A coalition of 19 states has filed a legal brief with the 5th Circuit Court of Appeals urging it to keep the block in place on the dangerous abortion pill that kills unborn babies and injures women.
Mississippi Attorney General Lynn Fitch today led a 19-statecoalition in filing an amicus brief in the U.S. Court of Appeals for the Fifth Circuit in the case of Alliance for Hippocratic Medicine v. U.S. Food and Drug Administration(FDA).
In the brief, the Attorneys General argue that the Biden Administration and the FDA’s attempt to roll back safety mechanisms for the abortion-inducing drug mifepristone and to make it widely available through the mail violates both federal law and state laws. Current federal criminal law plainly prohibits the distribution of abortion-inducing drugs through the mail. (18 U.S.C. §§ 1461,1462).
Last week, in ruling against the FDA, Texas U.S. District Court Judge Matthew Kacsmaryk stated, “The Court does not second-guess FDA’s decision-making lightly. But here, FDA acquiesced on its legitimate safety concerns — in violation of its statutory duty — based on plainly unsound reasoning and studies that did not support its conclusions.” On the same day, in a separate case and while reaching different conclusions, a federal district court in Washington also faulted the FDA’s actions.
“On one day, even while considering two very different cases, two judges found that the FDA’s approval of chemical abortion was flawed,” said Attorney General Lynn Fitch. “One thing is evident: Over the past two decades, the FDA has engaged in political calculations, not scientific ones, when it comes to chemical abortion. It is our hope that the Fifth Circuit sees how the FDA’s brazen attempt to trample on federal and state laws endangers both the health of women and democracy and takes decisive action to uphold the people’s right to regulate abortion.”
In the brief, the Attorneys General write, “Rather than respect the Constitution, the Supreme Court, and the democratic process, the Biden Administration and its FDA has attacked and worked to undermine the considered judgments of the elected representatives of States. The Biden Administration has, following Dobbs, doubled down on its efforts to impose on the country an elective-abortion policy that it could never achieve through the democratic process….”The brief concludes, “The serious nature of the FDA’s unlawful actions, and the agency’s decision to invite lawbreaking by private parties and government actors across the country, favors the relief the district court ordered….The district court’s decisive action was warranted. And this Court’s is too. This Court should deny any stay relief.”
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Attorneys General from Alabama, Arkansas, Florida, Georgia, Indiana, Iowa,Kansas, Kentucky, Louisiana, Montana, Nebraska, Ohio, South Carolina, South Dakota, Tennessee, Texas, Utah, and Wyoming joined General Fitch on this brief.
Meanwhile, Joe Biden made it official yesterday, as his administration filed papers with a federal appeals court asking it to block a federal judge’s ruling blocking the abortion pill nationwide. Biden followed up the legal papers with additional condemnation, calling it “completely out of bounds” for a federal judge to block the destructive pill that has killed millions of babies before birth.
“My thoughts are it’s completely out of bounds what the judge did,” Biden said when asked about last week’s ruling from U.S. District Court Judge Matthew Kacsmaryk.
As LifeNews reported, a federal judge has issued a ruling that will stop the sales of abortion drugs nationwide and possibly save hundreds of thousands or even millions of babies from abortions.
The abortion drug mifepristone is used for more than half of all abortions in the U.S. every year, or hundreds of thousands of unborn babies, according to the pro-abortion Guttmacher Institute.
But a new lawsuit, filed by a group of doctors with the Alliance for Hippocratic Medicine, challenges the U.S. Food and Drug Administration’s approval and later expansion of the deadly drug under the Clinton, Obama and Biden administrations. Represented by the Alliance Defending Freedom, the doctors point to evidence that the FDA ignored safety problems and failed to properly study the risks of mifepristone.
Judge Matthew Kacsmaryk of the Northern District of Texas issued the ruling blocking approval of the dangerous abortion pill. Kacsmaryk issued a ruling in Alliance for Hippocratic Medicine v. FDA that halts Food and Drug Administration (FDA) approval of the chemical abortion drug mifepristone and gave Biden seven days to appeal the ruling.
Yesterday, the Justice Department asked the 5th Circuit Court of Appeals to put the ruling on hold. It is seeking a short-term administrative stay as well as a long-term stay pending appeal on a lower court ruling. The Justice Department is asking for the 5th Circuit to act on its emergency request by noon on Thursday, “to enable the government to seek relief in the Supreme Court if necessary.”
Biden’s lawyers told the appeals court that if Kacsmaryk’s ruling were to go into effect, it “would thwart FDA’s scientific judgment and severely harm women, particularly those for whom mifepristone is a medical or practical necessity.”
“This harm would be felt throughout the country, given that mifepristone has lawful uses in every State,” the DOJ filing said. “The order would undermine healthcare systems and the reliance interests of businesses and medical providers. In contrast, plaintiffs present no evidence that they will be injured at all, much less irreparably harmed, by maintaining the status quo they left unchallenged for years.”
Danco, the maker of the abortion pill, joined the lawsuit.
Alliance Defending Freedom Senior Counsel Erin Hawley emailed LifeNews about the emergency request.
“By illegally approving dangerous chemical abortion drugs, and imposing its mail-order abortion regime, the FDA put women in harm’s way, and the agency should be held accountable for its reckless actions,” she said. “Pregnancy is not an illness, and chemical abortion drugs don’t provide a therapeutic benefit—they can cause serious and life-threatening complications to the mother, in addition to ending a baby’s life. The district court’s ruling last week was a significant victory for the doctors and medical associations we represent and, more importantly, the health and safety of women and girls. ADF remains committed to their protection.”
Biden issued a statement blasting the decision, calling it a “political, ideological” attack.
“Today a single federal district judge in Texas ruled that a prescription medication that has been available for more than 22 years, approved by the FDA and used safely and effectively by millions of women here and around the world, should no longer be approved in the United States. The Court in this case has substituted its judgment for FDA, the expert agency that approves drugs,” he said in a statement.
“If this ruling were to stand, then there will be virtually no prescription, approved by the FDA, that would be safe from these kinds of political, ideological attacks,” he said, ignoring the fact that other drugs are not designed to kill babies and are injuring women.
Biden views abortion as “freedom” for women and thinks killing a baby is somehow health care.
“The lawsuit, and this ruling, is another unprecedented step in taking away basic freedoms from women and putting their health at risk,” he said. “This does not just affect women in Texas – if it stands, it would prevent women in every state from accessing the medication, regardless of whether abortion is legal in a state. It is the next big step toward the national ban on abortion that Republican elected officials have vowed to make law in America.”
“My Administration will fight this ruling. The Department of Justice has already filed an appeal and will seek an immediate stay of the decision,” he said.
Separately, a district court judge, Judge Thomas O. Rice, issued a ruling in the State of Washington v. FDA that preliminarily enjoins the FDA from “altering the status quo and rights as it relates to the availability of Mifepristone under the current operative January 2023 Risk Evaluation and Mitigation Strategy under 21 U.S.C. § 355-1 in Plaintiff States.”
In his decision, Judge Kacsmaryk noted the following:
Over twenty years ago, the United States Food and Drug Administration (“FDA”) approved chemical abortion (“2000 Approval”). The legality of the 2000 Approval is now before this Court. Why did it take two decades for judicial review in federal court? After all, Plaintiffs’ petitions challenging the 2000 Approval date back to the year 2002, right? Simply put, FDA stonewalled judicial review — until now. Before Plaintiffs filed this case, FDA ignored their petitions for over sixteen years, even though the law requires an agency response within “180 days of receipt of the petition.” (pg. 1)
Most readers would not define pregnancy to be a serious or life-threatening illness. Even FDA does not earnestly defend that position. True, complications can arise during pregnancy, and said complications can be serious or life-threatening. But that does not make pregnancy itself an illness. (pg. 44)
One study revealed the overall incidence of adverse events is “fourfold higher” in chemical abortions when compared to surgical abortions. Women who underwent chemical abortions also experienced far higher rates of hemorrhaging, incomplete abortion, and unplanned surgical evacuation. (pg. 45)
Contrary to popular belief and talking points, the evidence shows chemical abortion is not “as easy as taking Advil.” Compelling evidence suggests the statistics provided by FDA on the adverse effects of chemical abortion understate the negative impact the chemical abortion regimen has on women and girls. When women seek emergency care after receiving the chemical abortion pills, the abortionist that prescribed the drugs is usually not the provider to manage the mother’s complications. Consequently, the treating physician may not know the adverse event is due to mifepristone. Studies support this conclusion by finding over sixty percent of women and girls’ emergency room visits after chemical abortions are miscoded as “miscarriages” rather than adverse effects to mifepristone. Simply put, FDA’s data are incomplete and potentially misleading, as are the statistics touted by mifepristone advocates. (pg. 47)
The Court does not second-guess FDA’s decision-making lightly. But here, FDA acquiesced on its legitimate safety concerns — in violation of its statutory duty — based on plainly unsound reasoning and studies that did not support its conclusions. There is also evidence indicating FDA faced significant political pressure to forego its proposed safety precautions to better advance the political objective of increased “access” to chemical abortion — which was the “whole idea of mifepristone.” (pg. 57)
The Texas judge ruled that the FDA cannot allow chemical abortion to be prescribed via telemedicine or without an in-person doctor’s visit, while the Washington judge ruled that the FDA must continue providing the abortion pill in accordance with the Biden-era rule changes
While the ruling in the Washington case technically only applies to 12 states, it still stands in direct conflict with the Texas ruling. With two rulings that directly contradict with each other, it is certain that this issue will be resolved by the United States Supreme Court, which just last summer overturned Roe v. Wade.
“This decision shines a light on something that the Biden Administration wants to sweep under the rug – that these drugs do not treat or cure disease but kill unborn children and expose their mothers to dangerous side effects. The FDA should be in the business of ensuring safety, not in taking lives,” said Carol Tobias, president of National Right to Life.
Tobias continued, “The abortion industry has pushed for lowering protections for women undergoing a chemical abortion, while it peddles lies about the ease of the method.”
Mifepristone is used in combination with misoprostol, a prostaglandin, to cause an abortion. Mifepristone blocks progesterone, leading to the death of the unborn baby, while the second drug, misoprostol, causes powerful, painful uterine contractions to expel the dead or dying baby.
The FDA recently weakened the Risk Evaluation and Mitigation Strategy (REMS) requirements for the drug to allow it to be dispensed and even mailed by pharmacies.
“Promoters of these pills like to trumpet high safety rates, but neglect to mention how that with hundreds of thousands of women taking these pills, even a couple of percentage points of women hemorrhaging, dealing with infections, and ectopic pregnancy, represents thousands of women desperately seeking treatment, which may or may not be nearby,” said Dr. Randall K. O’Bannon, Ph.D., director of Education and Research for National Right to Life.
First approved under the Clinton administration, mifepristone is used to abort unborn babies up to about 10 weeks of pregnancy – although some abortionists use it later. It works by blocking the hormone progesterone and basically starving the unborn baby to death. Typically, abortion groups also prescribe a second drug, misoprostol, to induce labor and expel the baby’s body.
Since the overturning of Roe v. Wade, the pro-abortion movement has been pushing abortion drugs even more heavily, and some groups send the drugs to women in pro-life states illegally.
Meanwhile, the Biden administration has been trying to expand the life-destroying drugs even further, first by allowing abortion drugs to be sold through the mail without any direct medical supervision, and, more recently, by allowing pharmacies like Walgreens, CVS and RiteAid to sell them.
In California, public colleges and universities also are required to provide abortion drugs for free on campus, and other Democrat-run states are considering similar mandates.
Along with millions of unborn babies’ deaths, the FDA has linked mifepristone to at least 28 women’s deaths and 4,000 serious complications. However, under President Barack Obama, the FDA stopped requiring that non-fatal complications from mifepristone be reported. So the numbers almost certainly are much higher.
Studies indicate the risks of the abortion drug are more common than what abortion activists often claim, with as many as one in 17 women requiring hospital treatment. A recent study by the Charlotte Lozier Institute found that the rate of abortion-related emergency room visits by women taking the abortion drug increased more than 500 percent between 2002 and 2015.
Another new study from the University of Toronto, “Short-Term Adverse Outcomes After Mifepristone–Misoprostol Versus Procedural Induced Abortion,” published in the Annals of Internal Medicine, found that one in ten women who took the abortion pill had to go to the emergency room, according to Pregnancy Help News.
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