Should You File a Taxotere Hair Loss Lawsuit?

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Taxotere was approved by the FDA in May 1996. The medicine was suggested for the treating patients with advanced or metastatic breasts malignancy after chemotherapy when any another medicine failed. But it has been found to cause permanent alopecia or hair loss in women.

The suits claim, however, that Sanofi allegedly advertised the medication for use in patients with early-stage breasts cancer. The suits also declare that the company advertised the medicine in a far better way than the rivals’ drugs even though studies proved that Taxotere didn’t offer any increased benefits.

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Actually, research posted in the brand new Great Britain Journal of Treatments in 2008 discovered that the competitor medicine of Taxotere, Taxol was actually far better than Taxotere. In 2009, the FDA send Sanofi a caution letter accusing the company of making false and misleading assertions about the effectiveness of its medication.

Across the country, women who consumed Taxotere during chemotherapy are filing lawsuits saying that they have lost their hair permanently due to medication. They’re seeking payment from the maker for mental suffering, bills and for their psychological destruction. If you too are have been cheated by Sanofi, you may file a Taxotere lawsuit by hiring a lawyer via http://www.taxoterehairlawsuit.com/taxotere-lawsuit-lawyers.aspx.

       

The lawsuits are filed to help patients recover money from the drug’s company for the damage they suffered due to their hair loss. The suits claim that the maker of the drug, Sanofi:

  • Paid doctors for prescribing Taxotere for off-label uses to the cancer patients at early stages.
  • Didn’t properly alert patients about the chance of long lasting, chemotherapy-induced alopecia (hair thinning).

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  • Subjected patients to a medication that was more harmful than other alternatives.
  • Trained their team to misrepresent the efficiency of the medicine.
  • Knew that the chance of everlasting hair thinning was much increased with Taxotere than competitor drugs.

As a result, Sanofi is in charge of providing reimbursement to women who experienced long-term hair loss due to the drug usage.

Lawsuits can help women retrieve compensation for injuries that they experienced after losing their hairs. These damages range from:

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  • Mental hurting (anxiety, despair, etc.)
  • Medical expenses, including remedy and counseling
  • Lost of income to work due to emotional destruction
  • Disfigurement
  • Loss of standard of living

The lawsuits can also help ensure that Sanofi and other medication producers market their products for FDA-approved uses only.

Risperdal Causes Male Breast Growth – Cosmetic Surgery Claim

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Risperdal (generically known as risperidone) is an antipsychotic drug that is used to treat delusional psychoses. Dopamine is a key neurotransmitter that the brain uses which allows a person to experience pleasure and desire. Risperdal acts to reduce the amount of dopamine the brain produces so that a natural balance of chemicals in the brain. This can reduce or eliminate many psychotic disorder that people experience.

How Risperdal affect?

The right cause of male breast enlargement among Risperdal users is unidentified, but is claimed that risperidone may boost production level of prolactin; a hormone that produced by the forward pituitary; in females, it induces growth of the mammary glands. As a result, teen boys got increased production of this hormone may also cause breast muscles development and in a few cases cause breast & nipple pain or nipple lactation.

Unfortunately, the use of Risperdal is known to cause several harmful side effects for its users. Dangerous side effects of Risperdal are similar to those of many other antipsychotic medications. Potential fatal side effects include tardive, dyskinesia, extrapyramidal disorders, and serious neuroleptic malignant disorders.

Non-fatal, short-term side effects of Risperdal nausea, anxiety, dizziness, insomnia, low blood pressure, muscle stiffness, fatigue and weight gain. For more information about Risperdal lawsuit, you can also visit http://www.risperdalgynecomastialawsuitcenter.com/risperdal-male-breasts-lawsuit.asp.

A study data released in 2006 in the Journal of Clinical Psychopharmacology provides facts to pay Risperdal court situations that the medicine considerably enhances prolactin creation level, directing to the person boob enhancement.

Medical specialists in the study notified of potential injury: “Risperidone directed at teen at dosages generally used for the healing of psychotic indications can significantly increase prolactin secretion levels, with medical implications for illustration gynecomastia.

So long as the very long time effects of antipsychotic drug-created hyperprolactinemia aren’t well equipped with documents, specifically involving lower bone relative density, infertility, development, and past due puberty, Risperidone should be studied carefully to children and young adults.”

Risperdal Lawsuit Compensation

The first Risperdal gynecomastia lawsuit was filed by a young adult who developed breasts while taking Risperdal between the ages of 9 and 14. The young man required surgery to remove the breast tissue, and suffered from a great degree of social and emotional trauma. This and subsequent Risperdal lawsuits have asserted that Jansen and its parent company Johnson & Johnson failed to adequately warn consumers that boys could grow breasts while taking Risperdal. If you or a loved one developed male breasts while taking Risperdal, you may be entitled to compensation through a Risperdal gynecomastia lawsuit.

Car Accident Attorneys – Auto Accident Causes, Distractions and Legal Representation

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Accidents are a given, they happen no matter how cautious one may try to be. The responsibilities of owning and driving a car are much greater than one may think.

It doesn’t matter that the car is parked or the owner is driving it, a car accident can still occur.

There are many car accident attorneys available in every community and you should select an attorney who has a positive reputation.

Most accidents are caused by distractions; distractions can be due to internal or external sources.

Internal distractions are one’s thoughts about activities that have nothing to do with driving.

External distractions are those that others, either inside or outside of the vehicle, create.

If you are looking for car accident lawyer, you can visit http://www.onderlaw.com/motor-vehicle-accidents/car-accidents.aspx.

Both are common occurrences that an experienced car accident attorney will be familiar with.

Internal types of distractions cause the driver to be inattentive and focus on their thoughts instead of driving.

Thoughts can be of, but not limited to: personal and some family problems, financial problems or maybe even a recent or future event that is of importance. External types of distractions can be caused by a large number of sources.

The weather, tuning the radio, eating/drinking, reading a map, texting or talking on a phone or CB radio or even by looking at another occupant of the vehicle.

Although it does not directly impact the actual cause of the accident, but the speed at which the vehicle is moving has a great impact as to how extensive the damage is done when an accident is occurring.

Most of the accidents can occur in one’s own driveway to happening on the highway. In addition, the collision can involve the driver’s car only or many other vehicles.

Depending upon where the accident occurs, who is involved and what has been damaged in an accident may require legal counsel.

Many times, accidents are minor and the incident is relatively easy to resolve but there are unfortunately times in which the matter is more complicated and an attorney is necessary.

 

How to Choose Hernia Mesh Lawyers for Ethicon Physiomesh

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Ethicon Physiomesh appears to be an unreasonably dangerous and defective hernia mesh product, which has been linked to reports of high failure rates and the frequent need for revision surgery.

In May 2016, Ethicon removed certain Physiomesh products from the market, after failing to identify a cause of the problems.

The hernia mesh lawyers at Saiontz & Kirk, P.A. are reviewing cases for individuals worldwide.

And it is not necessary to know whether Ethicon Physiomesh was used during your hernia repair.

The financial compensation may be available through Ethicon Physiomesh lawsuits for individuals who experienced complications like:

  • Bowel Adhesions, Bowel Perforation and Organ Perforation
  • Infections
  • Mesh Erosion Or Failure
  • Hernia Revision Surgery
  • Abdominal Pain
  • There are no charges unless a recovery is obtained.

Johnson & Johnson’s Ethicon subsidiary first received approval to market its Physiomesh Flexible Composite Mesh products in March 2010.

If you are looking for Ethicon physiomesh lawyer you can visit http://www.ethiconphysiomeshlawsuits.com and can find the best physiomesh lawyer.

Ethicon Physiomesh was introduced under the FDA’s controversial 510K fast-track approval process, meaning that the manufacturer only had to demonstrate that it was “substantially equivalent” to a previously approved hernia mesh system.

 As a result, the manufacturer was not essential to conduct thorough testing or research to establish whether users may face an unreasonable risk of problems following Physiomesh hernia repair.

In its FDA application, Ethicon described Physiomesh as “a sterile, low profile, flexible composite mesh designed for the repair of hernias and other facial deficiencies.”

The product is composed of a no absorbable, macroporous polypropylene mesh laminated between two undyed polyglecaprone-25 films.

An undyed polydioxanone film provides the bond between the polyglecaprone-25 film and polypropylene mesh. The polypropylene component is constructed of knitted filaments of extruded polypropylene.

Ethicon Physiomesh Hernia Repair Problems

After obtaining approval to the market and sell the product, Ethicon Physiomesh was widely adopted within the medical community amid aggressive marketing by the manufacturer, which attempted to promote the hernia mesh as superior to other hernia repair products.

 

Talcum Powder Ovarian Cancer Lawsuits

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Made from talc or talcum powder, baby powder is one of the most commonly purchased items found in the “baby aisle” at the store. It’s a product that’s been used for years, and one whose smell and feel can bring back affectionate memories for many. Recently, however, talcum powder has been related to several allegations that its use may cause ovarian cancer.

Talc is a mineral made up of various elements including magnesium, silicon and oxygen. It’s ground up to make a powder which is effective at absorbing excess moisture. It’s a mineral used in many products, from body and facial powders to certain kinds of cosmetic makeup.

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For many decades, talcum powder has enjoyed great success as a consumer product. While young mothers often enthusiastically sprinkle it on their infants during diaper changes to help absorb wetness and prevent diaper rash, other women used the powdery substance as a regular part of their feminine hygiene practices.

Johnson & Johnson is preparing to fight another legal battle as the number of lawsuits is increasing day by day. Thousands of women have filed lawsuits across the country against Johnson & Johnson alleging that the use of talcum powder leads to ovarian cancer.

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Several investigations on talc increase the medical sign which suggest Women should not use talcum powder as an intimate hygiene powder because of its link to ovarian cancer. The more often a woman uses it on her genital area, the more likely she will experience ovarian cancer.

If you’ve developed ovarian cancer and used talcum-based Johnson & Johnson powder product, such as Shower to Shower or Johnson’s Baby Powder then you may visit at  http://www.247lawsuitnews.com/ for a free talcum powder lawsuit case review.

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Our accomplished lawyers are dedicated to protecting consumers through class action and individual litigation, and are committed to ensuring that all victims have access to the type of aggressive legal advocacy that assures success.

Any women that have been diagnosed with ovarian cancer and that have also regularly used talcum powder for perineal hygiene may be eligible for compensation for their injuries and should contact us for a free case evaluation.  Compensation could include payment for medical bills, pain & suffering, and compensation for other damages that may have been caused.

If you’re currently suffering from ovarian cancer and know that you’ve been using Johnson & Johnson talcum powder in your vaginal area for years you should immediately contact our law firm so we can help you decide whether we need to file a lawsuit for damages on your behalf.