports were made to the FDA regarding faulty DePuy Pinnacle Ultamet Hip Implants.

Need a DePuy Pinnacle Ultamet Hip Implant Product Lawyer?

A personal injury caused by DePuy Pinnacle Ultamet Hip Implant can result in pain and suffering, thousands of dollars in unnecessary medical bills, repeated surgeries, permanent disability and possibly even death. If you or a loved one has been injured by a DePuy Pinnacle Ultamet Hip Implant after a hip replacement procedure, we can help you.

If you have been injured by a Zimmer Durom Cup in Connecticut, knowing your legal rights can provide both financial relief and peace of mind.

We are currently evaluating Zimmer Durom Cup injury claims in Connecticut and throughout the U. S. Victims of Defective Medical Devices, negligence, and personal injury have the right to seek compensation for their injuries, damages, loss of wages, and medical expenses. Our defective product injury lawyers handle all types of Defective Medical Device claims. We also handle every type of Defective Medical Device claim and injury compensation cases.
A Zimmer Durom Cup can cause life-threatening physical injuries and trauma that can include financial damage to victims of negligent drivers. Injured victims must deal with large and unforeseeable medical expenses, loss of wages, pain, suffering and loss of quality of life. Family members also can suffer economic loss, mental anguish and loss of companionship in caring for an injured family member.

Many Defective Medical Device injuries occur due to negligence on the part of the manufacturers. When a Defective Medical Device injury is caused by another party’s negligence you are entitled compensation for medical expenses, pain and suffering as well as other damages.