Alliance Defending Freedom, a nonprofit organization, sued the Food and Drug Administration on Friday, asking the organization to withdraw approval for the abortion drugs Mifepristone and misoprostol.
“Pregnancy is not a disease and chemical abortion drugs provide no therapeutic benefit – they end the life of the baby and create serious and life-threatening complications for the mother,” said ADF Senior Adviser Julie Marie Blake in a news release. “The FDA never had the authority to approve these dangerous drugs for sale. We urge the court to listen to the doctors we represent who seek to protect girls and women from the documented dangers of chemical abortion drugs.
ADF is committed to protecting religious freedom, freedom of speech, parental rights and the sanctity of life, according to its website.
“The FDA failed American women and girls when it chose politics over science and approved chemical abortion drugs for use in the United States,” the lawsuit says. “And it continues to fail them by repeatedly removing even the most basic safety requirements associated with their use.”
ADF claims that tThe FDA has never studied the safety of the drugs under the conditions of use indicated.
“The FDA’s approval of chemical abortion drugs has always stood on shaky legal and moral ground, and after years of shirking responsibility, it’s time for the government to do what is required by law: protect the health and safety of vulnerable girls and women,” , ADF Senior Advisor Eric Baptiste said in a statement.
FDA first approved mifepristone in 2000. Then in 2016, it was approved in combination with misoprostol to terminate pregnancies up to 70 days’ gestation, meaning 70 days or less from the first day of a woman’s last menstrual period.
The FDA did not immediately respond to a request for comment.
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