Abortifacient Brief: The Intrauterine Device

Brian Clowes
January 5, 2022
Reproduced with Permission
Human Life International

The intrauterine device (IUD) is a foreign body inserted into the uterus. IUDs are made of a non‑reactive plastic such as polyethylene and may include active chemicals or elements such as progesterone or copper which slowly diffuse into the uterus over a period of several years.

Is the IUD Abortifacient?

Short answer: sometimes.

But IUDs also irritate the endometrium (the lining of the uterus) and make it inhospitable to the blastocyst (the very early developing human being), which is an abortifacient effect .1

Nearly half a century ago, the American Medical Association recognized that "the action of the IUDs would seem to be a simple local phenomenon. That these devices prevent nidation [implantation] of an already fertilized ovum has been accepted as the most likely mechanism of action."2 The Food and Drug Administration (FDA) concurred in this assessment, finding that "IUDs seem to interfere in some manner with the implantation of the fertilized egg in the lining of the uterine cavity. The IUD does not prevent ovulation."3

Nothing has changed. The patient information pamphlets for all of the IUDs made today describe in detail this abortifacient action. For example, the PIP for the Skyla IUD says that one of its mechanisms of action is "alteration of the endometrium."

In summary, every IUD ever manufactured prevents implantation, meaning that they are all abortifacients.

These devices ensure that the uterus is as barren and hostile to new life as a desert. In fact, this abortifacient action is so efficient that scientists recommending the IUD for "emergency contraception" note that only one in 1,100 women will remain pregnant after inserting the device from two days to two weeks after their last unprotected intercourse.4

Controversy over the IUD

The first modern‑day IUD, the Grafenberg Ring, was placed on the market in 1915. Several other companies immediately saw the opportunity for profit, and by the mid‑1930s, there was a proliferation of IUDs for sale. They sported intimidating names such as the Sterilette, the Collar‑Button, the Wishbone, the Silkworm Pust, and the Star.

Some of the devices were of good quality, but many were made of "cheaper, noncorrosive metals, or of celluloid, bakelite, and chromium‑plated metals rather than gold."5

According to one expert at the time, "Sometimes these [cheaper IUDs] were claimed to be made of solid gold in order to enhance the price, and a few practitioners took economic advantage of the need and ignorance of women."6

More than 70 different types of IUDs have been manufactured over the last century. Some of these have consisted of polyethylene with barium sulfate so they could be detected by X‑rays. The Dalkon Shield, which was the most popular IUD in use for several years in the United States, was of this type. It was withdrawn from the market in 1984 due to a number of maternal deaths.7

Other IUDs, including the Progesterone‑T, were loaded with varying doses of progesterone crystals that were usually suspended in silicone oil. This IUD released about 24 milligrams of progesterone a year. It was originally promoted under the truly Orwellian label "Uterine Therapeutic System."8

The copper IUDs (including the "Copper‑7," "Copper‑T" and "Tatum‑T") discharged from 50 to 75 micrograms of ionic copper into the uterus each day. These copper ions interfere with the life‑sustaining functions that regulate implantation of the new human life in the uterus. Copper has been proven to be the active agent in these IUDs because identical devices are ineffective without the element. Each copper IUD is effective at causing early abortions for about four years.9

There are five IUDs currently [in 2022] available on the American market:

Complications Associated with IUD Use

According to their patient information pamphlets, complications associated with the IUDs in current use include:

This is nothing new. Until about 1960, the medical community generally condemned IUDs because of their severe side effects. Alan Guttmacher, former President of the Planned Parenthood Federation of America, said in 1959, "Intrauterine devices are mentioned only to be thoroughly condemned because of their ineffectiveness, their potential source for infection and irritation, as well as their carcinogenic potential."11

Although IUD technology had not advanced in the slightest, the entire medical community performed an abrupt about‑face in the mid‑1960s and began to accept the device. But serious complications were documented almost immediately. In 1974, the FDA summarized complaints received about the various IUDs on the market at that time.

The FDA had received reports of 238 cases of spontaneous septic abortion from women who had become pregnant with IUDs in place. Of these women, 21 died. The Dalkon Shield was involved in 14 of these deaths and 209 cases of septic abortion, and the Lippes Loop caused 5 deaths and 21 septic abortions.12

Overall, there were about 15,000 IUD‑related hospitalizations annually in the early 1970s. 13

A.H. Robin Pharmaceuticals made the Dalkon Shield IUD from 1971 to 1974. Documented reports of severe injuries began to surface almost immediately after initial distribution, and on 29 June 1975, the FDA announced it intended to "require special warning notices for users of the intrauterine devices, the contraceptives that were linked to 43 deaths in recent years."14

A.H. Robin pulled the Dalkon Shield from the market in 1975. By 1985, 13,000 women had sued the company for damages relating to sterility, miscarriages and pelvic infections. Incredibly, some population controllers, including Stephen Mumford and Elton Kessel ― who peddle the dangerous sterilizing chemical quinacrine in developing countries ― have tried to sanitize the image of the Dalkon Shield so that it can make a comeback.15

Ortho Pharmaceuticals withdrew its Lippes Loop from the American market in 1985, and G.D. Searle withdrew its Copper‑7 and Tatum‑T IUDs in 1986 when its liability insurance lapsed. Searle also faced 775 lawsuits from women who suffered injuries from their IUDs or who conceived babies with birth defects when the devices did not work properly.

Because of widespread negative publicity, only 1% of women using birth control were on the IUD by 1995, but this number had risen to about 9% by 2017.16

Why Is This Abortifacient Called a Contraceptive?

When discussing abortifacient means of birth control, the "family planners" call us pro-lifers "anti-science" when we claim that the IUD causes early abortions. They say that human life begins at implantation, not fertilization.

But there is no logical reason to make this claim. What is the difference between the early human being (blastocyst) the hour before it implants and the hour after?

Whenever there is such confusion, we may find the answer in the dishonest manipulation of terminology by the "family planners."

In 1963, the United States Department of Health, Education and Welfare (HEW) defined "abortion" as "all the measures which impair the viability of the zygote at any time between the instant of fertilization and the completion of labor."17

Until the mid‑1960s, scientists universally acknowledged that conception happened at the moment of fertilization of the ovum by the spermatozoa somewhere in the Fallopian tube. But pro-abortionists and population controllers already had their sights set on a shift from contraceptive to abortifacient methods of birth prevention, and abortifacient research was already ongoing in Japan and several European countries.

To make abortifacients acceptable to women, and to circumvent laws designed to prohibit abortion, the "family planners" realized that they had to blur the line between contraceptive and abortifacient action.

They could do this only by changing the definition of "conception" from fertilization [union of spermatozoa and ovum] to implantation. Under the new definition of "conception," if a device or drug ― such as an IUD or Depo‑Provera ― prevents implantation, then no abortion takes place. Under the new definition, abortion would only occur if a chemical or device killed a preborn child who had already implanted in the endometrium (lining) of the uterus.

The pro‑abortionists' continuing agitation for a change in terminology finally bore fruit in 1965, when the American College of Obstetrics and Gynecology (ACOG) published its first Terminology Bulletin , stating, "Conception is the implantation of a fertilized ovum." This semantic subterfuge resulted in the Bulletin inventing two misleading terms for early abortion: "Post‑conceptive contraception" and "post‑conceptive fertility control."18

The deception by the medical establishment regarding the definition of "conception" coincided exactly with its devaluation of the preborn child. Neither change in attitude nor terminology was based upon some revolutionary discovery in medical technology or knowledge: the changes were made purely to further the anti‑life goals of the medical profession and the pro‑abortionists.

The IUD and Population Control

IUDs have confronted the anti‑fertility industry with a number of forbidding problems, the greatest of which was the proven danger of the devices. This did not stop the IUD manufacturers from turning a tidy profit by dumping their products on the poor women of developing countries.19

Despite being faced with an avalanche of lawsuits claiming damage from its Copper‑7 and Tatum‑T IUDs, Searle said that it would continue to make IUDs for women in developing countries under population control programs funded by the United States and other Western countries.20 This is yet another example of the West's " " ― a willingness to dump unsafe and even lethal products on poor women of the developing world after judging them to be too risky for Western women.

Health risks associated with IUDs are a serious matter with grave implications that are not immediately evident. All of the IUDs currently on the market have patient information pamphlets that warn about the possibility of uterine perforation, especially among women with unusually-shaped uteri, or among women who have IUDs inserted immediately after childbearing. This shows that IUDs are especially ill‑suited for use in developing countries, where anemia and malnutrition are often endemic, especially among women and children.21

Naturally, long-acting birth control that women cannot control is ideal for use by coercive governments . For three decades, right up to the alleged end of its dreaded "one-child" program, nearly half of all Chinese women of childbearing age had IUDs implanted after their first birth because the only alternative the government gave them was immediate sterilization.22

Final Thoughts

The IUD is the perfect example of nature's lack of tolerance for abuse. The very idea of having a piece of plastic or metal inserted into the body in order to cripple a healthy reproductive system should be repugnant to women, but the anti-life mentality has advanced so far that millions of women are willing to risk the consequences.