205 CMR 3.29
Medications and Prohibited Substances
(1) Aggravating and Mitigating Factors. Upon a finding of a violation of 205 CMR 3.29, the
judges shall consider the classification level of the violation as listed at the time of the violation
in the Uniform Classification Guidelines for Foreign Substances as promulgated by the
Association of Racing Commissioners International (ARCI) and impose penalties and
disciplinary measures consistent with the recommendations contained therein. The judges shall
also consult with the official veterinarian, laboratory director or other individuals to determine
the seriousness of the laboratory finding or the medication violation. All medication and drug
violations shall be investigated and reviewed on a case by case basis. Extenuating factors
include, but are not limited to:
(a) The past record of the trainer, veterinarian and owner in drug cases;
(b) The potential of the drug(s) to influence a horse's racing performance;
(c) The legal availability of the drug;
(d) Whether there is reason to believe the responsible party knew of the administration of
the drug or intentionally administered the drug;
(e) The steps taken by the trainer to safeguard the horse;
(f) The probability of environmental contamination or inadvertent exposure due to human
drug use;
(g) The purse of the race;
(h) Whether the drug found was one for which the horse was receiving a treatment as
determined by the Medication Report Form;
(i) Whether there was any suspicious betting pattern in the race; and
(j) Whether the licensed trainer was acting under the advice of a licensed veterinarian.
As a result of the investigation, there may be mitigating circumstances for which a lesser or
no penalty is appropriate for the licensee and aggravating factors, which may increase the penalty
beyond the minimum.
(2) Penalties.
(a) In issuing penalties against individuals found guilty of medication and drug violations,
a regulatory distinction shall be made between the detection of therapeutic medications used
routinely to treat racehorses and those drugs that have no reason to be found at any
concentration in the test sample on race day.
(b) If a licensed veterinarian is administering or prescribing a drug not listed in the ARCI
Uniform Classification Guidelines for Foreign Substances, the identity of the drug shall be
forwarded to the official veterinarian to be forwarded to the Racing Medication and Testing
Consortium for classification.
(c) Any drug or metabolite thereof found to be presenting a pre- or post-race sample which
is not classified in the version of the ARCI Uniform Classification Guidelines for Foreign
Substances in effect at the time of the violation shall be assumed to be a ARCI Class 1 Drug
and the trainer and owner shall be subject to those penalties as set forth in schedule "A"
therein unless satisfactorily demonstrated otherwise by the Racing Medication and Testing
Consortium, with a penalty category assigned.
(d) Any licensee of the Commission, including veterinarians, found to be responsible for
the improper or intentional administration of any drug resulting in a positive test may, after
proper notice and hearing, be subject to the same penalties set forth for the licensed trainer.
(e) Procedures shall be established to ensure that a licensed trainer is not able to benefit
financially during the period for which the individual has been suspended. This includes, but
is not limited to, ensuring that horses are not transferred to licensed family members.
(f) Multiple positive tests for the same medication incurred by a trainer prior to delivery of
official notice by the Commission may be treated as a single violation. In the case of a
positive test indicating multiple substances found in a single post-race sample, the Stewards
may treat each substance found as an individual violation, depending upon the facts and
circumstances of the case.
(3) Medication Restrictions.
(a) A finding by the Commission approved laboratory of a prohibited drug, chemical or
other substance in a test specimen of a horse is prima facie evidence that the prohibited drug,
chemical or other substance was administered to the horse and, in the case of a post-race test,
was present in the horse's body while it was participating in a race. Prohibited substances
include:
1.
Drugs or medications for which no acceptable threshold concentration has been
established;
2. Controlled therapeutic medications in excess of established threshold concentrations
or administration within the restricted time period as set forth in the version of the ARCI
Controlled Therapeutic Medication Schedule in effect at the time of the violation;
3. Substances present in the horse in excess of concentrations at which such substances
could occur naturally; and
4. Substances foreign to a horse at concentrations that cause interference with testing
procedures.
(b) Except as otherwise provided by 205 CMR 3.00, a person may not administer or cause
to be administered by any means to a horse a prohibited drug, medication, chemical or other
substance, including anyrestricted medication pursuant to 205 CMR 3.00 during the 24-hour
period before post time for the race in which the horse is entered.
(4) Medical Labeling.
(a) No person on association grounds where horses are lodged or kept, excluding licensed
veterinarians, shall have in or upon association grounds which that person occupies or has
the right to occupy, or in that person's personal property or effects or vehicle in that person's
care, custody or control, a drug, medication, chemical, foreign substance or other substance
that is prohibited in a horse on a race day unless the product is labeled in accordance with
205 CMR 3.29(4).
(b) Any drug or medication which is used or kept on association grounds and which, by
federal or state law, requires a prescription must have been validly prescribed by a duly
licensed veterinarian, and in compliance with the applicable state statutes. All such
allowable medications must have a prescription label which is securely attached and clearly
ascribed to show the following:
1. The name of the product;
2.
The name, address and telephone number of the veterinarian prescribing or
dispensing the product;
3. The name of each patient (horse) for whom the product is intended/prescribed;
4.
The dose, dosage, duration of treatment and expiration date of the prescribed/
dispensed product; and
5. The name of the person (trainer) to whom the product was dispensed.
(5) Non-steroidal Anti-inflammatory Drugs (NSAIDs). The use of one of three approved
NSAIDs shall be permitted under the following conditions:
(a) Not to exceed the following permitted serum or plasma threshold concentrations which
are consistent with administration by a single intravenous injection at least 24 hours before
the post time for the race in which the horse is entered:
1. Phenylbutazone. two micrograms per milliliter;
2. Flunixin. 20 nanograms per milliliter;
3. Ketoprofen. two nanograms per milliliter.
(b) These or any other NSAID are prohibited to be administered within the 24 hours before
post time for the race in which the horse is entered.
(c) The presence of more than one of the three approved NSAIDs in the post-race serum or
plasma sample is not permitted.
1. A finding of phenylbutazone below a concentration of .5 microgram per milliliter of
blood serum or plasma shall not constitute a violation of 205 CMR 3.29(5).
2. A finding of flunixin below a concentration of three nanograms per milliliter of blood
serum or plasma shall not constitute a violation of 205 CMR 3.29(5).
(d) The use of all but one of the approved NSAIDs shall be discontinued at least 48 hours
before the post time for the race in which the horse is entered.
(e) The presence of any unapproved NSAID in the post-race serum or plasma sample is not
permitted.
(6) Furosemide.
(a) In order for a horse to be placed on the Furosemide List the following process must be
followed.
1. After the horse's licensed trainer and licensed veterinarian determine that it would be
in the horse's best interests to race with furosemide, the official veterinarian or his or her
designee shall be notified, using the prescribed form, that the horse is to be put on the
Furosemide List.
2. The form must be received by the official veterinarian or his or her designee by the
time of entry.
3. A horse placed on the official Furosemide List must remain on that list unless the
licensed trainer and licensed veterinarian submit a written request to remove the horse
from the list. The request must be made to the official veterinarian or his or her designee,
on the proper form, no later than the time of entry.
4. After a horse has been removed from the Furosemide List, the horse may not be
placed back on the list for a period of 60 calendar days unless it is determined to be
detrimental to the welfare of the horse, in consultation with the official veterinarian. If
a horse is removed from the official Furosemide List a second time in a 365-day period,
the horse may not be placed back on the list for a period of 90 calendar days.
5. Furosemide shall only be administered on association grounds.
6. Furosemide shall be the only authorized bleeder medication.
7. The use of furosemide shall not be permitted in two year olds.
(b)
The use of furosemide shall be permitted under the following circumstances on
association grounds where a detention barn is not utilized:
1. Furosemide shall be administered by single intravenous injection no less than four
hours prior to post time for the race for which the horse is entered.
2. The furosemide dosage administered shall not exceed 500 mg. nor be less than 150
mg.
3. After treatment, the horse shall be required by the Commission to remain in the
proximity of its stall in the care, custody and control of its trainer or the trainer's
designated representative under general association and/or Commission security
surveillance until called to the saddling paddock.
(c) Test results must show a detectable concentration of the drug in the post-race serum,
plasma or urine sample.
1.
The specific gravity of post-race urine samples may be measured to ensure that
samples are sufficiently concentrated for proper chemical analysis. The specific gravity
shall not be below 1.010. If the specific gravity of the urine is found to be below 1.010
or if a urine sample is unavailable for testing, quantitation of furosemide in serum or
plasma shall be performed;
2. Quantitation of furosemide in serum or plasma shall be performed when the specific
gravity of the corresponding urine sample is not measured or if measured below 1.010.
Concentrations may not exceed 100 nanograms of furosemide per milliliter of serum or
plasma.
(d) A horse which has been placed on the Furosemide List in another jurisdiction pursuant
to 205 CMR 3.00 shall be placed on the Furosemide List in this jurisdiction. A notation on
the horse's electronic eligibility certificate of such shall suffice as evidence of being on a
Furosemide List in another jurisdiction.
(7) Bleeder List.
(a)
The official veterinarian shall maintain a Bleeder List of all horses, which have
demonstrated external evidence of exercise induced pulmonaryhemorrhage from one or both
nostrils during or after a race or workout as observed by the official veterinarian.
(b) Every confirmed bleeder, regardless of age, shall be placed on the Bleeder List and be
ineligible to race for the minimum following time periods:
1. First incident - 14 days;
2. Second incident - 30 days;
3. Third incident - 180 days; and
4. Fourth incident - barred for racing lifetime.
(c) For the purposes of counting the number of days a horse is ineligible to run, the day the
horse bled externally is the first day of the recovery period.
(d) The voluntary administration of furosemide without an external bleeding incident shall
not subject the horse to the initial period of ineligibility as defined by 205 CMR 3.29(7).
(e) A horse which has been placed on a Bleeder List in another jurisdiction pursuant to rules
similar to 205 CMR 3.29(7) shall be placed on a Bleeder List in this jurisdiction.
(8) Androgenic-anabolic Steroids (AAS).
(a) No AAS shall be permitted in test samples collected from racing horses except for
residues of the major metabolite of nandrolone, and the naturally occurring substances
boldenone and testosterone at concentrations less than the indicated thresholds.
(b) Concentrations of these AAS shall not exceed the following plasma or serum thresholds
for unchanged (i.e., not conjugated) substance or urine threshold concentrations (i.e., free
drug or metabolite and drug or metabolite liberated from its conjugates):
1. Boldenone: 15 ng/ml of total boldenone in urine of male horses other than geldings,
or 25 pg/ml of boldenone in plasma or serum of all horses regardless of sex;
2. Nandrolone: 1 ng/ml of total nandrolone in urine for fillies, mares, and geldings,
or 45 ng/ml (as 5á-estrane-3â, 17á-diol)) in urine, in male horses other than geldings,
or 25 pg/ml of nandrolone in plasma or serum for geldings, fillies, and mares.
3. Testosterone:
a. In Geldings. 20 ng/ml total testosterone in urine, or 25 pg/ml of testosterone in
plasma or serum; and
b.
In Fillies and Mares. 55 ng/ml total testosterone in urine, or 25 pg/ml of
testosterone in plasma or serum.
(c) Any other anabolic steroids are prohibited in racing horses.
(d) Post-race urine samples must have the sex of the horse identified to the laboratory.
(9) Alkalinizing Substances. The use of agents that elevate the horse's TCO2 or Base excess
level above those existing naturallyin the untreated horse at normal physiological concentrations
is prohibited.
(a) The following levels also apply to blood gas analysis:
1. The regulatory threshold for TCO2 is 37.0 millimoles per liter of plasma/serum or a
Base excess level of 10.0 millimoles; and
2. The decision level to be used for the regulation of TCO2 is 37.0 millimoles per liter
of plasma/serum plus the measurement uncertaintyof the laboratoryanalyzing the sample
or a Base excess level of 10.4 millimoles per liter of plasma/serum.
(b) 1. If the level of TCO2 is determined to exceed 37.0 millimoles per liter of plasma/ erum
plus the laboratory's measurement of uncertainty and the owner or trainer of the horse
certifies in writing to the judges within 24 hours after the notification of the test results
that the level is normal for that horse, the owner or trainer may request in writing that the
horse be held in quarantine. If quarantine is requested, the licensed association shall
make guarded quarantine available for that horse for a period of time to be determined
by the steward or judges, but in no event for more than 72 hours.
2. The expense to maintain the quarantine shall be borne by the owner or trainer.
3. During quarantine, the horse shall be retested periodically by the Commission
veterinarian.
4. The horse shall not be permitted to race during a quarantine period, but it may be
exercised and trained at times prescribed by the licensed association and in a manner that
allows monitoring of the horse by a Commission representative.
5. During quarantine, the horse shall be fed only hay, oats, and water.
6.
If the Commission veterinarian is satisfied that the horse's level of TCO2, as
registered in the original test, is physiologically normal for that horse, the judges:
a. Shall permit the horse to race; and
b. May require repetition of the quarantine procedure established in 205 CMR
3.29(9)(b)1. through 6. to reestablish that the horse's TCO2 level is physiologically
normal.