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CABIRI Big Pharma Research – Reproductive Health

BAYER PHARMACEUTICALS WARNING LETTER

DEPARTMENT OF HEALTH & HUMAN SERVICES

Public Health Service

Food and Drug Administration Silver Spring, MD 20993

“FDA Warning Letter To Bayer”

Fadwa Almanakly, Pharm.D.

Associate Director, Advertising and Promotions

Bayer HealthCare Pharmaceuticals Inc.

6 West Belt Wayne, NJ 07470-6806

RE: NDA 21-225 Mirena® (levonorgestrel-releasing intrauterine system) MACMIS # 18166

Dear Dr. Almanakly:

The Division of Drug Marketing, Advertising, and Communications (DDMAC) has reviewed a script for a live consumer-directed program (program) entitled “Mirena Simple Style Statements Program” (150-74-0002-09) for Mirena® (levonorgestrel-releasing intrauterine system) (Mirena), submitted by Bayer HealthCare Pharmaceuticals Inc. (Bayer) under cover of Form FDA-2253.

The program overstates the efficacy of Mirena, presents unsubstantiated claims, minimizes the risks of using Mirena, and includes false or misleading presentations regarding Mirena. Thus, the program misbrands the drug in violation of the Federal Food, Drug, and Cosmetic Act (the Act), 21 U.S.C. 352(n), and FDA’s implementing regulations. See 21 CFR 202.1(e)(3)(i), (e)(5) & (e)(6)(i).

Background According to the DESCRIPTION section of its FDA-approved product labeling (PI),1 “Mirena® (levonorgestrel-releasing intrauterine system) consists of a T-shaped polyethylene frame (Tbody) with a steroid reservoir (hormone elastomer core) around the vertical stem.” The steroid reservoir contains the progestogen levonorgestrel, which is secreted slowly into the uterus over time upon the insertion of Mirena by a trained healthcare provider. According to the INDICATIONS AND USAGE section of its PI, Mirena is approved for the following indication: Mirena is indicated for intrauterine contraception for up to 5 years.

Thereafter, if continued contraception is desired, the system should be replaced. Mirena is recommended for women who have had at least one child. The PI for Mirena also includes numerous contraindications, including “[u]ntreated acute cervicitis or vaginitis, including bacterial vaginosis or other lower genital tract infections until infection is controlled,” and “[c]onditions associated with increased susceptibility to pelvic infections.”

1 The most current version of the FDA-approved PI as of the dissemination date indicated on Form FDA-2253 was the July 21, 2008, version, and that is the version referred to in this letter. We note that the PI for Mirena was updated on October 1, 2009. Fadwa Almanakly, Pharm.D.

Page 2

Bayer HealthCare Pharmaceuticals Inc. NDA 21-225 / MACMIS 18166 The use of Mirena is associated with a number of risks, including warnings regarding the increased risk of pelvic inflammatory disease (PID), ovarian cysts, and irregular bleeding and amenorrhea.

Additional warnings include the risk of Mirena embedding in, perforating, or being expelled from the uterus, as well as the increased risk of ectopic pregnancy, and the risks to an intrauterine pregnancy that occurs with Mirena in place. Should a woman become pregnant while using Mirena, serious risks include pregnancy loss and a permanent loss of fertility. In addition to the warnings noted above, the PI details the common adverse reactions that were observed during the clinical trials for Mirena.

According to the PI, “Very common adverse reactions” (>10% of clinical trial patients) included “uterine/vaginal bleeding (including spotting, irregular bleeding, heavy bleeding, oligomenorrhea and amenorrhea), and ovarian cysts.” Adverse reactions that were reported by 5% or more of clinical trial patients include, among others, abdominal/pelvic pain, nausea, headache, nervousness, back pain, weight increase, breast pain/tenderness, acne, decreased libido, and depressed mood. The PI also includes precautions that patients should be counseled that Mirena does not protect against HIV infection (AIDS) or other sexually transmitted diseases, and that patients should be instructed to check that the threads attached to Mirena are still in place after each menstrual period, as there is no contraceptive protection if Mirena is displaced or expelled.

Additionally, in regards to patient follow-up following the insertion of Mirena, the DOSAGE AND ADMINISTRATION, Patient Follow-up section of the PI states (in pertinent part): • Patients should be reexamined and evaluated 4 to 12 weeks after insertion and once a year thereafter, or more frequently if clinically indicated. Overstatement of Efficacy/Unsubstantiated Claims Promotional materials are misleading if they represent or suggest that a drug is more effective than has been demonstrated by substantial evidence or substantial clinical experience.

The Mirena program is a live presentation designed for a consumer audience of “busy moms.” The program is presented in a consumer’s home or other private setting (e.g. private restaurant party) by a representative from Mom Central (a social networking internet site) and a nurse practitioner (Ms. Barb Dehn).2 The script of this program submitted to FDA includes an introduction from the Mom Central representative, a presentation given by Ms. Dehn regarding the use of Mirena, and a “post-party” questionnaire for the audience. The script includes the following statements to be delivered by the Mom Central representative (emphasis added):

• “This party was brought to you by Mom Central in partnership with Bayer HealthCare Pharmaceuticals’ Mirena which may help couples keep life simple!” 2 The Mirena program submitted to FDA also references a presentation given by a fashion stylist (Ms. Angela Hastings) that immediately follows Ms. Dehn’s presentation regarding the use of Mirena. The script of Ms. Hastings’ presentation regarding fashion tips was not submitted to FDA.

Fadwa Almanakly, Pharm.D.

Page 3

Bayer HealthCare Pharmaceuticals Inc. NDA 21-225 / MACMIS 18166 • “Barb Dehn is a practicing Women’s Health Nurse Practitioner, award-winning author and nationally recognized health expert from San Francisco. Barb is going to kick things off with a discussion about romamance and how to find simple ways to reconnect with our partners.” The script also includes the following statements to be delivered by Ms. Dehn (emphasis added): •

“. . . And, let’s face it, when we feel good about the way we’re put together, we feel better about approaching the romance in our lives.” • “What we’re here to talk about today – is how to find those simple ways to reconnect with ourselves and our partners.” Following the introduction of the program, the script states that “Barb [Dehn] will begin presentation with an icebreaker – an interactive Q&A – which will touch upon issues such as busy schedules, barriers to intimacy and contraception” (emphasis added). The “icebreaker” questions include the following (in pertinent part; emphasis added): • “How many of you feel so busy that you often can’t find time to take care of yourself? And do you think this impacts your level of intimacy?”

• “Do you ever feel so overwhelmed by your schedule that intimacy is much more of a “to do” on a list than a desire?” • “If you didn’t have to worry about contraception, do you think you would be more likely to be intimate with your partner?”

• “Do you think if you didn’t have to worry about taking your birth control everyday, it would help you be more intimate?” Immediately following the “icebreaker” questions, the script for Ms. Dehn states (emphasis added):

• “So you mentioned that convenience and reliability are among the most important benefits of your birth control method. One strategy that I recommend for busy couples is choosing a birth control method that allows for spontaneous intimacy and which you don’t have to think about every day, such as the intrauterine contraceptive Mirena®.”

The above statements clearly indicate that the use of Mirena instead of other means of contraception will result in increased levels of intimacy, romance, and by implication, emotional satisfaction. These claims misleadingly overstate the proven efficacy of Mirena. Mirena has been proven to be an effective intrauterine contraceptive device. While we note that Mirena does not involve a daily routine and is not a barrier method of contraception, FDA is not aware of any evidence that suggests that women using Mirena for birth control experience an increase in reconnection, romance, or intimacy with their partners. Claims that state or suggest such quality of life outcomes, such as those described above, must be Fadwa Almanakly, Pharm.D.

Page 4

Bayer HealthCare Pharmaceuticals Inc. NDA 21-225 / MACMIS 18166 supported by substantial evidence, as demonstrated through adequate and well-controlled trials using validated patient assessment instruments to measure the outcomes of interest. If you do, in fact, have data to support these claims, you should submit them to FDA for review. We note that, according to the Mirena PI, at least 5% of clinical trial patients reported decreased libido as a side effect of Mirena use. Patients also experienced abdominal/pelvic pain, nausea, headache, nervousness, and depressed mood, which could adversely affect a woman’s feelings relating to romance or intimacy. The script also includes the following statements, to be presented by Ms. Dehn (emphasis added):

• “But what this party is really about is looking at the whole picture and figuring out steps to take to simplify your lifestyle while still looking and feeling great. One of those ways is finding a birth control that is compatible with your busy lifestyle.” The above statement goes beyond the suggestion of increased intimacy to suggest that Mirena can help patients “look and feel great.

” Again, FDA is not aware of any evidence suggesting that women who are using Mirena for birth control look great or feel great. Patients using Mirena may experience various side effects, such as irregular bleeding, ovarian cysts, back pain, weight increase, breast pain/tenderness, and acne, in addition to the side effects indicated above. The experience of these side effects can prevent patients from “looking and feeling great.” Such claims of improved patient-reported outcomes must be supported by substantial evidence, as demonstrated through adequate and well-controlled trials using validated instruments to measure these outcomes of interest.

If you do, in fact, have data to support these claims, you should submit them to FDA for review. Omission and Minimization of Risk Information Promotional materials are misleading if they fail to reveal material facts in light of the representations made by the materials or with respect to consequences that may result from the use of the drug as recommended or suggested by the materials. The script includes the following risk presentation, to be presented by Ms. Dehn (emphasis in original):

• Only you and your healthcare professional can decide if Mirena is right for you. Mirena does not protect against HIV or STDs. Candidates for Mirena have had a child, and do not have certain cancers or acute pelvic inflammatory disease. In rare cases, perforation or embedment may occur. Mirena may become completely or partially dislodged. In the uncommon event you think you’re pregnant, contact your healthcare professional without delay.

Ovarian cysts may occur and typically disappear. Changes in bleeding are common in the first few months followed by shorter, lighter periods. Periods, however, may remain irregular. The risk presentation omits the contraindications regarding untreated lower genital tract infections and conditions associated with increased susceptibility to pelvic infections, and does not adequately convey that should a woman become pregnant while using Mirena, she may lose her baby or her fertility. Fadwa Almanakly, Pharm.D.

Page 5

Bayer HealthCare Pharmaceuticals Inc. NDA 21-225 / MACMIS 18166

We refer you to the December 17, 2008, advisory letter from DDMAC to Bayer, regarding the promotion of Mirena. This advisory letter includes a change of opinion regarding the risk presentation for Mirena. The letter states (in pertinent part, emphasis added): Because this constitutes a change in our position, you will be provided a reasonable period of time to revise any Mirena promotional materials currently in use that omit this important risk information.

Accordingly, the revisions should be completed within 90 days of receipt of this letter or at the next production of new promotional materials, whichever comes first. The promotional program at issue here was newly developed, and as stated on the Form FDA-2253 accompanying the materials, it was disseminated on February 28, 2009, after the change of opinion letter was issued.

We also refer you to your January 5, 2009, response to the change of opinion letter, stating that you intend to comply with our request. Additionally, the script minimizes the risks associated with Mirena. Specifically, the “looking and feeling great” statement referenced above, in the context of the program as a whole, minimizes the risks associated with the use of Mirena.

As stated in the Background section above, the PI for Mirena includes “very common” (experienced by >10% of clinical trial patients) adverse reactions, in addition to other serious warnings, precautions, and safety issues associated with the use of Mirena. The suggestion that Mirena will help patients “feel great” minimizes the side effects that patients may experience as a result of using the drug. False/Misleading Statements The script includes the following statements to be presented by Ms. Dehn (emphasis added):

• “. . . Mirena has no daily, weekly, or monthly routines to comply with as compared to the negatives associated with other birth control methods.” The above claim that Mirena has “no . . . monthly routines” directly contradicts information contained in Mirena’s PI.

According to PRECAUTIONS, Continuation and Removal section (repeated in the DOSAGE AND ADMINISTRATION, Patient Follow-up section) of the PI for Mirena, “[Patients should be] reexamine[d] and evaluate[d] . . . 4 to 12 weeks after insertion and once a year thereafter, or more frequently if clinically indicated.”

The PRECAUTIONS, Patient Counseling Information section of the PI also states that patients should check that the threads attached to Mirena are in place after each menstrual cycle (thus on a monthly basis), to ensure that Mirena has not become displaced or expelled, which would result in a loss of contraceptive efficacy. Therefore, the claim that there is no “monthly routine to comply with” is a false statement.

We note that the script includes instructions to check the Mirena threads monthly in a separate part of the presentation; however, this does not correct the false statement highlighted above. Fadwa Almanakly, Pharm.D.

Page 6 Bayer HealthCare Pharmaceuticals Inc. NDA 21-225 / MACMIS 18166 Conclusion and Requested Action For the reasons discussed above, the program is misleading in violation of the Act, 21 U.S.C. 352(n), and FDA implementing regulations.

See 21 CFR 202.1(e)(3)(i), (e)(5) & (e)(6)(i). DDMAC requests that Bayer immediately cease the dissemination of violative promotional materials for Mirena such as those described above.

Please submit a written response to this letter on or before January 14, 2010, stating whether you intend to comply with this request, listing all promotional materials (with the 2253 submission date) for Mirena that contain violations such as those described above, and explaining your plan for discontinuing use of such violative materials.

Please direct your response to me at the Food and Drug Administration, Center for Drug Evaluation and Research, Division of Drug Marketing, Advertising, and Communications, 5901-B Ammendale Road, Beltsville, MD 20705-1266; facsimile at 301-847-8444. In all future correspondence regarding this matter, please refer to MACMIS # 18166 in addition to the NDA number for Mirena. We remind you that only written communications are considered official.

The violations discussed in this letter do not necessarily constitute an exhaustive list. It is your responsibility to ensure that your promotional materials for Mirena comply with each applicable requirement of the Act and FDA implementing regulations. Sincerely, {See appended electronic signature page} Carrie Newcomer for Cynthia Collins, Ph.D. Regulatory Review Officer Division of Drug Marketing, Advertising, and Communications

Sincerely,

Carrie Newcomer for Cynthia Collins,

Ph.D. Regulatory Review Officer Division of Drug Marketing, Advertising, and Communications

“CandyK’s Communication Outreach”

Dec 9, 2018

DRUGINFO@fda.hhs.gov

Thank you for contacting the Division of Drug Information (DDI). This message is an automatic acknowledgment of your inquiry.

Dec 9, 2018

Automatische Antwort: Mirena Claim

Thank you very much for your email. I’m not in the office until Monday, December 10th. During this time, I have no access to my emails. In case of emergency, you will reach my colleague Ms. Heber,mailto:kerstin.heber@bayer.com

Date: Thu, Mar 6, 2014

Subject: Incident #01980MMJ-42104CCO

To: <complaint@jointcommission.org HYPERLINK “”>

Oct. 21st, 2014

Your Comment Submitted on Regulations.gov (ID: CMS-2014-0115-0002)

Jan. 23, 2015

@aclufl.org

Legal Director – American Civil Liberties Union of Florida

Hello Candace-

I got your voicemail yesterday, but had a filing due in court. I just sent you an email copying Jeff Weinberger so I hope the two of you will follow up. I’m supposed to be in Palm Beach on Wed., Feb. 4, for a meeting at noon. However, if you have time that morning, I could probably get there by 10 a.m. and meet you someplace convenient. Please let me know if that works for you

Jan, 28th, 2015

Hello Candace-

Are you available to meet next Wed. at 10 a.m.? My meeting is at 11:30 a.m. and then I have to head back to Miami, but we can talk about this and the homeless rights work you’ve been doing then. If that time works, just let me know where you’d like to meet

Apr 10, 2014

Ellen Malcolm, National Partnership

Dear Candance,I’m the chairwoman for the National Partnership’s board of directors, and tomorrow I plan to mention you at our semi-annual meeting. Yes, you.

Apr 15, 2014

Balboa Press – jstogsdill@balboapress.com

I want to help you tell your story

To get started publishing right away or to discuss your options. I look forward to speaking with you again soon.

Mar 6, 2014

PATIENTSAFETY-L@LISTSERV.NPSF.ORG

LISTSERV@listserv.npsf.org

May 7, 2015

Cecile Richards, Planned Parenthood – NO Response

pponline@ppfa.org

Jul 23, 2014 – Planned Parenthood – No Response

Lisa.Murano@ppsoflo.org

Tue, Jul 31, 2018

CDER DRUG INFO <DRUGINFO@fda.hhs.gov>

druginfo@fda.hhs.gov

Incident #01980MMJ-42104CCO – Reporting to MedWatch

Division of Drug Information – Center for Drug Evaluation and Research

Thank you for writing to DICE@fda.hhs.gov. Your inquiry was forwarded to the Division of Drug Information in the FDA’s Center for Drug Evaluation and Research for a response.

Stay Tuned: Episode 7 – More Adverse Complications Continued

CABIRI Business Services

Canada Notices Big Pharma Chemical Dangers

Hello Fellow Americans and Leaders Of The United States,

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For the past several years I’ve been advocating about the dangers of the United States Pharmaceutical industry – Chemical Concoctions, that are harming, altering, and killing the American people.

My name is Candance Camper, I’m a 46yr., old Mother of 2, and a Vietnam Veteran daughter, with a college degree, with 30 years of Corporate business accounting experience in almost every market industry, including working for Local Government! So I’m well aware of what goes on behind closed doors that’s kept quiet!

“I started,” my social media business CABIRI, due to a personal medical nightmare that doctors, hospitals, and  pathologists left me wondering if I was going to live or die, from unknown illnesses, 6yrs. after getting a medical-device removed. As always being a healthy woman my illness was a blow to myself and my entire family, being that I’ve always been the backbone of my family! My children and family were petrified that I was not going to live due to being excessively hospitalized undiagnosed and living with permanent medical problems that involved disease, surgeries and credit ruined, and all my hard work of my life and children’s belonging just gone.

Well if that doesn’t wake you up, I don’t know what will! Truly, I had no other choice but to stand up and save my life, that’s when my Knowledge, Athletic, and Parents guidance kicked in! My parents, nurses, doctors, and many other professionals told me not to give up and I didn’t!

My two sons and my family mean the world to me! …And anyone deliberately trying to take me away from them, “By no fault of my own”, I had no choice to fight for them and myself in order to live! I’ve been fighting diseases, and other illnesses due to the ‘Toxic’ medical-device! I joined the, “Facebook Mirena-Iud support group,” where women all around the world, like myself speak about the dangers, side-effects and nightmares they’ve had due to this Toxic Device!

Since doctors, hospitals, nor pathologists could identify why I had a Mirena-Iud piece that broke off inside of me, migrated and embedded itself into my lymph nodes for 6yrs! I decided to take matters into my hands to save my own life! So I began researching the Pharmaceutical – Biotech Corporations in America!

When I completed my research it was so “Alarming” I sent my research to the “Office Of The President, FDA, HHS and many other Federal Agencies! All I kept hearing, “Oh maam, where sorry to hear that happened to you!” Well if you almost were taking away from your children and family by a “Toxic Device” those are not the words you want to hear!”

Advocating has been my only out, since my own Government, State, Lawyers, would not help me and left me homeless, sick and misdiagnosed! Well I’ve been overcoming this “Medical Nightmare,” and have been trying to find my own medical answers too heal my own body, since it seemed no body cared and doctors were left scratching there heads. The only country that reached out to me is Canada back in 2013, a woman from Lawsuits and Settlements reached out to me after reading one of my blogs, she understood what I was dealing with, being that women in Canada were experiencing the same type of medical-issues pertaining to the Mirena-Iud, the Lawyer stated she would help me, by doing a personal story about what I’ve been through!

Taking it a step further I began communicating my research to the entire world to prevent anymore deaths, permanent illnesses, due to the carelessness of “U.S. International Big Pharma Industry!”

As a advocate, I’ve found the dangers of the Healthcare industry and many other market industries in the United States! The entire United States is now catching own, many organizations, and other leaders, and fellow citizens who care about “Human Beings” are now stepping up and helping me save lives! The first step was to bring awareness, which now the United States Federal Government now see’s my point please view: http://thehill.com/regulation/238187-new-regs-for-thursday-toxic-chemicals-food-facilities-and-deepwater-ports

Their findings has, are a day late, in my case! They did not do anything to help me or acknowledge me for bringing this to their attention! Does the U.S. Federal Government truly feel that it’s okay to allow a “Foreign Country” to import chemical products into the United States, be approved by the FDA, CDC, NIH as safe for human consumption! Only to find out that the imported medical products have dangerous chemicals inside of them that can harm human beings!

Well United States, you don’t get a free pass, just as my “Father” didn’t get a free pass when he was drafted to the “Vietnam War!” My life and millions of “American Citizens,” are and have been impacted by these deadly chemically concocted drugs, medical-devices, and products!

As a American born citizen I’m appalled, frustrated, and upset, that Canada is the only country that is hearing me and millions of Americans! Actually, I must say I’m very pleased to see the news media, and other organizations have now caught on! See links below for yourselves, as the owner of CABIRI, everyone is forwarding me pertinent information too protect All American Citizens, since our Federal Government is refusing to do so! I had to save my own life, stand for all of Americans, and especially our children who need us to protect them from these type of medical dangers!

Too protect your friends, families, colleagues, please take a look at all my information! I have tons information that relates to my research @ https://www.facebook.com/kaila.truths! Although, the U.S. Government and the Medical Industry sold me out and left me to die and homeless, I refused not sell out my ‘Fellow Americans,’ in order too save their families lives, from the “International Controlled Big Pharma – Biotech leaders in the United States!

I’m not going to continue on and on there’s so much I can say, and have said, please see below links to enlighten yourselves about what truly happening behind the scenes in America, that could be deadly to you or your children!

Please see all attached articles: Some articles are “International Research Articles,” by professional medical researchers who’ve also have been finding strange harmful chemicals in drugs and products, due to the Chemical Industry working with the Big pharma industry!

View Link: Chemical Industry Increases Contributions and Lobbying as Congress Takes up Chemical Bill – http://www.cbgnetwork.org/6011.html

Appropriate Taxes for Multinationals!The chemical and pharmaceutical company BAYER has systematically moved profits to low-tax countries. The corporation thereby reduces its tax burden at the expense of taxpayers in Germany, the United States or France. http://www.cbgnetwork.org/5963.html

America, Thank you for continuing to read and support CABIRI, if it wasn’t for my business, family, friends, and colleagues, I may have  given up on myself! Now I’m facing a autoimmune disease, that I was told 2yrs ago were Ulcers. Thanks to the Mirena-Iud support group, it was brought to my attention from another young lady on the other side of the world, who happened to be having the same symptoms, as I. There actually were a few of us speaking about it, and they sent me their research to help me! I thanked the ladies from the bottom of my heart, the doctors in the United States were way off base and had no clue, and left me worried and undiagnosed!

I’ll tell ya America it’s been a fight, although I refused to give up, I now see it as my calling from above to help those who can’t help themselves, between my fathers VA treatment, and my personal medical experience 17 hospitals and 8 surgeries, there was no way a strong woman such as myself, would let this fly and not find out why, what, when, when, where and how!

Here’s to staying alive in the United States! Please see below articles for your knowledge:

The Dangers of ‘Pharma Partnering – http://www.bcam.qc.ca/content/dangers-pharma-partnering (Canada article)

Drug minister bans five legal highs from midnight – http://www.theguardian.com/science/2015/apr/09/government-advised-ban-substance-adhd-drug-ritalin-ethylphenidate?CMP=share_btn_fb&fb_action_ids=1577512209156547&fb_action_types=og.shares

FDA Asked Big Pharma to Self Police on Dangerous Chemicals http://t.co/P8cYGrbO2Y via @sharethis Be aware of toxic drugs still on market

Bernard Merkel: Measuring the performance of health systems—a troubled history – http://blogs.bmj.com/bmj/2015/04/09/measuring-the-performance-of-health-systems-a-troubled-history/?fb_action_ids=1577527129155055&fb_action_types=og.shares

An open letter from Giubilini and Minerva – http://blogs.bmj.com/medical-ethics/2012/03/02/an-open-letter-from-giubilini-and-minerva/

UK Ecstasy strength quadruples in light of competition from legal highs – http://pulseradio.net/articles/2015/04/ecstasy-strength-quadruples-in-light-of-competition-from-legal-highs

AstraZeneca’s Onglyza ‘mortality’ risks noted by FDA reviewers – FiercePharma: http://t.co/3XUrFyvO9d

US states face fierce protests from anti-vaccine activists – http://www.theguardian.com/us-news/2015/apr/10/anti-vaccine-protest-california-facts?CMP=share_btn_tw

Why Women Are Getting Breast Cancer on the Job – http://www.bcam.qc.ca/content/why-women-are-getting-breast-cancer-job

More International Big Pharma news:

Sale of BAYER plastics division: Countermotion to ASM – http://www.cbgnetwork.org/6051.html

Pesticides Linked to Honeybee Deaths Pose More Risks, European Group Says – http://www.cbgnetwork.org/6035.html

Bayer sells Institute plant back to Dow – http://www.cbgnetwork.org/2627.html

UK Regulators Prepare for Review of ‘Forgotten Thalidomide – http://www.cbgnetwork.org/6019.html
Lawsuit Launched to Protect Endangered Wildlife From New, Toxic Pesticide – http://www.cbgnetwork.org/6009.html

Victory for Bees and Freedom of Speech – http://www.cbgnetwork.org/6004.html

New TDI plant: Environmental groups affirm criticism – Friends of the Earth Germany and the Coalition against BAYER Dangers reconfirm their criticism towards the new chemical plant at Dormagen (Germany): http://www.cbgnetwork.org/5960.html

Drug companies spend lavishly to woo veterinarians – Drug companies, veterinarians tight-lipped about cash connection – http://www.cbgnetwork.org/5926.html

Hope your getting the message America! Here’s some interesting translated information

Coalition against Bayer Dangers- The street names changed Carl Duisberg

Current: Discovery Health: Interview with Philipp Mimkes ++++ Colombia: Three injured after fire ++++ The use of toxic pesticides continues to grow ++++ World War: “BAYER does not recognize its responsibility” ++++ “It is an unquestionable duty to help Franco” ++++ Advertising heroin in Spanish newspapers
More: Large multinational companies determine the political game in all parts of the globe. One of the biggest “global players” is the BAYER AG. No country on earth where BAYER is not active. The subsidiaries of the former IG Farben (BASF, Bayer and Hoechst) dominate the German and European chemical industries and have a combined annual 90 billion Euros volume. No government, political or institution can escape the influence of this powerful bloc. Any criticism of BAYER is primarily criticism of multinational companies in general and the chemical industry in particular. WONDERS AND DANGERS

America I had to include this information! Now will the U.S. Government and all Leaders now WAKE UP AND PROTECT U.S. CITIZENS: READ BELOW

Spanish – Translated
150 YEARS OF BAYER
Coalition against Bayer Dangers – The street names changed Carl Duisberg

Current: Discovery Health: Interview with Philipp Mimkes ++++ Colombia: Three injured after fire ++++ The use of toxic pesticides continues to grow ++++ World War: “BAYER does not recognize its responsibility” ++++ “It is an unquestionable duty to help Franco” ++++ Advertising heroin in Spanish newspapers

Coalition against Bayer Dangers (since 1983) supervises the multinational BAYER and coordinates activities against the violation of human and environmental rights by BAYER. “KEYCODE BAYER” contains annexes to the German magazine “Stichwort BAYER” – if you send a message (CBGnetwork@aol.com), you will receive the newsletter “KEYCODE BAYER” regularly via e-mail.

Please help us!
Scientific Committee

Prof. Juergen Junginger, designer
Prof. Dr. Juergen Rochlitz, chemist, former member of the Bundestag (Federal Parliament of Germany)
Prof. Rainer Roth
Wolfram Esche, legal attorney
Dr. Sigrid Müller, pharmacologist
Eva Bulling-Schroeter, member of the Bundestag
Prof. Dr. Anton Schneider, biologist
Dr. Janis Schmelzer, historian
Dr. Erika Abczynski, pediatrician
GLOBAL PLAYER

Large multinational companies determine the political game in all parts of the globe. One of the biggest “global players” is the BAYER AG. No country on earth where BAYER is not active. The subsidiaries of the former IG Farben (BASF, Bayer and Hoechst) dominate the German and European chemical industries and have a combined annual 90 billion Euros volume. No government, political or institution can escape the influence of this powerful bloc. Any criticism of BAYER is primarily criticism of multinational companies in general and the chemical industry in particular.
WONDERS AND DANGERS

The “wonders of chemistry” were a day applauded lightly as “progress of the human race”, but the dangers of producing chemical poisons have made us hostages: No one can escape, it affects us all. Reviews and alternatives are needed. Coalition against Bayer Dangers, which began as a citizens’ initiative in 1978, has worked to publish the risks of large-scale chemical production, eliminate potential hazards and develop alternatives.
ASPIRIN TO FORCED LABOR

Products like ASPIRIN are not the only things related to BAYER through its history, which extends until the nineteenth century. The company also identified with chemical warfare agents, with “drugs” such as HEROIN (an early BAYER registered trademark), and countless homemade insecticides and poisons. The company thinks only of his own benefit and works continuously with dictators and war criminals, from Hitler to Pinochet. BAYER director Carl Duisberg personally propagated the concept of forced labor during World War II. The idea stemmed after the mass murder in the concentration camp IG Farben owned company: Auschwitz-Monowitz. The company was positioned under a huge burden of guilt due to its strong complication in planning, preparation and conduct of the two world wars. The International War Crimes Tribunal for the company pleaded guilty for his role in the war and crimes of the Nazi dictatorship.
SOLIDARITY AGAINST THE POWER OF LARGE COMPANIES

Coalition against Bayer Dangers has been successful in combating global dangers and the seemingly omnipresent power of the BAYER group using action, information, and international solidarity. Coalition against Bayer Dangers unifies people and organizations in a network that continually fighting against BAYER to impose respect for human life, the dignity of working conditions and environmental security. The strength of Coalition against Bayer Dangers comes from solidarity and cooperation. Many volunteers throughout Germany and other countries work together on Coalition against Bayer Dangers, companeras cooperating with 46 countries.
PUBLISH ABUSES:

In their work, Coalition against Bayer Dangers assumes that large multinational companies are decisively responsible for the ecological, social, ethical and global political. Coalition against Bayer Dangers BAYER seen as one of the hounds of the chemical industry as an example of a company with multinational policy. The goal of the Coalition against Bayer Dangers is to make more transparent company policy and publish cases of abuse in factories around the world, helping those affected by abuse, organize resistance, fighting for improvements and propose alternatives, as well as ensure environmental protection, human rights and social security BAYER. Coalition against Bayer Dangers use their knowledge to help ensure that these acts of resistance from neighbors, relatives of employees, environmental groups and others succeed throughout the world. The activists Coalition against Bayer Dangers work together in the same place, if necessary to ensure that BAYER pay attention to environmental protection, social security and human rights. The prospectuses and KEYCODE STICHWORT BAYER BAYER are published quarterly and inform their readers of the latest actions.
ACTION TO ACTION:

Gone are the days of peace and tranquility enjoyed by BAYER at its annual shareholder meeting in Cologne. Provided voting rights of small shareholders, BAYER Critical Shareholders have faced the direction of the company, banks and large shareholders using the benefits of BAYER since 1982. It has become tradition to invite all affected world to meet to talk personally present at the shareholders meeting. A very special form of international solidarity.


THANK YOU FROM CABIRI,
Founder/Owner: Candance Camper
HELP ME SAVE AMERICA YOUR COUNTRY THE U.S. GOVERNMENT IS NOT PROTECTING YOUR FAMILIES!

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Eugenics Theory – Male Sterilization

 Men of America, Eugenics Theory Sterilization applies to you also, please view below many medical disparities that will Alarm you personally and emotionally!

Many American males may not be aware of the numerous Internationally controlled, “Big Pharma” lawsuits in the United States,” which impacts millions of American males livelihoods,  right the to reproduce, and possibly cause permanent life altering deadly problems.

The top American International pharmaceutical corporations are experimenting with various drugs via human beings, which are not only impacting women, also men. Please view all of the links below see the disturbing medical impacts that may hit home to you and your family! Before taking any drug please do your own due diligence for your own health, safety and well-being, if possible try natural healing and home remedies, “Like grandma or your mother may have taught ya”!

View Below International U.S. Big Pharma Male Lawsuits:
Axiron & Heart Attack or Stroke – Axiron is a topical testosterone replacement therapy (TRT) gel manufactured by Lilly USA, Inc. Axiron is a prescription medication that treats “Low T,” or low testosterone levels in men. Symptoms of Low T can include decreased strength and energy, mood changes, decreased libido, and erectile dysfunction.
Axiron was approved by the Food and Drug Administration in November 2010 and remains the only TRT product that is applied directly to the underarms. http://www.girardgibbs.com/axiron-lawsuits/

Testosterone Lawsuit News: Second Testim User Files Testosterone TreatmentLawsuit in Pennsylvania State Court, Bernstein Liebhard LLP Reports

Among other things, the lawsuit claims that Auxilium Pharmaceuticals Inc. and GlaxoSmithKline knew or should have known about the cardiovascular risks associated with Testim, including myocardial infarction,…

Testosterone therapy lawsuits are appearing more frequently as thousands of men report injuries shortly after beginning treatment. New research has shown the increased risk of complications in men that have been undergoing testosterone therapy, or low T treatment. The treatment, intended as a supplemental therapy for men with hypogonadism, could cause increased risk of ischemic stroke, myocardial infarction (MI) or even death.
On January 31, 2014, the U.S. Food and Drug Administration released a safety announcement warning consumers of the potential risk of testosterone therapy and announced that they will be conducting further investigation. Concern arose from two published studies that indicate higher risks of adverse effects in patients within the first three months of treatment. http://www.drugdangers.com/testosterone/lawsuit.htm#sthash.pcwtmsdd.dpuf

Axiron Lawsuit – http://www.axironlawsuit.com/
If you’re a middle-aged or older man, you’ve probably seen commercials urging you to talk to your doctor about testosterone replacement therapy (TRT). If you’re feeling tired, depressed, or lacking in sex drive, the commercial tells you, you may be suffering from low testosterone and could benefit from a supplement like Axiron. What the commercials don’t tell you is that testosterone boosters have recently been linked to serious side effects including heart attack, stroke, blood clots, and death.

Manufactured and marketed by Eli Lilly, Axiron was approved by the FDA in 2010. Sales reached nearly $50 million the following year, and the company spent twice that on a marketing campaign to promote the entire TRT industry. The target audience of these ads were men over the age of 30, the approximate age at which testosterone levels begin to decrease.
Testosterone Lawsuit News: Second Testim User Files Testosterone Treatment Lawsuit in Pennsylvania State Court

Read more: http://www.virtual-strategy.com/2014/03/25/testosterone-lawsuit-news-second-testim-user-files-testosterone-treatment-lawsuit-pennsyl#ixzz2x7uwlKbd
Read more at http://www.virtual-strategy.com/2014/03/25/testosterone-lawsuit-news-second-testim-user-files-testosterone-treatment-lawsuit-pennsyl#qplwXzrGTxM6MmUA.99

Court documents filed in the U.S. District Court, Northern District of Illinois indicate that five AndroGel lawsuits are currently pending in that jurisdiction. These include four cases filed on February 4th on behalf of men who allegedly suffer heart attacks, strokes and heart failure due to their use of the medication.

(Case Nos: 1:14-cv-00776, 1:14-cv-00780, 1:14-cv-00777, and 1:14-cv-00772) The Fifth AndroGel lawsuit was filed on February 10th and claimed that the Plaintiff suffered pulmonary embolism, deep vein thrombosis, and other serious cardiovascular injuries after using multiple doses of the drug. (Case: 1:14-cv-00917)

All of these filings followed an alert issued by the U.S. Food & Drug Administration (FDA) on January 31, 2014, that revealed the agency had undertaken a review of low testosterone therapies, after two studies indicated the drugs might increase the risk for heart attacks, strokes, and sudden death in certain men.

http://www.virtual-strategy.com/2014/03/25/testosterone-lawsuit-news-second-testim-user-files-testosterone-treatment-lawsuit-pennsyl

AndroGel Class Action Lawsuit 2014
Our unsafe prescription drug side effect law firm is currently investigating possible class action and single party claims against manufacturers of testosterone medications including AndroGel for the development of harmful side effects amongst users. In 2000 AndroGel 1.0% was approved by the FDA. Since then several studies have shown a significant, 30% in some cases, increase in the risk of Coronary Angiography and other cardiac based illnesses. In response the FDA issued a black box warning for the product in 2009. According to recent FDA warnings the use of AndroGel 1% and AndroGel 1.62% manufactured by Abbot Laboratories can result in cardiac complications including, heart attack, stroke, and pulmonary embolism.

Androgel Manufacturers Face Class Action for Antitrust Violations
A class action complaint filed last week in New Jersey federal court claims damages for violations of the Sherman Antitrust Act by brand-name and generic manufacturers of the drug, Androgel.

The suit alleges that brand name and generic manufacturers conspired to fix and raise the price of Androgel, by overcharging Plaintiffs and others by millions of dollars and depriving them of cheaper generic versions of the drug. The complaint estimates that hundreds or thousands of people or companies have been economically injured by the drug manufacturers’ conduct.

http://www.bigclassaction.com/lawsuit/androgel-class-action-antitrust.php
Propecia Side Effects – Lawsuits have been filed against Merck & Co. aka Merck KgaA alleging seriousPropecia side effects including Propecia sexual dysfunction and other Propecia side effects in men. Among allegations in the most recent Propecia lawsuit are that Propecia (Finasteride) can cause anxiety attacks and insomnia.

Plaintiffs allege that Propecia long term side effects, such as the emotional symptoms, remain years after patients have stopped taking the medication. Some Propecia patients may be taking Proscar, which is a higher dose version of finasteride. http://www.lawyersandsettlements.com/lawsuit/propecia.html#.UzOShPldXww

Two Navy Veterans Win Asbestos Mesothelioma Settlements
New York, NY: The lawsuits of two men who alleged a lifetime of working with asbestos led to their developing mesothelioma, a rare cancer that attacks the lining of the lungs have been successfully settled. http://www.bigclassaction.com/settlement/navy-veterans-asbestos-mesotheliom..

Risperdal Gynecomastia (Breast Development in Males)
The antipsychotic drug has also been linked to an increased risk of young males developing gynecomastia, an increase in breast tissue. This condition is thought to be caused by increased levels of prolactin, a hormone involved in lactation and increased in Risperdal patients. In November 2008,The Wall Street Journal reported that Risperdal can stimulate the production of prolactin.

Although Risperdal carries a warning about the risk some doctors have called on the FDA to strengthen the warning. Boys who have developed gynecomastia may experience pain or nipple discharge. Mild cases can be resolved with liposuction, while more severe cases will require a mastectomy.

http://www.lawyersandsettlements.com/lawsuit/risperdal.html#.UzOTxfldXww
http://www.lawyersandsettlements.com/articles/risperdal/interview-risperdal-lawsuit-side-effects-3-19603.html#.UzOUz_ldXww

Canada’s Supreme Court strips Viagra patent from Pfizer
http://www.reuters.com/article/…/us-viagra-idUSBRE8A70XG2012110&#8230; Nov 8, 2012 – A box of Viagra, typically used to treat erectile dysfunction
In the past, Pfizer has successfully defended patent lawsuits from Teva
NAION: Another Name for a Serious Condition Pfizer, the manufacturer of Viagra, faces numerous defective drug lawsuits claiming they failed to adequately warn the public about the dangers of NAION, the acronym for a condition known as “non-arteritic anterior ischemic optic neuropathy,” also called eye stroke. Pfizer has argued that no evidence exists linking Viagra to NAION, but attorneys are seeking a class action lawsuit on behalf of the 24 million men who have used Viagra since it came on the market.

Viagra lawsuits focus on physician reports claiming Viagra affects blood circulation to the optic nerve, resulting in vision loss. Attorneys are seeking to force Pfizer to place a ‘black box’ warning on the drug’s label, the strongest warning any medication can receive. Use of Viagra has been linked to; Sudden death – Cardiac events – Blindness – A sudden drop in blood pressure in some patients

Generic Viagra’s US Launch Set for 2017 as Teva, Pfizer Settle genengnews.com/gen-news…viagra-s…pfizer…lawsuit/81249269/ Dec 18, 2013

Viagra’s U.S. Launch Set for 2017 as Teva, Pfizer Settle Lawsuit … and Pfizer agreed to resolve a longtime patent lawsuit over the male – It is not worth your life Gentlemen!!

Pfizer Inc. Rigged Canadian Viagra Patent Filing Lawsuit – BioSpace http://www.biospace.com/News/pfizer-inc-rigged-canadian-viagra…/282068 Dec 12, 2012 – Pfizer illegally gamed the Canadian patent system to monopolize the market for Viagra and overcharge customers, a class action claims in.

Viagra, Cialis, and Levitra | Dennis Herron and Associates… dennisherron.com/hot-issues/viagra-cialis-and-levitra/ Viagra, Cialis, and Levitra Blindness Class Action Lawsuit. Viagra. Viagra was introduced in 1998 and had $1.68 billion in sales last year. The impotence drug.

Cialis (tadalafil) Side effects and lawsuit claims Eli Lilly http://www.resource4thepeople.com/defectivedrugs/cialis.html – by WJ Callahan Mar 6, 2013 – Cialis side effects such as vision impairment and heart pains, lawsuitsfor. … Accutane Lawsuit: Recall Class Action Lawyer…
Just for men – Disfigurement, pain, chemical burns, Review 637411 http://www.complaintsboard.com/…/just-for-men-disfigurement-pain-chemical&#8230; Oct 19, 2012 – Please include me in any class action lawsuit against Just For Men, my injuries need Justice. I am a public figure in the Fashion Industry,
Just For Men Chemical Burns Alleged in Lawsuits Being – PRWeb ww.prweb.com/releases/2014/01/prweb11482171.htm Jan 12, 2014 – Wright & Schulte LLC Launched Just For Men Lawsuit Investigation After … most powerful corporations take responsibility for their actions.
http://www.AgelessMaleresettinSettlement.com – Burmeister v NAC http://www.classactionsettlementnews.com/www-agelessmaleresettinsettlement- April 20, 2013 Filed Under: Class Action Lawsuit The Ageless Male lawsuit claim that state and consumer protection laws were violated in … The defendants deny any actions of wrong doing in the case but have agrees to settle.
Ageless Male is a Fraud they got sued in a Class Action Lawsuit – https://www.youtube.com/watch?v=x3S6dYFv5uU
Penis Enlargement Lawsuits – A New Jersey man has filed a false advertising lawsuit against a maker of herbal penis enlargement pills, alleging the medicine does not fulfill its promises, the plaintiff’s lawyer said on Monday. Two similar cases, filed last year in Colorado and Ohio, accuse manufacturers of herbal dietary supplements, VigRx and Enzyte, of falsely claiming to be able to add substantial length and girth to a man’s penis. All three suits seek class action status and claim to represent more than 1 million total plaintiffs. http://www.4-men.org/penis-enlargement/penis-enlargement-lawsuits.html

Proscar Lawsuits Claim Drug Caused Irreversible Sexual Side Effects – Men who suffered from sexual side effects or were diagnosed with prostate or breast cancer following use of Proscar. Damages Proscar sexual side effects can include impotence, problems with orgasm, erectile dysfunction, loss of libido, and ejaculation problems.

Proscar has also been associated with the development of prostrate cancer and male breast cancer in users. Merck – Proscar is a drug used to treat enlarged prostate glands. http://www.classaction.org/proscar

Finasteride Side Effects, Erectile Dysfunction Lawsuit http://www.yourlawyer.com›Topics› Defective Drugs Finasteride side effects increases erectile dysfunction (ED) risk,lawsuits are being evaluated by Parker Waichman LLP for Finasteride users reporting male sexual …

Nationwide Mr. Magic Male Enhancer Recall | Male http://www.schmidtandclark.com/mr-magic-male-enhancer-recall Free Male Enhancement Drug Recall Case … of trial lawyers that focus exclusively on the representation of plaintiffs in male enhancement drug recall lawsuits.

Drug Information – DrugAlert.org -Drug Recalls, Drug Lawsuit http://www.drugalert.org Recently, the U.S. Food &Drug Administration called for http://www.HardMenStore.com, an erotic retailer geared towards men, to recall 430 lots of its Silver Sword and Clalis

Men Claim Merck Baldness Drug Causes Impotence http://www.breakinglawsuitnews.com/men-claim-merck-baldness-drug-causes…Nine men have filed a lawsuit against Merck for their male pattern baldness drugsPropecia and Proscar, alleging the drugs cause sexual dysfunction, even after they …

Lyrica Side Effects Lawsuit – Do I Have A Lawsuit Lawyer doihavealawsuit.com/lawyer-attorney/70-side-effects-lawsuit/382…Lyrica Side Effects Lawsuit.

Pfizer’s antiepileptic drug Lyrica has been … the FDA alerted consumers about painful gynecomastia and breast enlargement in male due …

http://www.lawyersandsettlements.com/search.html?keywords=male+lawsuits Regenerect Supplement Consumer Fraud Class Action Filed
Los Angeles, CA: A consumer fraud class action lawsuit has been filed against Regenerect Natural Male Erectile Stimulant, claiming the product is mislabeled as a “drug-free,” “natural” diet supplement, when it contains active ingredients found in the prescription drugs Cialis and Viagra. According to the lawsuit, the male enhancement pro…

Male Power Plus
An over-the-counter pill, Male Power Plus, that is used to treat impotence, is being recalled because it may contain the unlabeled prescription drug ingredient tadalafil, which can cause dangerous side effects in people taking nitrates to treat such diseases as diabetes, heart disease and hypertension. Tadalafil, also known as Cialis, was approved by…

Nationwide Recall of Dietary Supplements X-Hero and Male Enhancer
Mar-28-11 Washington, DC: USA Far Ocean Group Inc is conducting a nationwide recall of the Company’s two supplement products sold under the names X-Hero and Male Enhancer. The Company has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of X-Hero sample found the product contains sulfosildenafil, the analogue of…

FDA Warns Dietary Supplement Contains Potentially Harmful Synthetic Steroids
Washington, DC: The US Food and Drug Administration is advising consumers to immediately stop using a product called Mass Destruction, marketed as a dietary supplement for muscle growth. The product is labeled to contain at least one synthetic anabolic steroid and has been linked to at least one reported serious illness. The FDA was alerted by t…http://www.lawyersandsettlements.com/search.html?keywords=male+lawsuits&page=8

Nature & Health Recalls Male Enhancement Products
Opteron 1 Inc., doing business as Nature & Health Co., is conducting a nationwide recall of the company’s 5 supplement products sold under the following names: LibieXtreme, Y-4ever, Libimax X Liquid, Powermania Liquid and Capsule, Herbal Disiac. Lab analysis conducted by the the Food and Drug Administration (FDA) of these five samples found they contain…

PAXIL DAMAGES DNA IN MEN’S SPERM – http://www.lawyersandsettlements.com/search.html?keywords=male+lawsuits&page=10

Investigators Find Paxil Effects Male Fertility New research just released shows that the antidepressant Paxil, also known as paroxetine, has a disturbing and potentially far-reaching effect on men who are taking the drug: it damages men’s sperm through DNA fragmentation, effecting fertility. While the researchers noted that they did not study. Asbestosis – Asbestosis Lung Disease, Asbestosis Lawsuit

Asbestosis disease is a serious breathing disorder caused by inhaling asbestos fibers. To ensure asbestosis compensation , it is recommended that you get help from an experienced asbestosis lawyer , who will file your complaint against all your employers and the companies that may have caused asbestos exposure. Asbestosis Asbesto…http://www.lawyersandsettlements.com/lawsuit/paxil-side-effects-fertility.html#.UzO8n_ldXww

Family Blames Propecia Finasteride for Son’s Suicide – Montgomery, NJ:A Propecia lawsuit is serious enough, as it suggests ultimate dissatisfaction with a product and the impact it has on an individual. The following case, however, is troubling in that a promising life has been lost, allegedly due to the effects of Propecia finasteride. http://www.lawyersandsettlements.com/articles/propecia/propecia-lawsuit-finasteride-side-6-17827.html#.UzO96fldXww

Cialis: Side Effects and FDA Updates – Since its introduction to the market, the FDA has issued two updates regarding Cialis side effects. These warnings have not led to significant litigation against the erectile dysfunction medication. While some people may have obtained a Cialis settlement due to adverse reactions to the drug, these results have not yet been made public.

In 2005, the first warning issued by the FDA concerned the risk of developing a vision condition known as NAOIN. This is a temporary or permanent sudden loss of vision in one eye. Many of those who have experienced this Cialis side effect had another contributing condition, such as hypertension. – See more at: http://product-liability.laws.com/cialis-lawsuit#sthash.JrY96nYk.dpuf

Cialis Lawsuit Information & Causes – The drug Tadalafil, marketed under the name Cialis, was approved by the Federal Drug Administration, FDA, in 2003 for use as a treatment for impotence and erectile dysfunction in men. Since that time, there have been numerous reports of severe side effects including non-arteritic anterior ischemic optic neuropathy, NAION, blindness and hearing loss http://www.acostawilliams.com/cialis-lawsuit/

Prostate Cancer and Male Bladder Sling Implant Problems – Occasionally men need bladder sling implants, especially those that have had prostatectomies, or the removal of the prostate. It can significantly improve longevity, but it also leads to stress urinary incontinence. While some implants do well, synthetic bladder sling implant failures are common among both sexes. http://www.topclassactions.com/lawsuit-settlements/prescription/3474-prostate-cancer-and-male-bladder-sling-implant-problems/

Male circumcision lawsuit – antimisandry.com – Articles antimisandry.com/campaigns-news/male-circumcision-lawsuit-10605.html Hmmmm? I hate to dump cold water on you lawsuits because its an important project but such lawsuits will be brushed aside by the agents of Satan in black robes of hell

Lipitor Diabetes Lawsuit – http://www.nastlaw.com/lipitor-diabetes-lawsuit/
Lipitor FDA Warning In February 2012 the U.S. Food and Drug Administration added new warnings to the labels of

Lipitor and other cholesterol drugs. The new warnings were based on the results from a study that showed statins may raise blood sugar levels, leading to memory loss and increasing the risk of developing Type II diabetes. Lipitor has been linked to an increased risk of Type 2 Diabetes.

A study by the University of Massachusetts showed women taking lipitor have a 48% higher risk of developing diabetes.The chance of developing diabetes from Lipitor is even higher in women with common risk factors such as obesity, high blood sugar, or a history of family diabetes.

Virilis Pro Sued By Adrian Carter For Male Enhancement Pill’s Alleged DISGUSTING Side Effect – If it does, meet Adrian Carter, who claims in a lawsuit filed on Monday that a Virilis Pro pill made his penis bleed and led to a terrifying surgery in which much of his manhood’s skin had to be removed.”During sexual intercourse, plaintiff experienced significant pain and observed a large quantity of blood squirting out of his penis onto the sheets, walls and mirror in the hotel room; his penis and scrotum were visibly swollen http://www.huffingtonpost.com/2012/08/29/virilis-pro-male-enhancement-adrian-carter-lawsuit_n_1840561.html

FAQ: Mesh patch injury, symptoms, lawsuits, hernia damage http://www.anapolschwartz.com/practices/surgical-mesh/faq.asp
FAQs FAQ: Mesh Patch Injury, Symptoms,Lawsuits, Hernia Damage. I’ve had hernia repair surgery. How do I know if I have one of these recalled mesh patches?

Depo-Testosterone Lawsuit TRT Lawsuits ww.depotestosteronelawsuit.com Depo-Testosterone Lawsuits are being filed in record numbers as thousands of men around the country report injuries after undergoing treatment.
osteoporosis in men – Fosamax Femur Fracture Lawsuits http://www.fosamaxlawsuitscenter.com Men taking Fosamax could also be at risk for injuries worse than their Osteoporosis, however, Fosamax studies have not focused on men.
Enzyte Scam Exposed! The Shocking Truth of Male Enhancement – http://www.enzytescam.com/

Kugel Hernia Mesh Patch Dangers – The Composix Kugel Mesh Patch is manufactured by Davol, Inc. (parent company: C.R. Bard, Inc.) and used in hernia surgery repair. Problems with the “memory recoil ring” that opens the Composix Kugel Mesh Patch can break under the stress of placement of the large sized products in the intra-abdominal space. This can lead to bowel perforations and/or chronic intestinal fistulae, or abnormal connections or passageways between the intestines and other organs. http://www.herniameshlawsuit.com/ – Hernia Mesh Recall Lawsuit Davol Bard Kugel Patch Lawyer

Testosterone Lawsuit Filings Continue, as New Study Questions Accuracy of Blood Tests Used to Diagnose Hypogonadism in Men – NEW YORK, March 14, 2014 /PRNewswire/ — As testosterone lawsuit (http://www.testosteronelawsuitcenter.com/) filings continue to mount against the manufacturers of AndroGel and similar medications, Bernstein Liebhard LLP notes that a new study is raising questions about the accuracy of blood tests used to diagnose hypogonadism (low testosterone) in men.

Testosterone therapies are approved to treat hypogonadism in men who suffer from the condition due to an underlying illness or injury. Drugs in this class include: Axiron- AndroDerm – AndroGel- Bio- T Gel- Delatestryl – Depo-Testosterone – Foresta – Striant – Testopel -Testim – The U.S. Food & Drug Administration (FDA) announced on January 31, 2014 that it had launched a safety review of prescription testosterone treatments after two studies indicated the medications might be associated with an increased risk of heart attack, stroke, and death in certain men. http://www.prnewswire.com/news-releases/testosterone-lawsuit-filings-continue-as-new-study-questions-accuracy-of-blood-tests-used-to-diagnose-hypogonadism-in-men-250351241.html

Axiron- AndroDerm – AndroGel- Bio- T Gel- Delatestryl – Depo-Testosterone – Foresta – Striant – Testopel -Testim

http://www.fda.gov/safety/medwatch/safetyinformation/safetyalertsforhumanmedicalproducts/ucm384225.htm&#8221; U.S. The Food & Drug Administration (FDA) Arial, announced on January 31, 2014 that it had launched a safety review of prescription testosterone treatments after two studies indicated the medications might be associated with an increased risk of heart attack, stroke, and death in certain men.

http://www.prnewswire.com/news-releases/testosterone-lawsuit-filings-continue-as-new-study-questions-accuracy-of-blood-tests-used-to-diagnose-hypogonadism-in-men-250351241.html

Additional information you may find interesting –

Schering AG struggled to rebuild its business during the difficult conditions that prevailed following the war. The company used its expertise in steroids to produce the first birth control pill, simply known as “the Pill,” introduced to the European market in 1961. With the profits from this product, Schering was able to diversify and one again try the U.S. market. In 1972 it acquired a half-interest in New Jersey-based Knoll Pharmaceutical, the first of several acquisitions Schering would make in the United States over the next several years.

“http://articles.chicagotribune.com/2013-04-16/lifestyle/sns-rt-us-bayer-yasmin-patentbre93f13y-20130416_1_yaz-lupin-ltd-yasmin&#8221;

Baby Boom Forces Brazil To Confront Fake Medicines
By David Willman, Tribune Newspapers: Los Angeles Times.

“http://www.bizjournals.com/eastbay/stories/2007/09/17/story15.html?
Bayer is locking in production and royalties from

“http://www.bizjournals.com/profiles/company/ch/basel/novartis_ag/3010243&#8221;
Novartis AG which is selling the former Chiron facility and launching its own version of the drug. The deal, with points still being negotiated, allows Bayer’s Berkeley biotech subsidiary, Bayer HealthCare Pharmaceuticals, to add 550 people, and gives Bayer greater control over its Betaseron business, which had second-quarter sales of $353.7 million.

“This is a different environment, but it’s still an exciting opportunity,” said Alfred Merz, who heads Bayer’s Emeryville transition team. “It’s really forward-looking.”As Novartis brings its version of Betaseron to the market in 2009, Bayer will produce it, shed the royalties it currently makes to Novartis, and, instead, receive royalties from the Swiss drug giant. Bayer, says Michael Schuppenhauer, a biotech consultant in Half Moon Bay, must prove it has the attention span to build a strong biotech business. Bayer doesn’t appear to know its long-term strategy, he said. “Bayer has a lot of strategic decisions to make and a lot to do in their pipeline to be a serious, good biotech player,” he said.

Meanwhile, Novartis is expected eventually to market an oral multiple sclerosis drug that could be made elsewhere, whittle Bayer’s MS drug market share and Bayer’s Betaseron royalty receipts. Plus, other companies – including Alameda’s Pepgen Corp. and Palo Alto’s Bayhill Therapeutics Inc., both of which have products in Phase 2 clinical testing – are working on new-generation drugs for an MS market valued by drug-development companies at more than $5 billion. At the same time, Bayer is digesting last year’s acquisition of Schering AG, and rumors have surfaced that Novartis is targeting Bayer as a merger target.Leading Causes of Death by Age Group, Race/Ethnicity Males, United States, 2010* – http://www.cdc.gov/men/lcod/2010/LCODrace_ethnicityMen2010.pdf

Doctors of Death: Understanding THE HIPPOCRATIC OATH by – http://www.youtube.com/watch?v=B7ehZVZUXbs

Please Read Men of America
http://www.worldlifeexpectancy.com/usa/african-american-death-rate
African Death Rate Per 100,000 … CDC official final death report

Death by Medicine Trailer

Potential Testosterone Treatment Lawsuits Being Evaluated by Sim –

Men

TOP PRODUCERS IN AMERICA –
Medicine Or Mass Murder? Guideline Based on Discredited Research May Have Caused 800,000 Deaths In Europe Over The Last 5 Years
http://www.forbes.com/sites/larryhusten/2014/01/15/medicine-or-mass-murder-guideline-based-on-discredited-research-may-have-caused-800000-deaths-in-europe-over-the-last-5-years

Special Report: Hangar 1 The UFO Files E02 Underground Bases – http://www.youtube.com/watch?v=5iMJXnoQrO8

CABIRI,
Web Content Freelance Writer

CABIRI Business Services

NEXIUM LAWSUITS – HIDDEN DEBACLE – Win Your Lawsuit

CABIRI – Consumer Advocacy Business Industry Research and Investigation 

If you can figure out the below piece’s of this puzzle you will come up with your answer to 

win your Nexium Cases! If you can not please email with will be more than happy to assist you! 

NEXIUM – 

Astrazeneca – Headquarters – London United Kingdom

Astrazenca – Astra AB – Zeneca Group – Sweden + British = AstraZenca plc,

ICI – Imperial Chemical Industries – Netherlands

ASTEX – London U.K.

Bayer Health Care (Bayer AG)  –  Adrea – Astrazeneca

GlaxoSmith Kline – The Wellcome -Trust – Sanger Instituute – UK

Unilever –  Netherlands

BASF – Germany

Henkel AG & Company, KGaA – Germany

http://www.consumer2savlives.comImage

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TODAY’S PHARMA NEWS IMPACTING LIVES

http://www.katv.com/story/24206652/medical-test-surprises-what-should-you-be-told

Medical test surprises: What should you be told?

Leukemia Drug Boosts Endocrine Breast Tx

http://www.medpagetoday.com/MeetingCoverage/SABCS/43426

 MI Admissions on Upswing in Younger Women

Published: Dec 13, 201

http://www.medpagetoday.com/Cardiology/MyocardialInfarction/43424

Kidney Group Ditches LDL Targets for Statin Tx

http://www.medpagetoday.com/Endocrinology/GeneralEndocrinology/43348

Salmonella Outbreak Traced to Chicken

http://www.webmd.com/food-recipes/food-poisoning/news/20131008/salmonella-outbreak-chicken

Navigating the NHS

 A third of GP practices ‘fail standards’

 

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The United States Medical Board does not accept international degree’s, although the government allows international business owners with green cards to run billion dollar U.S. corporation. The top U.S. Big Pharma and Biotech corporations are run by other countries along with many other business & corporations in the United States!

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