CABIRI RELEASES 2013 BIG PHARMA RESEARCH ARTICLES:
CABIRI Research: Big Pharma Research & Investigations IG Farben – Berlex – Schering Plough
Schering – Plough – Berlex – Bayer AG
Mirena IUD – Bayer AG & Subsidiaries
Corporate History – Lawsuits – Plaintiff Emails
To: Bayer AG – Executive Members & Subsidiaries
RE: Mirena – Bayer AG, Bayer Healthcare, Schering AG, Berlex Corporation, I.G. Farben
Schering Plough – Founded in 1851, by Ernest Christian Friedrich Schering
Company Formed: Schering AG – Germany
History: Following the entry of the United States into World War II in 1941. U.S. President
Franklin D. Roosevelt ordered Schering AG’s, U.S. Assets to be seized. The company was placed under Government administratorship until, 1952, by which all prior assets were sold to corporates his business and generated $254.5 million in sales by 1954. That figure doubled by 1962.
In 1971 Plough merged Plough Chemical Company Incorporated with Schering Corporation. The Schering corporation was a manufacturer of prescription pharmaceuticals, the merger name of the two corporations was named, Schering-Plough. Schering was able to gain entry back into the United State’s by merging with Plough in the pharmaceutical industry.
Release date from U.S. – 1941 to Re-entry date back into U.S. – 1971
Mr. Abe Plough, exhausted his full business ownership in his company and became chairman of the new merging corporation. Five years after the merger in 1976, Plough retired from his company he’d started in 1908.
Schering – Plough remained in America, growing there corporation no back in the United States. By 2005 Schering-Plough had 1.4% market share in the United States., becoming 17th in the top 20 pharmaceutical corporations by sales compiled y IMS Health of America.
Schering-Plough was a full member of the “European Federation of Pharmaceutical Industry and Associations” (EFPIA).
In November 2009, Schering-Plough merged with Merck & Company, or Merck KGAA in a reverse merger. Merck became a subsidiary of Schering-Plough. The two companies manufactured several pharmaceutical drugs, Claritin, and Clarinex, an anti-cholesterol drug Vytorin and a brain tumor drug Temodar.
Clarinex, Claritin, Vytorin, Temodar, Pipeline pharmaceutical Products
Class-Action Lawsuit Filed Against Claritin’s Maker – 2003
Consumer groups have filed a class-action lawsuit against pharmaceutical giant Schering-Plough – http://product-liability.laws.com/claritin-lawsuit – The [agency] has reviewed these ads and concluded that they are misleading and violate the Federal Food, Drug and Cosmetic Act and applicable regulations and should be discontinued immediately,” says the letter from Joan Hankin, JD, a consumer promotion analyst at the FDA.
The complaint, brought to a New Jersey state court, accuses the drug company of “deceptive advertising and overpricing” for Claritin, America’s most widely prescribed allergy drug.
Schering-Plough Settles Clarinex Class Action for $165 Million –
class-action.php– 2010 Specifically, the suit alleged that between May 2000 and February 2001 Schering-Plough made false statements that did not adequately disclose “serious and widespread deficiencies” in its quality and manufacturing operations. This, in turn, risked delay of FDA approval of Clarinex, a successor drug to Claritin.
Vytorin Class Action Lawsuits Mount as Justice Department Investigates – See more at: http://www.aboutlawsuits.com/vytorin-class-action-lawsuits-mount-1636/#sthash.nl7O9PnQ.dpuf – 2008 Vytorin lawsuits have been filed against Merck and Schering-Plough involving consumer fraud actions for selling a medication which provides no benefits, cases alleging personal injuries caused by the drug and claims to establish medical monitoring for users who were given
Temodar Bone Marrow Injury & Birth Defects –
Two Temodar lawsuits were filed against the drug’s parent companies, regarding illicit marketing and sales practices. In 2006, Schering-Plough, the former Temodar manufacturer, faced a Department of Justice investigation which uncovered mis-marketing and illegal sales practices.
The Temodar lawsuit found that the company marketed Temodar for unapproved forms of brain cancer, bribed doctors and promoted the sale of its Temodar products. For these charges, the company was ultimately forced to pay $435 million fines. – See more at: http://product-liability.laws.com/temodar
Following the resolution of this Temodar lawsuit, the drug was purchased by Merck. In 2011, the Department of Justice issued a subpoena seeking materials concerning marketing of Temodar dosage products.
This Temodar lawsuit was issued as part of an investigation which could lead to a Temodar concerning marketing abuses committed by Schering-Plough. In the past, similar Temodar lawsuits have included a fund for victims of adverse effects as a condition of settlement. http://product-liability.laws.com/temodar-lawsuit
Summary: Schering-Plough 1971 – Merck & Company or Merck KGAA merger – 2009
Merck & Company – Schering Plough Schering Products: sugammadex, Cerazette, Desloratadines, Neoclarit, Esmeron, Famvir, Famcilovir, Intron A & PEG-Intron, Levitra, Livial, Marvelon, NuvaRing, Quazepam, Remeron, Buprenorphine, Zetia; OTC: Afrin, Coricidin, Coppertone, Dr. Scholl’s, Zinka, Bain de Soleil, PD-1 antibody.
Schering-Plough – Merck & Company
Organon Research Analysis
2004 – Schering – Plough was accused of marketing gimmicks and payoffs to doctors for prescribing the company’s pharmaceutical products. At that time Schering entered into a consent decree with the FDA in 3/2002, from their manufacturing problems with Albuterol inhaler. Schering-Plough was ordered to pay $500 Million US dollars to the US Treasury.
Bridon (sugammadex’s) – Rejected 3x by U.S. FDA – 2008 due to hypersensitivity reaction concerns to the drug. Clinical trial
Approved by the European Union – 2008
Sugammadex’s – PD-1 antibody, repoductive medicine, contraception, psychiatry, HRT, anesthesia, Diosynth, birth control pills,
Marvelon, asenapine: some products acquired by purchase of Organon of Scotland
Organon Company Analysis:
Orgination: Akzo Nobel: 1646 – Sweden-Denmark-1777-
Organon: Human health business unit of Akzo Nobel – 80yrs.(Pharmaceutical industry)
Founded: Dr. Saal van Zwanenberg in Oss, Netherlands – 1923
Zwanenberg-Organon – New House Research – Scotland, United Kingdom, Courtaulds
Products – estrogens, insulin, cortisone, fibre
Koninklijke Zawnenberg Organon (KZO) – Fiber company AKZO
Base: New Jersery – Arnhem, Amsterdam
Manufacturing: Netherlands, Germany, United Kingdom, Ireland, China, Japan, Americas. High-Tech coatings, artificial fibers, paint,
2007 Schering-Plough New Jersey, acquired Organon, 2009 Schering-Plough mergered with Merck and Company aka Merck Sharp &
Dohme or MSD
Schering-Plough, N.J. The American Drug Maker agrees to purchase Akzko Nobel’s Organon Biosciences Unit – valued @ 14.4Billion –
The merger astounded many investors, who were waiting for the announcement of a planned IPO offering of Organon, the maker of birth control pills, for about $10 billion.
Azko Nobel world’s largest paint maker and coatings, chemicals – Amsterdam
Akzo – Last European company with chemical and pharmaceutical
1895 – Akzo Nobel’s: Eka Chemicals Pulp and paper chemicals
1923 – Produced Insulin from pancreases of animals
1968- Courtaulds acquires international paints
1969 – Merger AKU – KZO = AKZO
1994 – Akzo Nobel industries merge Akzo Nobel
1998 Akzo acquires – Courtaulads
2007 – Akzo Nobel sells Organon Biosciences NV – New Jersey Schering – Plough
Organon – Akzo Nobel Analysis
CFO: Organon Biosciences N.V. – Arhem, Netherlands – Dr. Jorg Spiekerkotter – 2006
Prior: Schering AG executive board member responsible for Leader of Finance Administration and Human Resources – Also prior, Head of Legal Hoescht Schering Agrevo. Organon hire’s Dr. Spiekerkotter as CFO, U.S. Schering-Plough New Jersey purchases
Organon a year later – 2007
Dr. Spiekerkotter CFO and board member of management leaves Organon Biosciences N.V., 2007. After the Schering-Plough purchase of Organon, Akzo Nobel, reduced pension liabilities, debt and paid for a share buy back of 1.3Million
Organon Pharmaceutical Inconsistencies:
Akzo Nobel Feels the pinned as Organon contraceptive sales drop in 2002
The Organon units of Akzo Nobel NV faired poorer than competitor Schering AG reporting a two perecent a year – on – year decline in the use of the contraceptive pill in the Netherlands in the first half of 2002. Sales of third-generation pills recorded the worst fall, declining 13% over a review period. Sales of Organon’s third-generation pills Marvelon & Mercilon fell 19% and 21%, while Schering’s Femodeen fell 18%.
Media – 2001 Alerts:
Users of third-generation pills had 70% greater chance of developing thrombosis than users of second-generation pills.
Dutch Foundation Pharmaceutical Statistics: Market leader Microgynon, Schering’s second generation pills, appears to have benefited from a drop in sales of third-generation pills – research published by the Dutch Foundation (SFK) indicates 13%
increase in the first half of sales. In addition, third-generation pills are were losing ground to Schering’s “Yasmin,” a pill launched in the Netherlands 4/2001. Organon was battling negative news regarding Implanon – a contraceptive inserted under the skin.
Women filed lawsuits, some claims stating they had fell pregnant while using the product, headaches, vein inflammation, bleeding and more lawsuit claims.
http://www.nytimes.com/1999/08/27/us/maker-of-norplant-offers-a-settlement-in-suit-over-effects.html Maker of Norplant Offers a Settlement In Suit Over Effects
(Plaintiff: Also participated in Norplant lawsuit and settlement)
Norplant II developed by Population Council Schering (OY) & Norplant 1 by Wyeth
Schering AG, Akzo Nobel’s Unit to end collaboration on Male Contraceptives – 2006
Schering AG and Akzo Nobel’s Organon unit will terminate a research collaboration into male fertility control at the end of Phase II clinical trial, which was designed to test a combination of two hormones known to suppress sperm production.
Bayer – Berlex
Schering AG – Dates back to Chemische Fabrik auf Actien – Chemicals operations
1930’s – Company diversified for Schering AG
1876 – Schering Glatz – Medicine distribution company launched – 1929 dissolved
1929 – Established Schering Corporation hormone research and synthesize steroid drugs based in New York
Formed Berlex Corporation in 1979 after acquiring assets of the Internal Medicine division of Cooper Laboratories, New Jersey
Area’s – Cardiovascular disease, birth control, diagnostic imaging, endocrinology
1980’s: Iodinated contrast agents used in imaging launched in U.S.
1982: Oral contraceptives, Leveln and Tri-Leveln, Magnevist launched
Schering- Plough sued Schering AG, claiming Berlex infringed upon it’s trademark
Results: Schering AG agreed to use the Schering name in the U.S., and Canada in connection with its pharmaceutical products, relying on the Berlex trademark.
Triton and Codon U.S. Corporation consolidation and purchase to form Berlex Biosciences of California – prior Ortho Research Center – built by Ortho Division of Chevron Chemical Company – Purchased @ $53million
Schering acquired Shell Oil biotech portion 1990 – Fludura, Betaseron
Schering acquires in 1993 – Chevron Chemical Company
Co-Partnership: Abbott Laboratories to sell Magnevist and Ultravist
Berlex Products: Fludara, Betaseron, Climara, Feridex I.V.,
Berlex acquired by Bayer AG
Berlex Lawsuits – Magnevist, Fludara, Betaseron
FDA Panel Suggests Bayer, GE MRI Drugs Be Restricted
Critical Drug Recall and Drug Shortages http://www.gilmanlawllp.com/defective-drug-side-effect-lawsuits/ben-venue-and-novartis-drug-recalls-and-shortages/
In the case of Ben Venue Laboratories, the shut-down of its Ohio manufacturing plant has resulted in the recall of the Fludara leukemia drug, as well as shortages of vital medications, including the life-saving cancer drugs, methotrexate and Doxil.
Betaseron – BigClassAction.com: Class Action News … http://www.bigclassaction.com/lawsuit/betaseron.php –
Berlex, Inc., the manufacturer of the medication, recently contacted healthcare professionals to remind them about certain aspects of the prescribing information for Betaseron as it relates to liver toxicity.
Bayer AG – Berlex – Schering
Research & Analysis
1999 launched – Acutect and Neotect lmaging products
2000 – Berlex Products launched – Levulan Kerstick used to treat keratoses
Betapace AF – replacement for Betapace and generic sotalol
Campath, Refludan, Finevin, Mirena – Iud, Yasmin, Leukine, Finacea
Berlex marketed some 20 products such as oral contraceptives called Yasmin, and Mirena, a implanted contraceptive and medicines to treat multiple sclerosis, dermatology disorders and cancers
Berlex contributed $1.2 billion in annual sales, which was one-quarter of it’s parent corporation Schering AG total revenue’s.
Bayer AG- Founded Friedrich Bayer & Johann Freidrich Weskott – 1863
st Product – acetylsalicylic acid (Aspirin) discovered by French Chemist Charles Frederic Gernhardt in 1853
1899 Bayer trademark of Aspirin was registered After World War I U.S. confiscation of assets – Lost Trademark status in U.S., UK, France – Trademark name currently registered in 80 countries under Bayer AG
1904 – Established Bayer Cross logo only for doctors and pharmacists Bayer’s U.S., confiscated assets acquired by U.S. Sterling Drug aka Sterling Winthrop Bayer became a subsidiary of IG Farben, German Chemical company conglomerate
World War II
IG Farben known for using slave labor in factories attached to concentration camps
Mauthausen-Gusen, concentration camps with 42.5% ownership
IG Farben produced Zyklon B – Chemical used in gas chamber of Auschwitz
After World War II IG Farben – Bayer separated into individual corporations
IG Farben ordered closed by Soviet Union for war reparations although, known for currently trading on Germany stock exchange
Bayer AG – Berlex – Schering
Research and Analysis
Bayer AG Executive Fritz ter Meer, was sentenced to 7yrs. In prison by the Nuremberg War Crimes Tribunal, when released he was appointed on the supervisory board of Bayer AG in 1956 – On the facts proven on record, the defendants who were members of the [managing board of I.G.] were accessories to and took a consenting part in the commission of war crimes and crimes against humanity as alleged in count three of indictments.
1978 – Bayer purchases – Miles laboratories and subsidiaries, Miles Canada, Cutter Laboratories – Products: Alka Seltzer, Flinstone Vitamins, One-A-Day vitimans, and Cutter insect, repellant
1994 – Bayer purchase Sterling Winthrop’s – OTC portion from SmithKline Beachman aka – Galxo Smith Kline – Enabling Bayer to acquire U.S., Canadian trademark rights to Bayer and Bayer Cross, as well as Aspirin trademark in Canada, that was previously
Bayer AG reorganized into a Holding Company in 2003 – Core businesses were transformed into limited companies, controlled by
Bayer CropScience AG, Bayer Healthcare, Bayer Material Science, Bayer Chemicals AG, Bayer Business Services GmbH, and Bayer
Industry Services GmbH & Co. OHG,
Bayer shares: Frankfurt Stock Exchange, London Stock Exchange, N.Y. Stock Exchange
Bayers 2004 Chemical reorganization – Formed Lanxess excluding H.S. Starack and Wolff Walsrode – polymers – Lanxess listed on
Frankfort Stock Exchange – 2005
2004 – Bayer Healthcare AG – Acquired OTC Pharmaceutica divison of Roche Pharmaceutical
2006 – Merck Kga $14.6 billion dollar take over Schering AG surpassed Bayer $19.5 bid
2007 – Bayer Healthcare Diagnostic Division acquires Siemens Medical Solutions
2008 – Bayer Healthcare acquires OTC U.S. Company Sagmel, Inc – which distributed
to most of common wealth countries, Russia, Ukraine, Kazakhstan, Belarus etc.,
Currently holding subsidiaries all over the world – Bayer’s holding company located in Germany
Bayer specialty area’s: Bayer Healthcare – Pharmaceutical and medical product sub-group – Bayer Healthcare 4 divisions – Bayer
Consumer Care, Bayer Animal Health, Bayer Medical Care, Bayer Schering Pharma
2007 Bayer Pharma took over Schering AG – Berlex and formed “Bayer Schering Pharma,” the largest take over in Bayer’s history. Named changed to Bayer Pharma in 2011.
Bayer AG – Berlex – Schering
Research and Analysis
Bayer Healthcare Pharmaceuticals is divided into two business units = General Medicine and Specialty Medicine. Women’s healthcare is example of General Medicine business unit.
Bayer’s Pharma unit produces birth control pills Yaz and Yasmin. Both pills use a newer type of progesterone a hormone called
drospirenone in combination of estrogen. (How many times had these products been passed through multiple mergers?)
Yaz was advertised as a treatment for premenstrual dysphroic disorder (PMDD), and moderate acne. Bayer also picked up Nexavar and Betaferon/Betaseron, and blood clotting drug, Kogenate,
(Many of these drugs were passed down by several prior German corporations)
2009 – U.S. Adrea, entered a global agreement with Bayer Healthcare AG, a subsidiary of Bayer AG. Where Bayer was in control of the completion of the ongoing phase I and phase II studies of RDEA119, which Bayer would be responsible for the further development and commercialization of RDEA119 and any of Adrea’s other MEK inhibitors.
*United States Adrea Biosciences, was acquired by AstraZeneca in 2012 a biotechnology company
AstraZeneca – Formed in 1913 in Sodertalje, Sweden by 400 doctors and apothercaries formed Astra AB. In 1993 British chemicals ICI consolidated it’s pharmaceutical business and its agrochemicals, specialty businesses, to form, The Zeneca Group plc.
1999 – Astra and Zeneca Group merged pharmaceutical companies to form AstraZeneca plc – U.S Headquarters in Wilmington,
Astra AB – British multinational pharmaceutical company based in U.K.
Products by Bayer AG and multiple subsidiaries: Women reproductive,
Aspirin, analgesic, antipyretic, anticoagulant medicine, Prontosil, Levitra,
Herion (diacetylmorphine) formerly sold as cough treatment, Sulonamide,
Ciprofloxacin, Polyurethane, Polycarbonate, CD’s, Makrolon, Suramin-Parathion, Insecticide Propoxur, Primodos – hormone pregnancy test
BAYER’S SPECIALTY AREA’S
Bayer Specialty Medicine business unit – Diagnostic Imaging
Contrast agents from his unit helps play crucial role in precise early diagnosis – Computed tomography (CT), magnetic resonance
imaging (MRI) and ultrasound
The Pet tracer Florbetaben, in Bayer’s pipeline is to recognize beta Amyloid, on of the pathological hallmarks of Alzheimer’s disease.
Bayer Consumer Care – Manages Bayer’s OTC medicine portfolio – Key products include, Aspirin, Aleve, food supplements, Redoxon, and Berocca, and skin products Bepanthen and Bepanthol.
Bayer Diabetes Care – Manages Bayer’s medical device portfolio, Key products; Mirena Iud, Blood glucose monitors, Contour Next EZ (XT), Contour USB, Breeze 2
Bayer Material Science: High-Tech Polymers, and develops solutions for a broad range of application relevant to everyday life
Bayer Business Services: Technology infrastructure and technical support, portion of Bayer USA and Bayer Canada – Bayer AG USA
Headquarters of North America Service Desk, and the Central IT Help Desk – Located in Robinson Township, Pennsylvania
Bayer Technology Services: Plant engineering, construction, optimization. Currenta; offers services for the chemical industry,
including utility supply, waste management, infrastructure, safety, security, analytic and vocational training
1904: Founded sports club, “Turn-und-Spielverein der Farbenfabriken vorm. Friedr. Bayer & Co., later SV Bayer 04, TSV Bayer 04
Levekusen, 1984 Bayer 04 Leverkusen
2014: Bayer, Novartis, Reckitt eye $10B-$12B bids for Merck consumer unit
Bayer AG -Berlex aka Schering
Lawsuit Research & Analysis
A cite from http://www.haemophilia-litigation.com/, access date 31 May 2006:
“After 1978, there were four major companies in the United States engaged in the manufacture, production and sale of Factor VIII and IX: Armour Pharmaceutical Company, Bayer Corporation and its Cutter Biological division, Baxter Healthcare and its Hyland
Pharmaceutical division and Alpha Therapeutic Corporation, which have been or are defendants in certain lawsuits.
The plaintiffs allege that the companies manufactured and sold blood factor products as beneficial “medicines” that were, in fact of
likely to be contaminated with HIV and/or HCV. This resulted in the mass infection and/or deaths of thousands of haemophiliac
Baycor – After 52 deaths were blamed on an alleged side effect of Bayer’s anticholesterol drug Baycol, its manufacture and sale were discontinued in 2001. The side effect was rhabdomyolysis, causingrenal failure, which occurred with a tenfold greater frequency in patients treated with Baycol in comparison to those prescribed alternate medications of the statin class
In January 2001, Bayer agreed to pay $14 million to the United States and 45 states to settle allegations under the federal False Claims Act that the company caused physicians and other health care providers to submit fraudulently inflated reimbursement claims to Medicaid Methyl parathion poisoning case – In October 2001, Bayer was taken to court after 24 children in the remote Andean village of Tauccamarca, Peru were killed and 18 severely poisoned when they drank a powdered milk substitute contaminated with the insecticide methyl parathion.
A Peruvian Congressional Subcommittee found significant evidence of criminal responsibility by Bayer and the Peruvian Ministry of Agriculture Liberty Link rice – In August 2006, it became apparent that the United States rice crop had been contaminated with unapproved genetically engineered Bayer CropScience rice. The genetically engineered rice has an herbicide-resistance trait. These forms of rice are commonly referred to among US rice growers as “Liberty Link rice 601” or “LL 601”. Approximately 100 varieties of rice are produced primarily in Arkansas,
Texas,Louisiana, Mississippi, Missouri, and California.
Bayer AG -Berlex aka Schering
2006 Trasylol safety advisory – In September 2006, Bayer was faulted by the FDA for not revealing during testimony the existence of a commissioned retrospective study of 67,000 patients, 30,000 of whom received Trasylol and the rest other antifibrinolytics. The study concluded Trasylol carried greater risks.
The FDA was alerted to the study by one of the researchers involved. Although the FDA issued a statement of concern, they did not change their recommendation that the drug may benefit certain patients. In a Public Health Advisory Update dated 3 October
2006, the FDA recommended “physicians consider limiting Trasylol use to those situations in which the clinical benefit of reduced
blood loss is necessary to medical management and outweighs the potential risks” and carefully monitor patients.The FDA took
Trasylol off the market on 5 November 2007.
Prostate cancer claims – In October 2009, the Center for Science in the Public Interest sued Bayer for “falsely claiming that the selenium in Men’s One-A-Day multivitamins might reduce the risk of prostate cancer
Yasmin / Yaz birth control pills – The FDA has repeatedly warned and punished Bayer for misstating the benefits of Yasmin (also known as Yaz) while understating its risks. In 2011, the FDA’s panel of experts voted 21-5 that the labeling on Yaz was inadequate and needed more information about the potential risk of blood clots in the legs and lungs. The former president of the Australian Medical Associationwas nearly killed by a blood clot that resulted from taking the pill.
The pill has been linked to 23 deaths in Canada. In April 2012, the FDA ordered Bayer to change its U.S. labeling to reference the increased risk for blood clots Neonicotinoid pesticides Clothianidin
In December 2010, a leaked memo from the EPA’s Environmental Fate and Effects Division asserted “Clothianidin’s (Bayer’s neonicotinoid pesticide) major risk concern is to non-target insects (that is, honey bees). Exposure through contaminated pollen and nectar and potential toxic effects therefore remain an uncertainty for pollinators.
“In January 2011,Avaaz.org launched an online petition to ban neonicotinoid pesticides Imidacloprid French and Nova Scotian beekeepers claim Bayer’s seed treatment midacloprid kills honeybees. France has since issued a provisional ban on the use of
imidacloprid for corn seed treatment pending further action. A consortium of U.S. beekeepers filed a civil suit against Bayer CropScience for alleged losses.
Bayer AG -Berlex aka Schering
Lawsuit Research and Analysis
Europe restrictions & challenge The European Commission has restricted the use of both of Bayer’s neonicotinoids. Bayer is challenging the restrictions.
Nexavar claims In an interview given to the Businessweek following controversies surrounding the Indian government’s decision to award a compulsory license to Indian company Natco Pharma Ltd. for Naxavar (Sorafenib), Bayer CEO Marijn Dekkers equated the compulsory license with theft. Regarding targeted markets, he said, “Is this going to have a big effect on our business model? No, because we did not develop this product for the Indian market, let’s be honest. We developed this product for Western patients who can afford this product, quite honestly. It is an expensive product, being an oncology product.”
In 28 August 2008, an explosion occurred at the Bayer CropScience facility at Institute,West Virginia. A runaway reaction ruptured a tank and the resulting explosion killed two employees. The ruptured tank was close to a methyl isocyanate tank which was undamaged by the explosion
Bayer Sued Over Unsupported Prostate Cancer Claims on One A Day 10/2009 http://www.cspinet.org/new/200910011.html
BAYER TO PAY $14 MILLION TO SETTLE CLAIMS FOR CAUSING PROVIDERS TO SUBMIT FRAUDULENT CLAIMS
TO 45 STATE MEDICAID PROGRAMS – January 2001 – http://www.justice.gov/opa/pr/2001/January/039civ.htm
Bayer Sold HIV-Risky Meds – 5/2003 http://www.cbsnews.com/news/bayer-sold-hiv-risky-meds/
BAYER FOUND RESPONSIBLE FOR POISONING OF CHILDREN IN PERU – http://www.twnside.org.sg/title/2410.htm
Bayer AG -Berlex aka Schering
Lawsuit Research & Analysis
FDA to Review Safety Issues Surrounding Leading Birth Control Pill Yaz – 12/2011
Yaz, Yasmin birth control pills linked to 23 deaths in Canada – 7/2013 http://www.nydailynews.com/life-style/health/yaz-yasmin-birth-
Yaz and Yasmin birth control pills linked to 23 deaths: Health Canada documents
1.1321110#ixzz2uD3dzpwU – 06/2013
Neonicotinoids: Syngenta and Bayer go to court against the European Commission
Leaked document shows EPA allowed bee-toxic pesticide despite own scientists’ red flags- http://grist.org/article/food-2010-12-10-leaked-documents-show-epa-allowed-bee-toxic-pesticide/ 12/2010
Bayer in settlement over Cipro pricing – http://www.cbgnetwork.org/5208.html 9/2013
The spying Scotsman who hunted the Nazis of New York: The amazing story of Britain’s clandestine war on Hitler’s agents… and his big- money backers in the US –
http://www.dailymail.co.uk/news/article-2530447/ The-spying-Scotsman-hunted-Nazis-New-York-The-amazing-story-Britains-clandestine-war-Hitlers-agents-big-money-backers 12/2013
Primodos victims from UK demand apology – Cologne, Germany – 26th April 2013 Bayer Shareholder Meeting – Speech Valerie Williams Lipobay/Baycol Victim Goes To Court – Argentina: BAYER Sentenced To Pay Compensation – http://www.cbgnetwork.org/4649.html
Bayer AG -Berlex aka Schering
Lawsuit Research Analysis
State ignored plan for tougher chemical oversight – West Virginia ignores a plan for tougher chemical oversight which
was worked out after an explosion in BAYER ́s Institute plant (more info). 300,000 residents are still without usable water
after a chemical spill – 1/2014 http://www.cbgnetwork.org/5405.html
Leaked Documents Reveal the Secret Finances of a Pro-Industry Science Group –
Whistleblower Lawsuit Filed Over Baycol Fraud – http://www.cbgnetwork.org/2703.html 4/2008
Bayer Held Back on Drug Dangers – http://www.cbgnetwork.org/288.html
Has died / Hemophiliacs infected by Bayer products – 8/2012 http://www.cbgnetwork.org/4607.html
Bayer, Baxter pay multimillion indemnity to haemophiliacs –
http://www.cbgnetwork.org/3678.html – Settlement in the US with victims from 22 countries / HIV
infections were preventable / “why is BAYER concealing the payments? 1/2010
NY Times: Bayer sold AIDS infected blood product – 5/2003
US elections: BAYER donates to Republicans and Tea Party-????? http://www.cbgnetwork.org/4595.html – 8/2012
Trial-related deaths in India – Open letter to BAYER – Bayer AG
CEO Marijn Dekkers -http://www.cbgnetwork.org/4109.html 10/2011
BAYER: Marketing Expenses Concealed – http://www.cbgnetwork.org/4317.html – 3/2012
Papantonio: Bayer’s Deceptive Marketing Is Killing Women – https://www.youtube.com/watch?v=19zwklFd9z0 3/2013
Bayer AG -Berlex aka Schering
Lawsuit Research & Analysis
$300 Million Compensation in the US
Settlements in Yaz litigation continue, mediator is “cautiously optimistic” that end is in sight – http://www.cbgnetwork.org/4512.html
Yaz: Food and Drug Administration to Discuss Dangerous Contraceptive Pills – http://www.cbgnetwork.org/4173.html 11/2011
Bayer contraceptive advert breaches Code of Practice – http://www.cbgnetwork.org/3922.html 5/2011
Newer Birth Control Pills Carry a Higher Risk of Blood Clots – http://www.cbgnetwork.org/3803.html
4/2011 – Complete Study “Risk of venous thromboembolism in users of oral contraceptives containing drospirenone”
(DownloadBMJ_Study_Drospirenone.pdf) and the study on US data
Yaz victims to appear in Bayer shareholder meeting
Ban demanded / Coalition introduces countermotions / more than 50 deaths in the US – http://www.cbgnetwork.org/3327.html
RISK OF THROMBOEMBOLISM ASSOCIATED WITH DROSPIRENONE-CONTAINING CONTRACEPTIVES (YASMIN, YAZ, MIRENA – IUD
Risk of thromboembolism in women taking ethinylestradiol/drospirenone and other oral contraceptives. –
Safety of a new oral contraceptive containing drospirenone. – http://www.ncbi.nlm.nih.gov/pubmed?
Bayer AG -Berlex aka Schering
Lawsuit Research and Analysis
Risk of hyperkalemia in women taking ethinylestradiol/drospirenone and other oral contraceptives. –
Schering AG Storms Birth Control Market http://www.forbes.com/2003/07/11/cx_ad_0710shr.html 7/2003
Coalition introduces Countermotion on blood thinner Xarelto – http://www.cbgnetwork.org/4337.html – 4/2012
Bayer Sells AIDS-Infected Drug Banned in U.S. in Europe, Asia –
IG Farben – Bayer AG
IG Farben to be dissolved -The company’s shares continue to trade on the German stock exchange even thought it went into
liquidation in 1952. IG Farben has been heavily criticized for not paying any compensation to former Nazi slave laborers after hundreds of Germany’s leading industrial companies contributed to a 10bn Deutschmark fund this year. Germany’s IG Farben, the company that made the Zyklon-B gas used in the Nazi death camps, has announced it will be dissolved by 2003?
In year 1928, the American holdings of IG Farben, namely, the American branches of Bayer Company, General Aniline Works, Agfa Ansco, and Winthrop Chemical Company, were organized into a Swiss holding company, which was christened Internationale Gesellschaft für Chemische Unternehmungen AG or IG Chemie, in short. The controlling interest of this entity rested with IG Farben in Germany. In the following year, 1929, just a decade before the outbreak of the Second World War, these American firms merged to become American IG Chemical Corporation, or American IG, later renamed General Aniline & Film. –
In 1952, IG Farben was split into BASF, Bayer, an Hoechst again.
German chemical companies —Badische Anilin- und Sodafabrik Ludwigshafen (BASF), Bayer, Agfa, Hoechst,Weiler-ter-Meer, and Griesheim-Elektron. These six companies were merged intoInteressen-Gemeinschaft Farbenindustrie AG or, IG Farben, for short.
Bayer AG -Berlex aka Schering
Lawsuit Research and Analysis
RAG To Take Over Degussa – http://cen.acs.org/articles/84/i1/RAG-Take-Over-Degussa.html 1/2006
Bayer Combination Aspirin Class Action Lawsuit Settlement –
http://www.topclassactions.com/lawsuit-settlements/lawsuit-news/14735-checks-go-bayer-combination-aspirin-class-action-settlement/ -Checks Go Out in
Bayer Combination Aspirin Class Action Settlement
Bayer HealthCare Pharmaceuticals Gender Discrimination Class Action Lawsuit Complaint
Female Bayer HealthCare Pharmaceuticals Employees File Gender Discrimination Class Action Lawsuit Complaint Against Bayer
HealthCare Pharmaceuticals. http://classactionlawsuitsinthenews.com/class-action-lawsuits/bayer-healthcare-pharmaceuticals-gender-discrimination-class-action-lawsuit-complaint/ 3/2011
Bayer’s Yasmin Lawsuit Settlements Rise to $402.6 Million – http://www.businessweek.com/news/2012-07-31/bayer-s-yasmin-lawsuit-settlements-rise-to-402-dot-6-million 7/2013
Bayer Combination Aspirin Multidistrict Litigation – http://www.douglasandlondon.com/legal-news/bayer-combination-aspirin-multidistrict-litigation/Yasmin/Yaz Litigation Heats Up, Bayer Accuses Litigation Lawyers of “Negative Advertising” –
MIRENA IUD and Risk of Uterine Perforation – http://www.lawyersandsettlements.com/lawsuit/mirena-IUD.html#.UwsElvldVQ4 1/2014
Bayer IUD Litigation Consolidated in New York – http://www.nationallawjournal.com/id=1202597081274?
Bayer Cipro Drug Litigation Settlement – ttp://classactionsnews.com/settlements/bayer-cipro-drug-litigation-settlement 3/2014
Mirena IUD Migration Problems Result in Lawsuit Against Bayer – http://www.aboutlawsuits.com/mirena-iud-migration-problems-lawsuit-31490/#sthash.6SHEPghs.dpuf 8/2012 – Mirena IUD Reported Problems and Complications Topped 70,000 –
CABIRI Research: Mirena IUD Maude Adverse Event Reports
MAUDE Adverse Event Report: BERLEX INC.MIRENA IUD
Sarah, see below information you requested concerning FDA Safety and adverse effects. In our conversation 2/28/2014, you stated that the FDA did not mention Mirena was a unsafe product for women – See Below Mirena Iud – FDA articles, I’ve outlined a few for your review:
|Lot Number 31218D|
|Event Date 04/11/2005|
|Event Type Other|
|Staff assisting physician handed the mirena box to the provider. The mirena iud was placed into the patient. After placement it was noted that the iud had an expiration date of 03/05. This was reported to the medical director. The mirena distributor was contacted & stated that if the device was placed a week after the expiration date it should not be a problem. Per the distributor, no ill effects have been noted if inserted 10 days after expiration date. The patient will be monitored for any adverse effects.|
|Brand Name||MIRENA IUD|
|Type of Device||IUD|
|Manufacturer(Section F) BERLEX INC. 340 Changebridge Rd. P.O. Box 1000 Montville NJ 07045 1000|
|Manufacturer (Section D) BERLEX INC. 340 Changebridge Rd. P.O. Box 1000 Montville NJ 07045 1000|
|Device Event Key||585173|
|MDR Report Key||595346|
|Device Sequence Number||1|
|Report Source||User Facility|
|Reporter Occupation||RISK MANAGER|
|Type of Report||Initial|
|1 Device Was Involved in the Event|
|1 Patient Was Involved in the Event|
|Date FDA Received||04/20/2005|
|Is This An Adverse Event Report?||No|
|Device LOT Number||31218D|
|Was Device Available For Evaluation?||No|
|Is The Reporter A Health Professional?||No Answer Provided|
|Was the Report Sent to FDA?||Yes|
|Date Report Sent to FDA||04/20/2005|
|Is the Device an Implant?||Yes|
|Is this an Explanted Device?||No Answer Provided|
|Patient TREATMENT DATA|
|Date Received: 04/20/2005 Patient Sequence Number:1|
MAUDE Adverse Event Report: MIRENAIUD HORMONE FILLED
|MIRENA IUD HORMONE FILLED|
Event Date 01/08/2004Event Type Injury Patient Outcome Life Threatening,Other Event Description – Pt had the mirena iud inserted in 04 – the pain upon insertion nearly made pt pass out – double painkillers didn’t help.
Pt whole body broke out in a severe sweat. Since having the iud inserted pt had severe cramps. Lower abdominal pain, pt had gained 30 pounds -size 4 to 14-, bloating, severe fatigue, mood swings – irritability, severe leg cramps, tingling in their fingers, joint pain and chest pain. Pt went back to the dr who steered the conversation away from the mirena and put them on estrogen for menopause. They took an ultrasound and said the iud appeared to be fine. Pt bled after the ultrasound for three days. They say “no one has any complaints about the mirena” yet this site http://www. Dysmenorrhea. Org/forum/documents all and more of the same symptoms pt is having and pt going to have their IUD removed. Pt hopes that their experience is not like others where the mirena has traveled on its own into their uterus, their stomach and even up to their head. Pt feels FDA needs to do something about the mirena. Consumers should be alerted to the side effects a huge amount of women are having from this product. Also, pain upon insertion is said to be negligible – but it is not negligible. It is severe in many cases.
|Type of Device||IUD HORMONE FILLED|
|Device Event Key||550739|
|MDR Report Key||561031|
|Device Sequence Number||1|
|Type of Report||Initial|
|1 Device Was Involved in the Event|
|1 Patient Was Involved in the Event|
|Date FDA Received||10/27/2004|
|Is This An Adverse Event Report?||Yes|
|Is This A Product Problem Report?||Yes|
|Device Operator||Invalid Data|
|Was Device Available For Evaluation?||No Answer Provided|
|Is The Reporter A Health Professional?||No|
|Was The Report Sent To Manufacturer?||No|
|Is this a Reprocessed and Reused Single-Use Device?||No|
|Is the Device an Implant?||Yes|
|Is this an Explanted Device?||No Answer Provided|
Bribed Doctor Fraudulent Mirena Actions –
The FDA also reported in April 2013 – Counterfeit Device circulating
Shrum, Kelly Dean., D.O.
|Department of Health and Human Services||Public Health Service|
Food and Drug Administration
|Rockville, MD 20857|
RETURN RECEIPT REQUESTED
Kelly Dean Shrum, D.O.
PROPOSAL TO DEBAR
NOTICE OF OPPORTUNITY FOR HEARING
DOCKET No. FDA-2012-N-0246
Dear Dr. Shrum:
This letter is to inform you that the Food and Drug Administration (FDA) is proposing to issue an order permanently debarring you from providing services in any capacity to a person that has an approved or pending drug product application. FDA bases this proposal on a finding that you were convicted of a felony under Federal law for conduct relating to the regulation of a drug product under the Federal Food, Drug, and Cosmetic Act (the Act). This letter also offers you an opportunity to request a hearing on this proposal.
Conduct Related to Conviction
On November 17, 2010, you were convicted by a jury of one count of Misbranding, a class A misdemeanor in violation of 21 U.S.C.§§ 331(a), 333(a)(1), 352(c) and 352(f)(1), and one count of
Health Care Fraud, a class C felony in violation of 18 U.S.C.§§ 1347 and 2. On September 30, 2011 the United States District Court for the Eastern District of Arkansas entered judgment against you. The underlying facts supporting this conviction are as follows.
You were a licensed physician practicing in the state of Arkansas. You offered gynecological and obstetric services to women, including providing forms of birth control. Your favored form of contraception was a levonorgestrel-releasing intrauterine device (IUD) known as Mirena. Mirena was made for BHCP, Inc. by Bayer Schering Pharma OY (Bayer). The only version of Mirena approved by FDA for marketing in the United States was approved on December 6, 2000 in New Drug Application (NDA) 21-225.
From in or about June of 2009, in the Eastern District of Arkansas and elsewhere, you purchased a foreign version of Mirena for use in your patients that was not FDA-approved. The labeling of the unapproved IUD was not in English, and did not include adequate directions for use. Arkansas Center for Women, Ltd. was registered with the Arkansas Medicaid Program. You were listed as the only physician affiliated with that clinic, and you signed the Medicaid provider contract on behalf of the Arkansas Center for Women. You submitted claims to the Arkansas Medicaid Program under the clinic’s provider number for procedure code J7302, Levonorgestrel Releasing Intrauterine Contraceptive (Mirena). This procedure code is specific to Bayer’s FDA-approved Mirena product and any item billed under this procedure code must be the FDA-approved version of Bayer’s Mirena.
From on or about January 15, 2008 through on or about June 12, 2009, you caused to be submitted claims for reimbursement to the Arkansas Medicaid Program, which included false representations. Specifically, you billed the Arkansas Medicaid Program as if you were administering the FDA approved version of Mirena, when you were actually administering a non-FDA-approved IUD.
Section 306(a)(2)(B) of the Act (21 U.S.C. § 335a(a)(2)(B)) requires debarment of an individual if FDA finds that the individual has been convicted of a felony under Federal law for conduct relating to the regulation of any drug product under the Act. As described above, you knowingly and willfully caused to be executed and attempted to cause to be executed a scheme and artifice to defraud the Arkansas Medicaid Program, and to obtain by fraudulent pretense and representations money under the custody and control of the Arkansas Medicaid Program, in connection with the delivery of or payment for health care benefits, items, or services, all in violation of Title 18 U.S.C. §§ 1347 and FDA finds that the conduct underlying this felony conviction relates to the regulation of a drug product under the Act because the use of an unapproved and misbranded drug undermines the drug approval process and FDA’s regulatory oversight over drug products marketed in the United States.
Section 306(c)(2)(A)(ii) of the Act (21 U.S.C. § 335a(c)(2)(A)(ii)) requires that your debarment be permanent. Proposed Action and Notice of Opportunity for Hearing – Based on the findings discussed above, FDA proposes to issue an order under section 306(a)(2)(B) of the Act (21 U.S.C. § 335a(a)(2)(B)) permanently debarring you from providing services in any capacity to a person having an approved or pending drug product application.
In accordance with section 306 of the Act and 21 CFR Part 12, you are hereby given an opportunity to request a hearing to show why you should not be debarred as proposed in this letter.
If you decide to seek a hearing, you must file the following: (1) on or before 30 days from the date of receipt of this letter, a written notice of appearance and request for hearing; and (2) on or before 60 days from the date of receipt of this letter, the information on which you rely to justify a hearing. The procedures and requirements governing this notice of opportunity for hearing, a notice of appearance and request for a hearing, information and analysis to justify a hearing, and a grant or denial of a hearing are contained in 21 CFR part 12 and section 306(i) of the Act (21 U.S.C. 335a(i)).
Your failure to file a timely written notice of appearance and request for hearing constitutes an election by you not to use the opportunity for a hearing concerning your debarment and a waiver of any contentions concerning this action. If you do not request a hearing in the manner prescribed by the regulations, FDA will not hold a hearing and will issue a final debarment order as proposed in this letter.
A request for a hearing may not rest upon mere allegations or denials but must present specific facts showing that there is a genuine and substantial issue of fact that requires a hearing. A hearing will be denied if the data and information you submit, even if accurate, are insufficient to justify the factual determination urged. If it conclusively appears from the face of the information and factual analyses in your request for a hearing that there is no genuine and substantial issue of fact that precludes the order of debarment, the Commissioner of Food and Drugs will deny your request for a hearing and enter a final order of debarment.
You should understand that the facts underlying your conviction are not at issue in this proceeding. The only material issue is whether you were convicted as alleged in this notice and, if so, whether, as a matter of law, this conviction permits your debarment under section 306(a)(2)(B) of the Act (21 U.S.C. § 335a(a)(2)(B)) as proposed in this letter.
Your request for a hearing, including any information or factual analyses relied on to justify a hearing, must be identified with Docket No. FDA-2012-N-0246 and sent to the Division of Dockets Management, Food and Drug Administration, 5630 Fishers Lane, Room 1061, Rockville, MD 20852. You must file four copies of all submissions pursuant to this notice of opportunity for hearing. The public availability of information in these submissions is governed by 21 CFR 10.20(j). Publicly available submissions may be seen in the Division of Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
This notice is issued under section 306 of the Act (21 U.S.C. § 335a) and under authority delegated to the Director, Office of Enforcement within the Food and Drug Administration.
Office of Enforcement
Office of Regulatory Affairs
As noted above, you were also convicted of causing the introduction and delivery for introduction into interstate commerce of a misbranded drug in violation of 21 U.S.C. §§ 331 (a), 333(a)(1), 352(c), and 352(f)(1), a misdemeanor. This conviction independently could form the basis for permissive debarment under section 306(b)(2)(B) of the Act; however, FDA declines to make a determination regarding permissive debarment at this time in light of your felony conviction.
Page Last Updated: 07/16/201
Website: FDA Safety & Adverse Effects – Related Articles: http://google2.fda.gov/search?q=mirena+iud&client=FDAgov&site=FDAgov&lr=&proxystylesheet=FDAgov&requiredfields=-archive%3AYes&output=xml_no_dtd&getfields=*
ARTICLES: Search Results
Showing 1 – 10 of about 36 for mirena iud in All of FDA.MAUDE Adverse Event Report: BERLEX INC.MIRENA IUD
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=595346- 39k- 2014-02-21-|
…MAUDE Adverse Event Report: BERLEX INC.MIRENA IUD.…BERLEX INC.
MIRENA IUD, Back to Search Results. Lot Number 31218D….
MAUDE Adverse Event Report: MIRENAIUD HORMONE …
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=561031 39k- 2014-02-21-|
…MIRENA IUD HORMONE FILLED, Back to Search Results. Event Date
01/08/2004….Brand Name,MIRENA. Type of Device,IUDHORMONE FILLED…. More results from www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm
Shrum, Kelly Dean., DO REGULATORY INFORMATION]
|http://www.fda.gov/regulatoryinformation/foi/electronicreadingroom/ucm312157.htm- 41k- 2012-07-16-|
…Your favored form of contraception was a levonorgestrel-releasing intrauterine
device (IUD) known as Mirena. Mirena was made for BHCP, Inc….
[PDF] HIGHLIGHTS OF PRESCRIBING INFORMATION These…
|http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021225s027lbl.pdf- 153k- 2009-10-14 Text Version|
…For the contraception indication, Mirena was compared to a copper UD
(n=1,855), to another formulation of levonorgestrel intrauterine system (n…
[PDF] Mirena® (levonorgestrel-releasing intrauterine system)…
|http://www.accessdata.fda.gov/drugsatfda_docs/label/2008/021225s019lbl.pdf- 148k- 2009-03-31-Text Version|
…The following are serious but uncommon side effects of Mirena: • Pelvic
inflammatory disease (PID). Some IUD users get a serious pelvic infection…
[PDF]Department of Health and Human Services Public Health…[ADVISORY COMMITTEES]
|http://www.fda.gov/…/advisorycommittees/committeesmeetingmaterials/pediatricadvisorycommittee/ucm288710.pdf- 72k-Text Version…and older, approximately 59% of drug use mentions for Mirena® were|
associated with the health care encounter code of “Insertion of IUD” (V251….
Adverse Effects Continued
[PDF]American College of Obstetrics and Gynecologists[DRUGS]
|http://www.fda.gov/…/enforcementactivitiesbyfda/selectedenforcementactionsonunapproveddrugs/ucm219965.pdf- 10-Text Version|
…use, and distribution of unapproved intrauterine devices (IUD) and intrauterine …
of FDA-approved products such as Mirena, Implanon, Copper-T, and…
September 30, 2011: Pine Bluff Doctor Sentenced in Health…[INSPECTIONS AND COMPLIANCE]
|http://www.fda.gov/iceci/criminalinvestigations/ucm274435.htm- 46k- 2011-10-04|
…the Arkansas Medicaid Program as if he was providing Medicaid beneficiaries with the FDA-approved, Bayer manufactured IUD Mirena®, when in…
FDA Cautions Against Using Unapproved IUDs[FOR CONSUMERS]
|http://www.fda.gov/forconsumers/consumerupdates/ucm219837.htm- 43k- 2010-07-22|
…“Federal law requires that IUD/IUSs (intrauterine systems) be FDA-approved prior to marketing….What advantages are there for keeping my IUD in?..
[PDF]Prescriber Contraception Counseling Guide [FOR INDUSTRY]
|http://www.fda.gov/downloads/forindustry/userfees/prescriptiondruguserfee/ucm361078.pdf- 201k Text Version|
… IUD insertion for emergency contraception is not recommended for female…7. Mirena® Prescribing Information, Berlex Corporation, April 2006….
|http://www.accessdata.fda.gov/drugsatfda_docs/nda/2013/203159Orig1s000ClinPharmR.pdf- 297k- 2013-10-04-Text Version|
…Mirena®, the only LNG-IUD currently on the market, was approved
in the US on December 6, 2000 under NDA 021225.…
[PDF]An Oncologist’s Perspective on the Clinical Use of Teratogenic…[ADVISORY COMMITTEES]
|http://www.fda.gov/…/drugs/drugsafetyandriskmanagementadvisorycommittee/ucm333370.pdf- 79k-Text Version|
…IUD– Copper only, progesterone-containing LNG-IUD (Mirena) • Permanent contraception…28 Page 29. What About LNG-IUD (Mirena)?…
[PDF] N203-159 Clinical PREA[DRUGS]
|http://www.fda.gov/downloads/drugs/developmentapprovalprocess/developmentresources/ucm350706.pdf- 302k-Text Version …low (0.2%) and is similar to the risk of ectopic with Mirena (0.1…Pelvic inflammatory disease and endometritis are historically associated with IUD…|
Adverse Effects Continued:
[PDF] N22252 Natazia Clinical PREA [DRUGS]
|www.fda.gov/downloads/drugs/developmentapprovalprocess/developmentresources/ucm283121.pd f- 1255kText Version …of efficacy ISS Integrated summary of safety IUD Intrauterine device IUS…such as fibroids or uterine cancer) •Mirena® (levonorgestrel-releasing… More results from www.fda.gov/downloads/drugs/developmentapprovalprocess|
October 8, 2009: Pine Bluff Doctor Indicted on Misbranding…[INSPECTIONS AND COMPLIANCE]
|http://www.fda.gov/iceci/criminalinvestigations/ucm271159.htm- 49k- 2011-09-08|
…Center for Women, LTD in Pine Bluff, Arkansas, federal agents located several non-approved versions of the Bayer manufactured IUD,Mirena®.…
[PDF]iPledge (isotretinoin) REMS [DRUGS]
|http://www.fda.gov/…/drugs/drugsafety/postmarketdrugsafetyinformationforpatientsandproviders/ucm234639.pdf- 1888k-Text Version|
…20 Page 31. Unacceptable Forms Of Contraception Include: • Progesterone- only “mini-pills,” eg: – Ortho Micronor® Tablets* •IUDProgesterone T...
FDA News Releases–Women’s Health [FOR CONSUMERS]
|http://www.fda.gov/forconsumers/byaudience/forwomen/ucm118628.htm- 45k- 2009-04-16-cached|
…October 16); FDA Approves Additional Use for IUD Mirena to Treat Heavy Menstrual Bleeding in IUD Users (October 1); FDA…
…MG X 1$$$$$69941665$6994166$1$PS$MIRENA$1$IU…$2$SS$COPPER-
CONTAINING INTRAUTERINE DEVICE (IUD)$1$$$$$Does…
[PDF] Human Drugs Program [ABOUT FDA]
|http://www.fda.gov/downloads/aboutfda/reportsmanualsforms/reports/budgetreports/ucm298355.pdf- 253k-Text Version|
… in patients, Mirena IUDs (Intrauterine Devices) from foreign sources that were not approved for use in the United States. The IUD’s were labeled in…
Adverse Effects Continued
MAUDE Adverse Event Report: BERLEX…
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=428416- 37k- 2014-02-21|
…BERLEX LABORATORIES MIRENA IUD, Back to Search Results. Event Date
04/01/2002….Brand Name,MIRENA. Type of Device,IUD….Event Date 04/01/2002
MAUDE Adverse Event Report: HERNIAMESH SRL …
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=2076427 – 42k- 2014-02-21|
…She had a mirena iud in place for contraception and the bleeding was
attributed to the iud which was eventually removed.…
MAUDE Adverse Event Report: CONCEPTUS OR…
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=3580915- 41k- 2014-02-21-|
…liters of blood, coded twice. I had the mirena iud at the time which the
surgeons left in place. Two days later, i requested…
MAUDE Adverse Event Report: CONCEPTUSESSURE
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=3339279- 41k- 2014-02-21-|
…can have essure. Pt’s body rejects foreign objects as two mirena iud’s fell out, one resulting in pregnancy. The pain was…
MAUDE Adverse Event Report: HERNIAMESH, SR1T…
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=1393932- 41k- 2014-02-21-cached|
…vaginal bleeding. She had a mirena iud placed by her primary md which
was removed approx after 1 year. Granulation tissue…
October 8, 2009: Pine Bluff Doctor Indicted on Misbranding…[INSPECTIONS AND COMPLIANCE]
|http://www.fda.gov/iceci/criminalinvestigations/ucm271159.htm- 49k- 2011-09-08|
…Center for Women, LTD in Pine Bluff, Arkansas, federal agents located several non-approved versions of the Bayer manufactured IUD, Mirena®….
|http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=3101345- 40k- 2014-02-21|
…I desired no more children. My gyno suggested the iud mirena. It was
unsuccessful, so they suggested essure. I had the coils inserted in 2010….
|Model Number ESS305-R1|
|Event Date 02/25/2013|
|Event TypePatient Outcome – Event Description I am a mother of 3. My last two pregnancies were 2007 and 2008. I desired no more children. My gyno suggested the iud mirena. It was unsuccessful, so they suggested essure. I had the coils inserted in 2010. First 6 months was fine. Normal period. Even light at times. But i started to feel like i had the flu everyday and i was bleeding through my clothes. Constant headaches. Depression increased. Was told i had a hormone imbalance. Had an ablation the summer of 2011. One day surgery at (b)(6) hospital. Periods were somewhat normal for about 8 months. Then the side effects mentioned previously progressed. My periods were unstable and heavy and put me in the bed. How can you be a mother, wife, employee when you feel like you are dying?|
|InvegaLawsuit | Gynecomastia, Hyperprolactinemia –http://www.classaction.org/invega-Lawsuits have been filed against Janssen Pharmaceuticals alleging that Invega can increase a user’s risk of developing gynecomastia and/or hyperprolactinemia. Invega Breast Lawsuit – Victim of Male Breast Enlargement? – MaleBreastLawsuit.com/InvegaLawsuit Lexapro Lawsuits | Lawyers for Heart, Birth Defects … http://www.classaction.org/lexapro If you took the antidepressant Lexapro and delivered a child with a birth defect, contact ClassAction.org. You may be entitled to damages. Free consultations. Develop Pancreatic Cancer – After Taking Diabetes Drugs? diabeticdruglawyers.com –JanuviaLawsuit | Januvia Side Effects Lawsuits –www.januvialawsuit.net – Januvia lawsuits for Januvia patients who experienced side effects such as pancreatic cancer, thyroid cancer, and pancreatitis,|
|Additional Research Links|
Prempro settlements cost Pfizer $896M; 4,000 lawsuits remain http://www.yourlawyer.com Articles Pharmaceutical giant Pfizer Inc. has disclosed that it has paid at least $896 million to settle 6,000 Prempro injury lawsuits filed by or on behalf of women who … Pfizer Settles Class Action Lawsuit by Former Wyeth … http://www.stollberne.com/…/pfizer…lawsuit-by-former-wyeth-shareholders Pfizer Inc. (“Pfizer”), the world’s largest pharmaceutical company, has agreed to pay $67.5 million to settle a class action lawsuit by shareholders of the … Remicade Lawsuit and Side Effect Information – i-Lawsuit http://www.i-lawsuit.com/remicade-lawsuit-and-side-effect-information Remicade is sold by Jansessen Biotech, Inc., … Vaginal Mesh Lawsuits– What You Need to KnowJanuary 28, 2013; Adderall Linked to Heart Failure and Sudden Death … Janssen Keeping Risperdal Side Effects a Secret Amidst … http://www.topclassactions.com/lawsuit-settlements/lawsuit-news/12396… A recent motion filed by Janssen Pharmaceuticals requests that plaintiffs may not use certain documents in court trials regarding Risperdal side effects. Gardasil Lawsuits | Gardasil Paralysis, Seizureswww.classaction.org/gardasil – Gardasil Lawsuits: Gardasil side effects may include death, paralysis, seizures and Guillain-Barre Syndrome. Lawsuit filed over side effects of HPV vaccine | Vaccine … vaccinenewsdaily.com/vaccine_development/212947-lawsuit-filed-over.-Lawsuit filed over side effects of HPV vaccine. … Merck & Co., the maker of Gardasil, allegedly caused the unnamed 16-year-old girl “physical and behavioral problems.” Takeda Pharmaceuticals – Manufacturer of Diabetes Drug, Actos www.drugwatch.com/manufacturer/takeda – Takeda Pharmaceuticals is a U.S. subsidiary of Takeda Pharmaceutical Company and manufactures Actos, a type 2 diabetes drug. Actos Litigation – Class Action Lawsuit, MDL Against Takeda injurylawyer-news.com/actos/class-action-lawsuit Actos litigation is pending in several U.S. courts as MDL, mass torts and individual claims, with patients alleging injuries like bladder cancer Crestor Diabetes Lawsuit | ClassAction.org – orLawsuit – A Drug Recall – w.adrugrecall.com/crestor/lawsuit.html –Sn patients taking Crestor developed life-threa tening rhabdomyolysis only a few months after the FDA approved the drug. Nine patients suffered from severe kidney … www.classaction.org/crestor – AstraZenecae Crestor lawsuits are mass tort cases, ng Diabetes Drugs? diabeticdruglawyers.com – You May Have A Case. Call Us Today. Januvia Lawsuit | Januvia Side Effects Lawsuits www.januvialawsuit.net – Januvia lawsuits for Januvia patients who experienced side effects such as pancreatic cancer, thyroid cancer, and pancreatitis, Click here to learn more. Federal Lipitor Diabetes Lawsuits Consolidated as MDL 2502 – Androderm® Lawsuit Filed in California Court After Testosterone Therapy Linked to Cardiac Events – Injury Lawyer News – IT Business Net
|Additional Research Links Yaz, Yasmin Lawsuit Settlements Continuehttp://www.classaction.org/blog/yaz-yasmin-lawsuit-settlements-continue|
Yaz, Yasmin Lawsuit Settlements Continue Jul 13, 2012 … After allegations of serious blood clotting complications and deaths as a result of Yaz and Yasmin use, Bayer is progressing smoothly in the…
Gadolinium Lawsuits | Gadolinium NSFhttp://www.classaction.org/gadolinium-injection-risk
Gadolinium Lawsuits | Gadolinium NSF Company(ies): Bayer Schering Pharma, GE Healthcare, Mallinckrodt, Inc. and Bracco Diagnostics, Inc. Additional Details: Gadolinium contrast dyes are injected
Levaquin and Cipro Tendon Injuries | Levaquin Cipro Lawsuitshttp://www.classaction.org/levaquin-and-cipro
Levaquin and Cipro Tendon Injuries | Levaquin Cipro Lawsuits Company(ies): Ortho-McNeil Pharmaceuticals, Bayer Pharmaceuticals; Additional Details: Part of the fluoroquinolone group of antibiotics, Levaquin and Cipro… http://www.classaction.org/levaquin-and-cipro
clipped from Google – 3/2014-Mirena Petition Signed by 1500 Womenhttp://www.classaction.org/blog/mirena-petition-signed-by-1500-women
Mirena Petition Signed by 1500 Women Lawsuit List … The FDA sent a letter to Bayer in 2010 which said their direct advertising program “overstates the efficacy of Mirena, presents unsubstantiated Trasylol Black Box Warning | Trasylol Side Effects – http://www.classaction.org/trasylol
Another Blood Thinner Prompts Concerns Over Serious Injurieshttp://www.classaction.org/…/another-blood-thinner-prompts-concerns-over- serious-injuries
Another Blood Thinner Prompts Concerns Over Serious Injuries As Pradaxa lawsuits continue to mount, the newest blood thinner approved by … Johnson) and Bayer, reports that it believes the number of adverse reports is
Monsanto Genetically Modified Wheat –http://www.classaction.org/monsanto-genetically-modified-wheat Bayer eventually agreed to a settlement. … Lawsuits are already being filed seeking compensation from Monsanto for negligence, loss of income, product News about Daiichi Sankyo Inc. Lawsuits Firms Kick Off Benicar Diarrhea Suits Against Daiichi – Two plaintiffs firms are planning to launch lawsuits against Daiichi Sankyo Inc. later this week in New Jersey that claim the company’s blood pressure drug Benicar… Daiichi Sankyo Accused Of Gender Discrimination – http://www.manufacturing.net/news/2013/02/daiichi-sankyo-accused-of… TRENTON, N.J. (AP) — Six current and former female sales representatives are accusing drugmaker Daiichi Sankyo of gender discrimination in a
Additional Research Links
Byetta Thyroid Cancer Lawsuit Filed Against Amylin, Eli …
Greg Abbott (R) pushes to block disabled Texans’ lawsuits …
http://www.dallasnews.com› News› Politics› Politics Headlines
Abbott Laboratories and Hospira retirement
Abbott Labs Sued by Five Men Claiming Androgel Injuries …
Pfizer’s Wyeth Pharmaceuticals Exposed By Whistleblower
Additional Research Links
Bayer Hiv Scandal – World Newshttp://www.definitionofnegligence.com/bayer-scandal-hiv-contaminated-drug-1000s-contracted-hiv/
FDA MAJOR COVER UP FOR BAYER~ Spreading HIV/ Aids Virus.wmv.mp4,BAYER scandal – HIV Contaminated Drug – 1000’s contracted HIV,Bayer…
Drugs company Bayer realised their product had been contaminated with AIDS, so what did they do, they still sold it because they didn’t want to lose money, and when …
Jan 28, 2011· … of dollars to end a scandal in which the company sold HIV.. in which the company sold HIV–contaminated…contracted HIV from the blood. You …
BAYER scandal – HIV Contaminated Drug – 1000′s contracted HIV – See more at: http://www.definitionofnegligence.com/bayer-scandal-hiv-contaminated-drug-1000s-contracted-hiv/#sthash.UimVMQVp.dpuf
Pfizer Unit Sued by Regulator for ‘Deterring Competition’ -http://wallstcheatsheet.com/business/pfizer-unit-sued-by-regulator-for-deterring-competition.html/?a=viewall – As full disclosure nears, doctors’ pay for drug talks plummetsSan Jose Mercury News
New England Compounding Center: Avoid Drugs From Company Tied To Meningitis, FDA Says http://www.huffingtonpost.com/2012/10/04/new-england-compounding-center-fda-drugs-meningitis_n_1940564.html
Multistate Outbreak of Fungal Meningitis and Other www2c.cdc.gov/podcasts/download.asp?f=8625771 – Oct 23, 2013· FDA reports conditions observed at NewEnglandCompoundingCenter facility (FDA Press Release: Oct. 26, …
Lawsuit on Behalf of Affymax, Inc. (AFFY) Investors Over …
EUGENICS CRIMES AGAINGST WOMEN
There is a influx of international corruption throughout America – Against women and this is now being brought to the forefront.
NO WOMAN DESERVES TO BE USED FOR MEDICAL EXPERIMENTS OR BECOME STERALIZED DUE TO PAST DICTACTOR’S EUGENICS THEORIES OF USING WOMEN’S BODIES AND THEIR CHILDREN BORN OR UNBORN TO CONTROL THE WORLD POPULATION!
PLEASE FEEL FREE TO RESEARCH AND INVESTIGATE ALL STATED FACTS IN THIS RESEARCH ANALYSIS! FOR YOUR FURTHER KNOWLEDGE! CABIRI, HAS MORE HIDDEN FACT’S TO REPORT!
Is Cyber Security A JOKE???
Whose Monitoring & Protecting U.S. Consumers…There’s So Much To Unpack Here….
Over the past several years Cabiri Research & Investigations has uncovered massive fraud on/offline it’s too much to list. Although if you have the time please read the numerous articles written dating back to 2014.
As the years have gone by it’s hasn’t gotten any better in fact it’s much worse! ‘To be honest ‘Folks’ you can’t trust anything online. Although were forced; to use these platforms for business purposes and livelihoods. These culprits are utilizing to their benefit social media platforms, websites, autoresponders, emails, text messaging, to catch their next victims. They sit back watching and waiting to attack.
And many of these platforms can careless; as long as they get their monthly subscription, membership or platform fees.
CABIRI’s recent catches were GeekSquad/Best Buy impersonators located in Frankfurt Germany, and Warrior + Plus a 3rd party vendor allowing fraudulent merchants from India and other countries to scam consumers out of money utilizing false advertisement, videos, paid promoters, and ‘Fake DFY’ product/service schemes. There’s a entire slew of them on there! Just stealing from U.S. Citizens as U.S. Citizens fight back and report to authorities; although caseloads are so extensive it’s like a needle in haystack so the American people are just out of their hard earned money.
These culprits are playing the game by using prominent U.S. business platforms to carry out their agendas. At the expense of the American people. We wonder why the U.S. Debt Clock has tipped over beyond repair…We’ll never see in this lifetime.
The Social Security Administration reported during Covid 19; there were over 800K Identity Theft Cases in the U.S. we should asking why is Equifax, Transunion, Experian still in business. Do they know who is who with all those Identity Fraud cases unsolved? What credit reporting system are they using? Do they know if the people are real or fake?
As well; does the Federal Government truly know whose who in the United States. There’s lots of unanswered questions to think about?
CABRI has been incredibly successful in catching many culprits over the years. If you read through the entire blog, you will be amazed at what has been uncovered through the investigative work and personal experiences. In some cases, even going into the trenches to dig deeper to uncover the truth. However, it can be very dangerous to know too much, as you may be subject to gang-stalking, blackballing, and other forms of persecution.
We really need to do better to prevent these culprits from defrauding consumers and the United States! We wonder why CCP has been monitoring U.S. and U.S. Citizens via TikTok “Right Under Are Noses!’ China isn’t the only country using U.S. platforms to carry out there hidden agendas.
In my opinion every business online doing business within the U.S. should have a Contact number, Face/ID recognition of all employees, and board members, Local U.S. address, and have a encrypted Business ID between Business/SBA/Federal Government; All Business Information should be posted on a separate public platform.
If the U.S. business partners with an international business all above will apply to them as well; besides having a encrypted International Business ID. The U.S. business will be held responsible for any fraud or illegal actions of the international 3rd party business or it’s employees using their platforms or website platforms who defrauds the American people. The company may be fined or penalized by the SBA/Government. Which means the U.S. business owner should their due diligence before partnering with any International Business! Doing business internationally could me a “National Security” issue for the U.S. depends upon what that international businesses hidden agenda may be.
The internet has become an increasingly complex place, with humans, artificial intelligence, bots, and metaverses all interacting with each other. With people from all over the world online at any given time, it is difficult to know who is doing what. For this reason, the United States should implement more stringent regulations for internet usage. These regulations should be designed to protect the safety and security of users, and to ensure that everyone is held accountable for their actions online. With the right guidelines in place, the internet can be a safe and secure place for everyone to enjoy.
Let’s add just as they don’t truly know who owns guns; we don’t know whose flying drones.
CABIRI – Research & Investigations
Daughter Of Vietnam Veteran – Helping Keep America Safe
The Internal Death: New Episodes & Medical Research On ‘Kindle Vella’
Pharmaceutical Fraud vs Quality of Life
Human lives are in the hands of corporate criminals racing to dominate the world, “one country, one human life at a time!”
Corporate Fraud against human lives considered a – “Misdemeanor”
“Billions of citizens around the world,” depend on pharmaceutical corporations, doctors, FDA, NIH, CDC, and many other Federal Government healthcare agencies and organizations, whom are to provide the human population with proper safe medical products, procedures, drugs and devices. We must question the actions of healthcare corporations, agencies, and organizations, who put their corporate interest before human lives. If we don’t do this how can we truly trust a “Corporation-Business” who’s previously engaged in criminal activity, whether it was directly or indirectly.
From recent market research it seems pharmaceutical, medical, oil, wall street corporate leaders and political lobbyists are altering these “specific industries” for their corporate benefits to gain world power! It’s truly sad to know there’s some individuals with leadership positions who care nothing about a ” Human life!” The main focus is corporate greed and the race to rule the world by any means necessary, which impacting human lives all around the world.
America it’s time for all of us to question the “credibility” of the “Quality of Healthcare” being administered by corporations, businesses, and organizations, who were previously or currently involved in fraudulent activities that could of negligentlycost a human life, or hit a families financial stability. How does anyone know if Pharmaceutical corporations behind schemes such as Medicare/Medicaid Fraud are now “Trustworthy?” And have learned there lesson, to not scheme the government or the U.S. Citizens! “We all know it’s not that easy.” Now don’t we! Glaxo-Smith Kline has been in the spot light being reprimanded in the U.S., China, and India for illicit business practices.
These Healthcare corporations are providing services, products and drugs for the human population, so how does one truly know if were safe from corporate negligence and greed.
Another question we must ask the U.S. Healthcare officials is; Why isn’t corporate fraud cases handled in the same manner as any other regular fraud or criminal case prosecuted in the court of law? If a regular citizens pleads guilty to fraud, there’s usually a financial penalty, as well as a probationary period, and other court order requirements to satisfy the fraud charge.
Along with the fraud penalty, is the United States Federal Court, imposing a probationary period with additional future audits for these corporations – business who are involved in fraudulent activities. If not it should be the case if human lives can be severely impacted by their fraudulent actions. In the real world fraudulent activities could involve jail time, so why does a corporation or business just get slapped with a monetary fine?
America here’s the “Root Case” of the problem, The United States Supreme Courts have granted Healthcare Corporations the power to alter and “Kill Human Beings!” Supreme Court rules Drug Companies exempt from Lawsuits http://www.whiteoutpress.com/articles/q32013/supreme-court-rules-drug-companies-exempt-from-lawsuits/
America, how is this legal or ethical, when these other human beings are making decisions, products, drugs and procedures for other human beings. Who is the U.S. Supreme court really protecting, in my opinion it may be the beliefs of the “Roman Catholic church?” The top elitists who are ‘Believer’s’ in the “Eugenics Theory” to depopulate those who are a waste to society! Including those who they feel are unworthy to society. Their actions are being played out in many “Executive Board Rooms,” plotting to harm innocent lives by lying to the poor patients using them as clinical trial guinea pigs! This is awful although very true in our society and whether we realize it or not it’s “Very Realistic and True!” So just as the looming ‘Civil Right’s Violations’ in Ferguson the “Deadly Healthcare Industry” in America must receive just as much attention in order to save lives!
As a Florida resident, I’ve personally seen a abundance of new “Healthcare clinics” popping up all over the place, along with this comes excessive ads for clinical trial research companies seeking citizens to perform experiments on them for their man-made drugs, products and devices. America, please it’s time to think about what were putting into our bodies!
See below Healthcare corporations who have our lives in their hands and involved in fraudulent schemes
Coalition against BAYER Dangers – View All Articles @ http://www.cbgnetwork.org/4.html
Bayer agrees to biggest Medicaid fraud settlement – BOSTON (Reuters) — Germany’s Bayer will plead guilty to a criminal charge and pay $257 million in fines and civil damages in what U.S. prosecutors Wednesday called the biggest Medicaid fraud recovery in U.S. history. http://usatoday30.usatoday.com/money/industries/health/drugs/2003-04-16-drug-settlement_x.htm
Corporate Crime Reporter, APRIL 21, 2003 – BAYER PLEADS GUILTY IN MEDICAID FRAUD CASE – TO PAY $5.5 MILLION CRIMINAL FINE, $251 MILLION TO SETTLE CIVIL CASE – http://www.cbgnetwork.org/382.html
The Pharma Letter | 04 September 2013 – Bayer in settlement over Cipro pricing – A partial settlement has been reached in a US class action law suit involving the prescription antibiotic Cipro (ciprofloxacin), originated by German drug major Bayer, it was announced by a group of US law firms acting in the law suit on September 3 http://www.cbgnetwork.org/5208.html
Press Release, October 10, 2013 – Coalition against Bayer Dangers (Germany) – GMO patents held by BAYER and BASF – Not only MONSANTO! – The discussion on Genetically modified seeds is dominated by the criticism directed against MONSANTO. In the wake of MONSANTO the German company BAYER has become one of the largest agricultural corporations in the world. Already, BAYER is one of the leading suppliers of pesticides and seeds. A current enquiry at the European Patent Office shows that in terms of the number of GMO patents BAYER actually comes first. http://www.cbgnetwork.org/5242.html –
People & Power—Drug Money – http://www.cchrint.org/2010/08/17/people-power-drug-money/
Pradaxa Lawsuits Show Drug Manufacturer May Have Hidden Research http://blog.lawyerworks.com/2014/02/18/pradaxa-lawsuits-show-drug-manufacturer-may-hidden-research/
Study Finds An Underreporting of Injuries Associated With defective Medical Devices http://blog.lawyerworks.com/2014/01/21/study-finds-an-underreporting-of-injuries-associated-with-defective-medical-devices/
U.S., Nev. join lawsuit against hospice accused of fraud http://www.smartbrief.com/12/05/14/us-nev-join-lawsuit-against-hospice-accused-fraud#.VIVKZzHF-Yw
Hepatitis C plus hepatitis B raises risk of cirrhosis, liver cancer, death http://www.smartbrief.com/12/02/14/hepatitis-c-plus-hepatitis-b-raises-risk-cirrhosis-liver-cancer-death#.VIViijHF-Yw
Drugging our kids: RX alliance rewards doctors as drug companies get richer http://www.cchrint.org/2014/11/24/drugging-our-kids-rx-alliance-rewards-doctors-as-drug-companies-get-richer/
Behind the Epidemic of Military Suicides – http://www.cchrint.org/issues/the-hidden-enemy/
Corruption in the pharmaceutical industry –
Quality of Life Solution by CABIRI,
American Citizens Fed Up with International Citizen Control
Many Americans are fed up and speaking up about International country people who have come over to America!
The United States Government is failing to realize there is a ground war going on in America, that may not turn out
very pretty, if a handle is not put on all the Immigrants who have come over to America! Many Americans are getting fed up at this point young and old and the “Pot is slowly brewing and thickening!”
Many American born citizens have now realized that many International citizens now own Corporations, Businesses Real-Estate, and have taken many jobs away from hard working generatinoal American families! This is not good America, CABIRI, has been speaking and following the media for quite some time and the plot is thickening!
Americans are very upset with the United States Government for allowing International Countries people to come over to America on Visa’s and acquire anything they want! Which is now turning into a major problem. If nothing is done Americans will start a war in their own country to take back what is rightfully theirs. All these smart politicians are missing the boat on this, as the pot is brewing. Why do you think Americans are not giving up “Gun Control”, why do you think there are private American Militia Groups forming in America for a reason and many are missing what is truly going on!
The American Government, should United States back into the hands of the American people or their may be some not so nice things to occurr down the line! Americans have children and they want to live the American Dream, and if International Country people have taken over, how will this be possible! Which causes a grave problem in America, the United States Government is missing. The Department of Homeland Security has no control over International Visa holders or newcomers, this all in the hands of the United States Government whom are allowing all of these international country people to come take control over many of Americas Business Industries, which is wiping out the Naturalized American Born Citizens an their families and the Next American Generation.
Many Americans are realizing this is only occurring in America, No other country in the world is allowing other international country people to take over their country by visa entry! Also another factor brewing is American Citizens are fed up with International Country people evading Taxes, and Credit History requirements, and College Tuition perks, why American citizens are being scrutinized for every little thing possible, International Country people are getting away with Economical Murder in America, taking away from millions of American Families.
If the Government does not put handle on this Immediatley, they thought the “Bundy Ranch” was bad, what if they had that all across America! They have no idea Americans are buying guns and purchasing guns for a reason, and are refusing to give them up for a reason! In CABIRI, finding many Americans Citizens are fed up with every where they turn it’s a International Citizen whom is doing better than them in their own country and they were born and raised in America with deep family roots. So the pot is definitley brewing and the United States Government should realize Americans are going to stand for this too much longer! Many have expressed to CABIRI, the United States Government is Corrupt and for International Citizens and against it’s own American Citizens. Which is a major problems.
The United States Forefathers’ stated if ‘Internationalism’ every became a problem in America, there would be a turn over in Americas Government leadership and American Citizens will have to fight to take control back over thier country! This may happen sooner than later, many American Citizens tempers are looming and tired of seeing international visa holders and residents excelling and Americans dimishing. Which is a major problem!
Please tell your American Government Leaders to put America back in the hands of the American Citizens or prepare for some very uneasy times looming in American by millions of “Fed up American Citizens, who want their country back, which means, Land, Jobs, Schools, Oil, Food, Healthcare, Biotechnology, Technology, Wall Street, etc., basically all economical resources that have been stripped away from American Families.
How The international Banking Cartel Controls The World Through The U.S. Military And Economic Sabotage
International Pfizer – AstraZeneca Conspiracy
America, please read the attached articles, you’ll view corruption at it’s best! Read how foreign countries are side-stepping Americas taxes by running their “Big Pharma” Corporations based in U.S. in their international country or some other country! Not in the U.S.!
They’re only doing business in the U.S. to gain profits from American Citizens, who are buying their pharmaceutical drugs more than any other country! Americans are unknowingly, making other countries rich, while they have hidden-agendas brewing in America! Cancer, is growing rapidly in America for a reason, it’s called “Reverse Psychology” surprisingly, AstraZeneca pipeline is full of Cancer Drugs for “Pfizer! The below article will spell it out and many more debacles you’ll think twice about if you care for your well-being in America!
Pfizer AstraZeneca takeover attempt prompts job warning from Vince Cable Business secretary says he is committed to maintaining UK’s position in pharma industry, but investors welcome bid!
Headquarters: Tokyo, Japan
Additional locations: U.K., Sandwich – U.S., MIT – Boston MA, California, Michigan
U.S. – Germany mixed family partnership based out of (Ludwigsburg, Germany/U.S.) – presumed makers of “Citric Acid”
Area’s: Primary Care, Specialty Care, Oncology, Emerging Markets, Established Products, Consumer Healthcare, Nutrition, & Capsugel
Originally – Fine Chemicals Company – Known for Producing drugs through chemical synthesis
Mergers & Acquitsitions: Warner Lambert, Pharmacia, Searle, UpJohn, Monsanto, Wyeth, King Pharmaceuticals, Alacer Corp
Products: Zoloft, Lipitor, Norvasc, Zithromax, Aricept, Diflucan, Viagra, Celebrex, Emergen – C, Xanax, Xalatan, Depo-Provera, Feldene
Astra AB – Originated “Stockholm, Sweden
Formation of AstraZeneca
ICI – Imperial Chemical Industries – Acquired By:(Azko Nobel)
Prior British Chemicals Empire Largest Manufacturing Corporation
ICI aka Henkel AG Integration (Dusseldorf, Germany) – Chemical Manufacturing – Detergents, adhesives, brand technologies, industrial business,
“ICI” aka Zeneca Group, Zeneca Plc, Zeneca Farm-Foundation (British Multinational Pharmaceutical Company – U.K./Europe)
“ICI Acquired – Unilever Anglo-Dutch Multi-national Consumer Goods – Worlds 3rd Largest Consumer Goods Company
Areas: Foods, Beverages, Cleaning Agents, Personal Care, Shampoo, Deodorant, Hair-Care
U.S. – North Wilmington, Delaware, Millbank, Headquarters: London, U.K, New Jersey, Netherlands, Sweden, France, India, Japan, Brazil, Canada
Products: Paints, foods, polymers, electronic material, chemicals, fertilizers, insecticides, dyestuffs, non-ferrous metals, Biopol, Paludrine, Halothane, Inderal, Beta-Blocker, Tamoxifen, Synthetic pyrethroid insecticides, Synthetic fibres, Polyesters, Nylons, Industrial polymers, Various Paints, Personal, Consumer & Home Care, Vaccines, Pharamcokinetic, Isoenzymes, Biotechnology, H1N1 Intranasal Novel,Antibody, Raxibacumab, erythematosus, Benlysta, Inflammatory Disease, Gastrointestinal, Infection, Respiratory, Pathological, Oncology, Neurological
Human Health Services: Astrazeneca/MedImmune – 90 Million (Phase 1 H5N1)
$894M deal ends most of Pfizer’s lawsuits – http://abcnews.go.com/Business/story?id=6062389 Death’s
Tort Hell: Pfizer And A Lawsuit Over An Injury From A Generic http://www.forbes.com/sites/edsilverman/2013/06/14/tort-hell-pfizer-and-a-lawsuit-over-an-injury-from-a-generic/
Lipitor Lawsuit News: Pfizer, Inc. Named in Whistleblower Lawsuit Alleging Improper Marketing of Lipitor
$142 Million Award Against Pfizer Stands – What is Off-Label Marketing? – http://charlottesville.legalexaminer.com/uncategorized/142-million-award-against-pfizer-stands-what-is-off-label-marketing/
Lawsuits claim Pfizer drug Lipitor gave women type 2 diabetes
Pfizer enters final settlements in 660 Chantix lawsuits – http://blog.al.com/spotnews/2013/07/pfizer_enters_final_settlement.html
Pfizer resolving several lawsuits over its drugs – http://www.businessweek.com/ap/2012-11-12/pfizer-resolving-several-lawsuits-over-its-drugs
Pfizer Hit With $43 Million Settlement For Misleading Marketing Of Drugs – http://consumerist.com/2012/12/12/pfizer-hit-with-43-million-settlement-for-misleading-marketing-of-drugs/
Pfizer Recalls Antidepressant Effexor Because It Is Not A Heart Medicine – http://consumerist.com/2014/03/07/pfizer-recalls-antidepressant-effexor-because-it-is-not-a-heart-medicine/
Louisiana Woman Files Lipitor Lawsuit Against Pfizer – http://www.ringoffireradio.com/2013/10/louisiana-woman-files-lipitor-lawsuit-pfizer/
Nexium Use and Increased Risk for Fracture or Plavix and Nexium lawsuits? – http://www.lawyersandsettlements.com/lawsuit/nexium.html#.U2Cl-PldWDo
AstraZeneca Settles Most Seroquel Suits – http://prescriptions.blogs.nytimes.com/2011/07/28/astrazeneca-settles-most-seroquel-suits/
Scientist’s lawsuit accuses AstraZeneca of fudging Brilinta study
WSJ: Scientist’s lawsuit accuses AstraZeneca of fudging Brilinta study -http://www.fiercepharma.com/story/wsj-scientists-lawsuit-accuses-astrazeneca-fudging-brilinta-study/2014-02-03#ixzz30LvDKAb3
Statins | Crestor Lipitor Zocor | Diabetes | Lawsuit – http://www.torhoermanlaw.com/crestor
ASTRAZENECA PHARMACEUTICALS LP PLEADS GUILTY TO HEALTHCARE CRIME; COMPANY AGREES TO PAY $355 MILLION TO SETTLE CHARGES – http://www.justice.gov/opa/pr/2003/June/03_civ_371.htm
Pharmaceutical Giant AstraZeneca to Pay $520 Million for Off-label Drug Marketing – http://www.justice.gov/opa/pr/2010/April/10-civ-487.html
AstraZeneca to cut 2,300 more jobs – http://www.usatoday.com/story/money/business/2013/03/21/astrazeneca-cuts/2005357/
Test results take precedence over ethics – http://www.svd.se/nyheter/inrikes/provsvar-gar-fore-etik_2667047.svd
AstraZeneca Buys MedImmune for $15.6 Billion – http://www.nytimes.com/2007/04/24/business/24drug-web.html
Pfizer Proposes a Marriage With AstraZeneca, Easing Taxes in a Move to Britain – http://dealbook.nytimes.com/2014/04/28/pfizer-proposes-a-marriage-and-a-move-to-britain-easing-taxes/?src=meRing of Fire Fraud and Whistleblowers in Big Pharma
America, please ask yourselves – What benefits are these companies giving you and your families?
Should Americans trust International Pharmaceutical companies with their health and well-being, based in another country?
Freelance Corporate Research
Special Alert!! Women Taking Deadly Birth Control Toxins
All Women! Please be aware of “Birth Control” Toxic Dangers From 2nd, 3rd Generational toxins and Newer Birth Control Mixed Chemical Toxicities, That can severely harm your bodies internally and externally!
Please Read vital information and Save lives Pass this article Along!
Such as Yaz, Mesh, Mirena-Iud, etc.,
Please read article from the BMJ or British Medical Journal
RESEARCH via BMJ Group of U.K. – British Medical Journal
All women of America Please read for your own Reproductive Health Safety, in reading you’ll find it very interesting the health risks involved from taking these toxic Birth Control pills, and Birth Control Devices!
Please read below important information from actual “Research Journal,” that was compiled by several medial professionals:
Different combined oral contraceptives and the risk of venous thrombosis: systematic review and network meta-analysis –
BMJ 2013; 347 doi: http://dx.doi.org/10.1136/bmj.f5298 (Published 12 September 2013)
Many different combined oral contraceptives are available. We selected 10 frequently prescribed oral contraceptives for the network meta-analysis:
20 μg ethinylestradiol with levonorgestrel (20LNG)
30 μg ethinylestradiol with levonorgestrel (30LNG)
50 μg ethinylestradiol with levonorgestrel (50LNG)
20 μg ethinylestradiol with gestodene (20GSD)
30 μg ethinylestradiol with gestodene (30GSD)
20 μg ethinylestradiol with desogestrel (20DSG)
30 μg ethinylestradiol with desogestrel (30DSG)
35 μg ethinylestradiol with norgestimate (35NRG)
35 μg ethinylestradiol with cyproterone acetate (35CPA)
30 μg ethinylestradiol with drospirenone (30DRSP)
We categorised 20LNG, 30LNG, and 50LNG as second generation progestogens, and 20GSD, 30GSD, 20DSG, 30DSG, and 35NRG as third generation progestogens. 35CPA and 30DRSP were not used in this classification by generations.
Apart from adjustments in the dose of ethinylestradiol, the progestogen compound was also changed in an effort to reduce side effects. After the first generation progestogens (that is, norethisterone and lynestrol), new progestogens were developed. These new compounds were called second generation (that is, levonorgestrel) and third generation progestogens (that is, gestodene, desogestrel, norgestimate).15 However, users of combined oral contraceptives with third generation progestogens have a higher risk of venous thrombosis than those using second generation progestogens.16 17 18 19 Other progestogens have been developed after the introduction of third generation progestogens—that is, drospirenone (introduced in 2001). The thrombosis risk for contraceptives with drospirenone was found to be higher than for combined oral contraceptives with second generation progestogens.
Women of America are taking 2nd and 3rd generational toxic chemical compounds! Also, let’s not forget to discuss the Newer chemical compounds that weren’t clinically tested properly! The Clinical Trial Dates, Do Not surpass the amount of time needed, to deem a chemical product or drug safe for human consumption or usage! This would mean the FDA and the Pharmaceutical Industry providers are marketing new products to human beings, that are deadly and unsafe. Which is very disturbing and alarming in America!
Basically using women as “Guinea Pigs,” for their mixed chemically induced birth control products! Which are causing Reproductive Health life altering problems for all women!
The British Medical Journal tells the real truth about the serious findings of “Birth Control Dangers!
Thanks BMJ, for allowing the real truth to be known, saving millions of women lives in America and Abroad!
Here’s another one you may want to read!
Breast cancer screening pamphlets mislead women – BMJ 2014; 348 doi: http://dx.doi.org/10.1136/bmj.g2636 (Published 25 April 2014) Cite this as: BMJ 2014;348:g2636
Additional Full Content Link – http://www.bmj.com/search/thrombosis?filters=type%3Ahighwire_article
Freelance Business Research Copywriting
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