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How A Defective Medical – Device Turned Her Life Upside Down
Leading her to go down the Biggest Rabbit Hole Of Her Life

Digging Deep Into The United States ‘Top 10 Big Pharma Corporations’ United States Government and the U.S. Healthcare Industry.

Unleashing Research data dating back to 2013…
Provided to the Obama Administration

BY: Daughter Of Vietnam Veteran
2018 Prior Political Candidate
Homeless Women’s Advocate
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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

Event Description

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
Event Key	565764
Report Number	595346
Device Sequence Number	1
Product Code	HDT
Report Source	User Facility
Reporter Occupation	RISK MANAGER
Type of Report	Initial
Report Date	04/20/2005
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 Operator	Physician
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
Event Location	Other
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

http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=595346

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.

Brand Name	MIRENA
Type of Device	IUD HORMONE FILLED
Device Event Key	550739
MDR Report Key	561031
Event Key	532986
Report Number	MW1033889
Device Sequence Number	1
Product Code	HDT
Report Source	Voluntary
Reporter Occupation	Patient
Type of Report	Initial
Report Date	10/27/2004
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
Event Location	Unknown
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

http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfmaude/detail.cfm?mdrfoi__id=561031

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

CERTIFIED MAIL
RETURN RECEIPT REQUESTED

05-09-2012

Kelly Dean Shrum, D.O.
(b)(6)

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.

FDA’s Finding

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.
Sincerely,

/S/
rmando Zamora
Acting Director
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

http://www.fda.gov/regulatoryinformation/foi/electronicreadingroom/ucm312157.htm

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….

[PDF]203159Orig1s000

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…

[TEXT] primaryid$caseid$drug_seq$role_cod$drugname$val_vbm…[DRUGS]

http://www.fda.gov/…/guidancecomplianceregulatoryinformation/surveillance/adversedrugeffects/ucm350261.txt- 2560k- …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…

Additional Research Links

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®….

MAUDE Adverse Event Report…

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

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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/

wn.com/Bayer_HIV_scandal

FDA MAJOR COVER UP FOR BAYER~ Spreading HIV/ Aids Virus.wmv.mp4,BAYER scandal – HIV Contaminated Drug – 1000’s contracted HIV,Bayer…

http://www.ristoranti-napoli.it/v/cphkD-9NUe8/bayer_scandal_hiv…

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 …

http://www.cbsnews.com/news/bayer-admits-it-paid-millions-in-hiv…

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!

CABIRI Big Pharma Research – Reproductive Health

BAYER PHARMACEUTICALS WARNING LETTER

DEPARTMENT OF HEALTH & HUMAN SERVICES

Public Health Service

Food and Drug Administration Silver Spring, MD 20993

“FDA Warning Letter To Bayer”

Fadwa Almanakly, Pharm.D.

Associate Director, Advertising and Promotions

Bayer HealthCare Pharmaceuticals Inc.

6 West Belt Wayne, NJ 07470-6806

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

Dear Dr. Almanakly:

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

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

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

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

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

Page 2

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

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

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

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

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

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

Fadwa Almanakly, Pharm.D.

Page 3

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

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

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

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

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

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

Page 4

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

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

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

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

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

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

Page 5

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Sincerely,

Carrie Newcomer for Cynthia Collins,

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

“CandyK’s Communication Outreach”

Dec 9, 2018

DRUGINFO@fda.hhs.gov

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

Dec 9, 2018

Automatische Antwort: Mirena Claim

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

Date: Thu, Mar 6, 2014

Subject: Incident #01980MMJ-42104CCO

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

Oct. 21st, 2014

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

Jan. 23, 2015

@aclufl.org

Legal Director – American Civil Liberties Union of Florida

Hello Candace-

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

Jan, 28th, 2015

Hello Candace-

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

Apr 10, 2014

Ellen Malcolm, National Partnership

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

Apr 15, 2014

Balboa Press – jstogsdill@balboapress.com

I want to help you tell your story

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

Mar 6, 2014

PATIENTSAFETY-L@LISTSERV.NPSF.ORG

LISTSERV@listserv.npsf.org

May 7, 2015

Cecile Richards, Planned Parenthood – NO Response

pponline@ppfa.org

Jul 23, 2014 – Planned Parenthood – No Response

Lisa.Murano@ppsoflo.org

Tue, Jul 31, 2018

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

druginfo@fda.hhs.gov

Incident #01980MMJ-42104CCO – Reporting to MedWatch

Division of Drug Information – Center for Drug Evaluation and Research

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

Stay Tuned: Episode 7 – More Adverse Complications Continued

CABIRI – CandyK’s Boutique Wishes You A Happy & Safe Holiday Season

Is Cyber Security A JOKE???

Whose Monitoring & Protecting U.S. Consumers…There’s So Much To Unpack Here….

Over the past several years Cabiri Research & Investigations has uncovered massive fraud on/offline it’s too much to list. Although if you have the time please read the numerous articles written dating back to 2014.

As the years have gone by it’s hasn’t gotten any better in fact it’s much worse! ‘To be honest ‘Folks’ you can’t trust anything online. Although were forced; to use these platforms for business purposes and livelihoods. These culprits are utilizing to their benefit social media platforms, websites, autoresponders, emails, text messaging, to catch their next victims. They sit back watching and waiting to attack.

And many of these platforms can careless; as long as they get their monthly subscription, membership or platform fees.

CABIRI’s recent catches were GeekSquad/Best Buy impersonators located in Frankfurt Germany, and Warrior + Plus a 3rd party vendor allowing fraudulent merchants from India and other countries to scam consumers out of money utilizing false advertisement, videos, paid promoters, and ‘Fake DFY’ product/service schemes. There’s a entire slew of them on there! Just stealing from U.S. Citizens as U.S. Citizens fight back and report to authorities; although caseloads are so extensive it’s like a needle in haystack so the American people are just out of their hard earned money.

These culprits are playing the game by using prominent U.S. business platforms to carry out their agendas. At the expense of the American people. We wonder why the U.S. Debt Clock has tipped over beyond repair…We’ll never see in this lifetime.

The Social Security Administration reported during Covid 19; there were over 800K Identity Theft Cases in the U.S. we should asking why is Equifax, Transunion, Experian still in business. Do they know who is who with all those Identity Fraud cases unsolved? What credit reporting system are they using? Do they know if the people are real or fake?

As well; does the Federal Government truly know whose who in the United States. There’s lots of unanswered questions to think about?

CABRI has been incredibly successful in catching many culprits over the years. If you read through the entire blog, you will be amazed at what has been uncovered through the investigative work and personal experiences. In some cases, even going into the trenches to dig deeper to uncover the truth. However, it can be very dangerous to know too much, as you may be subject to gang-stalking, blackballing, and other forms of persecution.

We really need to do better to prevent these culprits from defrauding consumers and the United States! We wonder why CCP has been monitoring U.S. and U.S. Citizens via TikTok “Right Under Are Noses!’ China isn’t the only country using U.S. platforms to carry out there hidden agendas.

In my opinion every business online doing business within the U.S. should have a Contact number, Face/ID recognition of all employees, and board members, Local U.S. address, and have a encrypted Business ID between Business/SBA/Federal Government; All Business Information should be posted on a separate public platform.

If the U.S. business partners with an international business all above will apply to them as well; besides having a encrypted International Business ID. The U.S. business will be held responsible for any fraud or illegal actions of the international 3rd party business or it’s employees using their platforms or website platforms who defrauds the American people. The company may be fined or penalized by the SBA/Government. Which means the U.S. business owner should their due diligence before partnering with any International Business! Doing business internationally could me a “National Security” issue for the U.S. depends upon what that international businesses hidden agenda may be.

The internet has become an increasingly complex place, with humans, artificial intelligence, bots, and metaverses all interacting with each other. With people from all over the world online at any given time, it is difficult to know who is doing what. For this reason, the United States should implement more stringent regulations for internet usage. These regulations should be designed to protect the safety and security of users, and to ensure that everyone is held accountable for their actions online. With the right guidelines in place, the internet can be a safe and secure place for everyone to enjoy.

Let’s add just as they don’t truly know who owns guns; we don’t know whose flying drones.

.

CABIRI – Research & Investigations

Daughter Of Vietnam Veteran – Helping Keep America Safe

Website: http://www.cabiri-business-services.com

The Internal Death: New Episodes & Medical Research On ‘Kindle Vella’

Government Harrassment & Racial Profiling by Law Enforcement

American Citizen are being tracked and harrased by Americas Law Enforcement Officials

America, there is a new trend happening in the United States, many citizens are unaware of that needs to be addressed. CABIRI, has been speaking with numerous American born citizens, who are fed with the United States Government and their prawns working with them!

In states such as; Florida and New York, many citizens are complaining about police harrassment for minor infractions, which law enforcement agencies are targeting Latino’s, African-Americans and Hispanics, which is considered racial profiling and harrassment. These agencies are attacking poor and homeless citizens whom are already suppressed and some professional citizens whom have never had a run in with the law, all due to skin color.

Please read below some current scenario’s that were communicated to CABIRI! The scenario’s are very disturbing and should hit home to all American Citizens, for this could happen to you, a friend or a family member;

1. A well known Latino coach, on chemo-therapy, who choose not to disclose his name due to his professional status; Stated himself and wife whom are of Latino origin born in America with deep family roots, recently relocated from New York to Florida due to uncessary excessive police harrassment by NY Law Enforcement Officers, whom are stopping and harrassing anyone that is Latino, African-American or Hispanic! Apparently, for anything that they can find wrong or trump up against any of these nationalities they are doing it! They are giving citations for various minor things, due to the color of their skin. He stated they are also giving them excessive jail time and tickets for very small amounts of illegal substances, like one marijuana joint! Which is ridiculous when this may be legalized and is legal in many states! The gentleman stated; once you go to court it seems the judicial system is involved in these planned out scheme’s! The middle-aged many 55yrs of age stated all the racial profiling was supposed to be stopped by the new Mayor of New York after “Bloomberg.” He stated this is not the case instead, the racial profiling acutally has increased dramatically, he stated they are giving New York Citizens excessive citations; to boost State’s Revenue’s, and to promote or give pay raises to Law Enforcement offcials! They are being told the more “Busts” you make the better your pay and you can also get promoted within the department up the ranks by the number of busts or tickets you write! Is this legal America!

This is awful and should be very illegal in the United States! These actions are putting ultimatiums on Law Enforcement Officials, who now have to work hard to “Bust” as many citizens as they can, or they may lose their jobs or never get promoted! This also puts naturalized American born citizens of color at risk, backing them up against the wall, due to the color of their skin, which many of these citizens may be law abiding professional citizens! Why are many New York citizens being harrassed for ‘No reason at all?’ These actions by the Mayor of NY the Judicial System, and Law Enforcement Agency’s could be considered a “Pyramid Scheme” by New York’s State and Local Governments, targeting innocent citizens to boost there State and Local revenue’s! Which is illegal and unethical! Racial Profiling must stop! Also answer this; why aren’t other nationalities such as Whites, Europeans, Germans, Russians, Indians, Hungarian, Chinese, Japanese, Israel, Australians or any other nationality that have now moved into America, not being harrassed?

2. This next scenario was taking from a Mother in Florida who’s child was incarcerated for the first time in his life in Florida! Local Law Enforcement, tried to recruit her young adult son for other “Drug Busts” to take down other top drug consipators! Which would put her son in harms way, whom is a good kid just messed up one time trying to help his mother! She stated the Law Enforcement official told her son if he did not agree; they will issue a warrant for his arrest, although he had already been before a judge for his mistake! America no matter how you look at this situation this is very upsetting! The poor mother now is looking to move out of the area and State of Florida for fear her African-American son will be now profiled by Florida Law Enforcement officials. For not agreeing to become a ” Police Informant!” The mother and son, are now very frightenend and must stay in the area until all his court matters are taking care of, this is awful and very disturbing America! This young child whom has never been in trouble in his life, and was only trying to help his mother whom has been dramactically ill for 2yrs. and unable to work, both of them now have to fear for their lives against police brutality, due to her son not agreeing to become an “Informant”! Are you kidding me America!

The mother did not want her son to be known as a “Snitch,” which could result in her and her son’s death! Now they are very afraid to go out the house or live in the State of Florida, although stuck until her son has completed his Pre-Trial Services. She knows although, this was not right for her son to do, and he also understands and very frightened to ever to return to jail, since this was his first time! She stated they are very afraid, of what may happen in Florida! America this is awful and unlawful and all of Florida’s Local and State Law Enforcement officials should be investigated! “Again names will not be disclosed due to sensitivity and protection of family.”

3. This last scenario, was taken from a woman who was picking up a friend at a “Florida Jail!” Be aware to all American Citizens for this one, this is a “Shocker!” The woman stated; her license plates were run in the parking lot at the jail, to see if she had any outstanding warrants for her arrest. Although, she had none, she thought about “Entrapment,” for all the citizens who may visit, or come onto State property! Law Enforcement officials are becoming very sneaky by running license plates without citizns knowing it! She stated, if you happen to have a warrant for your arrest officers are coming out and arresting citizens as they are visiting or picking up family members. America this is Entrapment, illegal and unethical and also needs addressed!

4. This is a tidbit of information for “Bails Bondsmen” who depend on this field as their sole income! Guess What! State and Local Governments are now taking over your job, which will “Wipe Out” all “Bail Bondsmen!” How? Public Citizens can now pay bonds; Online, or use a 877# they can call and pay over the phone, and this does include “Surety and Cash Bonds!” So Please be aware!

America these scenario’s tooken from random citizens should be very disturbing and eye opening to many, this is abuse of power by Local, State and Government Officials against American Citizens, and ‘Must’ be addressed! As American citizens if we do not prevent such scenario’s like this from occuring, what else will State and Local Government officials, feel like they can get away with! Please pass along and help prevent this type of harrassment in America against American Citizens!

This is abuse of Power in America, and according to previous “ForeFathers” American Citizens have the last word, not other human being elected officials with a title, who feel they have the right to harm other human beings, whom are paying taxes and their salaries! They are not “Supreme Beings” and have no right!

Thank you for reading, and please pass along and stand up and fight for your rights in America! Another human being has no right to control you, this is your life and remember you only have one to live!

MUST READ RECENT POLICE CORRUPTION LINKS:

Prosecutor: Cops in rural California town preyed on poor drivers – http://www.cnn.com/2014/02/25/justice/california-police-corruption-arrests/

King City police officers arrested in corruption scandal
http://www.montereyherald.com/news/ci_25223763/king-city-police-officers-arrested-corruption-scandal

‘Injustice Anywhere’: A Philadelphia Story of Justice Denied – http://www.huffingtonpost.com/tag/police-corruption/

Police Corruption – http://stopthedrugwar.org/taxonomy/term/27

8 Officers Charged With Gun Trafficking in U.S. Corruption Case – http://cityroom.blogs.nytimes.com/2011/10
/25/officers-accused-of-smuggling-guns-in-federal-corruption-case/?_php=true&_type=blogs&_r=0

Baltimore City Police Officer Faces Drug Charges In Latest Corruption Case – http://baltimore.cbslocal.com/2013/05/31/charges-to-be-announced-in-law-enforcement-corruption-case/

Metro police officers arrested in federal corruption investigation – http://www.wsbtv.com/news/news/local/metro-police-officers-arrested-corruption-investig/nWMcg/

Tulsa man gets $425K in police corruption case – http://www.washingtontimes.com/news/2014/jan/30/suit-tied-to-tulsa-police-corruption-settled/

Racial profiling case against Sheriff Terry Johnson to head to trial
http://www.wxii12.com/news/racial-profiling-case-against-sheriff-terry-johnson-to-head-to-trial/26617302#xzz35VdBdsRk

Racial Profiling – http://www.huffingtonpost.com/news/racial-profiling/

I Was Racially Profiled in My Own Driveway – http://www.theatlantic.com/national/archive/2014/04/i-was-racially-profiled-in-my-own-driveway/360615/

Racial Profiling Rife at Airport, U.S. Officers Say – http://www.nytimes.com/2012/08/12/us/racial-profiling-at-boston-airport-officials-say.html?pagewanted=all

Race Matters: Blacks documented by police at high rate – http://www.thestar.com/news/crime/raceandcrime/2010/02/06/race_matters_blacks_documented_by_police_at_high_rate.html

CABIRI,
Freelance Business Research Reporting

Special Alert!! Women Taking Deadly Birth Control Toxins

All Women! Please be aware of “Birth Control” Toxic Dangers From 2nd, 3rd Generational toxins and Newer Birth Control Mixed Chemical Toxicities, That can severely harm your bodies internally and externally!

Please Read vital information and Save lives Pass this article Along!
Such as Yaz, Mesh, Mirena-Iud, etc.,

Please read article from the BMJ or British Medical Journal 

RESEARCH via BMJ Group of U.K. – British Medical Journal

All women of America Please read for your own Reproductive Health Safety, in reading you’ll find it very interesting the health risks involved from taking these toxic Birth Control pills, and Birth Control Devices! 

Please read below important information from actual “Research Journal,” that was compiled by several medial professionals:

Different combined oral contraceptives and the risk of venous thrombosis: systematic review and network meta-analysis – 

BMJ 2013; 347 doi: http://dx.doi.org/10.1136/bmj.f5298 (Published 12 September 2013)

Many different combined oral contraceptives are available. We selected 10 frequently prescribed oral contraceptives for the network meta-analysis:

20 μg ethinylestradiol with levonorgestrel (20LNG)
30 μg ethinylestradiol with levonorgestrel (30LNG)
50 μg ethinylestradiol with levonorgestrel (50LNG)
20 μg ethinylestradiol with gestodene (20GSD)
30 μg ethinylestradiol with gestodene (30GSD)
20 μg ethinylestradiol with desogestrel (20DSG)
30 μg ethinylestradiol with desogestrel (30DSG)
35 μg ethinylestradiol with norgestimate (35NRG)
35 μg ethinylestradiol with cyproterone acetate (35CPA)
30 μg ethinylestradiol with drospirenone (30DRSP)

We categorised 20LNG, 30LNG, and 50LNG as second generation progestogens, and 20GSD, 30GSD, 20DSG, 30DSG, and 35NRG as third generation progestogens. 35CPA and 30DRSP were not used in this classification by generations.

http://www.bmj.com/content/347/bmj.f5298 –
Apart from adjustments in the dose of ethinylestradiol, the progestogen compound was also changed in an effort to reduce side effects. After the first generation progestogens (that is, norethisterone and lynestrol), new progestogens were developed. These new compounds were called second generation (that is, levonorgestrel) and third generation progestogens (that is, gestodene, desogestrel, norgestimate).15 However, users of combined oral contraceptives with third generation progestogens have a higher risk of venous thrombosis than those using second generation progestogens.16 17 18 19 Other progestogens have been developed after the introduction of third generation progestogens—that is, drospirenone (introduced in 2001). The thrombosis risk for contraceptives with drospirenone was found to be higher than for combined oral contraceptives with second generation progestogens.

Women of America are taking 2nd and 3rd generational toxic chemical compounds! Also, let’s not forget to discuss the Newer chemical compounds that weren’t clinically tested properly! The Clinical Trial Dates, Do Not surpass the amount of time needed, to deem a chemical product or drug safe for human consumption or usage! This would mean the FDA and the Pharmaceutical Industry providers are marketing new products to human beings, that are deadly and unsafe. Which is very disturbing and alarming in America!

Basically using women as “Guinea Pigs,” for their mixed chemically induced birth control products! Which are causing Reproductive Health life altering problems for all women!

The British Medical Journal tells the real truth about the serious findings of “Birth Control Dangers!

Thanks BMJ, for allowing the real truth to be known, saving millions of women lives in America and Abroad!

Here’s another one you may want to read!

Breast cancer screening pamphlets mislead women – BMJ 2014; 348 doi: http://dx.doi.org/10.1136/bmj.g2636 (Published 25 April 2014) Cite this as: BMJ 2014;348:g2636

Additional Full Content Link – http://www.bmj.com/search/thrombosis?filters=type%3Ahighwire_article

CABIRI,
Freelance Business Research Copywriting

HEALTH ALERT! FDA proposes program for faster approval of medical devices – Americas Nightmare

BIG PHARMA DANGER ALERT! 

America, this is a total nightmare! The FDA has the nerve to want to speed up the process in killing off Americans by expediting the International Pharmaceutical products that are giving American Citizens, Cancer, Strokes, Heart Attacks,Life – threatening diseases, including causing many deaths! Every American must protect their own health at this point!

The international Top Big Pharma leaders in America has now conned the U.S. FDA into quickly approving, non-clinically tested products or clinically tested products that haven’t had the effective research to back the safety of the millions of drugs and medical devices American citizens are putting into their bodies! Please read CABIRI, articles where America is the only country who is funding all of these toxic products! Why is that America? Why are we the only country backing these international pharmaceutical companies who are killing us off one by one, with many of their deadly toxic drugs and products!

These Big Pharma corporations have infiltrated the American markets and have dominated the medical industry in America! All Americans are falling for their cycle of conspiracies, led by Greed-Money & Power! Not the best interest of a human life!! It’s time Americans wake up, Read – Research – Investigate before you take anything prescribed that comes from any of these top international corporations in America! Be Aware! They could cause you or your families life! Or you may be inundated with a disease that could cause your life.

This is article is not to scare anyone, this article is to “Wake Up” America, from a personal experience from someone who knows the truth, and is trying to save lives. This is no joke, and is real, if you don’t trust what is being presented, please do your own research, to protect yourself and your family! This is awful, and we all must do something about this, we can’t not let the FDA and Big Pharma, start killing us off quicker with their toxic products! READ, READ, READ!

If you can find other healthier organic alternatives, then it would be in you and your families best interest to try them out! If not prepare to face doctors, hospitals, surgeries, excessive medications that are not safe! Think about you and your childrens health, do you really want to continue playing “Russian Roulette” with your life by putting all your faith into a Internationally led pharmaceutical Industry who knows nothing about American Culture, and are paying off Americas medical professionals to get their products approved! The “AMA,” doesn’t except Foreign medical degree’s so how in the world can Internationally led pharmaceutical corporate owners supply pharmaceutical products in America? This is very contradictory and disturbing, and everyone must start realizing this Medical contradiction! 

Please save yourselves, find other alternatives for living healthy! There are natural organic products, and doctors available, who are not part of the Big Pharma conspiracy in America! It’s time to change in the 21st century, and start saving our own lives and not being co-dependent on Americas ” International Big Pharma!” By the way who also are raising Medical rates, Insurances, and Supplying millions of Americans with unsafe medical products! Do they really deserve this type of control in America! Again! Why is America the only country backing these companies, research shows many other countries have banned many of their products! 

Please see disaster waiting to happen: 
http://www.foxnews.com/health/2014/04/22/fda-proposes-program-for-faster-approval-medical-devices
Note: This is a form of “Eugenics Theory” – By Adolph Hitler, and it’s working in America! Be AWARE!! 

CABIRI, 
Freelance Writing Business Researcher
Website: http://www.consumer2savlives.com – (Read valuable life saving information) http://www.foxnews.com/health/2014/04/22/fda-proposes-program-for-faster-approval-medical-devices/</

URGENT ALERT! AMERICAN ECONOMICAL WARFARE COLLAPSE

NOTE: IF YOU DON’T CARE ABOUT WHAT HAPPENS TO YOU OR YOUR FAMILY, KEEP IT MOVING AND DON’T WASTE YOUR TIME READING THIS!  

FOR THOSE WHO CARE CONTINUE READING, SAVE YOUR OWN LIVES!
American Citizens: Please Read and Pass on to all your Family and Friends – Save your own lives

Please Read Along This is no JOKE!

Brief and to the point America!

America is urgently in danger of collapsing! Every American must read and view all attachments included in this article. There are a series of events currently and rapidly happening in America! CABIRI, has personally found due to a medical- device that almost took the founders life! Who decided to start CABIRI, due to the medical nightmare which she was hospitalized an entire year! The founder started researching who, what, when and how her life was almost taken from her, and why she lost everything she ever owned due too a trauma she didn’t see coming, as a healthy ex-athlete, professional prior corporate individual, and before her medical trauma a prior small business owner! Please see below Bayer Healthcare of Germany and all their economical subsidiaries killing and impacting American families, via sterilization and Cancer & Death’s!

The founder has always previously, dedicated her life in helping all human beings in need to the best of her capabilities, even going through her own personal struggles in life. Many of the founders family, friends and business colleagues who’ve come across her respects opinions, well-rounded business knowledge, and she also happens to be very well-travelled locally and internationally. She is known as a blunt, compassionate, “Truth Seeker”, who believes in protecting human beings. No matter if their young, old, child or of; any nationality that may be caused “Unnecessary Harm”!

All American’s are in jeopardy! So please listen, learn, and spread the word! CABIRI has found the disturbing truth! In researching CABIRI, has found very frightening things that we’ve been trying to communicate to all American Citizens of the United States which all holds very true, you can do your own research, below links will help you see the light!

Actually, many Americans and news reporters, journalists, book authors, and Tv programmers, have been trying to tell American citizens. America is in danger! All  American or international leaders who the have guts to stand up and fight for human lives must react now to what’s occurring in America and globally! A world take over is looming and the American dollar is quickly diminishing. Which means all Americans will suffer, What if all of a sudden you can’t use the American dollar anymore, what are you going to do how are you going to feed your family and supply the economical resources you need to survive?

An American economical warfare has been looming for the past decade and is now showing it’s “Ugly Head” in the United States! Every naturalized American citizens must watch all below video’s, the series of events are happening behind closed doors and many citizens are trying to tell all American Citizens. PLEASE Wake UP! America is truly in trouble, and all American’s must become one nation under whatever god you choose to represent to save you and your family. The “Eugenics Theory” is alive and prevalent in America!

Top Big American international corporations and countries have now brought America to it’s knee’s and every American citizen are now suffering or will suffer, including your children. Please do not take this information for granted, for it’s very true and real and everyone needs to stand up and listen to what is being communicated and shown to you!

This is not the time to sit back and do nothing, if you do nothing every American family will be hit harder than you could ever have possible imagined, with things you never thought could happen in this day and age!

Just as CABIRI’s founder never imagined she’d be hospitalized an entire year on/off all due to a faulty medical device that gave her a life-threatening disease, and had her in pre-cancer stages, the device was distributed by several merging international non American friendly countries, which dates back to World I and World II, and many of these countries have infiltrated American Economical Markets, Governments, Businesses, and have hidden agendas in America to bring it down. They’ve even had their own private international meetings excluding America! So what does that tell you! Germany Russia, China, U.K., Europe, Japan and many more including the middle-eastern countries are have been plotting against America!

They are winning big economically here in America and are privately taking American lives via “Big Pharma” to depopulate American citizens by Eugenics Theory!

There also are many other forms of current events that have occurred in America, these events aren’t just occurring for no reason, this is all the impacts of decades of planned out plots, you can view some @ http://www.consumer2savlives.com and http://www.consumer2savlives.wordpress.com, please take the time to read and pass along, it’s very urgent for every American to communicate this information, this is no joke, we all must save one another in America, if you care about your life and your families lives you will do something to help or contribute to your country and help save your children’s future in America.

CABIRI, has effortlessly been reporting, American Economical Warfare since November 2013, after stumbling across the hidden conspiracies and corruption occurring in America by International countries, via the pharmaceutical industry, and many other numerous industries in America, which have been brewing for over a decade, and now has hit American borders!

If your wondering why you or your family are struggling, or why a family member has suddenly become sick with cancer or any other unexpected medical trauma, you need to start clicking on all the links below and get educated of what’s occurring in your country! Also, please understand this does not matter if your rich or poor, you are a American. The collapse coming will hit all Americans from every angle you will be in the “Cross-Fire”, you are not immune to a country disaster, police state, communism, or no way to spend your American dollar, or being stricken from a disease, or anything else these international Top American business owners and conspirators see fit in harming the United State’s and it’s citizens taking control, and collapsing the American government, Wall Street, Banks and Businesses!

Please take this seriously, again this is no time to sit back and say “Yea Right” – What a bunch of Bull”! Many American citizens will not be saying this when everything in America comes crumbling down right in front of you! Then what are you going to do, will you be the American citizen who say’s “I could of, would of, or should of done something? By that time it may be too late for you and your family!

It’s here and real, getting worse day by day, so please take heed NOW! Do something NOW! We do not have time to waste this is why CABIRI, is reporting to all America, so everyone can start taking action to protect their precious families and assets. America needs leaders to stand up and start helping too save America! America needs their own “Private Non-Governmental Defense Team” to battle what’s coming and figure out a game plan to stop these, “Greedy international and U.S. Government conspirators,” from taking over United States and collapsing America, leaving it’s citizens in a “Great Depression!” Or even thrown into communist camps!

Note: The “Eugenics Theory,” was put in place by “Adolph Hitler” of Germany and explains it all, and there is no time to waste, so don’t take this lightly, or you, your family, kids and grandchildren will soon suffer, it’s all to go down this year in 2014, according to many you will view in the below video’s the collapse is coming sooner than later! Please pass this on get onboard, communicate to all who matter, most importantly start preparing to save and protect your family, to what is to come in the American Economical Warfare Collapse.

Take your money out of the banks, or you will not have any, go back to the olden days, protect your assets and your personal family interests before they are stripped away from you! Pay Cash it’s FAST! Many international countries are paying cash for all of America’s economical resources and business, to fly below the U.S. Government Radar! Also their inter-country international mergers in America are horrific they are selling American businesses to other international countries like “HOT CAKES!” Leaving America even more WEAK and citizens jobless and homeless!

AGAIN, PLEASE SAVE YOU AND YOUR FAMILY LIVES THIS IS NOT IN VAIN AND IS VERY CRITICAL TO EVERY CITIZEN OF AMERICA!

VIEW ALL VIDEO LINKS – BLOGS VIEW WEBSITE:
http://www.consumer2savlives.com – http://www.consumer2savlives.wordpress.com

http://forerunnerchronicles.com/glen-beck-warns-economic-impact-is-coming/
Glen Beck Warns Economic Implosion Coming

http://www.endofamerica.com/?gclid=CLW9-e6Zrr0CFcRi7AodqBEAtA
The Most Important Day in America in 50 Years – July 1st, 2014

https://www.youtube.com/watch?v=ACVWfcL8c7s – World Bank Whistleblower ***Exposes All*** (Pt.1)

https://www.youtube.com/watch?v=moTx2jQ0OQ0 – The British Banking Conspiracy Part 2 – America, Israel and The Federal Reserve (9/11)

https://www.youtube.com/watch?v=MkAn3VIe1yQ – U.S. Government Preparing for Collapse (and Not in a Nice Way)

https://www.youtube.com/watch?v=LvmqiQohXWA – AMerican Economic Collapse 2014 – Peter Schiff

https://www.youtube.com/watch?v=mldFxyQYMHk – Jesse Ventura America Economic Collapse Coming 2014 Martial Law!

https://www.youtube.com/watch?v=ZrYrKmFBetk – AMERICA ON THE BRINK 2014

https://www.youtube.com/watch?v=yZc2_OByeEs – HARVARD Economist Predicts USD COLLAPSE Will Occur 2014 – Time Running Out For AMERICA

https://www.youtube.com/watch?v=WiQIpDBjbf8 – PLANNED GLOBAL ECONOMIC COLLAPSE 2014

– America’s Depression Looming

http://www.theguardian.com/world/2014/mar/24/home-insulation-schemes-speedy-rollout-was-insane-and-unsafe – Home insulation scheme’s speedy rollout was ‘insane and unsafe’

http://www.theguardian.com/world/2014/mar/24/ukraine-1bn-aid-bill-clears-senate-hurdle-gop Ukraine aid bill clears Senate hurdle after Republicans drop resistance to IMF loans

Lawmaker Accuses GM of “Criminally Deceiving” the Gov’t http://www.thefiscaltimes.com/Articles/2014/03/25/Lawmaker-Accuses-GM-Criminally-Deceiving-Gov-t#sthash.BaaxarQh.dpuf

http://www.fiercepharma.com/story/suffering-eli-lilly-freezes-salaries-third-year-running-cuts-bonuses/2014-03-25?utm_source=rss&utm_medium=rss – Suffering Eli Lilly freezes salaries, cuts bonuses across the board

Suffering Eli Lilly freezes salaries, cuts bonuses across the board http://www.fiercepharma.com/story/suffering-eli-lilly-freezes-salaries-third-year-running-cuts-bonuses/2014-03-25#ixzz2x1vfGpN2

Politicians add fuel to the firestorm over Gilead’s hep C drug pricing http://www.fiercepharma.com/story/politicians-add-fuel-firestorm-over-gileads-hep-c-drug-pricing/2014-03-24#ixzz2x1w1TeqD

The top 10 pharma companies by 2013 revenue http://www.fiercepharma.com/special-reports/top-10-pharma-companies-2013-revenue#ixzz2x1wiTFKj

Humira – http://www.fiercepharma.com/special-reports/humira-best-selling-drugs-2013

Cost watchdogs demand efficacy data on new Bayer CANCER DRUGS http://www.fiercepharma.com/story/cost-watchdogs-demand-efficacy-data-new-bayer-cancer-drugs/2014-03-24#ixzz2x1xjTIj0

VIEW MORE OF BAYER OF GERMANY UNITED STATES BIG PHARMA MOVES!
http://www.fiercepharma.com/special-reports/bayer-healthcare-top-10-pharma-companies-2013-revenue
With Big 5, Bayer aims for 8% annual pharma growth through 2016
Aiming for big growth in top 5 meds, Bayer will stake an extra $600M on marketing, R&D
New drugs in hand, Bayer’s pharma sales leap ahead
With a sweetened $2.9B bid, Bayer nabs its Xofigo partner, Algeta

AbbVie CEO’s pay doubles to $18.2M in Abbott pharma spinoff’s first solo year

AbbVie CEO’s pay doubles to $18.2M in Abbott pharma spinoff’s first solo year – FiercePharma http://www.fiercepharma.com/story/abbvie-ceos-pay-doubles-182m-abbott-pharma-spinoffs-first-solo-year/2014-03-25#ixzz2x205xwAz – BE AWARE CONNECTED TO INERNATIONAL BIG PHARMA CULPRITS!!!!

In latest marketing-reform move, GSK recruits in-house doctors to speak for products – http://www.fiercepharma.com/story/latest-marketing-reform-move-glaxosmithkline-recruits-house-doctors-speak-p/2014-03-17#ixzz2x20l0egv

Gilead’s hot-selling Sovaldi draws more patent attacks – http://www.fiercepharma.com/story/gileads-hot-selling-sovaldi-draws-more-patent-attacks/2014-03-14#ixzz2x25T65Pg – INTERNATIONALLY OWNED!

Sanofi reportedly jumps into $12B race for Merck’s consumer unit http://www.fiercepharma.com/story/sanofi-reportedly-jumps-12b-race-mercks-consumer-unit/2014-03-25#ixzz2x25zz3ZB

UPDATED: J&J releases more Doxil, its popular cancer med that has been dogged by supply issues

UPDATED: J&J releases more Doxil, its popular CANCER med that has been dogged by supply issues – FiercePharma http://www.fiercepharma.com/story/janssen-releases-more-doxil/2014-03-24#ixzz2x26LZ5T5

Toothpaste factory line or F1 racetrack? McLaren revs up Glaxo’s production – http://www.fiercepharma.com/story/toothpaste-factory-line-or-f1-racetrack-mclaren-revs-glaxos-production/2014-03-24#ixzz2x278zh3E

Soriot notches a bigger bonus, but total $5.5M in pay is no record breaker

Soriot notches a bigger bonus, but total $5.5M in pay is no record breaker – FiercePharma http://www.fiercepharma.com/story/soriot-notches-bigger-bonus-total-55m-pay-no-record-breaker/2014-03-24#ixzz2x27aTIzy – AMERICAN’S TAX PAYING DOLLARS GOING INTERNATIONAL!!

THIS SHOULD BE ENOUGH TO SWALLOW TO SEE THE POINT AMERICA! START SAVING YOUR COUNTRY FROM THESE
PHARMACEUTICAL GIANTS, WHO ALSO OWN OR MERGED WITH MANY AMERICAN CONSUMER INDUSTRY BUSINESSES!