Nationwide: Fentanyl Used With Dog Tranquilizers To ‘Eat The Flesh’ Of Drug Users: Now Needing Amputations
WHAT IS GOING ON!
We truly despise articles as such bearing bad news to ‘Society’ which is already currently dealing with difficult
trying times. This article is necessary to ‘Save Families’ who may have a loved one fighting ‘Fentnayl Addictions!’
Many People Are Dropping Dead Out Of Nowhere & Now This!!!
Any ‘Sane Individual’ should be asking the below questions and be concerned about this ‘New’ drug crisis!
~The first question is; who is responsible for supplying, and marketing these drugs?
~How are drug users getting their hands on these dangerous cocktails?
~Why is a Tranquilizer used to sedate ‘Horses’ on the open market?
~Why is this not getting more attention? This is modern-day genocide at best!
The sad part it’s being reported, there is no cure for this dangerous ‘Flesh Eating’ chemical drug cocktail.
Individual flesh is being eaten to the point their bones are exposed.
“Could you imagine walking down the street and seeing this?”
The individuals (Human beings) who have to get their body parts amputated. Now is on permanent disability!
As well drug Users’ can get the disease “Gangrene” in their open flesh wounds by not getting the proper medical
If the crisis is not addressed this could cause massive deaths on our U.S. streets, no matter what ‘State’ you reside in!
This crisis may cause other issues; Many individuals will have to depend upon Drug, Disability, and Homeless Services & Programs from the Government, Non-Profits, etc. in order to survive and to continuously purchase and support their Drug Addictions Of Fentanyl & Xylazine (Horse Tranquilizer).
From MSBC Article:
Xylazine is strong enough to sedate a horse and according to data from the city, it was found in more than 90% of the Philadelphia drug samples in 2021.
It is not just a Philadelphia problem. The DEA warns that the drug is leading to a major spike in overdose deaths across the nation. Officials say Tranq was first found in the drug supply in Puerto Rico and is mixed in with fentanyl to extend the high.
Animal tranquilizer found in 90%+ of Philly drug supply, ‘Tranq’ is eating users’ skin leading to amputations (msn.com)
People need to be very mindful that if this isn’t addressed immediately; This could cause irreversible damage to many “Human Beings and the U.S. Economy!”
This dangerous ‘Drug Chemical Concoction’ of “Fentanyl and Xylazine” and its producers and sellers are preying upon vulnerable
human beings! ‘ALL FOR PERSONAL PROFIT GAINS’ OR A NEW DEPOPULATION TACTIC’
What is wrong with people. It begs to question of how ‘Evil’ some people and their ‘Souls’ truly are! ‘Why is money more important than a human life’ – ‘We all only have one life!’
Maliciously harming others is against the ’10 Commandments,’ when any human being passes away ‘they can’t take any amount of profits with them!’ So why destroy another ‘Humans Beings’ life for Money, Greed, and Power, you can’t take with you?
Everyone should be truly concerned about this problem! As ‘A Socioeconomic Journalist’, Homeless Women’s Advocate, and Humanitarian Consultant, I felt it extremely necessary to ‘Publicly’ bring awareness to this horrible discovery.
Let’s add with all the current ‘Nationwide’ job lay-offs and cutbacks; there may be a wave of individuals and families who fall on financial hard times, becoming vulnerable, and turning to these types of drugs as a coping mechanism. Leading to more possible ‘Drug Over Doses, Suicides, Mental-Illness and Permanent Disabilities.
IF YOU CAN HELP TAKE ACTION
Please support those who are helping ‘Fight’ against ‘Fentanyl and Xylazine! As well please contribute to all those developing programs and services to help fight this new dangerous ‘Epidemic!’
Xylazine, drug known as ‘tranq,’ eats flesh, is linked to thousands of heroin, fentanyl ODs: Report – silive.com
What is xylazine? Animal tranquilizer shows up in US drug supply (usatoday.com)
Freelance Investigative Journalism
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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!
Political Bureaucracy Violating U.S. Citizens Required Humanitarian Needs
The U.S. Government, International Corporate Business Owners are concerned with Only $$$$$$$$
Humanitarian Right’s Violations – Against “Chronically Homeless Medically Ill Citizens”
It’s hard in this day in age, to really believe a word that comes out of any of our politicians mouths. There’s so much corruption in the U.S. Government, Federal Agencies, Corporations, Organizations, Wall Street, IMF, Technology, Agriculture, Environmental Industry, Judicial and Healthcare systems, it’s ridiculous there is no trust or honesty anywhere in our Federal Government leaders. It’s time for all Americans to come to a realization that the United States is a “Socio-Economic Disaster Area” that must be fixed immediately, for the good of the American people!
Recently, our research consisted of investigating the crisis into America’s ‘ Chronic Homeless Epidemic’ the U.S. Government is keeping hidden, boosting economic growth, and unemployment numbers which are fallacies. These higher ups are living in their million dollar “Bubbles” and making “Deadly Decisions for the American people or lack thereof; and these Government officials have the slightest clue about the “Real world humanitarian nightmare” millions of Middle-Income, and Poor Citizens are experiencing on the “Lower Economic Level!’
Does anyone not realize what goes on in the dark always comes to light. Sometimes all it takes is ‘A Voice, real world experience’s, education and plain common sense’ to figure out there’s a serious problem in our society.
“When speaking with,” Federal, State and local government representatives, about the medically ill and other disabled, elderly citizens whom are currently chronically homeless in a the United States for periods between 1 – 3yrs. It was disturbing to find out there’s no help for citizens of the United States in need of desperate economical help. The age ranges of the “Chronic Homeless Epidemic,” in the U.S. varies from the elderly, middle-aged, and children.
“Many citizens as well as myself,” are frustrated with the U.S. Federal Government leaders who’s allowing ‘Political Bureaucracy” to stand in the way of saving human lives in America! These entities don’t realize good standing ‘American Citizens’ who previously worked hard paid their taxes faithfully, are also being denied any help or support if they become chronically homeless due to a sudden medical or non-medical illnesses. What are U.S. citizens paying taxes for?
The more frustrating part comes into play, when you try contacting these agencies for any help. Here’s some barriers you’ll face when you contact any agency on the Federal, State or Local government levels. You’ll have a hard time getting insurance if your medically ill and unemployed, You’ll be unable to seek proper medical treatment due to being uninsured, You’ll be subjected to taking radiation treatments for your cancer while living in a hotel and you can’t afford it, You’ll need multiple surgeries and living in hotel and can’t afford it, You’ll apply for SSI/Disability 2 – 3x and be “Denied” although you’ve given the Social Security Administration medical, doctor, and homeless certificate proof, You’ll be denied rental assistance HUD, Public Housing, on State/Local levels due to lack of State/Local funding and 3yr. housing waiting lists, You’ll be discharged from multiple hospitals homeless and medically ill, You’ll find your State/Local/and Non-Profit Organizations do not have any resources available for medically disabled citizens, including Veterans, You’ll find your Emergency Hotline for local citizens doesn’t have any current homeless referrals due to again, lack of funding.
“When investigating we also found,” when you contact Federal/State/Local Government agencies you’ll be put into a “Whirl-Pool’ of transferred “Non-helpful phone calls,” which your lucky if you get a call back or a email response. You’ll be given multiple contact numbers on the “Federal level” for the State and Local Community level, which also are all dead end phone calls, each blaming the United States Economic problems on one another. It gets better America “No agency” on any level will accept responsibility for the “Broken” Public Assistance Programs in the United States all American Citizens require for their family’s basic “Humanitarian Needs!”
If people of the United States are “Chronically Homeless” this distinctively means basic humanitarian needs are not being met for the American people. Which is a direct violation of our “Constitutional rights.” The right to health encompasses not only health care but also the underlying determinants of health such as adequate sanitation and safe drinking water and adequate housing!
The right to health is “an inclusive right extending not only to timely and appropriate health care but also to the underlying determinants of health, such as access to safe and potable water and adequate sanitation, an adequate supply of safe food, nutrition and housing, healthy occupational and environmental conditions, and access to health-related education and information” – Committee on Economic, Social and Cultural Rights– http://www.ohchr.org/EN/Issues/ESCR/Pages/Health.aspx
The right to have your health intersects with many issues, including Disease, Disability, Job Loss, Housing and Financial stability. If a citizens health is failing and they aren’t being provided basic “Humanitarian Needs” (Required By Law), this makes it virtually impossible for a human being to live a normal life which is a direct violation of there ‘Human Rights!’
The Federal/State/Local Agencies are denying millions of United States Citizens there basic ‘Humanitarian Needs’ to live a normal healthy safe life. If citizens of ‘America’ getting their basic humanitarian needs met! It’s time for immediate “Government Action” or “Immediate U.S. Citizens Action” – Against Federal, State and Local Governments for not providing citizens with basic “Humanitarian” needs!
Per the United Nations State’s and Governments are to adhere to the following “Humanitarian Needs For All Citizens”
What are human rights?
Human rights are rights inherent to all human beings, whatever our nationality, place of residence, sex, national or ethnic origin, colour, religion, language, or any other status. We are all equally entitled to our human rights without discrimination. These rights are all interrelated, interdependent and indivisible.
Universal human rights are often expressed and guaranteed by law, in the forms of treaties, customary international law , general principles and other sources of international law. International human rights law lays down obligations of Governments to act in certain ways or to refrain from certain acts, in order to promote and protect human rights and fundamental freedoms of individuals or groups.
Interdependent and indivisible
All human rights are indivisible, whether they are civil and political rights, such as the right to life, equality before the law and freedom of expression; economic, social and cultural rights, such as the rights to work, social security and education , or collective rights, such as the rights to development and self-determination, are indivisible, interrelated and interdependent. The improvement of one right facilitates advancement of the others. Likewise, the deprivation of one right adversely affects the others.
Both Rights and Obligations
Human rights entail both rights and obligations. States assume obligations and duties under international law to respect, to protect and to fulfil human rights. The obligation to respect means that States must refrain from interfering with or curtailing the enjoyment of human rights. The obligation to protect requires States to protect individuals and groups against human rights abuses. The obligation to fulfill means that States must take positive action to facilitate the enjoyment of basic human rights. At the individual level, while we are entitled our human rights, we should also respect the human rights of others.
America, there is no help or support in the United State’s so it’s up to the American people to demand our Humanitarian Rights for our Family’s safe, health and well-being! We must ensure all basic humanitarian needs are being met whatever our nationality, place of residence, sex, national or ethnic origin, color, religion, language, or any other status. We are all equal, bleed red blood, and entitled to our human rights without discrimination or unfair treatment due to “Political Bureaucracy.”
Thank you for taking the time to read! Check Out: http://www.consumer2savlives.com view ‘CABIRI’s “Luv Thy Neighbor project” that will help bring your local community organizations, churches and citizens together which will ensure all community citizens basic needs are being met, leaving no family behind.
* America maybe it’s time for the ‘American People’ to request adjustments in the U.S. Government laws! As per our prior “Fore Fathers” if the United States Government is not working for the American people, the people have the authority and power to make changes! Although, in this day and age American citizens will face “Military Style Police Resistance” for fighting for basic “Human Rights!”
Political Solution: What if politicians and government leaders were required to live in the “Real World” for a period of 6 months to a year before they can run for office. It’s important for Political leaders to get a taste of what it’s like to live a normal life without wealth. Maybe this will help ‘Leaders’ become more compassionate about another human life, and it also may help them understand what it’s like to live as a regular white-collar or blue-collar citizen. The “Real World” stipulation will ensure all elected officials will be working hard for the American people not “Corporations” or to line their own “Pockets.”
Freelance Business Research For America
America not immune to human rights violations – http://www.vanguardngr.com/2014/09/america-immune-human-rights-violations/
UN Condemns America on Human Rights’ Violations – http://thesovereigninvestor.com/asset-protection/un-condemns-america-human-rights-violations/
Uncle Sam is Driving Americans to Let Go of Their Citizenship – http://thesovereigninvestor.com/asset-protection/expatriate-taxation-laws-driving-americans-let-go-citizenship/
WORLD REPORT 2014 – http://www.hrw.org/world-report/2014/country-chapters/united-states
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,
Florida Corruption = Rick Scott & Leaders
Palm Beach County System Flaws
1. Lack of Homeless Shelters Rehabilitation Assistance Programs for Women & Children – 10yr. Homeless Program Adopted by Palm Beach County – No return phone calls lack of shelter, funding etc. W.P.B. Mayor blames county for homeless crisis! County we have no $$!
2.No family orientated transitional monitoring faith based 12 Step Treatment/Substance Abuse/alcohol programs – Separate from court order drug program, half way houses, pre-trial intervention.
3.United States Census For Palm Beach County – Omits Statistical Information for White Owned Firms – Includes Black, Asia, Native Hawaiian, Pacific Islander, Native-America, Latino, and Women
http://quickfacts.census.gov/qfd/states/12/12099.html & Omits PBC male percentage, No account of PBC Foreign Citizens Visa statuses
4. No Immediate Temporary Disability and/or Medical Insurance for unknown medical emergencies extending over a 6mth period of time.
5. Lack of Shore Security – Via Waterways – preventing drug smuggling and human trafficking, or non-monitoring of foreign visitors docking for long periods of time.
6. Lack of auditing and monitoring local Governments, organizations, political leaders, who are accountable, and responsible for other human lives – Current Governor Health Con-Artist himself!
7. Lack of affordable Housing for Veterans, Elderly, Single-Parent Mothers, & the Medically Ill
8. Lack of International Educational Programs – Assisting International children and families with English, History, Laws, Schooling, etc.,
9. Debt to Income Ratio Inequality – Poverty – Hidden Homelessness Crisis in Florida
10. Outdated Programs listed as services – Stating available for assistance when in fact their not.
11. UN Condemns U.S. Police Brutality, Calls For ‘Stand Your Ground’ Review – Florida has a bad case of racial profiling
12. HUD RELEASES JULY 2014 HOUSING SCORECARD – “The market indicators for the housing market recovery were mixed in July as foreclosure filings continue to improve, but home sales, particularly for new homes, showed unexpected weakness,” said HUD Assistant Secretary for Policy Development and Research Katherine O’Regan. http://portal.hud.gov/hudportal/HUD?src=/press/press_releases_media_advisories/2014/HUDNo_14-097
13. Rehabilitate or punish? – Psychologists are not only providing treatment to prisoners; they’re also contributing to debate over the nature of prison itself. http://www.apa.org/monitor/julaug03/rehab.aspx
Palm Beach Post Article: Posted: 6:51 a.m. Monday, July 2, 2012
By Sonja Isger and Jennifer Sorentrue
Palm Beach Post Staff Writer
After more than a decade of planning, Palm Beach County will open its center for the homeless today.
It is the first time that the county’s homeless have had a single place to go for shelter, medical care, job training and other social services.
Although a handful of local charities and churches have always helped the homeless with emergency shelter, meals and job training, the county has lacked a central place for the homeless to go to easily navigate those services.
Homeless advocates say the center’s opening is the culmination of a perfect set of circumstances — a county commissioner advocating the project; a partnership between the county and nonprofits working with the homeless; and $8.5 million in federal grant money. What happened to the funding, who monitors and disburses has federal funding disbursement went toward homelessness assistance? If so why has homelessness increased in the Palm Beach County area.
“Everything came together,” said Marilyn Munoz, Executive Director of the county’s Homeless Coalition.
County commissioners first talked about providing an emergency shelter for the homeless in 2001, when former Commissioner Addie Greene formed a task force to help craft the plan.
But the next year, Greene said that the shelter should no longer be the task force’s top priority, acknowledging that political pressure from other commissioners had persuaded her to change her mind. Many worried about finding a location for the facility and complained that they would simply be “warehousing” the homeless.
Greene’s decision came after the county’s director of human services issued a report in 2002 saying that building a shelter for the homeless would be “cost prohibitive.” Instead, the director said he wanted more money for social workers to provide counseling for homeless people. He also said he would pay for more room nights and motels and halfway houses for the homeless while the social workers worked to find permanent help.
“In the beginning, (county managers) sort of encouraged you not to build permanent shelters,” said Commissioner Karen Marcus, who was first elected to the board in 1984. “It was, ‘if you start building them, you are actually going to get more homeless.”
By 2005 the county had partnered with CARP, Inc., which stands for Comprehensive Alcoholism Rehabilitation Programs, to help fund a 16-bed Homeless Residential Assessment Center at CARP’s campus in West Palm Beach.
But advocates kept pushing for a county-owned facility.
Meanwhile, an impromptu homeless shelter at Westgate Tabernacle in suburban West Palm Beach was drawing attention to the county’s growing homeless problem. The tabernacle drew the ire of county officials for opening its own shelter to house as many as 150 people a night. County officials argued that the shelter violated both fire code and zoning laws.
The tabernacle sued the county in 2007 and 2009, seeking relief from the fines. It argued that county officials had denied the homeless problem existed.
At the same time, then-Commissioner Jeff Koons was urging the commission and county administrators to address the county’s homeless problem. Working with nonprofits, he ultimately helped establish a homeless advisory board, responsible for crafting a 10-year plan to end homelessness in the county.
Koons resigned from the commission in 2010 amid an extortion scandal and was sentenced to five years’ probation but has since returned to advocating for the homeless. In an interview Thursday, he recalled urging advocates for the homeless to talk to commissioners about the county’s problem.
“I’d tell people whenever you bump into a commissioner, tell them how proud you are that they are working on homelessness,” Koons said.
The resource center became a critical piece of the 10-year plan, which was approved by the commission in 2008.
“Without Jeff Koons pushing it, I don’t know that it would have gotten this far,” Marcus said of the center. “It just became a real priority for him. He reached out to all the providers.”
Homeless in Palm Beach County
• A 2011 count found there were 3,228 homeless people in Palm Beach County.
• In county schools this year, there were 1,590 students between the ages of 5 and 17 who were considered homeless or in danger of becoming homeless.
• Fifty-six percent of the students in the county’s school system qualify for free or reduced-cost lunches.
• The leading causes of homelessness in the county are unemployment and lack of affordable housing, officials say.
• The county’s homeless outreach team placed 1,423 adults in emergency shelter last year.
Homeless Resource Center
Cost: $9.2 million
Location: 1000 45th St., West Palm Beach
Capacity: 60 beds, opening in three phases; 20 beds will open July 2; 20 beds will open Oct. 1; and 20 beds will open by Jan. 2. (non – existing)
Operation: Palm Beach County has contracted with three local nonprofits to run the facility and provide the social services. The county’s homeless outreach team will also be based at the center.
Lead operator: Gulfstream Goodwill Industries, responsible for overseeing the on-site interim housing and providing individual housing placement. (2013 No Services Available for homeless)
Adopt-A-Family: Will help families find services and housing. (2013 No services available)
The Lord’s Place: Will help refer people to the center and will provide employment and life skills services. (2013 No services available)
Lewis Center – (No services Available)
Homeless coalition – No return phone call – Governors R. Scott office – We can’t help you we have no $$ (How can you trust a man who’s had previous healthcare fraud, to do right by his citizens?)
Medical services: Staff from the county’s health department will provide on-site medical service.
Report: Heroin epidemic in South Florida -The problem has become an epidemic, according to the National Institute on Drug Abuse, in the aftermath of the crackdown on pill mills that dispensed high-potency painkillers. By Dan Christensen – BrowardBulldog.org –
U.S. Healthcare Hell – Woman Faints In Florida Office Applying For Healthcare
Woman Faints Waiting For Medical Insurance – Palm Beach County – Healthcare District
Healthcare Hell In America costing lives
The following is a story, about dangerous’Healthcare’ debacle’s in America concerning hospitals where I personally received treatment from on 13 separate occasions undergoing 6 surgeries, and ironically still currently going through constant life-threatening medical issues pre and post hysterectomy and other medical concerns where I could of lost my life at any given moment!
While all healthcare agencies, organizations, hospitals, politicians, doctors, and many healthcare leaders and decision makers sat around, and did nothing to acknowledge any of my life-threatening severe medical issue’s.
Attacks against U.S. women is currently occurring and no political figure, corporation or top 1% cares if “Women” live or die in America, so please be careful on who you vote for it may be the difference between your “life or death.
World pharmaceutical greed, corruption, and Healthcare political bureaucracy, has millions of Floridians and many U.S. citizens currently uninsured, requiring medical attention! My story proves they don’t care about your health!
It’s not rocket science people “Come On” if people aren’t receiving proper healthcare, this could be very well construed as direct violations of humanitarian rights, by not receiving proper, safe, medical treatment.
All Americans must ask themselves; Why are there so many problems in the United States healthcare industry? and..Who can citizens really trust with their health, safety and well-being? Why are there still currently thousands of “uninsured citizens” in the “State of Florida,” and elsewhere whom are in desperate need of life-saving medical attention, just as my personal “healthcare hell,” which is ongoing!
Currently I reside in West palm beach, Fl area and I don’t have any healthcare insurance, due to not having a proper residence or mailing address, which ironically was caused by my excessive hospital visits from 2012 up until recently.
As a woman who’s been at the bottom dealing with this “Healthcare Hell” in America, this has been a living nightmare, and trust and believe out of 2 years of fighting the Healthcare system in America, and Florida, no political figure or any other leader cares about a human life, let alone a woman’s life!
I’ve been fighting for immediate Healthcare re-certification to receive healthcare coverage for additional surgery and a needed mammogram. My life is currently at a stand still and in the hands of a faulty re-certification system at the Healthcare District of Palm Beach County! The ordeal left me lethargic passed out on a cement restroom floor with a elevated B.P. of 229/108 and more bodily injuries.
Currently, I’m unable to receive proper medical treatment that’s been ongoing since 2012, due to lack of medical insurance, although previously insured by the Health Care District of Palm Beach County a few months prior!
Several hospitals and ER rooms provided me with minimal treatment due to my lack of insurance, referring me to my primary care doctor and others, along with providing prescriptions for my dangerously high hypertension, after giving a B.P. injection to lower my B.P. while I was in the E.R., then soon after came my discharge papers! Amazingly, no healthcare professional directly addressed the root cause of my medical problems that landed me into the E.R. They gave me a band-aid and brushed me off like my life didn’t matter!
Getting discharged by both doctor and hospital was a slap in the face, when they all knew very well I had no medical insurance for follow up or prescriptions, none of the so-called caring compassionate, nurses, doctors, or hospital staff seemed to care! I thought to myself how can you discharge a “High Risk” re-occurring patient knowing they don’t have access to follow up healthcare, and they could die?
Now get this one my initial healthcare district insurance coverage was first activated February 2013, due to the persistence of my doctors office at the time who phoned the Healthcare District Management office and explained, to them I was there new patient and in need of immediate surgery and I really needed medical coverage for surgery. At that time of course the Healthcare District approved my medical coverage from 2/2013 – 3/2014 under option 1. Unknowingly months later post-surgery, I started having additional medical complications that landed me right back into the hospital in 2014.
Currently I’m still undergoing life-threatening medical problems stemming back from 2012! Due to recent life-threatening medical problems from previous surgeries that went unexplained, and now new cancerous concerns, where I’ve recently visited 3 ER rooms and hospitalized 2 times in the month of 6/2014, recent as 9/30/2014, each visit uninsured!
When I phoned the Healthcare District of f Palm Beach County in 6/2014, after being released from the hospital, they explained to me my coverage was dropped due to my “lack of response” from there office mailing my re-certification information to a previous incorrect address, where I’d been evicted 2 weeks after my 5th major surgery 8/2013, which was the start of my homelessness being uninsured, and after 8 months of hospital visits and 5 surgeries.
Now October 2014, I’m currently experiencing more life-threatening medical problems that need to be immediately addressed. So with no insurance, and being afraid for my life possibly having cancer. In a recent visit the ER doctor at Wellington Regional suggested; if I was hospitalized multiple times in the West Palm Beach area and still having medical problems maybe it was time to go out of the “State” and seek proper medical attention elsewhere! Surprisingly, this was not the first time I was told this, “many organizations stated,” this when I was seeking homelessness help and additional medical help! This doesn’t speak well of Florida!
Relocating as some wished me to do was virtually impossible, due to my extensive ongoing medical trauma’s and multiple surgeries it made no sense to leave and start my medical problems over elsewhere? I hope there is hope in my future, because several South Florida Hospitals and Doctors failed on several occasions to find the cause of my ongoing medical problems which has lasted for a long period of time, basically putting my life on hold. How can a person live their life not knowing, if they may end up in the hospital at any time?
So trying again to re-qualify for somebody’s healthcare insurance, I’ve been fighting to stay healthy and alive, while continually fighting the Government, State, and Local Healthcare agencies for fair and proper healthcare for all human beings! Politicians are supposed to protect the health, safety and well-being of American citizens, which is not being done, American citizens are dying in the hands of “United States Healthcare, Hell Of A Faulty System.”
Palm Beach County Healthcare District Hell
Back to the Palm Beach County Health Care District, in September 2014 after another E.R. discharge, I contacted the Healthcare District and spoke with the customer service department. This is when the agent stated, since my case was already closed, they would re-send me new paperwork to my mailing address to re-apply.
After 2 months the application never arrived, when calling to check the CSR states they have nothing to do with mailing the applications, and it’s best I come in, this was 3 weeks later! Needless to say I was furious! So I went in and I was told since I only had a mailing address and was homeless, I needed to show proof of my homelessness and needed a Homeless Declaration form filled out from a agency proving so, this form was filled out the very same day as per request.
After visit two and turning in all paperwork, a few days later I called the Healthcare district to check the status of my application, which I thought would be immediately re-activated, being that I was homeless and just previously covered the following year from 2/2013- 3/2014, only lapsing a few months which nothing changed besides more hospital and ER visits. I couldn’t understand the problem, when the Healthcare District had numerous medical bills from my recent previous 6 surgeries and multiple hospital visits, and prescriptions from the prior year 2013 when I was insured.
On 10/14/2014, I spoke with the customer service department for the Healthcare district who preceded to tell me I was not approved yet because their system mysteriously, now showed I owned a business! “Needless to say, I hit the roof!” This was totally wrong and crazy being that I’d just given them a ‘Homeless Declaration Form’ proving my homelessness, and the Healthcare District billing department surely should have medical proof in their systems of many medical bills from coverage 2/2013 – 3/2014, are you serious.
Please tell me how in the world could I own a business, when they knew good and well I’ d been hospitalized and undergoing life-threatening surgeries since 12/2012 when my doctors office initially called them to let them know I needed immediate surgery. Very frustrated I called to speak with the west palm beach area coordinator, to talk about why all of a sudden after being covered for a year and not even a few months lapsing time I now own a business? I explained to her I needed immediate health coverage to be seen and treated for a lump in my breast and other medical conditions dating back from the prior year.
The area coordinator stated, I needed to write a letter stating that I didn’t have a business that never existed! I asked her why in the world would I have to do that, when I gave them a homeless declaration form proving being homeless, along with them having proof of me being hospitalized and under doctors care since 2012, I’m sure the county has paid numerous amounts of medical bills on my behalf from 2/2013 – 8/2014 where I underwent 6 surgeries and was hospitalized numerous times. The area coordinator didn’t want to hear anything I stated, and told me to bring in the letter, or not be approved and hung up the phone. I thought wow, my life is in her hands!
America this has been a medical nightmare I wish upon no human being. I still have no medical insurance and a untreated lump in my breast that could be cancerous, along with having other related life-threatening reproductive health medical problems. In the meantime, I’m being unnecessarily taken through the ringer by the Healthcare District of Palm Beach County!
In my own defense to save my life from possible cancer, I’m writing this for all eye’s to see what’s currently occurring to women and many citizens in America due to a broken healthcare system involving political bureaucracy!
Please realize if this is happening to me, how many others is this happening too? Lives are precious and should not be put through such red tape especially when a citizens life is in danger, and they’ve been in the system a year and few months prior. At this moment my life sits in the hands of a woman at the Healthcare district, I don’t know! In 5 attempts in contacting the area coordinator again this time leaving several messages, I received no return phone call from the area coordinator.
The Healthcare system flaws is not only Florida based it goes all the way up to Washington, who apparently is missing the boat, if millions of U.S. citizens are still currently uninsured, and facing poverty due to a mis-diagnosed medical trauma’s, that are now haunting America’s healthcare industry. Something and many things are off in United States Healthcare and Automobile industries.
All bets are off, when it comes to saving human lives people deserve the right to proper medical treatment, and proper shelter. These are basic necessities in life to survive. The healthcare system is broken in every facet, insurance, pharmaceutical industry, Agencies, Doctors, etc., All of these agencies are gambling with human lives by not providing the basic necessities a human being needs to survive.
By not providing citizens with the bare living necessities such as quality healthcare, and shelter this a direct violation of humanitarian rights. According to the ACLU 3/2014 – U.N. Holds U.S. Accountable for Human Rights Violations at Home and Abroad
“The United States is abandoning its role as the global champion of human rights,” warned Jimmy Carter in a 2012 New York Times op-ed. Less than two years later, Carter’s warning has been vindicated. Yesterday, the U.N. Human Rights Committee issued a blistering report on the U.S. government’s role in perpetuating injustices both within its borders and abroad.
My once healthy product life has been medically turned upside down in a instant! Yours can be to, so be careful, and watch who you vote for! Ensure that the person your voting for will care totally for you and your families best interest. Now is the time to replace all healthcare killers, who are impacting human lives!
All leaders, must ensure every American citizen has all basic necessities to live a normal functional, healthy, stable life while on earth! If fair humanitarian treatment isn’t being provided for U.S. citizens, why should citizens pay taxes, or support leaders who don’t care about the well being of a human life?
Freelance Consumer Advocacy
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