MARK TAYLOR’S FIGHT FOR COLUMBINE

mark

FEAT-IMGsm-Mark_Taylor-01

 MARK ALLEN TAYLOR

On April 20, 1999 Eric Harris opened fire outside Columbine High School. Standing with his friends having a discussion on the Bible was Mark Allen Taylor. The first bullets hit Mark with anywhere from 7 – 13 entering his body. The damage was so great that doctors could not determine the number of bullets that entered. The following video documents Mark’s life from that moment on. Click to view: http://youtu.be/XH7m-YNApU4

https://www.facebook.com/ReleaseMarkTaylor

Our webmaster for the International Coalition for Drug Awareness at www.drugawareness.org, Todd Bentley, who is Mark’s best friend and my incredible son-in-law and best father to my grandchildren anyone could ask for, put this video together and entered it in an Infowars contest (thus the reference to Infowars. I encourage you to share this everywhere!

I am extremely concerned about Mark’s health due to the damaging effects of the drugs he has been forced to take. He has worked long and hard in fighting this battle to bring awareness about the dangers of antidepressants and the truth about the cause of school shootings. And I do believe what he has been through is payback for the effectiveness of the battle he fought.

Now Mark needs our help to set him free from the system that is destroying him! What damage he suffered at Columbine is NOTHING in comparrison to the damage he has suffered from the past several years of forced drugging with the same drugs he was working so hard to warn society about!

Go to www.drugawareness.org to donate and help us raise the necessary funds to get the legal help he needs to set him free and safely withdraw from the medications that are killing him!

WARNING: In sharing this information about adverse reactions to antidepressants I always recommend that you also give reference to my CD on safe withdrawal, Help! I Can’t Get Off My Antidepressant!, so that we do not have more people dropping off these drugs too quickly – a move which I have warned from the beginning can be even more dangerous than staying on the drugs!

The FDA also now warns that any abrupt change in dose of an antidepressant can produce suicide, hostility or psychosis. And these reactions can either come on very rapidly or even be delayed for months depending upon the adverse effects upon sleep patterns when the withdrawal is rapid! You can find the CD on safe and effective withdrawal helps here: http://store.drugawareness.org/

Ann Blake Tracy, Executive Director,
International Coalition for Drug Awareness
www.drugawareness.org & www.ssristories.net
Author: Prozac: Panacea or Pandora? – Our Serotonin Nightmare – The Complete Truth of the Full Impact of Antidepressants Upon Us & Our World” & Withdrawal CD “Help! I Can’t Get Off My Antidepressant!”

About the Author: Ann Blake Tracy is the author of PROZAC: PANACEA OR PANDORA? –OUR SEROTONIN NIGHTMARE!, and the director of the International Coalition For Drug Awareness [www.drugawareness.org]. She has testified before the FDA and has testified as an expert in legal cases involving serotonergic medications since 1992.

BOOK: Prozac: Panacea or Pandora? – Our Serotonin Nightmare! Anything you ever wanted to know about antidepressants is there along with everything drug companies hope you never find out about these drugs. SAFE WITHDRAWAL CD “Help! I Can’t Get Off My Antidepressant!” on how to safely withdraw from antidepressants & most psychiatric medications is saving lives! Both available at www.drugawareness.org

BOOK TESTIMONIALS:

“Very bold & informative”

“Priceless information that is giving me back to me”

“The absolute best reference for antidepressant drugs”

“Well documented & scientifically researched”

““I was stunned at the amount of research Ann Tracy has done on this subject. Few researchers go to as much trouble aggressively gathering information on the adverse reactions of Prozac, Zoloft and other SSRIs.”

WITHDRAWAL HELP CD TESTIMONIALS:

“Ann, I just wanted to let you know from the bottom of my heart how grateful I am God placed you in my life. I am now down to less than 2 mg on my Cymbalta and I have never felt better. I am finally getting my life back. I can feel again and colors have never been brighter. Thanks for all that you do!!” … Amber Weber

“Used your method of weaning off of SSRI’s and applied it to Ambien. Took 6 months but had been on 15 mg for years so what was another 6 months. I have been sleeping without it for 2 weeks and it is the first time I have been able to sleep drug free for 15 years. What a relief to be able to lay down and sleep when I need or want to. Ambien may be necessary for people at times but doctors giving a months worth of it at a time with unlimited refills is a prescription for disaster. It is so damn easy to become dependent on. Thanks for your council Ann.”… Mark Hill

 

CELEXA & LEXAPRO: CLASS ACTION FOR FRAUD FILED AGAINST DRUG MAKER

Drug-Product-Injuries

Celexa and Lexapro are two of the most deadly of all the antidepressants and I can think of few who deserves a lawsuit like this more than they!!!

Baum Hedlund files class action for fraud against the makers of Celexa & Lexapro!!!!

“If either you or your child took Celexa or Lexapro between 2001 and the present and were under the age of 18 at the time, you may have a claim against the manufacturer, Forest Labs.

“Forest Labs, the manufacturer of the antidepressants Celexa and Lexapro, paid the government a settlement in 2010 because it illegally promoted Celexa for use in children and adolescents despite the fact it had not been approved for marketing in the United States. The Justice Department sued Forest Labs because it is illegal for a pharmaceutical company to promote a drug through “off-label marketing,” which means for uses that have not been approved by the Food and Drug Administration (FDA).

“Forest Pharmaceuticals, a subsidiary of Forest Labs, also was penalized for only publicizing positive Celexa study results in adolescents to doctors, while choosing to withhold the negative results. The company pled guilty to several crimes, including misbranding Celexa by marketing the antidepressant drug for use in children from 1998 to 2002 and paying kickbacks to doctors to encourage them to prescribe the drugs.”

(GET DETAILS FOR FILING BY CLICKING ARTICLE BELOW:)

www.baumhedlundlaw.com/consumer-class-actions/celexa-lexapro-consumer-fraud.php

WARNING: In sharing this information about adverse reactions to antidepressants I always recommend that you also give reference to my CD on safe withdrawal, Help! I Can’t Get Off My Antidepressant!, so that we do not have more people dropping off these drugs too quickly – a move which I have warned from the beginning can be even more dangerous than staying on the drugs!

The FDA also now warns that any abrupt change in dose of an antidepressant can produce suicide, hostility or psychosis. And these reactions can either come on very rapidly or even be delayed for months depending upon the adverse effects upon sleep patterns when the withdrawal is rapid! You can find the CD on safe and effective withdrawal helps here: http://store.drugawareness.org/

Ann Blake Tracy, Executive Director,
International Coalition for Drug Awareness
www.drugawareness.org & http://ssristories.drugawareness.org
Author: Prozac: Panacea or Pandora? – Our Serotonin Nightmare – The Complete Truth of the Full Impact of Antidepressants Upon Us & Our World” & Withdrawal CD “Help! I Can’t Get Off My Antidepressant!”

ZOLOFT: MULTIPLE LAWSUITS FILED FOR MULTIPLE BIRTH DEFECTS

Zoloft-mother-and-child[1]

ZOLOFT: MULTIPLE LAWSUITS FILED FOR MULTIPLE BIRTH DEFECTS

I do not believe it is clear to many people how serious these SSRI birth defect cases really are. This is to give you an idea of just how serious the birth defect cases are going against these drug companies…

Child was born with multiple birth defects…The complainant states that she took Zoloft throughout her pregnancy after it was prescribed by her treating physicians. She gave birth to a child with numerous congenital birth defects. The baby has been diagnosed with spina bifida, scoliosis, vater syndrome, tracheoesophageal fistula, and mitral valve regurgitation.

CASE #1

New Jersey Woman Files Zoloft Birth Defects Lawsuit

Perry Larkin | November 6th, 2012 | Posted in Zoloft Lawsuits

A New Jersey woman filed a new Zoloft litigation on October 17, 2012 seeking damages against manufacturer Pfizer, Inc. According to the filing the woman took the antidepressant Zoloft during her pregnancy and it caused multiple birth defects in her newborn son.

The case was filed in the U.S. District Court, Southern District of New York (Foley Square). She makes complaints of product liability, defective design, failure to warn, negligence and misrepresentation and seeks punitive and actual damages.

Zoloft accused of showing “willful disregard” to informing the public of risks

According to studies, Zoloft has long been linked to birth defects in newborns. In spite of FDA regulations that the new medical evidence requires Pfizer to update the warning label, the company has yet to do so.

The plaintiff’s attorney states that the company showed a willful disregard to informing the medical community and public of the risk of congenital birth defects due to Zoloft and this caused permanent harm to his client’s son. The label still fails to warn of the dangers and risks of congenital birth defects of Zoloft if it’s taken during pregnancy.

The plaintiff claims that her baby suffered from the following side effects of Zoloft: spina bifida, vater syndrome, clubfoot and other related defects.

Pfizer alleged to have known of side effects as early as 2007

The lawsuit alleges that Pfizer carelessly marketed the product and failed to provide sufficient warning as to the possible side effects to pregnant women. This case joins other designated cases for the pilot program of the district court, which aims to address complex civil cases.

The complaint says that in 2007, Pfizer knew that selective serotonin reuptake inhibitors (SSRIs) like Zoloft doubled the risk of septal heart defects in babies who were born to mothers who took the medication. In studies published in the New England Journal of Medicine, it indicates that a four-fold increase in heart defects was connected to pregnant women using Zoloft during their first trimester. Other studies showed that using the medication while pregnant is also linked to a higher occurrence of heart malformation.

Child was born with multiple birth defects

The complainant states that she took Zoloft throughout her pregnancy after it was prescribed by her treating physicians. She gave birth to a child with numerous congenital birth defects. The baby has been diagnosed with spina bifida, scoliosis, vater syndrome, tracheoesophageal fistula, and mitral valve regurgitation.

The plaintiff seeks compensation for medical costs, as well as punitive and special damages.

injurylawyer-news.com/2012/11/new-jersey-woman-files-zoloft-birth-defects-lawsuit/

CASE #2

Zoloft Caused Daughter’s Birth Defects, Tennessee Parents Claim in Lawsuit

Tracy Ray | October 24th, 2012 | Posted in Zoloft Lawsuits

In a lawsuit against Pfizer that was recently added to the Zoloft MDL, parents Michael and Shana Reid of Tennessee charge that their daughter was born with birth defects resulting from Zoloft. The Reids originally filed their lawsuit on June 8, 2012, in the Court of Common Pleas in Philadelphia County, and the case was transferred to the Zoloft MDL in the U.S. District Court, Eastern District of Pennsylvania, on August 16, 2012.

Baby needed surgery for life-threatening defects

According to the Reid’s lawsuit, Shana Reid was prescribed Zoloft by her physician during her pregnancy. She read the drug’s warning label, but did not see anything about birth defects, so she trusted that the antidepressant was safe to use while pregnant. Had she been warned about the risk of birth defects resulting from Zoloft, she would not have taken it during her pregnancy, she states in the lawsuit.

The Reid’s baby was born on October 14, 2004 with life-threatening congenital birth defects, the lawsuit states. As a result, the child has undergone corrective surgery and is likely to require further surgeries in future.

Plaintiffs accuse Pfizer of failure to warn mothers of Zoloft’s risks

The Reid’s lawsuit alleges that Pfizer was aware of the risk of side effects after taking Zoloft, but failed to adequately warn the public or the medical community. Their lawsuit charges that Pfizer’s marketing and advertising for Zoloft misled pregnant women and their doctors by giving inaccurate or misleading information about the danger Zoloft poses to a fetus when the drug is taken during pregnancy.

The lawsuit bring counts of failure to warn, design defect, fraud, negligence, gross negligence, negligent design, and breach of warranties. The plaintiffs are seeking compensation in excess of $75,000 in damages.

FDA issued warning about Zoloft birth defects

The FDA issued a warning in July 2006 stating that studies had shown that babies born to mothers who took Zoloft or other SSRI antidepressants during pregnancy were six times more likely to be born with PPHN than babies born to mothers who did not take antidepressants.
The following year, a 2007 study published in the New England Journal of Medicine found that women who took Zoloft during the first trimester had double the risk of giving birth to an infant with heart defects, compared to those who did not take antidepressants.

injurylawyer-news.com/2012/10/zoloft-caused-daughters-birth-defects-tennessee-parents-claim-in-lawsuit/

CASE #3

A Lawsuit Alleging Birth Defects From Zoloft is Filed in Pennsylvania
Perry Larkin | October 15th, 2012 | Posted in Zoloft Lawsuits
On September 10, 2012, a new lawsuit alleging birth defects from the use of Zoloft while pregnant was filed on behalf of ten plaintiffs by Zoloft attorneys. The case, Lentz et. Al. v. Pfizer Inc., was filed in the U.S. District Court for the Eastern District of Pennsylvania and alleges that the antidepressant Zoloft (sertraline) is responsible for the birth defects in their children.

This lawsuit joins the increasing number of plaintiffs who are seeking compensation for the alleged problems as a result of the medication.

Pfizer is accused of knowing of the risk of birth defects and failing to alert the public

The lawsuit alleges that Pfizer knew of the possibility of birth defects from preclinical and published studies and took no action to properly study the drug and its aftereffects. In addition, they chose not to publish these studies due to the revelation of increased risks with the drug. The manufacturer is accused of concealing, suppressing the results, and failing to warn consumers of the potential dangers. Pfizer continues to deny these accusations.

Many side effects from Zoloft can affect the heart, the gastrointestinal system, and cranial malformations

The children were born between 1998 and 2011. A correlation was demonstrated in studies between 2007 and 2009 that indicated the increased risk of birth defects when women take Zoloft while pregnant, but the plaintiffs were unaware of these studies. The plaintiffs claim that if they’d known of the risks, they never would have taken the drug.
Some of the side effects resulting from Zoloft use described in the lawsuit include gastrointestinal problems such as anteriorly displaced anus and omphalocele; heart defects such as right-sided aortic arch, patent ductus arteriosus, cleft mitral valve, transposition of the great arteries, atrial and ventrical septal defects, anomalous pulmonary venous return, and aotrtic stenosis; and craniofacial malformations such as cleft lip and palate, and multiple-suture craniosynostosis.

Pfizer’s safety information posted online doesn’t mention birth defects
On their website, Pfizer has posted “Important Safety Information” about possible complications of Zoloft, but doesn’t specifically mention birth defects. The site does state that “[w]omen who are pregnant, plan to become pregnant, or who are breastfeeding should not take any antidepressant without consulting their doctor,” but to date doesn’t acknowledge any risk of birth defects, nor does it indicate that Zoloft poses any risk to a pregnancy that other antidepressants don’t also pose.

injurylawyer-news.com/2012/10/a-lawsuit-alleging-birth-defects-from-zoloft-is-filed-in-pennsylvania/

CASE #4

Zoloft Drugmaker Blamed for Child Death

Elise Kramer | October 11th, 2012 | Posted in Zoloft Lawsuits

A New York couple has filed a lawsuit against Zoloft drug maker Pfizer, claiming that the antidepressant Zoloft is responsible for the birth defects experienced by their deceased son. The lawsuit was filed on August 17, 2012, in the United States’ District Court for the Eastern District of Pennsylvania, where the current Zoloft multidistrict litigation case is taking place. Jessica and Shawn Coon are claiming that Zoloft was responsible for the side effects experienced by their child, as Jessica took the medication during her pregnancy; they claim that they were not adequately informed of potential side effects associated with the medication at the time.

Negligence claimed by couple

The plaintiffs claim that the deceased minor, known as J.A.C., was born with congenital heart defects caused by birth defects after Zoloft use. He passed away just one month after he was born at the West Chester Medical Center in New York. They claim that because of Pfizer’s negligence and misrepresentation, Jessica Coon continued to take the SSRI drug Zoloft while she was pregnant with her child, which resulted in the birth defects he suffered and in his subsequent death.

The lawsuit claims that Pfizer and its subsidiaries, including Greenstone LLC, did not demonstrate reasonable care in the production, marketing, and distribution of their antidepressant, which caused a number of patients to suffer from birth defects as a result of the drug’s use by pregnant mothers. A number of studies have shown that Zoloft can be linked to an increased risk in birth defects, including PPHN and congenital heart disorders, which can be fatal in serious cases.

Numerous birth defects associated with antidepressant

The growing number of plaintiffs who have chosen to file a birth defects lawsuit related to Zoloft indicates the serious concern about birth defects related to the drug. Studies published in the New England Journal of Medicine revealed that infants born to women taking SSRI medications such as Zoloft were 50 percent more likely to develop heart defects and other serious heart problems.

injurylawyer-news.com/2012/10/zoloft-drugmaker-blamed-for-child-death/

About the Author: Ann Blake Tracy is the author of PROZAC: PANACEA OR PANDORA? –OUR SEROTONIN NIGHTMARE!, and the director of the International Coalition For Drug Awareness [www.drugawareness.org]. She has testified before the FDA and has testified as an expert in legal cases involving serotonergic medications since 1992.

BOOK: Prozac: Panacea or Pandora? – Our Serotonin Nightmare! Anything you ever wanted to know about antidepressants is there along with everything drug companies hope you never find out about these drugs. SAFE WITHDRAWAL CD “Help! I Can’t Get Off My Antidepressant!” on how to safely withdraw from antidepressants & most psychiatric medications is saving lives! Both available at www.drugawareness.org

BOOK TESTIMONIALS:

“Very bold & informative”

“Priceless information that is giving me back to me”

“The absolute best reference for antidepressant drugs”

“Well documented & scientifically researched”

““I was stunned at the amount of research Ann Tracy has done on this subject. Few researchers go to as much trouble aggressively gathering information on the adverse reactions of Prozac, Zoloft and other SSRIs.”

WITHDRAWAL HELP CD TESTIMONIALS:

“Ann, I just wanted to let you know from the bottom of my heart how grateful I am God placed you in my life. I am now down to less than 2 mg on my Cymbalta and I have never felt better. I am finally getting my life back. I can feel again and colors have never been brighter. Thanks for all that you do!!” … Amber Weber

“Used your method of weaning off of SSRI’s and applied it to Ambien. Took 6 months but had been on 15 mg for years so what was another 6 months. I have been sleeping without it for 2 weeks and it is the first time I have been able to sleep drug free for 15 years. What a relief to be able to lay down and sleep when I need or want to. Ambien may be necessary for people at times but doctors giving a months worth of it at a time with unlimited refills is a prescription for disaster. It is so damn easy to become dependent on. Thanks for your council Ann.”… Mark Hill

“I’m so thankful for AnnTracy and all her work. Also for taking the time out to talk to me and educate everyone! She has been a blessing to me during this awful time of antidepressant hell!” … Antoinette Beck

Amby Cole vs. Eli Lilly

Eli LillyAmby Cole vs. Eli Lilly

Lilly faces another Prozac lawsuit
Tennessee widow says husband hanged himself 13 days after drug was prescribed.

By Jeff Swiatek
jeff.swiatek@indystar.com
The Indianapolis Star

The lawsuit, filed last week in U.S. District Court for the Western District of Tennessee, is the latest in more than 200 lawsuits against Prozac maker Eli Lilly and Co.  since the early 1990s.

Amby Cole vs. Eli Lilly

6/25/2002

Lilly faces another Prozac lawsuit
Tennessee widow says husband hanged himself 13 days after drug was prescribed.

http://www.starnews.com/article.php?prozac25.html,business

By Jeff Swiatek
jeff.swiatek@indystar.com
The Indianapolis Star

To read the lawsuit go to: http://www.justiceseekers.com/files/NLPP00000/060.PDF

A Tennessee woman charges that Prozac caused her husband to hang himself 13 days after being prescribed the drug by his cardiologist for chest pain and loss of weight.

The lawsuit, filed last week in U.S. District Court for the Western District of Tennessee, is the latest in more than 200 lawsuits against Prozac maker Eli Lilly and Co. since the early 1990s.

Plaintiff Amby Cole, joined by her two children, says in the lawsuit that Milton Cole’s death in June 2001 “fits the signature pattern” of suicide caused by the Prozac family of antidepressants.

Cole wasn’t seriously depressed or suicidal and “became nervous, jittery and aggravated” after taking Prozac, the lawsuit says.

The wrongful-death and product-liability lawsuit charges that Prozac causes violent side effects that are dose-related, but Lilly “chose not to pursue” a lower-dose Prozac and put a once-weekly version on the market only last year.

“Lilly did not start marketing a once-a-week Prozac until its patent rights had been adjudicated as over and it was threatened in the marketplace with a generic formulation,” the lawsuit says.

Lilly has always maintained that Prozac’s side effects don’t include suicidal or violent thoughts. In the only two Prozac civil suits to come to trial, juries have sided with Lilly.

Attorneys for plaintiffs in the latest suit are J. Houston Gordon of Covington, Tenn., and Andy Vickery of Houston. Call Jeff Swiatek at 1-317-444-6483.

Copyright 2002 The Indianapolis Star