{"id":282751,"date":"2023-01-04T18:41:07","date_gmt":"2023-01-05T00:41:07","guid":{"rendered":"https:\/\/www.liveaction.org\/news\/?p=282751"},"modified":"2023-01-24T16:36:12","modified_gmt":"2023-01-24T22:36:12","slug":"us-abortion-pill-lives-lost-adverse-obscured","status":"publish","type":"post","link":"https:\/\/archive.liveaction.org\/news\/us-abortion-pill-lives-lost-adverse-obscured\/","title":{"rendered":"US abortion pill use up 14% in a year with 5.6M lives lost, as adverse events on women are further obscured"},"content":{"rendered":"
<\/div>

The abortion pill has ended the lives of 5.6 million babies in the U.S. since its approval in 2000, according to\u00a0updated<\/a>\u00a0data\u00a0published<\/a>\u00a0by the U.S. Food and Drug Administration (FDA). And in just the past year, two additional deaths have been added to the agency’s reported deaths attributed to the abortion pill.<\/p>\n

The abortion pill, mifepristone (brand name Mifeprex), was approved by the FDA in\u00a02000<\/a>\u00a0for the termination of pregnancy in a regimen along with a second drug, misoprostol.<\/p>\n

In\u00a0December of 2018<\/a>, the FDA\u00a0reported<\/a>\u00a024 deaths\u00a0associated with abortion pills since its approval. Then, on December 16, 2021<\/a>, the FDA\u00a0published<\/a>\u00a0an updated \u201cPost-Marketing Adverse Events\u00a0Summary<\/a>\u201d\u00a0revealing that as of June 30, 2021, that number had climbed to 26.<\/p>\n

But on January 4, 2023, the FDA updated<\/a> that death count again, writing that “As of June 30, 2022, there were 28 reports of deaths<\/a> in patients associated with mifepristone since the product was approved in September 2000, including two cases of ectopic pregnancy (a pregnancy located outside the womb, such as in the fallopian tubes) resulting in death; and several fatal cases of severe systemic infection (also called sepsis).” The reported deaths come with several caveats (see image below for clarification).<\/p>\n

\"Image:

28 Abortion Pill Deaths as stated by FDA as of June of 2022<\/p><\/div>\n

Accumulative abortion pill totals since approval\u00a0<\/b><\/p>\n

The FDA report<\/a> also\u00a0tragically revealed that “[t]he estimated number of women who have used mifepristone in the U.S. for medical termination of pregnancy through the end of June 2022 is approximately 5.6 million women” \u2014an increase of 700,000 (over 14%) from the 4.9 million\u00a0reported<\/a>\u00a0through the end of June 2021.<\/p>\n

It is important to note that since abortion pill use has been increasing more rapidly in recent years, the 14% accumulative increase between 2021 and 2022 is likely to be much lower than the increase of abortions reported between the years 2021 and 2022, once that data becomes available.<\/p>\n

\"\"

Reporting of abortion pill use by FDA (comparison)<\/p><\/div>\n

Just this week, the Biden-Harris FDA\u00a0weakened<\/a>\u00a0important safety regulations (REMS) on abortion pills further by allowing retail brick and mortar pharmacies to dispense the abortion regimen months after they eliminated<\/a>\u00a0the in-person requirement by permanently allowing the abortion pill to be shipped by mail.\u00a0REMS, or Risk Evaluation and Mitigation System<\/a>, is a \u201cdrug safety program that the\u2026\u00a0FDA<\/a>\u00a0can require for certain medications with serious safety concerns.\u201d<\/p>\n

According to the FDA, \u201cThe adverse events cannot with certainty be causally attributed to mifepristone because of concurrent use of other drugs, other medical or surgical treatments, co-existing medical conditions, and information gaps about patient health status and clinical management of the patient.\u201d<\/p>\n

Abortion pill-related deaths began shortly after approval<\/strong><\/p>\n

The Population Council, a\u00a0eugenics-founded<\/a>\u00a0\u201cnon-profit,\u201d\u00a0brought<\/a>\u00a0the abortion pill (known then as RU-486) into the U.S. and\u00a0later<\/a>\u00a0set up<\/a>\u00a0the pill\u2019s manufacturer,\u00a0Danco Laboratories, LLC,<\/a>\u00a0a\u00a0sub-licensee<\/a>\u00a0of the Population Council. The FDA\u2019s abortion pill approval process, which culminated in 2000, has been\u00a0highly secretive<\/a>\u00a0as Live Action News has documented.\u00a0Tragically, shortly after approval, deaths were reported, and over the ensuing years, abortion pills deaths climbed.* Read more about this tragic history\u00a0here<\/a>.<\/p>\n

In May 2020, Columbia University journalists Lauren Mascarenhas and\u00a0Abigail Brone\u00a0interviewed<\/a>\u00a0early abortion pill advocates including Dr.\u00a0Beverly Winikoff,<\/a>\u00a0who was\u00a0employed<\/a>\u00a0at the time by the\u00a0Population Council<\/a>\u00a0as the Program Director for Reproductive Health \u2014 and was the person in charge of the abortion pill\u2019s clinical trials.<\/p>\n

In a stunning admission to these journalists,\u00a0Winikoff<\/a>\u00a0credited the 9\/11 terrorist attacks with \u2018saving\u2019 the abortion pill, after news of the attack overshadowed the news of a woman\u2019s death attributed to the abortion pill.\u00a0In 2003, Winikoff left the Population Council to\u00a0found<\/a>\u00a0Gynuity Health Projects,\u00a0which is\u00a0heavily funded<\/a>\u00a0by abortion pill investors.\u00a0Under Winikoff\u2019s direction, Gynuity sponsored abortion pill clinical trials, including\u00a0experiments<\/a>\u00a0on African women, and a\u00a0TelAbortion<\/a>\u00a0trial willing to mail abortion drugs to girls as\u00a0young<\/a>\u00a0as 10.<\/p>\n

Adverse Events\/Complications<\/strong><\/p>\n

In\u00a0April of 2011<\/a>, the FDA\u00a0reported<\/a>\u00a0over 2,200 adverse events associated with the abortion pill. At the same time, post-marketing reports at that time\u00a0showed<\/a>\u00a014 women had died, 612 were hospitalized, 339 women had experienced blood loss severe enough to require transfusions, and several hundred reported cases of infection \u2014\u00a0some severe.<\/p>\n

It was in this year\u00a0that the FDA\u00a0determined<\/a>\u00a0that a\u00a0REMS<\/a>\u00a0was\u00a0necessary<\/em>\u00a0for mifepristone.<\/p>\n

\"Image:

Abortion Pills placed under REMS in 2011 (FDA REMS defined as of 6\/3\/2020)<\/p><\/div>\n

According to the June 30, 2022 report, the\u00a0data showed<\/a>\u00a0(image below) an increase to 4,203 adverse events, including 1,048 hospitalizations, nearly 604 instances of blood loss requiring transfusions, and other serious complications. The FDA also recorded 414 infections, with 71 being categorized as \u201csevere based on medical review of the available case details.\u201d<\/p>\n

Keep in mind that under\u00a02016 changes<\/a>\u00a0put in place by the Obama administration\u2019s FDA, the FDA\u00a0no longer mandated<\/a><\/strong>\u00a0abortion pill manufacturer Danco Laboratories or GenBioPro (the pill’s generic manufacturer) to notify the FDA of\u00a0complications<\/a>\u00a0(adverse events) other than death<\/strong><\/em>. Therefore, there is no way to truly know the number or types of adverse events that took place due to the abortion pill after 2016.<\/em><\/p>\n

READ:\u00a0ER doctors should falsify records to hide abortion pill complications in a post-Roe era, suggests media\u2019s favorite abortionist<\/a><\/em><\/strong><\/p>\n

\"Image:

Abortion pill adverse events (complications) reported to FDA as of June of 2022<\/p><\/div>\n

\u201cSevere infections generally result in death or hospitalization for at least 2-3 days, require intravenous antibiotics for at least 24 hours and total antibiotic usage for at least 3 days, or have other physical or clinical findings, laboratory data, or surgery that suggest a severe infection,\u201d the FDA also wrote.<\/p>\n

No national requirements<\/a> to report abortion complications exist.<\/p>\n

The FDA wrote<\/a>, “The following information is from United States (U.S.) post-marketing reports received by FDA of adverse events that occurred among patients who had taken mifepristone for medical termination of pregnancy. Because FDA has eliminated duplicate reports, and in some cases, reclassified the adverse event terms for individual cases after reviewing the narrative details, the numbers provided here may differ from the numbers of the reports that may be obtained through Freedom of Information Act requests.”<\/p>\n

“Health care providers should review the approved labeling for Mifeprex and the approved generic, Mifepristone Tablets, 200 mg. The signs and symptoms they should watch for are included in the labeling, available\u00a0here<\/a>,” the FDA added<\/a>.<\/p>\n

Susan B. Anthony Pro-life America previously\u00a0pointed out<\/a>\u00a0that \u201c[m]ultiple peer-reviewed studies<\/a>\u00a0confirm that women are at risk of\u00a0severe side effects<\/a>\u00a0after taking chemical abortion pills, including hemorrhaging, the need for follow-up surgery, and even death. Studies have found that\u00a0chemical abortion has four times the complication rate of surgical abortion<\/a>, and these risks only increase with advanced pregnancy and lack of medical supervision. Peer-reviewed research from Charlotte Lozier Institute has also\u00a0found<\/a>\u00a0that after a chemical abortion there is a 53% greater risk for an ER visit for abortion complications than after a surgical abortion.\u201d<\/p>\n

Hiding abortion pill complications<\/strong><\/p>\n

Abortion insiders suggested that women should lie when they present to the emergency room with abortion pill complications. This also dampens any chance that accurate numbers on abortion pill complications or deaths will be reported as such to authorities.<\/p>\n

Recently, Dr. Daniel Grossman, who has led the charge to expand use of the abortion pill,\u00a0reiterated<\/a>\u00a0his\u00a0previous position<\/a>\u00a0that emergency room doctors should avoid documenting abortion pill complications to hide information from law enforcement in a post-Roe environment.<\/p>\n

Stunningly, the FDA appears to be moving in lock step with this idea by eliminating specific text (see images below) from the black box warning and the patient counseling section of the abortion pill’s January 2023 labe<\/a>l.<\/p>\n

The text, according to the FDA’s 2019 Mifepristone label<\/a> (as well as older labels), previously stated, “Advise the patient to take the Medication Guide with her if she visits an emergency room or a healthcare provider who did not prescribe MIFEPREX, so that the provider knows that she is undergoing a medical abortion<\/strong> (emphasis added).”<\/p>\n

\"Image:

Abortion pill label changes (2019 to 2023) edits to Black Box Warning and counseling section<\/p><\/div>\n

\"Image:

Abortion Pill Label Changes 2023 no longer tells women to bring medication guide to ER<\/p><\/div>\n

In\u00a02020<\/a> alone, abortion pills took the lives of nearly 500,000 preborn babies while sales from the pill regimen comprised an astounding 53% of nationally reported abortion numbers, according to updated data\u00a0published<\/a>\u00a0by\u00a0Guttmacher Institute<\/a>\u00a0researchers. Abortion pill use is only expected to grow with the Supreme Court’s decision to overturn Roe v. Wade.<\/p>\n

The “no-test” protocol<\/a> as well as politically motivated lax regulations on the part of the Biden Administration’s FDA regarding imported and domestic abortion pill sales will have the potential to place women’s lives at greater risk even as increased numbers of unregulated\u00a0virtual abortion pill businesses<\/a> surge.<\/p>\n

*The FDA has received reports of serious adverse events in patients who took mifepristone. As of June 30, 2022, there were 28 reports of deaths in patients associated with mifepristone since the product was approved in September 2000, including two cases of ectopic pregnancy (a pregnancy located outside the womb, such as in the fallopian tubes) resulting in death; and several fatal cases of severe systemic infection (also called sepsis). The adverse events cannot with certainty be causally attributed to mifepristone because of concurrent use of other drugs, other medical or surgical treatments, co-existing medical conditions, and information gaps about patient health status and clinical management of the patient. A summary report of adverse events that reflects data through June 30, 2022, is\u202fhere<\/a>. The FDA has reviewed this information and did not identify any new safety signals. The FDA intends to update this summary report as appropriate.<\/h6>\n

Editor’s Note, 1\/15\/23: This post originally listed an increase at 70,000. This should have read 700,000. We regret the error. A note of clarification regarding cumulative totals was also added.<\/em><\/p>\n

\"\"<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

The abortion pill has ended the lives of 5.6 million babies in the U.S. since its approval in 2000, according to\u00a0updated\u00a0data\u00a0published\u00a0by the U.S. Food and Drug Administration (FDA). And in just the past year, two additional deaths have been added to the agency’s reported deaths attributed to the abortion pill. The abortion pill, mifepristone (brand […]<\/p>\n","protected":false},"author":303,"featured_media":282840,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"om_disable_all_campaigns":false},"categories":[15,8],"tags":[],"yoast_head":"\nUS abortion pill use up 14% in a year with 5.6M lives lost, as adverse events on women are further obscured<\/title>\n<meta name=\"description\" content=\"Abortion insiders suggest women should lie when visiting ERs for abortion pill complications, decreasing reporting accuracy, and the FDA may be aiding this.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/archive.liveaction.org\/news\/us-abortion-pill-lives-lost-adverse-obscured\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"US abortion pill use up 14% in a year with 5.6M lives lost, as adverse events on women are further obscured\" \/>\n<meta property=\"og:description\" content=\"Abortion insiders suggest women should lie when visiting ERs for abortion pill complications, decreasing reporting accuracy, and the FDA may be aiding this.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/archive.liveaction.org\/news\/us-abortion-pill-lives-lost-adverse-obscured\/\" \/>\n<meta property=\"og:site_name\" content=\"Live Action News\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/liveaction\" \/>\n<meta property=\"article:published_time\" content=\"2023-01-05T00:41:07+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2023-01-24T22:36:12+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/archive.liveaction.org\/news\/wp-content\/uploads\/2023\/01\/GettyImages-1443809780-embryo-fetus-pill.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" 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Action"},"image":{"@id":"https:\/\/archive.liveaction.org\/news\/#\/schema\/logo\/image\/"},"sameAs":["https:\/\/www.facebook.com\/liveaction","https:\/\/twitter.com\/liveaction","https:\/\/www.instagram.com\/liveactionorg\/","https:\/\/www.pinterest.com\/LiveActionFilms\/","https:\/\/www.youtube.com\/user\/LiveActionFilms"]},{"@type":"Person","@id":"https:\/\/archive.liveaction.org\/news\/#\/schema\/person\/81ff4ca810d98b0b5b376a640452d9e6","name":"Carole Novielli","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/archive.liveaction.org\/news\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/df095be9fa34b48e50413a07102ab289?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/df095be9fa34b48e50413a07102ab289?s=96&d=mm&r=g","caption":"Carole Novielli"},"description":"Carole Novielli has over thirty years of research experience on abortion, Planned Parenthood and eugenics. Her work has been published by many reputable media outlets. As a woman opposed to abortion, Carole is a committed Christian who refuses to be silenced by the main stream media and the nation's pro-abortion feminist minority.","sameAs":["https:\/\/twitter.com\/https:\/\/twitter.com\/CaroleNovielli"],"url":"https:\/\/archive.liveaction.org\/news\/author\/carole\/"}]}},"_links":{"self":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts\/282751"}],"collection":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/users\/303"}],"replies":[{"embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/comments?post=282751"}],"version-history":[{"count":28,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts\/282751\/revisions"}],"predecessor-version":[{"id":284204,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/posts\/282751\/revisions\/284204"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/media\/282840"}],"wp:attachment":[{"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/media?parent=282751"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/categories?post=282751"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/archive.liveaction.org\/news\/wp-json\/wp\/v2\/tags?post=282751"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}