AN UPDATE FROM LIFE
ISSUES INSTITUTE
RU 486 Advocates Plan for the Millennium
From the time of the first announcement about RU 486 in 1982,
abortion advocates have consistently talked about introducing
it worldwide, especially into so-called developing
or Third World countries where surgical abortion
is not widely available. But that has not occurred. The dangerous
RU 486/Cytotec prostaglandin chemical abortion technique (RU
486/PG) is currently licensed in three European countries
and only one non-European nation, the People's Republic of
China.
Action is underway to market RU 486/PG more widely. A group
of 46 leading RU 486 advocates and researchers held a 2_-day
conference in Bermuda from January 10 to 13, 1998 to explore
the issues surrounding the introduction of a practicable means
of safe and effective early medical (chemical) abortion in
the developing and re-restructuring world, stated the
report of the meeting. (Presumably, the re-structuring
countries would include Eastern European countries formerly
under Soviet domination.)
According to the published reports, formal presentations
during the first two days described the status of research
and licensing, policy issues, and providing chemical abortion
services. During the final half-day session, the conferees
formulated a consensus statement recommending specific actions
for researchers, funding organizations, abortion providers,
and policymakers.
The conference was sponsored by the New-York-City-based Population
Council and the Wellcome Trust from the United Kingdom. The
Council published a 29-page report titled Towards Safe
and Effective Use of Medical Abortion, and representatives
from both organizations published a 2-page article summarizing
key aspects of the deliberations in the July 24,1998 issue
of the leading U.S. journal Science. (Unless otherwise
noted, all citations below to statements made at the meeting
are from the Population Council's report. Both publications
summarized the proceedings and seldom presented direct quotations
from the speakers.)
The published reports of the conference provide valuable
insights for Pro-Family and Pro-Life supporters in two ways.
First, speakers at the meeting gave some new information about
the hazards of RU 486/PG abortion. Second, the publications
outlined details of the ambitious plans to overcome some of
the medical and practical hurdles that the abortion advocates
believe are impeding world-wide use of RU 486.
Chemical Abortion Dangers
Scattered among the usual rhetoric proclaiming the safety
of RU 486/PG abortion, abortionists offered some new information
about the dangers of chemical abortion.
A representative of the Special Programme of Research, Development
& Research Training in Human Reproduction of the World
Health Organization (HRP/WHO) stated that there have been
three reported cases of anaphylactic shock from RU 486/PG
abortion. This complication is an allergic, life-threatening
drug reaction and had not been previously reported.
During a discussion period, someone raised concerns about
the counseling that pregnant women who are considering RU
486/PG abortion should receive about the potential damage
to the unborn baby. The report stated that women should be
informed that if they don't abort and pregnancy continues,
there is a higher incidence of congenital abnormalities.
Lawsuits may occur in cases of mis-counseling. There
is one pending law case of a baby who had a birth defect in
the United Kingdom, stated the report.
A point of contention among the conferees was using the anti-cancer
drug methotrexate (MTX) for abortion. Opinion diverged
widely, stated the report, with strong support
for its use from delegates from the U.S. The Science
article noted that MTX is not as inexpensive as misoprostol
(Cytotec) or as easy to administer as mifepristone (RU 486).
In addition, many physicians remain uneasy about methotrexate
because of its possible toxicity and teratogenic effects.
Spreading RU 486/PG Worldwide
The fundamental premise underlying the Bermuda meeting was
that introducing chemical abortion into developing countries
would reduce the purported high rates of morbidity and mortality
from unsafe abortion around the world. Citing a WHO report
in 1993, the Science article claimed 70,000 deaths
per year from unsafe surgical abortion around the world, almost
all in developing countries. (The Population Council report
claimed 100,000 without citing a source.) Neither report presented
any documented proof of their claim.
The Science article asserted that chemical abortion
methods may be particularly important in resource-poor
conditions where inadequate surgical services for abortion
may entail a very high risk of infection and reproductive
tract injury. Based on ten years of experience, there
was unanimous agreement that mifepristone (RU 486) has
`come of age' for use in early medical (chemical) abortion,
stated the authors.
The final report of recommendations on how to overcome the
medical and political obstacles hindering introduction of
RU 486/PG grouped the findings into four major categories.
Here are some highlights.
First, in the area of Biomedical Research and Development,
there was strong interest in finding a way to use the anti-ulcer
drug Cytotec (misoprostol) for abortion because it is already
on the market around the world. The report called for abortion
tests to determine the optimum dose, route of administration,
upper limit of gestational age for use, and how it can be
employed in places where RU 486 is not available. The Science
article observed that in Brazil women use it to induce
bleeding and then seek help from medical services as they
would for spontaneous miscarriage. A speaker from South
Africa, Dr. Helen Randera-Rees, described how her abortion
facility uses Cytotec vaginally followed by manual vacuum
aspiration.
Second, concerning Providing Mifepristone
(RU 486), the conferees advocated taking an indirect approach
similar to Cytotec. They recommended licensing RU 486 for
uses not prohibited by current legislation, such as
inducing labor after fetal death or oncology. Once the drug
was on the market for a non-abortion use, they expect it could
be used for abortion.
The Science article also noted the considerable uncertainty
concerning possible problems with a supply of RU 486 for clinical
use in developed countries, especially with the reluctance
of some pharmaceutical manufacturers to associate themselves
with any abortifacient drug. The conferees noted that
production was well under way in China, and they encouraged
western manufacturers to become partners with the Chinese.
Third, discussions about Local Health Service Delivery
provided several illuminating revelations. Dr. Beverly Winikoff,
a senior official at the Population Council, which controls
the U.S. patent for RU 486, indicated once RU 486/PG is on
the U.S. market, some of the tight restrictions on its use
may be changed or eliminated. She argued that is not
essential to establish elective surgical abortion services
as a back-up before medical (chemical abortion) services are
introduced, stated the report. The abortion facility
would not have to have surgical abortion services since women
could receive treatment at any facility equipped to handle
a miscarriage. Moreover, Winikoff noted that non-physicians
can provide medical (chemical) abortion, just as they provide
IUDs. Ultrasound is not essential to every setting,
stated the report. She also explained that tests in the U.S.
and four other countries indicated that it may not be
necessary for women to visit the abortion facility to
take the prostaglandin and that the cut off for using RU 486/PG
could be extended well beyond 49-days (7-weeks).
In countries where abortion is illegal, the conferees stated
that there is a need for post-abortion care, and to
examine how medical (chemical) abortion would fit into this
service. The published reports did not elaborate on
this point, but the implication is that abortion drugs might
somehow be introduced under the guise of providing women with
medical care for miscarriages.
The fourth set of recommendations on Advocacy and
Legal Issues was based on the assertion that Advocacy
for medical abortion is essential, irrespective of the prevailing
legal position regarding abortion. In other words, abortion
proponents should ignore the legal restrictions on abortion
in their effort to promote chemical abortion methods. One
crucial component of their strategy is to focus opinion
on the social injustice of unsafe abortion. That problem
could of course be fixed by chemical abortion.
Conclusion
The published reports of the Bermuda conference offer a brief
glimpse of the messianic zeal that the Population Council
and other organizations have to spread the gospel of chemical
abortion around the world. They are committed to push ahead
despite the ever-growing body of information about the physical
and psychological dangers from their own tests and clinical
experience.
Fortunately, in order to garner wide support, the abortion
advocates publish reports such as these, which offer Pro-Life
and Pro-Family advocates some insights into their long-range
plans and better ammunition against RU 486/PG in the public
debate.Subject Index to The RU 486 Report
(September 1994 - December 1998)
(Listed by article name, date of publication, and page, with
oldest article first)
Cytotec (misoprostol)
Misused with RU 486, Jan. 1995, p. 1.
Citizen Petition side effects, Feb./Mar. 1995,
p. 3-4.
Misused for 2nd Trimester Abortion, Feb./Mar. 1995, p. 6.
Used with methotrexate (MTX), see methotrexate
listing.
Methotrexate (MTX) and Cytotec (misoprostol) Prostaglandin
Abortion Method
Poses Threat, Apr. 1995, pp. 1-4.
More Tests Begin, May 1995, p. 2-4.
Study Ignores Dangers, Nov. 1995, pp. 2-4.
Researcher Opposes Abortion Use, Dec. 1995 p. 1.
Not "Standard of Care," Dec. 1995, p. 2.
Two Chemical Abortion Methods May Be On U.S. Market Soon,
Apr. 1996, p. 1.
FACT SHEET, Comparison of Chemical Abortion Methods: RU 486/Prostaglandin
and Methotrexate (MTX)/ Prostaglandin, Oct. 1996, p. 2.
Planned Parenthood Starts Nationwide Methotrexate/Prostaglandin
Abortion Test, Oct. 1996, p. 3.
Methotrexate/Cytotec Prostaglandin Abortion: An Annotated
Chronology and Bibliography, Jan.-Feb. 1998, p. 5.
RU 486 (mifepristone) Boycott
Status, Sept. 1994, p. 2.
Gathers Steam, Feb./Mar. 1995, p. 5.
New Boycott Target, June 1995, p. 1.
21 National Groups Declare Renewed RU 486 Consumer Boycott,
Mar. 1996, p. 1.
RU 486: Where Do We Go From Here?, Sept. 1996, p. 1.
Renewed Boycott Pressure on Hoechst Needed, Dec. 1996-Jan.
1997, p. 1.
Hoechst Donates European RU 486 Patent to Avoid
Consumer Boycott, Apr. 1997, p. 1.
RU 486 (mifepristone)/ Action Items
What You Can Do, Nov. 1994, p. 4
RU 486 as Medicine, Nov. 1994, p. 3.
Citizen Petition Follow up, Feb./Mar. 1995, p.
4.
Soundbites, Feb./Mar. 1995, p. 6.
Sample Speech Against RU 486, Aug. 1995, p. 1.
Safety Concerns at Center of Debate, Sept. 1995, p. 1.
What Is Happening With RU 486? Questions, Answers, and Theories,
Feb. 1996, p. 1.
Two Chemical Abortion Methods May Be On U.S. Market Soon,
Apr. 1996, p. 1.
Local Opposition Vital To Prevent More Doctors From Performing
RU 486 Abortions, May 1996, p. 1.
Assessing the Acceptability of Chemical Abortion
Methods, June 1996, p. 1.
Quick Response to Media On Upcoming RU 486 Publication Essential,
July 1996, p. 1.
FDA Advisory Committee Recommends RU 486 Approval, Aug. 1996,
p. 1.
RU 486: Where Do We Go From Here?, Sept. 1996, p. 1.
RU 486 Approvable for U.S. Market by mid-1997,
Oct. 1996, p. 1.
FACT SHEET, Comparison of Chemical Abortion Methods: RU 486/Prostaglandin
and Methotrexate (MTX)/ Prostaglandin, Oct. 1996, p. 2.
Hoechst Donates European RU 486 Patent to Avoid
Consumer Boycott, Apr. 1997, p. 1.
Great Opportunity to Refute Myths about the Non-Abortion
Uses of RU 486, Sept.-Oct. 1997, p. 1.
The Facts Against RU 486 Abortion: An Update, Mar.-Apr. 1998,
p. 1.
The RU 486 Abortion Technique From Discovery to Marketing,
1980-1988: A Chronology and Bibliography, Jun.-Jul.-Aug.,
1998, p. 1.
RU 486 Edging Closer to Marketing in U.S., Sept.-Oct.-Nov.,
1998, p. 1.
Chinese Clone of RU 486 Slated for Non-Abortion
U.S. Tests, Sept.-Oct.-Nov., 1998, p. 2.
Chinese Marketing RU 486 Technique, Sept.-Oct.-Nov., 1998,
p. 2.
RU 486 Marketing May Spread Across Europe, Sept.-Oct.-Nov.,
1998, p. 3.
RU 486 Labeled Abortion Drug in Emergency Contraception
Publicity, Sept.-Oct.-Nov., 1998, p. 3.
RU 486 Prominent in Congressional Deliberations, Sept.-Oct.-Nov.,
1998, p. 6.
RU 486 (mifepristone) Proponents / Food and Drug Administration
(FDA)
Goal of Adding Abortionists, Nov. 1994, p. 1.
Citizen Petition Given to FDA, Feb./Mar. 1995,
pp. 1-2.
FDA Wary of Citizen Petition, May 1995, p. 1.
Key Post to RU 486 Advocate, May 1995, p. 4.
Objective Evaluation Impossible for FDA, Oct. 1995, p. 1.
What Is Happening With RU 486? Questions, Answers, and Theories,
Feb. 1996, p. 1.
Federal Research Underway on New Abortion Drug, Feb. 1996,
p. 3.
RU 486 Hits Roadblock In Australia, July 1996, p. 4.
FDA Advisory Committee Recommends RU 486 Approval, Aug. 1996,
p. 1.
RU 486 Approvable for U.S. Market by mid-1997,
Oct. 1996, p. 1.
Details Emerge About Stealth Abortion-Pill Company,
Nov. 1996, p. 1.
Lawsuits May Delay RU 486 Debut, Dec. 1996-Jan. 1997, p.
2.
With Key RU 486 Lawsuit Settled, Proponents Aim for U.S.
Sales by Year's End, Feb.-Mar. 1997, p. 1.
Hoechst Donates European RU 486 Patent to Avoid
Consumer Boycott, Apr. 1997, p. 1.
New Contract Dispute Delays U.S. RU 486 Marketing, July 1997,
p. 1.
Status of Chemical Abortion Drugs Under Development in the
U.S., Aug. 1997, p. 2.
Lawsuits Partially Settled, But Obstacles Remain to RU 486
Sales in U.S., Nov.-Dec. 1997, p. 1.
Key RU 486 Marketing Effort Stalled, But Research Continues,
Jan.-Feb. 1998, p. 1.
RU 486 Prominent in Congressional Deliberations, Sept.-Oct.-Nov.,
1998, p. 6.
RU 486 Proponents Plan for the Millennium, Dec. 1998, p.
1.
RU 486 (mifepristone) Side Effects / Dangers
Dangerous Fallout, Nov. 1994, p. 2.
Citizen Petition filed, Feb./Mar. 1995, pp. 1-4.
Not As Easy As Promised, Part I, July 1995, p. 1.
List of side effects and dangers in sample speech, Aug. 1995,
pp. 3-4.
Safety Concerns at Center of Debate, Sept. 1995, p. 1.
Not As Easy As Promised, Part II, Oct. 1995, p. 4.
Safety and Efficacy Questions, Nov. 1995, p. 1.
Not As Easy As Promised , Part III, Dec.1995, p. 4.
RU 486 Near-Death Accident in Iowa Raises Safety
Questions, Jan. 1996, p. 1.
Assessing the Acceptability of Chemical Abortion
Methods, June 1996, p. 1.
FDA Advisory Committee Recommends RU 486 Approval, Aug. 1996,
p. 1.
FACT SHEET, Comparison of Chemical Abortion Methods: RU 486/Prostaglandin
and Methotrexate (MTX)/ Prostaglandin, Oct. 1996, p. 2.
New Insights from Abortion-Pill Test, Aug. 1997, p. 1.
The Facts Against RU 486 Abortion: An Update, Mar.-Apr. 1998,
p. 1.
Article on U.S. RU 486 Test Gives More Details About Dangers
to Women, May, 1998, p. 1.
RU 486 Proponents Plan for the Millennium, Dec. 1998, p.
1.
RU 486 Testing
No News, Good News, Sept. 1994, p. 1.
No NY State Funding, Sept. 1994, p. 2.
Australian Tests Suspended, Sept. 1994, p. 3.
Status of tests (table), Sept. 1994, p. 4.
Tests Begin, Nov. 1994, p. 1.
Trial Starts in St. Louis, May 1995, p. 1.
12th Test Site Announced, July 1995, p. 4.
Trials End, Nov. 1995, p. 1.
Two Chemical Abortion Methods May Be On U.S. Market Soon,
Apr. 1996, p. 1.
Assessing the Acceptability of Chemical Abortion
Methods, June 1996, p. 1.
RU 486 Hits Roadblock In Australia, July 1996, p. 4.
Canadian Official Rejects Fast-Track Approval for RU 486
Abortion, May 1997, p. 1.
U.S. Testing of Chinese RU 486 Clone,
July 1997, p. 3.
New Insights from Abortion-Pill Test, Aug. 1997, p. 1.
Status of Chemical Abortion Drugs Under Development in the
U.S., Aug. 1997, p. 2.
Key RU 486 Marketing Effort Stalled, But Research Continues,
Jan.-Feb. 1998, p. 1.
Article on U.S. RU 486 Test Gives More Details About Dangers
to Women, May, 1998, p. 1.
The RU 486 Abortion Technique From Discovery to Marketing,
1980-1988: A Chronology and Bibliography, Jun.-Jul.-Aug.,
1998, p. 1.
Chinese Clone of RU 486 Slated for Non-Abortion
U.S. Tests, Sept.-Oct.-Nov., 1998, p. 2.
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