Dietary Supplements: Ephedra

Dietary Supplements: Ephedra
Updated January 23, 2007
Donna V. Porter
Specialist in Life Sciences
Domestic Social Policy Division

Dietary Supplements: Ephedra
Ephedrine is a natural constituent of the herb ephedra and a synthetic compound
present in certain over-the-counter drug products. The herbal form, known as Ma
Huang in China, has been used as a remedy for asthma. In western cultures,
ephedrine, the active drug product ingredient, has been used as a bronchodilator and
decongestant for various respiratory problems. More recently, dietary supplements
containing ephedra have been promoted for weight reduction and as a performance
enhancer in body building and other sports.
Under the provisions of the Dietary Supplement Health and Education Act of
1994, the Food and Drug Administration (FDA) must show that a supplement is
unsafe and causes harm before it can be removed from the market. In 1997,
following several hundred reports of adverse effects alleged to be caused by ephedra
use, FDA proposed rules to restrict the dosage, prohibit supplements containing
ephedrine to be combined with other known stimulants, and require specific warnings
on ephedra-containing supplements. The proposed rule was criticized for the lack
of scientific evidence to support dosage limitations and the labeling requirements,
which led the agency to withdraw part of the proposal in 2000. However, several
high profile deaths attributed to ephedra led FDA to repropose the original regulation
in 2003 and publish a final rule prohibiting the sale of ephedra under the safety
provisions of Dietary Supplement Health and Education Act in February 2004. In
April 2005, the FDA ban was overturned in federal district court, but subsequently
upheld in the U.S. Court of Appeals in August 2006.
Several congressional hearings have focused on the limitations of FDA’s current
adverse events reporting system, which was used by the agency to conclude that
dosage restrictions and mandatory labeling were needed, and specific cases of death
attributable to ephedra. A Government Accountability Office report examined the
scientific basis for FDA’s 1997 ephedra proposal and concluded that the number of
adverse event reports related to ephedra warranted agency attention to safety
concerns, but failed to provide adequate evidence to support the dosing levels and
duration of use limits. In June 2002, HHS announced that it planned expanded
research on the safety of ephedra, following completion of a RAND Corporation
report commissioned to review the existing science. The RAND report indicated that
the literature showed that, while ephedra can promote a modest short-term weight
loss in clinical trials, there was insufficient data on long-term benefits for weight-loss
and body building and combined with other stimulants, it was associated with
increased health risks.
In the 108th Congress, several resolutions were introduced that would have
expressed the sense of the Congress either that all major sports organizations should
ban the use of ephedra or that the Secretary of the Department of Health and Human
Services should remove ephedra from the market. Several bills introduced would
have established labeling and advertising rules for supplements containing ephedra,
prohibited sales to minors, required premarket approval and post-market reporting
of serious adverse effects. These bills received no further action. No bills concernedth
with supplements containing ephedra were introduced in the 109 Congress.

Background ..................................................1
FDA’s Regulation of Herbal Ephedra..............................3
1997 Proposed Regulations..................................3
Continued Adverse Events Reporting..........................4
Recent Efforts to Regulate...................................5
Prohibition on Sale.........................................7
Congressional Attention.........................................9
Published Research...........................................12
NIH — Office of Dietary Supplements............................13
Ephedra Status in Other Countries................................14
State Regulation of Ephedra....................................15
Industry Self-Regulation.......................................15
Observations ................................................17

Dietary Supplements: Ephedra
Ephedrine is the pharmaceutically active compound found in both natural form
in herbal ephedra and the synthetic ingredient present in certain over-the-counter
(OTC) drug products.1 Dietary supplements containing ephedra and their regulatory
status have been of on-going concern to Congress, the supplement industry and
consumers. This report will attempt to clarify the current regulatory status of dietary
supplement products containing ephedra.
Ephedra is a botanical whose herbal properties have been known for centuries
by the name of Ma Huang in China, where it was first used as a remedy for the
treatment of bronchial asthma. Although some 40 species are known worldwide, its
herbal and pharmaceutical effects are attributable to the contents of ephedrine and
related alkaloids found primarily in the species of Chinese origin. Historically,
practitioners of traditional medicine in China have been trained in the art and skills
of compounding small amounts of a variety of botanical ingredients, including
ephedra, to treat specific conditions. Ma Huang has generally been consumed in the
form of an invigorating tea or infusion with beneficial effects on respiration.
In western cultures, ephedrine has been used for years in various drug products.
Ephedrine is mainly used as an ingredient in bronchodilator and decongestants, for
treating asthma and hayfever, and to combat circulatory collapse in reaction to
anesthesia, poisoning, shock and allergic reactions. Most recently, ephedra in pill
form has been promoted for weight reduction and as a performance enhancer in body
building and other sports.
The pharmaceutical effects of ephedra are due to the ephedrine alkaloids, but the
herbal product may not have the same physiological effect as the pure compound,
which can be produced synthetically. The ephedra herb has been used for similar
medical purposes, although dietary supplement advocates claim that its action is
more gentle and less likely to cause adverse effects. However, a report that
investigated the pharmacokinetics of ephedrine from three commercially available
herbal Ma Huang products, compared to 25 milligrams (mg) ephedrine hydrochloride
capsules showed that the products had similar effect.2 The authors reported that

1 Note: Since ephedrine is the active chemical present in both dietary supplements and OTC
drug products, the term ephedra will be used to refer to the dietary supplement (natural)
form and ephedrine will refer to the drug (synthetic) form for purposes of this report.
2 Gurley, B., et al. Ephedrine pharmacokinetics after ingestion of nutritional supplements
containing Ephedra sinica (ma Huang). Therapeutic Drug Monitoring. 1998. v. 20, pp. 439-


recent increases in Ma Huang toxicity were not due to the differences in the
absorption rates of botanical ephedrine compared with synthetic ephedrine, but
instead resulted from accidental overdose often promoted by off-label claims and a
belief that natural medicinal agents are inherently safe.
The Dietary Supplement Health and Education Act of 1994 (DSHEA) exempted
dietary supplements from the type of premarket approval process that drugs, medical
devices and food additives must undergo before they are allowed to be sold. For
medical devices and food additives, manufacturers must demonstrate to the Food and
Drug Administration’s (FDA) satisfaction that the products are safe through adequate
scientific testing prior to marketing. In the case of prescription and OTC drugs,
manufacturers must prove, through adequate and well-controlled investigations, that
their products are safe and effective before they can be approved for marketing.
However, Congress effectively shifted the burden of proof under DSHEA from the
manufacturer to the agency to show that a dietary supplement is unsafe, a standard
significantly more difficult to meet. Moreover, the agency must demonstrate that the
dietary supplement causes harm before it can be removed from the marketplace. In
the case of herbal supplements, FDA has only voluntary reports from consumers to
rely on, along with generally limited scientific evidence. Very often ephedra is one
of several supplements consumers are using, thus complicating a determination of the
actual cause of an adverse reaction. Because the law does not require that these
products undergo premarket testing and evaluation, there is no reliable baseline
information on the possible side effects that can be used to anticipate or compare
adverse events. Another confounding factor is research evidence that supplement
users are less likely than other consumers to report adverse effects from a product
they use.3
In contrast, when ephedrine is used in prescription or OTC products, it is
regulated as a drug by FDA’s Center for Drug Evaluation and Research (CDER).
Ephedrine is used for treating mild forms of asthma, and is also approved by the
agency for treating such conditions as hypotension, nasal congestion, and sinusitis.
FDA considers nonprescription ephedrine to be safe and effective as a
bronchodilator, preferably when used under a doctor’s care. The dosage
recommendations in adults and children over 12 years are 12.5 -25 mg every 4 hours,
not to exceed 150 mg per day.4 According to the industry handbook, the principal
adverse effects can include central nervous system (CNS) stimulation, sleeplessness,
nausea, loss of appetite, tremors, tachycardia, and urinary retention.5 The handbook
further indicates there are reports that chronic overdose of ephedrine may, in some
patients, result in either severe cardiac toxicity or psychosis. Ephedrine, along with
other CNS stimulants such as caffeine and phenylpropanolamine, are frequently used

3 Barnes, J., et al. Different standards for reporting ADRs to herbal remedies and
conventional OTC medicines: face-to-face interviews with 515 users of herbal remedies.
Journal of Clinical Pharmacology. v. 45, 1998, p. 496-500.
4 U.S. Department Health and Human Services (HHS). Food and Drug Administration.
Cold, cough, allergy bronchodilator, and antiasthmatic drug products for over-the-counter
human use. Federal Register. v. 56. April 1, 1991, p. 190-197.
5 American Pharmaceutical Association. Handbook of Nonprescription Drugs. 12th Edition.

1999. Chapter 10. Asthma by D. M. Williams and T. H. Self, p. 229-230.

as ingredients in products manufactured to physically resemble much stronger
controlled substances, such as amphetamines. To prevent both misuse and abuse
with the OTC version of ephedrine, an FDA drug advisory committee recommended,
and in 1995 the agency subsequently proposed an amendment for more stringent
regulation of ephedrine, which is primarily contained in bronchodilators.6 However,
the agency has not yet finalized the proposed rule on ephedrine in bronchodilators.
Denmark, which has considerable research and use experience with ephedrine for
weight loss, regulates it as a prescription drug. In 1999, the World Health
Organization had proposed a restriction on the manufacture and distribution of
ephedrine-containing bronchodilator products; however, no final restriction has been
FDA’s Regulation of Herbal Ephedra
1997 Proposed Regulations. In the 1990s, FDA began receiving reports
that consumers were experiencing a variety of adverse effects, allegedly caused by
ephedra use. After the agency accumulated several hundred reports of adverse
effects, including a number of deaths, attributed to the supplement’s use, it convened
on October 11-12, 1995 an ephedra working group, which included members of the
FDA Food Advisory Committee and outside experts. Following the testimony
presented at its first meeting, the group reached no conclusions or determination
whether FDA should take any action on regulating these supplements. At a second
meeting on August 27-28, 1996, when additional information was reviewed, some
group members indicated their concern that there was no safe level of this substance.
Others, however, believed that there were certain levels that were safe for use of
Subsequently, FDA proposed a rule for ephedra that addressed issues
concerning its dosing, labeling and warning statements.7 The agency proposed that
in supplement form a single dose should not exceed eight milligrams and products
should bear required labeling to indicate that no more than 24 mg should be taken in
a given day. Also, labeling information was to indicate that the product should not
be used for longer than seven days and required a warning statement that the product
was not for long-term use, such as for body building and/or weight loss. The agency
also proposed to prohibit the use of ephedra in dietary supplements in combination
with ingredients that have a known stimulant effect, such as caffeine, which might
cause an interaction. In addition, FDA proposed that a statement accompany any
claims that encourage short-term excessive intake to enhance a purported effect, such
as increased energy, stating that consuming more than the recommended serving
(dose) might result in serious adverse health effects, such as heart attack, stroke,

6 U.S. Department Health and Human Services (HHS). Food and Drug Administration.
Cold, Cough, Allergy, Bronchodilator, and Antiasthmatic Drug Products for Over-the-
counter Human Use. Proposed Amendment of Monograph for OTC Bronchodilator Drug
Products. Notice of proposed rulemaking. Federal Register v. 60, no.144. July 27, 1995,
p. 38643- 38647.
7 U.S. Department Health and Human Services (HHS). Food and Drug Administration.
Dietary Supplements Containing Ephedrine Alkaloids. Proposed rule. Federal Register v.

62. June 4, 1997, p. 30678-30724.

seizure, or death. FDA proposed that these specific warning statements be required
to appear on supplement labels when the product contained ephedra.
FDA’s proposed regulation generated considerable comment, primarily from
consumers and the dietary supplement industry. Most critical comments claimed that
FDA’s ephedra dosage limitations were not based on scientific evidence, and its
labeling requirements were excessive. The voluntary adverse events reporting
(AERs) system, which had been the source of the agency’s justification for proposing
the regulatory changes, also came under scrutiny. The AERs data were criticized for
being insufficient to determine whether the adverse events reported were actually
caused by ephedra use.
As a result of the continued criticism of the agency’s use of the AERs as the
basis for its rulemaking, FDA announced in April 2000 that it was withdrawing
certain provisions of the proposed rule on ephedra.8 The provisions that were
withdrawn included the dietary ingredient limit for ephedra on a per serving basis,
proposed compliance procedures for use of the high performance liquid
chromotography method (for sample analysis), limitations on the duration of the
product’s use, and the prohibition on claims for long-term use, such as for
bodybuilding and weight loss. The agency retained the sections of the proposed rule
that would prohibit use of ingredients with stimulant effects in combination with
supplements containing ephedra, and the requirement that products containing
ephedra carry a warning statement on its use by consumers with certain diseases or
health conditions or who use certain drugs, accompanied by a recommendation that
use be discontinued if they experience certain signs or symptoms.
Continued Adverse Events Reporting. On March 31, 2000, FDA released
140 additional recent cases of adverse events associated with ephedra use.9 The
agency indicated that these cases had been more fully reviewed and evaluated to
determine whether ephedra was the likely cause of the adverse events. FDA also
announced its intention to participate in a public forum to address these new adverse
events reporting data. By that time, about 1200 cases of adverse events allegedly
attributed to ephedra had been reported to the agency.
The Department of Health and Human Service’s Office of Women’s Health
convened the Safety of Dietary Supplements Containing Ephedrine Alkaloids Public
Meeting on August 8-9, 2000, to provide an opportunity to review the analysis of
adverse events reports by FDA and outside experts. Additional public testimony on
recent scientific information on ephedra use was also taken. The Federal Register
announcement of the meeting sought comments on several questions concerning
physiologic actions of ephedra, indications for its use, dosage and duration of use,
and risks based on user demographics. It also sought comments on combination use

8 U.S. Department of Health and Human Services (HHS). Food and Drug Administration.
Dietary Supplements Containing Ephedrine Alkaloids; Withdrawal in Part. Proposed Rule.
Apr. 3, 2000. Federal Register v. 65, no. 64, p. 17474-17477.
9 U.S. Department of Health and Human Services (HHS). Food and Drug Administration.
Dietary Supplements Containing Ephedrine Alkaloids; Availability. Notice. Federal
Register v. 65, no.64. Apr. 3, 2000, p. 17510-17512.

with stimulants, exercise stress and individual sensitivities, and the outcomes
associated with dose, user characteristics, and duration of exposure. The meeting
revealed the considerable difference of opinion between government and outside
reviewers on the evidence concerning the risks associated with using ephedra, based
on AERs. Numerous private citizens provided both positive and negative
testimonials regarding their personal experience with ephedra use: some reported
life-changing weight loss, improvements in other health conditions, and increased
energy, while others told of experiencing severe side effects after consuming even
minimal doses. Several scientific investigators currently engaged in research on the
use of ephedra for weight loss spoke at the meeting, but were unable to disclose the
final results of their studies because they had not yet been peer-reviewed and
accepted for publication. The summary of the meeting identified several needs: a
reliable system for monitoring adverse events; adequate labeling for warnings and
contraindications; consumer education; recognition that ephedra use for weight loss
and ergogenic purposes constitutes treatment for a health condition (not a dietary
supplement structure/function role); long-term trials to establish dose levels and
duration guidelines; good manufacturing practices; and a research agenda.10
Recent Efforts to Regulate. On June 14, 2002, the HHS Secretary Tommy
Thompson announced new efforts to expand scientific research on the safety of
ephedrine alkaloids and aggressively pursue the illegal marketing of non-herbal
synthetic ephedrine alkaloid products.11 On October 7, 2002, FDA stopped imports
of the ephedra-containing products by the Dutch operator selling these products in
the United States. In addition, the agency sent inspectors to the New Jersey firm that
was distributing the Dutch-made products in this country. When inspectors were
denied access to the building, a court order was obtained to enter the building and
inspect the company’s records. On October 8, 2002, Secretary Thompson announced
that he had asked FDA to evaluate the best scientific evidence available and
recommend the strongest possible mandatory warning labeling for ephedra-
containing products.
Following the deaths of several athletes, FDA reopened for 30 days its earlier
proposed rules for ephedra on March 5, 2003. The published document specifically
requested comments on the portions of the proposal that addressed dosing, labeling
and warning statements, based on new evidence concerning health risks associated
with the use of supplements containing ephedrine alkaloids. In addition, the agency
signaled its intention to consider whether in light of recent evidence it should
determine that ephedra-containing supplements present a “significant or
unreasonable risk of illness or injury under conditions of use recommended or
suggested in labeling.” FDA also sought comments on whether additional legislative
authorities would be necessary or appropriate to enable it to address this issue most
effectively. The agency had proposed the following warning statement to appear on
the principal display panel of the supplement product (see box 1). The additional

10 Jones, W. Safety of Dietary Supplements Containing Ephedrine Alkaloids. Public
Meeting August 8-9, 2000. Report, 5 p.
11 U. S. Department of Health and Human Services. HHS Announces Plans To Study
Ephedra; Steps Up Enforcement of Illegal Ephedrine Marketing. HHS News. June 14, 2002,
[ press/2002pres/20020614.html ]

information provided in box 2 was to appear on the outer product label or in product
labeling that is an integral part of the outer product packaging, such as information
at the point of purchase.
Box 1. Proposed Warning Label for Principal Display Panel
Warning: Contains ephedrine alkaloids. Heart attack, stroke, seizure, and death have
been reported after consumption of ephedrine alkaloids. Not for pregnant or breast-feeding
women or persons under 18. Risk of injury can increase with dose or if used during strenuous
exercise or with other products containing stimulants (including caffeine). Do not use with
certain medications or if you have certain health conditions. Stop use and contact a doctor if
side effects occur. See more information [...].
Box 2. Proposed Additional Information for Product Labeling
This product contains ephedrine alkaloids, which can have potentially dangerous effects on the
heart and central nervous system.

— > Do not use with
!a monoamine oxidase inhibitor (MAOI) or for 2 weeks after stopping an
MAOI drug;
!certain drugs for depression, psychiatric, or emotional conditions;
!drugs for Parkinson’s disease;
!drugs for obesity or weight control;
! methyldopa.
> Contact a doctor before using this product if you have or ever had
!heart disease, high blood pressure, thyroid disease, seizure, diabetes,
depression, and other mental, emotional or behavioral conditions, glaucoma,
or difficulty urinating due to prostate enlargement.
— > Stop use and contact a doctor immediately if these side-effects occur
!dizziness, severe headache, rapid and/or irregular heartbeat, chest pain,
shortness of breath, nausea, loss of consciousness, or changes in emotions or
behavior (such as depression, hallucinations or severe mood swings).
— > Your risks of serious side-effects from this product can increase
!with increased dose, frequency, or duration of use;
!if you take it with other dietary supplements containing ephedrine alkaloids
(such as ephedra, ma huang, Sida cordifolia);
!if you take it with additional products containing stimulants, such as
caffeinated beverages and foods (including dietary supplements containing
guarana, kola nut, mate yohimbine/yohimbe, Citrus aurantium);
!if you take it with medications synephrine, phenylephrine, ephedrine,
pseudoephedrine, or phenylpropanolamine;
!if you use it before or during strenuous exercise.

Prohibition on Sale. On December 30, 2003, HHS and FDA announced
plans to prohibit the sale of dietary supplements containing ephedra. The decision to
prohibit the sale of ephedra under the safety provisions of DSHEA represented the
first time that the statute has been used to remove a supplement ingredient from the
marketplace. The ban was to take effect 60 days after the agency published the final
rule. The 60-day period following publication of the final rule is required under the
Congressional Review Act. In the meantime, FDA released a consumer alert that
announced its plan to prohibit sales of ephedra-containing dietary supplements and
urged consumers to stop using these products. The agency also sent certified letters
to over 60 manufacturers who had been producing supplements containing ephedra
to provide the companies with advance notice of the final rule to be published to
facilitate their earliest compliance.
The final notice of the ephedra ban was published on February 11, 2004 and12
went into effect on April 12, 2004, without any congressional objection. By the
time the FDA ban was announced, several Members of Congress were calling for it
to be banned. However, several manufacturers sought a temporary restraining order
to prevent the ban from taking effect, pending further scientific testing, in U.S.
District Court for the District of New Jersey. The arguments were heard on April 12,
2004 and rejected from the bench on the same day, because the case put forth by the
plaintiffs did not meet certain legal standards. The judge would not immediately stay
the rule and ordered the plaintiffs to submit additional briefs so that the court could
reach a decision on whether to stay the ban permanently.
In its announcement of its plans to prohibit the sale of ephedra-containing
supplements, FDA indicated that it had reached this decision after conducting an
exhaustive and highly resource-intensive process that is required under the provisions
of DSHEA for banning a supplement that presents a significant and unreasonable risk
to human health. To meet the safety standard, FDA said it gathered and thoroughly
reviewed a prodigious amount of evidence about ephedra’s pharmocology, clinical
studies of ephedra’s safety and effectiveness, newly available adverse events reports,
the published literature and a seminal report by the RAND Corporation. The agency
also reviewed tens of thousands of public comments on its March 2003 request for
information about ephedra-associated health risks. Coupled with several high-profile
deaths alleged to be from ephedra use and the subsequent reopening of the comment
period on the previously-published proposed rule on ephedra regulation plus
increasing pressure from Congress, the agency’s decision was the culmination of a
process that began in 1997 when FDA first proposed to require warning statements
on the hazards of ephedra use.
Following the announcement on the ephedra ban, the agency had indicated that
it planned to move beyond its recent action against ephedra and increase its focus on
certain other supplements. Former FDA Commissioner McClellan had stated the
agency’s intention to examine kava, bitter orange (citrus aurantium), aristolochic

12 U.S. Department of Health and Human Services (HHS). Food and Drug Administration.
Final Rule Declaring Dietary Supplements Containing Ephedrine Alkaloids Adulterated
Because They Present an Unreasonable Risk; Final Rule. Feb.11, 2004. Federal Register
v. 69, no. 28, p. 6787-6854.

acid, usnic acid, and pyrrolizidine alkaloids, several of which are ingredients in
weight loss products. These supplement ingredients have been associated with
kidney and liver problems. In May 2004, then Acting FDA Commissioner Crawford
stated that the agency was developing approaches to systematically review the
evidence about the safety of individual dietary supplement ingredients. FDA plans
included evaluation of the available pharmacology, published literature (including
animal, in vitro, epidemiological and clinical trial data), evidence-based reviews and
adverse event information, which is the approach that formed the scientific
foundation for its rulemaking on ephedra.
However, on April 14, 2005 a federal district judge in Utah struck down the
FDA ban on supplements containing ephedra.13 The ruling was in favor of a Utah
supplement company that had challenged the agency’s ban, claiming that ephedra has
been consumed safely for hundreds of years, and that the agency had not proven that
supplements containing ephedra were harmful. The decision prevented FDA from
stopping the manufacturer from selling its product containing ephedra and sent the
case back to the agency to determine both safe and dangerous levels of ephedrine,
ephedra’s active ingredient. HHS officials and Department of Justice Department
lawyers took some time to examine the ruling to determine the next step. Some anti-
ephedra advocates viewed the ruling as falling short of an outright reversal of the
ban, and interpreted the language in the order as only applying to a specific, lower-
dosage (10 milligrams) segment of the market. The supplement manufacturer’s
attorney declared that the court’s ruling has lifted the FDA ban.
On August 17, 2006, the U.S. Court of Appeals for the Tenth Circuit in Denver
upheld the FDA’s final rule declaring all dietary supplements containing ephedrine
alkaloids adulterated, and therefore, illegal for marketing in the United States.14 This
decision reverses the 2005 decision in Utah. The Appeals Court’s ruling
demonstrated the soundness of the agency’s decision to ban dietary supplements
containing ephedrine alkaloids, consistent with DSHEA. It also found that Congress
required FDA to conduct a risk-benefit analysis under the provisions of the act.
Counsel for the supplement company that had originally challenged the FDA ban
plans to ask for a rehearing of the case by the full court, since the August 17, 2006
decision was made by two judges. Failing that, they plan to take the case to the
Supreme Court.

13 Government News. District judge orders FDA to reopen ephedra rulemaking. Natural
Products Industry Insider. May 23, 2005, p.14.
14 For further information, see [http://insidehealth

Congressional Attention
During a 1999 hearing of the House Committee on Government Reform, the
limitations of FDA’s current adverse events reporting system were scrutinized.15 The
agency acknowledged that all adverse event reporting cases were posted on its
website without being subjected to a vetting process to determine the likely cause of
the adverse reaction. According to FDA officials, this process was used to expedite
release of adverse cases to interested parties, in lieu of freedom of information
procedures which usually take up to a year to respond to specific requests. Thus, the
cases were reported as they were received due to the agency’s limited resources to
review the cases before they were released. Committee members acknowledged that
the resources needed to improve the adverse events reporting system were limited.
The House Committee on Science requested that the General Accounting Office
(GAO) examine the scientific basis for FDA’s ephedra supplement proposal and
determine whether the agency adhered to the regulatory flexibility analysis
requirements for federal rulemaking. On August 4, 1999, GAO released a report in
which it raised concerns about the process by which FDA had compiled the 800
reports on the harmful effects of ephedra.16 The report indicated that the agency was
justified in its determination that the number of adverse events relating to
supplements containing ephedra warranted agency attention and consideration of
steps to address safety concerns. However, GAO expressed concern about the
manner in which FDA used the adverse events reports in supporting the proposed
dosing levels and duration of use limits, and concluded that the agency needed
additional evidence to support these restrictions. The report indicated that while
ephedra might be harmful, the agency lacked adequate data to set dosage levels.
GAO concluded that FDA’s economic analysis contained the basic elements of a
federal agency’s cost-benefit analysis; however, the agency analysis was not
sufficiently transparent about how it reached its estimate of the costs and benefits of
the proposed actions. The GAO report led to FDA’s decision to withdraw portions
of the proposed rule in 2000.
In the FY2001 HHS appropriations report (S.Rept. 106-293 accompanying S.
2553), the Senate Committee on Appropriations indicated its continued support for
the work of the Office of Dietary Supplements (ODS) at the National Institutes of
Health (NIH) and the need for additional research to better inform consumers of the
health benefits of supplements. The Committee specifically encouraged ODS to
support research on ephedra within the funds provided.
On October 9, 2001, Representative Susan Davis introduced the Ephedrine
Alkaloid Consumer Protection Act (H.R. 3066), the first bill to specifically address
this dietary supplement ingredient. The bill would have required that supplements

15 U.S. House of Representatives. Committee on Government Reform. How Accurate is the
FDA’s Monitoring of Supplements Like Ephedra? 106th Cong., 1st sess. Comm. Print. 106-

60. May 27, 1999, 89 p.

16 U.S. General Accounting Office. (Now known as the Government Accountability Office.)
Dietary Supplements: Uncertainties in Analyses Underlying FDA’s Proposed Rule on
Ephedrine Alkaloids. GAO/HEHS/GGD-99-90. July 1999, 79 p.

containing ephedrine alkaloids be labeled with a warning against use by individuals
under 18 years of age, and during pregnancy or nursing. The label would also have
directed users to consult a physician before use, if an individual had a personal or
family history of a number of health conditions, or if certain drugs or dietary
supplement ingredients were being used. The label would also have required a
statement that consuming the product might cause adverse health effects, and
recommended discontinuing use and contacting a health professional immediately,
if certain severe side effects occurred. Labeling would have warned about use of the
products when additional caffeine was being consumed, and would have required
disclosure of the number of milligrams of ephedrine alkaloids and any other
stimulant present in a serving, standardized nomenclature for the ephedrine
ingredient, provided a toll-free number and internet address maintained by the
Secretary of HHS for reporting adverse effects, a labeling and advertising warning
that ephedrine alkaloids were present in the product which may cause adverse health
effects and directed the user to read the label and follow directions. The bill would
have also prohibited the sale to anyone under the age of 18 years and required
ephedrine alkaloid-containing products to be behind the counter in retail
establishments. The bill was referred to the House Committee on Energy and
Commerce and no additional action occurred.
Several hearings were held in 2002. On July 25, the House Committee on
Government Reform convened a hearing on the recent research on the impact of diet
and lifestyle on personal health, the growing trend toward obesity and the use of
supplements in promoting good health. The draft RAND Corporation report that
reviewed the literature on health problems associated with ephedra was discussed
during the hearing. Subsequently, the Committee requested that GAO review health-
related calls that one company collected from consumers from May 1997 to July
2002. GAO examined the extent to which consumer information in the records was
comprehensive, interpretable and consistently recorded, counted the number of call
records reporting types of adverse events that FDA had identified in 1997 as serious
or potentially serious, and compared its findings with those of six other reviews of
the call records, including one by the company.17 GAO reported in March 2003 that
it counted 96 reports that were for heart attacks, strokes, seizures, deaths and cardiac
arrest. The company had identified 78 cases, the other reviews had ranged from 65
to 107 cases.
On July 31, 2002, the Senate Committee on Governmental Affairs’
Subcommittee on Government Management, Restructuring and the District of
Columbia held a hearing entitled “When Diets Turn Deadly: Consumer Safety and
Weight Loss Supplements,” which focused on ephedra-containing supplements and
the current evidence linking them to serious health problems. Subsequently, the
subcommittee convened a hearing on October 8, following the death attributed to
ephedra of a 16-year-old athlete in the Chairman’s district. The hearing focused on
the illegal marketing of products containing ephedra to individuals, particularly
athletes, in certain age groups. A general consensus of the witnesses was that

17 U.S. General Accounting Office. Dietary Supplements Review of Health-related Call
Records for Users of Metabolife 356. GAO-03-494. Mar. 2003, 31 p.

availability of these products should be restricted for individuals under 18 years of
In the 108th Congress, several resolutions and bills that specifically addressed
ephedra/ephedrine alkaloids were introduced. H.Con.Res. 52 as introduced by
Representative Hooley on February 25, 2003, expressed the sense of Congress that
all major sports organizations should ban the use of ephedra and dietary supplements
containing ephedrine. Currently the National Football League, the National
Collegiate Athletic Association, the International Federation of Football Associations
and the International Olympic Committee have banned use of ephedra and
supplements containing ephedrine. On November 6, 2003, H.Res. 435 was
introduced by Representative Davis and S.Res. 260 was introduced by Senator
Durbin, expressing the sense of their respective chambers that the Secretary of
Health and Human Services should take immediate action to remove dietary
supplements containing ephedrine alkaloids from the market. Both House resolutions
were referred to the Committee on Energy and Commerce and subsequently to the
Subcommittee on Health, but no further action was taken. The Senate resolution was
referred to the Committee on Health, Education, Labor, and Pensions, but no further
action was taken.
H.R. 725 was introduced by Representative Susan Davis to amend the Federal
Food, Drug and Cosmetic Act to establish labeling and advertising requirements for
dietary supplements containing ephedrine alkaloids and prohibit sales to individuals
under 18 years of age. The bill would have required warning statements and dosage
information similar to that proposed by FDA as well as contact information for
purposes of the medical product reporting program. In addition to the prohibition of
sales to minors, the bill would have required that products be held in a portion of the
retail establishment not intended to be accessible to its customers. These provisions
are similar to the bill introduced in the 107th Congress. The bill was referred to the
House Committee on Energy and Commerce and subsequently to the Subcommittee
on Health, but no further action occurred.
On March 4, 2003, the Ephedra Public Protection Act (H.R. 1075) was
introduced by Representative Sweeney. It would have required premarket approval
for supplements containing ephedrine group alkaloids and subsequent reporting of
serious adverse effects once they were allowed to be marketed. The bill defined
‘ephedrine supplements,’ ‘serious adverse experiences’ and ‘documented incident.’
The bill also would have required that the Secretary of HHS publish the proposed
rules of good manufacturing practices with 120 days of enactment. (The proposed
rules for good manufacturing practices for dietary supplements were actually
published on March 13, 2003). Finally, the bill would have required the testing of
each production lot/batch of ephedrine containing product to ensure label accuracy
and carry an expiration date on the label. The bill was referred to the House
Committee on Energy and Commerce and subsequently to the Subcommittee on
Health, but no further action occurred.

Several hearings were held during the 108th Congress. The House Committee
on Energy and Commerce held a two-day hearing on issues related to ephedra-
containing dietary supplements.18 On the first day witnesses included victims’
families, researchers, several manufacturers and agency officials. The second day the
witnesses included representatives of collegiate and major league sports: baseball,
auto racing, football, and soccer. At a hearing convened by the Senate Committee
on Commerce, Science and Transportation on October 28, 2003, the Members heard
testimony from representatives of the FDA, the Federal Trade Commission, Anti-
Doping Agency, a supplement trade association, consumers and a scientist. The
hearing was designed to determine the availability of supplements to consumers of
all ages, industry marketing practices, the effectiveness of DSHEA to protect
consumers and whether the current level of domestic consumption exposes
consumers to unexpected long and short term effects.
No legislation was introduced in the 109th Congress that addressed the issue of
dietary supplements containing ephedra. Prior to the FDA ban, several Members had
supported banning supplements containing ephedra, so congressional interest may
depend on the outcome of further legal action.
Published Research
On November 6, 2000, the New England Journal of Medicine released an article
on the health effects of dietary supplements containing ephedra.19 The report was the
result of an FDA request for an independent review of adverse event reports related
to the use of supplements containing ephedra to assess causation, and to estimate the
level of risk that use of these supplements poses to consumers. The researchers
reviewed 140 reports of adverse events related to ephedra-containing supplements
submitted to FDA between June 1, 1997 and March 31, 1999. The results indicated
that 31% of cases were considered to be definitely or probably related to the use of
ephedra-containing supplements and 31% were deemed to be possibly related.
Among the adverse events, 47% involved cardiovascular symptoms (hypertension,
palpitations, tachycardia and stroke) and 18% involved the central nervous system
(seizures). Ten events resulted in deaths and 13 events produced permanent
disability. The authors concluded that the use of ephedra-containing dietary
supplements may pose a health risk to some individuals and the findings indicated
the need for a better understanding of individual susceptibility to the adverse effects
of these supplements. The final version of the report was published in NEJM on

18 House of Representatives. Committee on Energy and Commerce. Subcommittee on
Oversight and Investigations, and Commerce, Trade and Protection. Hearings. Issuesth
Relating to Ephedra-Containing Dietary Supplements. July 23 and 24, 2003. 108 Congress,st

1 session. Serial no. 108-43, 270 p.

19 Haller, C. A., and N. L. Benowitz. Adverse Cardiovascular and Central Nervous System
Events Associated with Dietary Supplements Containing Ephedra Alkaloids. New England
Journal of Medicine. Nov. 6, 2000.

December 21, 2000.20 The early release of the article was a decision of the editors
because of the potential public health significance of the study results.
Researchers at several institutions conducted a six-month clinical trial to assess
the safety and efficacy for weight loss of an herbal supplement containing Ma Huang
and caffeine.21 They concluded that herbal ephedra and caffeine lowered body
weight, fat and BMI (basal metabolic index). Blood pressure was transiently and
heart rate persistently increased, but cardiac arrhythmias were not increased. Self-
reported symptoms were similar to those for synthetic ephedrine and caffeine
A 2001 report on the use of herbal medicines prior to surgery suggested that
certain products may increase the risk of morbidity and mortality.22 Researchers at
the University of Chicago identified eight herbs (including ephedra) that potentially
pose the greatest hazard to care of patients undergoing surgery. The study found that,
for ephedra, the relevant pharmacological effects included increased heart rate and
blood pressure, which increased the risk for heart attack and stroke. Use of the
supplement needed to be discontinued at least 24 hours before surgery. The report
concluded by suggesting that during the preoperative evaluation, physicians need to
explicitly elicit and document a history of herbal medication use, as well as learn the
potential preoperative effects of the commonly used herbal medications to prevent,
recognize and treat potentially serious problems associated with their use and
A separate analysis of adverse reactions to ephedra and other herbal products
during 2001 documented by the Toxic Event Surveillance System was published.23
Products containing ephedra alone or in combination with other herbs or substances
accounted for 64% of all adverse reactions, while these products represented only
0.82% of herbal products sales. The relative risk for an adverse reaction from
ephedra was markedly elevated in comparison to all other individual herbs by 10 to


NIH — Office of Dietary Supplements
In January 2002, the congressionally mandated Office of Dietary Supplements
(ODS) at the National Institutes of Health and the Council for Responsible Nutrition
convened a two-day conference on the science and policy aspects of performance-
enhancing supplement ingredients, such as ephedra, androstenedione and creatine.

20 Haller, C. A., and N. L. Benowitz. Adverse Cardiovascular and Central Nervous System
Events Associated with Dietary Supplements Containing Ephedra Alkaloids. New England
Journal of Medicine. v. 343, no. 25, Dec. 21, 2000, p 1833-1838.
21 Boozer, C. N., et al. Herbal Ephedra/Caffeine for Weight Loss: A six Month Safety and
Efficacy Trial. Obesity Research v. 9, no 1. 2001, p. 68.
22 Ang-lee, M, J. Moss and C. Yuan. Herbal Medicines and Perioperative Care. Journal of
American Medical Association. July 11, 2001. v. 286, no. 2, p. 208- 216.
23 Bent, S. et al. The Relative Safety of Ephedra Compared with Other Herbal Products.
Annals of Internal Medicine. v.138, no.6. Mar. 18, 2003, p.468-471.

The sessions reviewed the scientific evidence on the benefits and risks of certain
supplements in performance enhancement, and the challenges facing regulators,
educators and sport health professionals in working with individuals consuming these
ODS initiated a systematic review of the literature on ephedra through the
Agency for Healthcare Research and Quality (AHRQ), which conducted the analysis
in its Evidence-based Practice Center at its RAND-Southern California unit. The
review addressed a series of questions related to safety and efficacy of ephedra, alone
and in combination with other ingredients, for use in weight management, athletic
performance and energy enhancement. The reviewers concluded that ephedrine and
ephedra promote a modest short-term weight loss in clinical trials.24 They determined
that there were no data on long-term weight loss, and insufficient evidence to support
the use of ephedra for athletic performance. The evidence did show that the use of
ephedra or ephedrine with caffeine was associated with increased risk of psychiatric,
autonomic or gastrointestinal symptoms, and heart palpitations. The report was to
have been used in shaping the ODS research agenda related to ephedra, until FDA
announced the ban on ephedra-containing products.
Ephedra Status in Other Countries
On June 14, 2001, Health Canada (HC) released an advisory, warning
consumers not to use products that contain ephedra, either alone or in combination
with caffeine and other stimulants, for weight loss, body building or increased
energy.25 The agency noted that it had authorized ephedrine only for use in nasal
decongestants in OTC cold products. Its last action was about three years earlier
when it addressed Ma Huang use in diet aids. Health Canada had been contemplating
issuing the advisory for some time, based on its review of FDA’s AER database and
60 AERs, two of which were deaths, related to ephedra use in Canada before October


In January 2002, Health Canada banned the distribution, sale and/or importation
of all ephedra-containing products that had a unit dose of more than eight milligrams
(mg) of ephedra or 32 mg per day, and combination products containing ephedra with
other stimulants (such as caffeine). It also banned ephedra products with labeled or
implied claims for appetite suppression, weight loss promotion, metabolic
enhancement, increased exercise tolerance, body-building effect, euphoria, increased
energy or wakefulness or other stimulant effects. Products were to be recalled to the
retail level and retailers were to remove the product from store shelves and return
them to their suppliers. Health Canada issued this ban under a Class I Health Hazard
for a high-risk population (individuals who suffer from certain pre-existing chronic
conditions) and a Class II Health Hazard for the general population. Products
containing ephedra, which are marketed for traditional medicine, will continue to be
available, provided that they do not contain caffeine or exceed the ephedra content

24 Shekelle, P.G. et al. Efficacy and Safety of Ephedra and Ephedrine for Weight Loss and
Athletic Performance. Journal of the American Medical Association. v. 289, no.12, Mar. 26,

2003, p. 1537-1545.

25 Ephedra in Canada. The Tan Sheet. June 25, 2001, p. 32.

of 8 mg per dose to a maximum of 32 mg per day. Products with drug identification
numbers that are sold as nasal decongestants and meet the same dose levels will also
continue to be available. Health Canada plans to continue to monitor reports of
adverse events associated with ephedra and will take further action as necessary. A
random market survey was to be conducted within six months of the requested recall
to determine whether these products have remained off the Canadian market.
Several other countries have either restricted sales or otherwise controlled
ephedra’s availability. The Council of the European Union lists ephedra in the
category of an illicit crop. Most European Union members have a long-standing
prohibition against its use in food and dietary supplements, while also strictly
regulating its use for medicinal purposes, by requiring physicians to write
prescriptions which allow for monitoring the quantity and duration of use. Germany
and the Netherlands have essentially banned it. The United Kingdom has restricted
its use under the category of herbal medicine and Ireland has banned it all together.
Australia lists ephedra and any product containing it as a controlled substance, along
with prohibiting its sale as a food or in a food product. In the Middle East, Jordan
has withdrawn an herbal weight loss product that contained ephedra from the market,
while Saudi Arabia has banned the importation and sale of dietary supplements
containing ephedra alkaloids. The primary country that has not changed EA’s status
is China, which has used ephedra for centuries in traditional herbal healing. The
Chinese government owns and operates ephedra farms and processes products for
pharmaceutical use, although some ephedra is available in stores alone and in
supplements, where use is less restricted.
State Regulation of Ephedra
In the absence of FDA regulation of dietary supplements containing ephedra, a
number of states attempted to take action to regulate ephedra following reported
adverse effects on consumers. State efforts have taken several different forms. Some
states have regulated the product by age group, some states have declared it an illegal
drug, while other states have adopted regulations on how and to whom it can be sold.
See the CRS Congressional Distribution memorandum entitled Ephedrine: Federal
and State Law Regarding Access and Control, by M. Ann Wolfe and Diana T. Duffy,
November 2, 2000, for further information on state action.
In March 2003, Suffolk County, New York banned the sale of ephedra and in
April the New York City Council introduced a bill to ban ephedra sales as well.
Subsequently the State of New York banned ephedra sales and California followed
suit. Illinois legislation banning the sale of ephedra was signed into law on May 25,
2003, following the death of a 16 year old high school athlete. Other states had bills
under consideration until the FDA banned ephedra nationwide.
Industry Self-Regulation
Since 1994, the major trade associations representing manufacturers of the
dietary supplement industry (the American Herbal Products Association-AHPA, the
Consumer Healthcare Products Association-CHPA, the Council for Responsible
Nutrition-CRN, the National Nutritional Foods Association-NNFA, and the Utah

Natural Products Association-UNPA) have participated in a voluntary program for
the formulation and labeling of ephedra-containing products. In many respects, the
voluntary program addresses the same issues that were included in the provisions of
FDA’s proposed rule. The industry’s self-regulation provisions were based on the
OTC drug standards for ephedrine.
Under the provisions of the voluntary program, a limit on serving size for
products containing ephedra is not to exceed 25 mg, for a total of not more than 100
mg per day. Product labeling is required to be in conformity with the standard
common name listed in the Herbs of Commerce.26 A listing of the amount of ephedra
per serving is required on the label. No synthetically derived ephedrine or their salts
are allowed either in the finished product or in raw materials used in their
manufacture. Claims that the product may be useful to achieve an altered state of
consciousness, euphoria or as a “legal” street drug are not permitted. A label
statement including the following information or a statement in conformance with
applicable OTC drug monographs must be included:
!not intended for use by anyone under the age of 18;
!do not use this product if you are pregnant or nursing;
!consult a health care professional before using this product if you
have heart disease, thyroid disease, diabetes, high blood pressure, a
psychiatric condition, difficulty in urinating, prostate enlargement or
seizure disorder, if you take monoamine oxidase inhibitor (MAOI)
or any other prescription drug, or you are using an over-the-counter
drug containing ephedrine, pseudoephedrine or phenypropanolamine
(ingredients found in certain allergy, asthma, cough/cold and weight
control products);
!exceeding recommended serving will not improve results and may
cause serious adverse health effects; and
!discontinue use and call a health care professional immediately, if
you experience rapid heart beat, dizziness, severe headache,
shortness of breath or other similar symptoms.
Several states have considered, and four (Ohio, Washington, Hawaii and
Michigan) have already implemented, adoption of the industry’s voluntary standards
as their requirements for herbal ephedra products. In May 1999, the supplement
industry suggested that FDA adopt the industry’s standards either as industry
guidance or the basis for developing a regulation.27 More recently, CHPA has
recommended that FDA adopt the industry program standards into regulation.28

26 American Herbal Products Association. Herbs of Commerce. Austin, Texas, 1992. 78 p.
(A compilation of common names of herbs standardized to botanical names in order to
reduce nomenclature problems for trade purposes.)
27 McGuffin, M. American Herbal Products Association. Statement. Presented at the
Safety of Dietary Supplements Containing Ephedrine Alkaloids Public Meeting. August 8-

9, 2000, 5 p.

28 Soller, R. W. Consumer Healthcare Products Association. Comments on the safety
evaluation of ephedra. Presented at the Safety of Dietary Supplements Containing

On October 25, 2000 a citizen’s petition on ephedra was filed with FDA by four
trade associations (AHPA, CHPA, NNFA, and UNPA).29 The petition requested that
the agency revoke the parts of the 1997 proposed ephedra rule that still stood and
implement an industry standard for the labeling and marketing of dietary supplements
containing ephedra. The industry standard for labeling and marketing of supplements
containing ephedra outlined in the petition was essentially the same as the provisions
(outlined above in this report) of the industry’s voluntary program that had been in
place for more than eight years. The industry indicated in the petition that virtually
all major manufacturers and distributors of ephedra products (represented by the
trade associations filing the petition) have already adopted the voluntary program
In December 2000, the Council for Responsible Nutrition announced the results
of the Cantox Health Sciences International Report that it had funded to review
recent clinical trials on the safe use of ephedra.30 Cantox analyzed in detail 19
clinical trials, AERs from FDA, case reports and published articles, including data
from human and animal studies. The report indicated that ephedra is safe to use at
a total daily dose of 90 mg, divided into smaller doses of up to 30 mg each, which
would cause no observed adverse effects. In addition, a 150 mg total daily dosage
was determined to be the lowest level at which moderate adverse effects were first
The HHS/FDA determination that ephedra was a risk to public health under the
standard for safety in DSHEA represented the first time that the 1994 statute has been
used to prohibit the sale of a dietary supplement. The process, which started in 1997,
was both time consuming and labor intensive for the Department to establish that it
had met the standard of significant and unreasonable risk. The FDA’s final decision
appeared to have been based on the collective information available: ephedra’s
pharmacology, clinical studies of its safety and effectiveness, hundreds of adverse
event reports (including 150 deaths), an extensive review of the published literature,
and a report of an independent scientific institute. Since the Department decided to
appeal the recent legal challenge to the ephedra ban and prevailed, the ephedra case
could serve as a model for the review process and procedures for a supplement that
raises public health concern in the future.
The current voluntary adverse reporting system continues to be controversial
due to its limitations in providing the information needed to determine causality
between the use of supplements containing ephedra and suspected health problems.
These limitations also make it difficult for FDA in its rulemaking to address safety,

28 (...continued)
Ephedrine Alkaloids Public Meeting. August 8-9, 2000, 5p.
29 APHA, CHPA, NNFA, UNPA. Citizen’s Petition to the Food and Drug Administration
on Dietary Supplements Containing Ephedrine Alkaloids. Oct. 25, 2000, 6 p.
30 Cantox Health Sciences International. Safety Assessment and Determination of a
Tolerable Upper Limit for Ephedra. Dec. 20, 2000.

duration of use and dosage levels for dietary supplements containing ephedra, or in
the future, any other supplement ingredient that seems to present a public health
concern. The AER reports are generally incomplete and difficult to use in
establishing whether ephedra was the “cause” of a particular adverse event in a given
individual. Furthermore, according to Barnes et al.,31 the number of adverse reports
received into the system may represent an under-reporting of the actual number of
adverse events occurring. Future research on the use of ephedra for weight reduction
may shed some light on its efficacy as well as on any adverse events that may occur
in a more controlled research environment, and holds out the possibility of evidence
of benefits outweighing the risks to the extent that it might be regulated and used as
a drug. Congress has continued to review the problems with the voluntary AERs
system for supplements through oversight hearings and reports. In 2006, it
introduced and enacted legislation that would require mandatory reporting of dietary
supplement AERs (see CRS Report RS22480 for further information).
Nevertheless, the number of adverse event reports relating to supplements
containing ephedra seems to indicate that there is a problem with its use in at least
a select group of consumers who experience severe adverse reactions, including life-
threatening events, following use of the supplements. Given the current dearth of
controlled clinical trials, it is impossible to ascertain which consumers, many of
whom seem to have no known health problems, might be adversely affected by
ephedra use. It seems plausible that determining a safe level of ephedra for the
general population as a whole may never be possible. An additional question to be
examined concerns the health effects of caffeine in combination with ephedra.
FDA’s decision to prohibit the sale of supplements containing ephedra signaled a
final agency determination that there was no safe level. To date, no new information
has been reported that changes that determination. The industry’s claim that ephedra
has been used for hundreds of years, while technically correct, fails to consider the
different dosage and uses to which it is being put today. Although the final rule was
still subject to the Congressional Review Act after it was published, Congress did not
alter the final rule, and by the time of the ban, a number of Members had been
advocating that FDA ban EA.
The congressional language encouraging NIH-ODS to conduct research on
ephedra was aimed at helping to generate the answers to numerous questions on the
health effects and the vulnerable populations that should avoid use of this
supplement. However, no specific funding has been provided for such an initiative;
Congress has indicated that it should be supported out of existing funds. While the
funding provided to ODS has been increased in recent fiscal years, there are a number
of areas of research investigation competing for the monies that the office receives.
Furthermore, the results of any research focused on a specific supplement ingredient
that is funded by NIH-ODS will not be available for three-five years because of the
time involved in initiating such a program, completion of the research, and
publication of the results in a peer-reviewed journal. Nevertheless, the recent
announcement concerning the expansion of research on the safety of these products

31 Barnes, J., et al. Different Standards for Reporting ADRS to Herbal Remedies and
Conventional Otc Medicines: Face-to-face Interviews with 515 Users of Herbal Remedies.
Journal of Clinical Pharmacology. v. 45, 1998, p. 496-500.

suggests that the Department recognized the need to seek additional information on
the health impact from the use of ephedra-containing supplements. The plans for
future research on supplement ingredients were placed on hold following FDA’s
decision to ban ephedra.
Given the number of adverse event reports associated with ephedra, including
the number of deaths, and the amount of controversy surrounding the strict
requirements that FDA had originally proposed for dietary supplements containing
EA, the final rule to prohibit the sale of EA as a dietary supplement was an
interesting development. The more moderate voluntary self-regulatory program for
the formulation and labeling of ephedra-containing products, that the supplement
industry has had in place for some time, was not adopted by all manufacturers of
ephedra-containing products, and was not considered as effective as it might have
been. Bills introduced in the 108th Congress would have mandated a number of the
provisions of both the FDA proposed rules and the self-regulatory program that the
supplement industry has endorsed. The regulatory stalemate might have been
resolved by the FDA decision to prohibit the sale of this supplement ingredient;
however, the recent court challenges may keep the question of regulation open.
The long-term impact of the ephedra ban and the court ruling may be to raise
concern among some lawmakers and others about changes needed to make DSHEA
more effective in addressing regulation of supplements in the future. Several bills
introduced in the 108th and 109th Congresses attempted to begin to address concerns
beyond the problems with ephedra-containing products alone (see CRS Report
RL30887 for further information). Congress has now made AERs mandatory for
dietary supplements with the enactment of S. 3546/P.L.109-462. FDA had indicated
it planned to complete rules on good manufacturing practices (GMPs) by the end of
2006; however, to date no final regulations have been published. In addition, the
agency also is reportedly developing approaches to systematically review the
evidence about the safety of individual dietary supplement ingredients. It remains to
be seen whether these various piecemeal changes will improve FDA’s ability to
regulate supplements in the future.