Treatment option for wombats with mange- second report from the
Treatment Options for wombats with Mange- Second report from the Wombat Protection Society of Australia Mange Clearing House
The current paper reviews and critiques information about acaricides that have been used or could potentially be used to remove the mite s.scabiei from naturally reared
free wombats. The means by which these conclusions are reached are contained in the body of the paper. 10 per cent Sulphur in oil, self applied by the wombat via a
distribution device hung over burrows rates as the method which best meets the criteria set down in paper number one.
The first report into Mange researched available literature, critiqued existing studies
and looked at impediments to action. Its’ main conclusions are contained in the summary given below.
1.Sarcoptic mange is caused by a mite that can be easily eradicated using a variety
of acaricides. These acaricides exist naturally,eg; sulphur, lemon juice, eucalyptus/tea tree oil or are synthesised eg; ivermectin, selamectin, benzyl
benzoate,and used in commercially registered products eg; revolution, ivomec or cydectin, amongst others.
2.The intensity of mite infestation correlates with the severity of clinical signs seen in infested animals.
3.If left, in general, sarcoptic mange progresses, mites increase incrementally and the affected wombat dies. We know this death is slow and painful and avoidable.
4.The death of an heavily infested wombat in its burrow, if shared with another wombat, is the most likely means by which an intense load of mites will be
transferred to another wombat, sufficient, irrespective of previous contact to the mite and possibility of immunity, to cause sarcoptic mange in that animal.
5.Mites do not live long off their host and burrows, even if infested via the death of a wombat from sarcoptic mange , will be mite free within three weeks. Leaving
wombats with sarcoptic mange to die is unethical and likely to lead to more wombats dying from mange.
6.Treating wombats with early stages of clinical signs will lead to complete resolution of mange and the wombat will be healthy and not more likely to become reinfested,
From what we know, we recommend;1. Action to eradicate mange in wombats should be taken.
2. Wombats with clinical signs of mange should be treated with an acaracide.
3. Wombats with severe mange should be targeted for treatment and need, in
addition to acaricidal treatment, antibiotics to assist secondary infections and thus prevent their deaths. Treatment of these animals is particularly important
not only to prevent their suffering but to ensure no other wombat becomes infested.
4. Carers of hand reared wombats turning these animals from captive to free should
avoid burrows where a wombat has died from sarcoptic mite infestation for at
5. Carers of wombats with severe mange should avoid allowing that animal to die
and if it does should ensure no other wombat has contact with its bedding, housing or burrow for a period of at least three weeks.
There are many methods that can be used to eradicate sarcoptes scabiei, the mite
that causes mange in wombats. This review is by no means a full coverage of those methods. Some techniques have been selected because they have been referred to
previously in the limited literature concerning scabies/mange, for example in Lee Skerratt’s 2001 Phd. thesis where ivermectin injections were used to completely
resolve all clinical signs of scabies/mange in wombats. Others have been selected because they present a good match with the criteria set by the first report into
scabies/mange and are considered to potentially do the most good and the least harm. We include non prescription treatments such as sulphur and oil which are
considered safe for use without supervision. Others are included because members or websites mention the use of such products on wombats. Phosmet, contained in
the now withdrawn Novartis product poron, and the now unavailable (in Australia) product porect, are included for that reason. The miticide Ectodex, containing
amitraz,is included because it too appears on a mange related site and there are new warnings not to use such products with other products such as Ivermectin (we
found one mange treatment procedure still on websites in Australia recommending the use of both these products in a single treatment program).Similarly where other
veterinary medications we are aware of are used on wombats, for example valium, for sedation and they are in conflict with a particular scabies/mange treatment, for
example the ivermectin group, we make mention of these. The inclusion of any product or treatment in this review should not be considered in anyway to constitute
an endorsement of that product for use on wombats. Individual eradication programs will need to consider a range of factors before deciding on treatment methods.
While we will use our evaluation schema developed previously to provide a ranking
for possible interventions, the individual circumstance of the proposed use situation must be taken into account and methods determined from those variables. Readers
are reminded that NO products anywhere in the world are registered for use on wombats and all uses of any manufactured product are off label uses. In some
States there may also be legal issues pertaining to using any product or treatment method on a native animal and contact regarding this with appropriate authorities in
Cost of treatment is another when trying to have an impact on a widespread problem like scabies/mange in wombats. Currently there are no State funded projects looking
into the issue and most costs of treatment are borne by those who volunteer their time and energy in the attempt to save wombats. This leads to uses of products that
are not only off label but often in variance with the product formulation, for example, using an oral version of a product as a pour on. While this can be technically done in
some cases, it must be remembered that dose rates for injections, oral use and pour -ons vary, as do the amounts of certain components in different formulations of
products. It is important when using any restricted product that an appropriate authority, such as a veterinarian, prescribe and oversee the management of its use
to avoid mistakes. We have noted that website information often fails to indicate that product formulations vary and we know of one case where the use of a formulation
for pigs rather than that for poultry may have been responsible for the death of a wombat.
There will also be issues specific to wombats that need to be taken into account and
may not have been considered in provided product information. Wombats , for example are hind gut fermenters and as such are likely to excrete metabolites of
products much more slowly than would be the case with usual experimental animals.
Many products shouldn’t be used on young or suckling animals, hence joeys in
pouches could be affected by applications on female wombats.
Many commercially available products are used in other ways, such as insecticides for crops. A great deal of the adverse impact information which exists about various
chemicals comes from testing of these uses of these chemicals and specific, limited use of animals products do not necessarily result in the same adverse outcomes. For
example, using a product as a foliar spray over many acres of sunflower crops has a different effect on non target species such as bees than does the use of the same
product in much smaller doses such as a spot on or in injectable form on an animal. Similarly, it needs to be recognized that often the tests undertaken to register a
product differ from country to country and product type to type. There are big differences in determining safety factors for products used as drugs versus those
used as crop pesticides. We urge you to follow through and read the references before quoting adverse impacts of particular chemicals. We remind you that no study
has been based on outcomes for wombats.
Acaricides that exist in nature without modification cannot be copyrighted and therefore less testing of such substances occurs and literature information is scarce.
It is registration boards that determine the type of testing required. In the first step of making any of the macrocylic lactone acaricides, which happen to be antibiotic as
well as acaricidal, naturally occurring bacteria are fermented. Were the resulting product used directly, it would be organic, be able to be registered as organic and as
such could not be “owned”, unless the fermentation process was novel and copyright. In the next stage chemical reactions and procedures are used to change
the final product’s molecular structure to a substance that is considered synthesized because it wouldn’t, in that format, be found in nature. This product can be owned.
Companies choose how they register products in particular countries, dependant on
market forces and registration requirements of that country. If a particular product is already registered and in use, for example, for scab or scabies or mange, a company
whose product also covers the same mites but is effective against fleas, for which no other product is registered, may not bother to include its miticidal properties in their
registration. Frontline, containing the miticide, Fipronil is an example of this. In Australia, Frontline is registered for fleas and ticks but not mites. Similarly, products
that are registered elsewhere (U.S.A. and U.K. for example) may have limited registrations in Australia. Synthesised products often have multi type uses, all the
avermectin acaricides are antibiotics as well, though in many cases their manufacturers have not applied for registration of the substance as an antibiotic.
This is a huge area of study and it is well beyond the scope of this paper to include
all chemicals, all means of application and all data concerning impact of chemical use. We have done our best and used information from as many countries and as
many applications as we could locate, while still focusing on the main aim of this work- to locate and critique available substances that can be used to eradicate
mange in the wild wombat population in Australia.
As with the first report into scabies/mange, we ask for input and feedback and see this report as a starting point that should change and develop as information and
The first report covered how mange is recognized and diagnosed. In terms of the
least invasive means of deciding whether to treat an animal showing apparent signs of scabies/mange, we recommend the “maybe mange” approach, described here by
“Since negative test results do not rule out mite infection, a "Maybe Mange" test is
frequently performed. This consists simply of treating for sarcoptic mange and observing for resolution of the signs within 2-4 weeks.” We believe the “maybe
mange test”, used with a safe acaricide is appropriate and overcomes stress that would be otherwise associated with other means of detecting mange such as capture
This research would recommend treating any wombat showing clinical signs of
mange and to treat prophylactically those not showing clinical signs, given products or treatments are selected which do no harm. The evaluation of the potential for
harm was established in the first report and the criterion developed is listed below.
1. The degree of interference with the wombat’s normal routine and lifestyle. The better
treatment will not interfere, or limits the degree of interference with the normal routine and behaviour of the naturally raised free wombat.
In regard to this there are methods of treating mange that do not involve capture or
confinement the wombat for that purpose. These methods rank above other methods requiring capture. A self administered spot on would rank 5,above one needing to be
administered by a person, which would rank 4, above catching the wombat and dosing it orally, which would rank 3, above capturing the wombat and injecting
substances into it once, which would rank 2, above having to recapture the animal progressively to give injections which would rank 1, above confining and removing
the animal for that purpose from its usual environment.
2. The degree of likely impact on the longer term health of the animal. The better
treatment has no new negative impacts on the long term well being of the wombat.
Here we look at how long the product stays in or one the wombat and whether any residual effects, impact on gut flora, reproductive rates, levels of toxicity and other
adverse event reports such as mutagenicity, phylogenicity of the product exist or are on record. Rankings start with 5 and for each area of concern one point is deducted.
3. The degree of ease with which the treatment can be supplied to the wombat. The better
treatment is simple, safe and able to be provided by a range of people.
This section is ranked giving remote, self applied products the higher recommendation, those requiring contact with the animal such as injectable a lower
ranking and those requiring specialized training due to toxicity or some other reason lower ratings.
4. The universality of treatment. The better treatment will be able to be used on wombats
whatever their stage of mange development and should cause no harm to any other wombat that may come in contact with the treatment modality.
Some products specifically are not recommended for young or sick animals or
animals that are lactating. Where these factors are known they are included in the evaluation of the product. Each product starts with five and a point deducted for any
5. The unintended consequences of treatment. The better treatment should have no or as
few unintended consequences to those using the treatment, other animals that may
inadvertently come in contact with the treatment and the environment in general.
These effects include impact on other creatures such as dung beetles or effects from run off from product use on aquatic creatures. Once again it is often broad acres use
of foliar or soil preparation uses of these chemicals that cause these problems where use as a spot on or injectable is not as problematic, however where these outcomes
are known they are taken into account.
Skerratt,L. Sarcoptic Mange in The Common Wombat, Vombatus Ursinus , Melbourne
University.2001.pp.1-290.Available on line from Melbourne University Library.
Wombat Protection Society of Australia Mange Report 1 . 2007 Available on site
www.wombatprotection.org.au Research section.
We have had two reports for successful mange mite removal using lemon juice. One is the straight application of juice to the mite affected area and the other, believed to
be derived from a herbal remedy involved letting lemons steep in a bucket of water until mouldy and then using this solution as a wash. It was successfully used on dogs
exhibiting clinical signs of mange in N.S.W. according to member 694301 and 694373 and one of the Society’s Directors, Macpherson, reports its use in the
Northern Territory in 2002 to remove scabies mites from camp dogs. In Arnhem land these dogs are known as “skin dogs” due to alopecia caused by mite infestation. Due
to the need to throw buckets of water at wombats to deliver this treatment method it is considered likely to impact on their normal behaviour and rates lower than a self
application method. As no testing could be found with lemon juice alone distributed from a self applicator, comment about this cannot be made. It is also possible that
the mould spores produced by the rotting lemons are involved in its miticidal activity but this has not been documented. 3,5,3,5,5 =21
Oil of some type to remove and soften crusting associated with mange should not be
considered a treatment in and of itself, although there is some evidence that oil will smother mites.
Davis and Skerratt recommended baby oil or if this had not softened the crusting
Glycerine and raw sugar.(Davis and Skerratt). As part of a treatment procedure.
Davis,C and Skerratt,L. Mange Update.Reproduced from Wildcry-newsletter of the Wildlife Care Network. 1995.
Sump oil was apparently used on pigs to remove mites . According to member
number 694374 this was still being used on pig farms up into the 1990s. It is likely to be the combined effect of oil smothering live mites and sulphur in the engine oil
that had effect. Sump oil while a history of its efficacy and use exist and its use on animals consumed by people exists, would not be recommended due to the likelihood
of heavy metals and carcinogens in the product, given that other products can be found which do not include these concerns. It would also involve capturing the
wombat for this treatment and possibly doing so on a number of occasions. 2,3,3,3,3 =15
Sulphur is an element represented by the symbol S. In recent times there have
been various spellings of the word sulphur and these now include as correct sulfur. According to the Wikipedia it is an abundant, tasteless, multivalent, non metal. It is
an essential element for life and is found in amino acids,eg; cysteine and methionine. (Wikipedia) . Sulphur is an essential element of protein, biotin and vitamin B1. It is
part of the chemical structure of the amino acids methionine, cysteine, taurine and gutathione. It is required for the synthesis of collagen ,needed for skin. (Zest). It is
an essential component of all living cells. S-S sulphur bonds between peptide chains
give proteins their strength and these are found in hair and feathers.(Wikipedia).
It is used commercially, amongst other uses, as an insecticide and fungicide. The smell occasionally associated with a sulphur compound is not due to sulphur itself
but the compound, usually hydrogen sulphide also known as rotten egg gas.
Sulphur has been used as an insecticide and fungicide for thousands of years, one of the earlier mentions of it was by Homer in the 8th Century B.C. as what he
referred to as “pest averting sulfur”. It is still recommended as a scabies cure for infants, mixed in its precipitated powder form ( 5 to 6 per cent) into petroleum jelly
and applied as a cream twice daily for a week. (Miller-Keane,1997,p.1444). In the only systemic study of mange in wombats, author Lee Skerrat writes “organic or
metabolized products of sulphur appear to have acaricidal activity and for many years sulphur was the drug of choice when treating scabies” (Skerratt,2001,p.32).
Skerratt also reports on an early explorer becoming infested with scabies from a wombat and resolving this with sulphur.
Sulphur occurs in its elemental form near hot springs and volcanic regions in many
parts of the world and in underground deposits beneath quicksand in the U.S.A. To extract the later, a procedure known as the Frasch process, was invented around
1867. Elemental sulphur is also present in salt domes in Mexico and evaporates in Eastern Europe and Western Asia. It can be reconstituted by the action of anaerobic
bacteria on sulphite minerals, especially gypsum, and through the process of hydrodesulphurisation of oil and gas, and it is also present in meteorites.
Sulphur is available in onions, skunk smell and brassicas (Wikipedia) as well as grapefruit, dried beans, cabbage, eggs, fish, garlic, kale, meats, soybeans, turnips ,
Sulphur in its elemental form is odorless and harmless, it is when compounded or in the process of breaking down that odor arises. Sulphur is consumed in large
quantities through food, the average person, according to Lenntech takes in 900mg of sulphur each day.
Sulphur dioxide is used in food additives and is meant to be safe in small amounts
except to insects where it prevents respiration (due to them having no lungs), but hydrogen sulphite is more toxic than cyanide and quickly deadens smell resulting in
exposures which can kill.(Wikipedia). Airborne sulphur compounds when mixed with water cause what has become known as acid rain. Sulphur as gas, in compounds in
the air, due to industrial processes, causes damage; in animals this is mainly brain damage through malfunctioning of the hypothalamus and damage to the nervous
system. Brain, heart and kidney damage, foetal and congenital effects can be caused by sulphur products and sulphur poisoning can be passed through mother’s milk.
Internal enzyme systems of animals can also be affected. (Lenntech). These effects are through inhalation of sulphur compounds in the air, not through transdermal or
Sulphur exists in many commercial products including Sulfa*Derm cream where the active ingredient is 99.96% Pure volcanic ash sulphur. This is used as a bactericide,
for dermatitis, rashes and ringworm, acne and fungal/yeast infections.
According to Zest’s table of toxicity for dietary and mineral intake there is no
toxicity associated with a high sulphur intake.
A number of members of the Wombat Protection Society have used sulphur mixed with oil to successfully treat scabies/mange and remove mange mites on wombats
with no reported negative or side effects. Members 694374, 694324, and 694321 have used this method. There are two ways such treatments have been employed.
The first involves captive wombats having the oil and sulphur mix rubbed over their bodies to a point of fur saturation over a long period of time, using the oil to assist
remove the keratotic plaques and feeding the wombat small doses of sulphur mixed into feed. This method causes saturation of fur with oil and may lead to thermo-
regulatory issues so it is only used on captive wombats able to be monitored and temperature controlled. 1,3,2,5,5=16
The second method using the same mixture of sulphur and oil is to hang an
applicator device over a burrow that delivers a small quantity of sulphur and oil onto the top of the wombat each time it enters and leaves the burrow. Using the
wombat’s natural grooming process, over a period of time, the oil and sulphur is gradually distributed over the entire body. This method does not involve saturating
the animal so thermoregulation is not an issue.
In trials with a hand reared captive wombat, given a 5ml delivery of sulphur and oil daily for a week as a pour on, no matting or sticking of hair occurred and after 24
hours in each case the mixture was well distributed throughout the fur despite it only being applied to the neck region. It also made no difference if this amount was
squirted along the back. Wombats generally only enter and leave burrows a few times at most nightly, and a delivery device of 5mls will not result in the animal
It should be noted that some proponents of this method believe that scabies/mange is the result of other environmental factors as well and merely eradicating the mange
mite will not ensure the ongoing health of the wombat per se. It is also important to note that a wombat with severe mange (more than 75% of body affected by
plaques, following Skerratt,2001) would, in most circumstances also require antibiotics to survive, however, there may be benefits to other wombats which may
share the burrow of such of wombat in removing the mites from it , even if it dies.
Sulphur has also been claimed to detoxify and enhance immune response (Zest) so it would seem that no further harm is likely to be done to a wombat with severe
mange which may die using the self application method and this method probably protects other wombats that may share a burrow with it.
The delivery device is a plastic screw top jar filled with 500mls of a carrier oil such as
advocado, neatsfoot or a vegetable oil, into which is mixed 50grams sulphur and agitated to make a 10% suspension. The sulphur does not fully dissolve into the oil
but rather is suspended and delivered via the oil onto the wombat. This container has a small hole 1/8” drilled into the lid and is screwed onto an upturned lid such as
a milo lid employing washers between the two lids. This is hung from a chain by a spike over the top of burrows at wombat height. The solution runs out onto the lid
and remains there airlocked until the wombat’s movement tips the amount on the lid down its back at which time the lid refills.
Lenntech Sulphur – S http://www.lenntech.com/Periodic-chart-elements/S-en.htm
Miller-Keane (Eds) Encyclopedia and Dictionary of Medicine, Nursing and Allied
Skerratt,L. Sarcoptic Mange in The Common Wombat, Vombatus Ursinus. Doctoral Thesis, Department of Veterinary Science. Melbourne University.2001.pp.1-
290.Available on line from Melbourne University Library.
These include two classes of acaricides, avermectin acaricides and milbemycin
acaricides. Ivermectin,(ivomec) selamectin (revolution)and eprinomectin (eg;ivomec eprimec) are avermectin acaricides and moxidectin (cydectin) is a milbemycin
acaricide.Macrocyclic lactone acaricides are also classed as antribiotic acaricides. This section covers these commonly used miticides.
Ivermectin is contained in a wide array of products used for combating a wide variety
of infestations, including scabies. IVOMEC®, HEARTGARD30 & ACAREXX are commercial names for products containing ivermectin. In the only systemic study
undertaken into mange on wombats Lee Skerratt successfully proved that Ivomectin by injection could be used to eradicate infestations of the mite (2001). Ivomectin is
contained in a number of formulations and formats including pour-ons, chewables, injectable, tablet and spot ons. It is present in different amounts depending on the
product formulation, so a sheep drench (worming medicine taken orally) contains a different amount of ivermectin per ml than does a pour-on for cattle (a substance
According to Marvistavat, In the mid-1980's, ivermectin was introduced as probably
the most broad-spectrum anti-parasite medication ever. It is effective against most common intestinal worms (except tapeworms), most mites, and some lice. It is not
effective against fleas, ticks, flies, or flukes. It is effective against larval heartworms (the "microfilariae" that circulate in the blood) but not against adult heartworms
(that live in the heart and pulmonary\arteries). It is commonly used for the treatment of a variety of mange mites including treatment of sarcoptic, notoedric or
In dogs,side effects generally do not occur with any anti-mange doses of ivermectin
except in Collies, Shetland sheepdogs, Australian shepherds, and Old English sheepdogs, though some individual animals that are not members of these sensitive
breeds may also be prone to side effects. Collies with Ivermectin sensitivity have
been found to have a mutant gene for what is called the "P-glycoprotein."
In dogs,side effects of concern are: dilated pupils and drunken gait that can progress
to respiratory paralysis and death if medication is not withdrawn and supportive care is withheld.
Ivermectin should not be used in combination withr related tranquilizers. It
should not be used in conjunction with Amitraz (Mitaban) dips nor with Amitraz tick prevention collars (Preventic collars). Amitraz is also contained in a wash available
in Australia called Ectodex and previously was suggested as part of a mange treatment for wombats in combination with Ivermectin. (see Mange Update, ….
website).This should be avoided. These medications (containing Amitraz) are all members of the monoamine oxidase inhibitor group and when they used together
their effects add together creating sedation and adverse neurologic effects.
Ivermectin use in pregnancy and lactation is not considered to be a problem. It is possible to test an individual animal’s response to Ivermectin by using a low dose of
ivermectin. According to Shipstone (2000) Ivermectin is able to cross the blood-brain barrier and cause neurotoxicity in some dogs. Collies and Old English sheepdogs are
predisposed. Toxicity effects include ataxia, mydriasis, tremors, stupor, salivation, bradycardia and respiratory arrest. Toxic side effects are noted at 100-200ug/kg so
Shipstone advises a regime beginning with 50ug/kg and gradually increasing to 300ug/kg. He also compares milbemycin (see moxidectin) favourably due to its lower
toxicity in general and specifically in ivermectin sensitive animals, but claims it is prohibitive due to cost. In his studies he used this orally at a dose rate of 200 to
The following information about Ivermectin was written by Shipstone ,2000 referring to Demodex , a mite that affects dogs. Three types , a follicular mite D canis, a short
bodied mite D cornei and a long bodied mite (unnamed) have been described. He
says that the published literature recommends a dose of 600ug/kg daily but he found
that 300ug/kg daily was effective. Shipstone uses the cattle injectable formulation administered orally (p241) at 300ug/kg daily until two negative skin scrapings are
found one month apart and continues treatment for at least two months after the initial negative skin scrape is obtained.
Davis (1995) using advice from Lee Skerratt used Ivomec® at the rate of 1ml/10
kilos body weight directly onto the skin over the shoulder area on days three, ten and seventeen. Ivomec®pour-on product information warns not to underdose and
that applications should not occur prior to rainfall.
The wombat Protection society recently corresponded with members using ivomec as a spot on / pour on product and noted that there is a difference in the amount of
active ingredient in different products. The sheep drench, is 0.8grams to the litre or 1000mls. This is the equivalent of 0.08% w/v which is how Merial explain it on their
web site. The cattle pour on Ivomec Pour- On® for cattle, (note also there is another cattle pour on product called ivomec eprinex® containing another ingredient) is
5mg/ml and is used at a rate of 1ml per 10kg. A 40kg wombat would receive 4mls which is 20mg of ivermectin. To deliver the same amount of invermectin using sheep
drench you’d need to use 25mls. We reiterate the caution given in the beginning of
this paper, It is important when using any restricted product that an appropriate authority, such as a veterinarian prescribe and oversee the management of its use to
It is also important to recognize that off label uses and uses of ivermectin type products with animals other than those specified by the manufacturers can cause
additional problems. Veale noted that in Victoria “ farmers often purchase any product containing avermectin/milbemycin intended for sheep use and apply it goats.
This is occurring despite manufacturer’s warnings that moxidectin, in particular, is not recommended for goats. Scott et al demonstrated that the clearance of
ivermectin from the plasma of goats after oral administration was faster than from sheep”p.304,2002. Veale comments that an ivermectin resistant strain of Ostertagia
sp isolated from goats was infective for sheep and that Trichostrongylus spp may
also pass from goats to sheep. This study was “the first report in Australia of the
recovery of Trichostrongylus spp nematodes after treatment of ruminants with the
avermectin/milbemycin ( macrocyclic lactone) antithelmintics.”p.304.
In addition to the development of resistances there is also evidence that dung
beetles, and hence by association the possibility of a wide array of insect life being affected by the excretion of these monocyclic lactones in the faeces of treated
animals. The avermectins (abamectin, ivermectin and doramectin) and particularly ivermectin, have “ been shown to have adverse effects on the development and
survival of more than 20 species of scarabeine dung beetles and dung feeding flies. Sublethal effects have also been displayed in progeny and include reduced fecundity,
impaired mating and developmental abnormalities.”. Wardhaugh,K.G. ’98,p.259 .In comparison,the millibemycins (moxidectin) when used in accordance with the
manufacturer’s instructions, appear to have minor effects on dung feeding insects.(ibid.p.259).,these will be covered further on in this paper.
Ivermectin as an Injectable using Skerratt (2001) 0,2,1,3,1 =7
Davis,C and Skerratt,L. Mange Update. Reproduced from Wildcry-newsletter of the Wildlife Care Network. 1995.
Pipano,E. Recent Developments in the Control of Ectoparasites and endoparasites of dogs and /Cats with selamectin. Israeli Journal of veterinary Medicine vol 58, No.2
Shipstone,M. Generalised demodicosis in dogs, clinical perspective. Australian Veterinary Journal. Vol 78. No.4. April 2000.pp.240-242
Veterinary Medicines containing Organophosphates. UK Parliament Publications.
Rendell,R.Dr. in New Zealand Veterinary journal. Ivermectin/ Moxidectin Resistances,
Veale,Pi. Resistance to Macrocyclic Lactones in Nematodes of goats. Australian Veterinary journal. Vol.80, No.5 May 2002.
Wardhaugh,K.G. and Ridsdill-Smith,T.J. Antiparasitic drugs, the livestock industry
and dung beetles- cause for concern.? Australian Veterinary journal. Vol 76. No.4, April 1998.
Wombat Protection Society of Australia. Correspondence with Members. Mange
Eprinomectin is the main content in Ivomec® Eprinex™ Pour-On and is registered against a number of endo and ecto parasites for use in dairy and beef cattle. It’s U.S.A. registration includes
Mange Mites Chorioptes bovis and Sarcoptes scabiei .It was approved for use in the U.S.A. in 1997. It was registered by Merk /research /labarotories in America and is made by Merial Australia
pty.Ltd. It is effective in killing a wide array of ecto and endo parasites, flies and worms. Ivomec eprinex® pour-on is a clear non aqueous solution containing 5mg per ml of eprinomectin. It is
applied by pouring the substance onto cows running a strip down their back. Its dose rate is 1ml per 10 kilos of body weight.
In cattle, radiolabelled eprinomectin was absorbed slowly after topical administration. The absorbed radiolabel was taken up mainly by the liver and to a lesser extent by the kidney, fat, and muscle.
The radiolabel disappeared from these tissues with half-lives of 7.8 and 8.6 days, except for muscle beneath the application site in which the half life was 36 days.
After oral administration of eprinomectin, the approximate LD50 values were 70
mg/kg bw for mice and 55 mg/kg bw for rats. Eprinomectin is moderately hazardous
In U.S. studies of Eprinomectin against s.scabiei on cows, treated once and compared to controls via weekly skin scrapings and mite counts, researchers found that by day 21 a standard dose of
eprinomectin achieved 100% efficacy controlling mange mites.(NADA data).
The World Health Organisation has produced a report on eprinomectin and in this report notes that most of the substance leaves the body via faeces and residual amounts left within the body remain
TOXICOLOGICAL EVALUATION OF CERTAIN VETERINARY DRUG RESIDUES IN FOOD
WHO FOOD ADDITIVES SERIES 41 Prepared by:The 50th meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA)
www.fda.gov/cvm/FOI/933.htm - 209k www.inchem.org/documents/jecfa/jecmono/v041je02.htm - 74k
Selamectin is the active chemical in Revolution, which is a topically applied as a(spot
on) and used for Cats and dogs. In cats, Pfizer, the manufacturer, claim it kills adult fleas and prevents eggs hatching, prevents cat heartworm disease, treats and
controls ear mites and treats and controls roundworms. In dogs it is approved for use against adult fleas, flea eggs, heartworm, ear mites, sarcoptic mites and the
American dog tick (in USA). The recommended topical dose rate is 6mg/kg of body weight and it comes in a variety of weight ranges including 20.1kg-40kg in which
there are three pack and six pack versions. There does appear to be an expiry date associated with the product, with a minimum of 12 months indicated by the
It is advertised as a prescription only medicine, not an insecticide (see Pfizer,dog, 2007) and is sold for dogs as a once monthly spot on. Pfizer comments its low
volume allows it to be placed in one spot and this is achieved on dogs by parting the hair at the base of the neck and placing the pre-measured tube there and squeezing
Selamectin, along with Ivermectin is one of the avermectin acaricides. These and the milbemycin acaricides ( which include moxidectin) are classed as a macrocyclic
lactones . Despite Pfizer’s comments , Selamectin is both an acaricide and an insecticide. (Wood,A.) It binds to glutamate gated chloride channels in the parasites’
nervous system, causing them to open. It is absorbed through the skin and distributed via blood. According to the Nolan (2004) it concentrates in the sebaceous
glands and active concentrations are found in plasma for at least 30 days. Most is excreted unmetabolised in feaces, and a small amount is excreted in urine. According
to a press release by Environmental protection agency (America) Revolution is recommended as a replacement for the banned chlorpyrifos Dursban where it is
registered as a parasiticide not an insecticide and was formulated specifically for dogs and cats.(EPA News Release)
Selamectin is a semi synthetic modification of doramectin produced from a bio-
engineered new strain of streptomyces avermitilis which has a half life of 11 days in
dogs and 8 in cats. Applied topically it has a substantially longer half life than when
Adverse Effects noted by Pfizer (2007) include up to 1% of dogs and cats experiencing digestive upset and 1% cats having hair loss at the applicator site. It
should not be used on sick, debilitated or underweight animals. For humans it may be irritating to skin and eyes.
According to Nolan (2004) a 10x dose given to dogs and cats starting at six weeks
old for 7 monthly treatments produced no adverse reactions, given orally at normal dose rate to cats 2 out of 6 vomit and a 3x normal doses produced no problems in
reproductive female dogs or heartworm positive dogs. 3 monthly doses of 5x normal
dose rate produced no adverse effects in ivermectin sensitive colliesEfficacy against mitesForty two dogs with naturally acquired infestation of S. scabiei obtained from
commercial dog kennels where an outbreak followed an inadvertent introduction
of infested dogs (USA) or from a private hunting kennel which experienced an outbreak of scabies (Europe) were treated on day 0 and day 30 with selamectin at
the recommended dose and or with an inert vehicle mixture. Counts of S.scabiei from skin scrapings were performed every 14-15 days up to 60 days after
treatment. S.scabiei mites were reduced 93.5 % (USA) and 98.1 % (Europe) on the first count after treatment and by 100 % for all remaining counts. There was
a clear reduction of the severity of the clinical signs for the selamectin treated dogs compared with those treated with the vehicle mixture (22).
In another study dogs and cats presented at veterinary clinics in the USA and Europe were treated against scabies infection with selamectin or other insecticides
containing phosmet or amitraz or N-(mercaptomethyl) phthalimide S-(0,0-dimethyl phosphoro-didithioate). No S. scabiei were detected in over 95 % of the
selamectin treated dogs, 30 days after a single dose and no mites were recovered from any of the selamectin treated dogs after the second treatment. A dramatic
improvement in all six clinical signs of S. scabiei (pruritus, erythema, crusting, papulae, alopecia and pyodermatitis) was observed in the course of treatment.
Similar results were achieved with the control products while repeat treatments were necessary to control the infestation. When a dog is diagnosed with S. scabiei
infestation it is recommended that all dogs in contact also be treated irrespective of whether they are showing clinical signs (23).Pipano (2003).
In controlled studies Selamectin in Revolution was safely used in animals receiving other typical veterinary products such as vaccines, antithelmintics,
antiparasitics, antibiotics, steroids, collars, shampoos and dips.
Storeage conditions store below 30 degrees C 86F. (prnewswire)
Selamectin in Revolution Spot on- 3,4,3,4,4=18
Nolan,Dr. University of Pennsylvania.
Pipano,E. Recent Developments in the Control of Ectoparasites and endoparasites of dogs and /Cats with selamectin. Israeli Journal of veterinary Medicine vol 58, No.2
2003. http://www.isvma.org/article/58_2_1.htmPRN New Wire
Revolution flea and Heartworm control IPET International.12_2.htm
Wood, Alan. Compendium of Peticide Common Names. Classified Lists of Peticides. 2006. http://www.alanwood.net/pesticides/class_pesticides.html
Moxidectin , like Ivermectin and Selamectin is a Macrocyclic lactones and an
antibiotic acaricide. It is in a separate class called milbemycin acaricides (Wood).
Moxidectin is found in a range of veterinary medicines including Advocate, a spot on
for dogs ( in combination with imidacloprid ); Pro Heart an anti heartworm treatment for dogs , Quest a horse wormer and Cydectin,for cattle.
Moxidectin is used in treatments prescribed for dogs, cats, horses cattle and sheep for endo and ecto parasites and can include oral, topical and injectable applications
according to the Wikipedia. It works by binding to parasite’s glutamate-gated chloride ion channels. This disrupts neurotransmission that paralyses and kills the
parasite. According to the Committee for Veterinary Medicinal Product of the European Agency for the Evaluation of Medicinal Products Moxidectin is intended for
the treatment of endo- and ecto-parasites in cattle and sheep at the recommended doseage of 0.2mg/kg bw administered by oral or subcutaneous routes. It is also used
In horses the recommended dose is 0.4mg/kg bw administered once orally. It is considered to have a NOEL( no observable effects level = no adverse effects
observed) of 0.3mg/kg bw/day. This study on horses found that peak serum concentration was attained 6 hours post does, that oral and intravenous routes gave
approximately the same rate of elimination of moxidectin from the animals, that is elimination half life is approximately 80 hours and by 168 hours post dose 77.3% is
excreted, 77% by faecal route and 0.3% in urine. Horses fed moxidectin orally at the recommended rate and later slaughtered were found to contain moxidectin in fat at
the rates of 222ug/kg at 28 days reducing to 131ug/kg at 49 days. In other tissues tested the residual was below measureable levels, less than 10ug/kg.(1999,p.2)
It has been used to eliminate demodex mange mites from dogs. Shipstone (2000)
compares milbemycin (moxidectin) favourably to ivermectin due to its lower toxicity in general and specifically in ivermectin sensitive animals, but claims it is prohibitive
due to cost. In his studies he used this orally at a dose rate of 200 to 400ug/kg per day.,but noted facial angio-oedema in 12.5% of treated dogs.(p.242).
It has been used to eradicate knemidocoptic mange (scaly face) in budgeriagars in a study by Toparlak et al (1999) where Cydectin injectable was used as a spot on at
the rate of 0.1ml Cydectin per bird. Cydectin’s active constituent is 10mg/ml moxidectin and in this study 0.1ml ( 1mg moxidectin) equivalent 25-29mg/kg was
used as a spot on on birds with 0.1ml dropped onto the skin between feathers on the bird’s neck. This rate is much higher than the recommended rate of 0.2mg/kg bw for
cattle but the authors whose study appears in the Turkish Journal of Veterinary Science report no side effects for the birds and complete resolution of all clinical
signs, including itching stopped within 10 days and spongy lesions healed in 30-40 days after one treatment. They found no better efficacy with two treatments. The
authors’ comment that this treatment was quicker and had better outcomes than treatment with ivermectin.
Moxidectin is contained in ProHeart a heart worm prevention treatment for dogs. .
ProHeart is considered able to treat external parasites ( fleas,ticks and mites) and internal parasites ( intestinal worms, lungworms, heartworms).
The Injectable form of proheart has been withdrawn from sale due to potential side effects according to Dr. D.Ruben The injectable form of ProHeart is blamed for the
death of “Tobie”, a Border Collie and cautions are now given to people using heartworm treatment with dogs that may be ivermectin sensitive such as herding
dogs which apparently carry a gene that responds to ivermectin.
Wooster et al (2001) reported in the Australian Veterinary Journal, tested
ivermectin and moxidectin against two field isolates of a worm that parasitises sheep, H.contortus in a study which suggests that resistance to these chemicals is
developing. The millibemycins (moxidectin) when used in accordance with the manufacturer’s instructions, appear to have minor effects on dung feeding insects.
In an assessment for registration as an organic product (denied as the product was considered synthesized) the technical advisory panel agreed that moxidectin did not
appear to have carcinogenic, developmental or teratogenic impact. Bacterial assays indicate it is not a mutagen mammalian tests are inconclusive. It appears to not
effect earthworms and fauna remains present in dung pats of treated versus untreated animals.(TAP,p5-6,2003)
Moxidectin alone in Cydectin Pour On for Cattle- 3,4,3,4,4 =18
PRODUCTS COMBINING MILBEMYCINS WITH OTHERS
Advocate is a patented combination of Imidacloprid (contained in Advantage) and
Moxidectin used to eliminate parasitic infestations and to prevent new infestations in dogs ,according to its maker, Bayer Australia. Bayer say that it provides continuous
protection following one “spot on” application which lasts for a month. In dogs fleas, heartworm and gastrointestinal worms are eliminated, ear mites and demodex (a
skin mite) are controlled and Bayer claim that sarcoptic mange is 100% eliminated after a single treatment. There are three types of Advantage for dogs 4-10kilos, 10-
25kilos and over 25 kilos. These products contain Imidacloprid at 100grams/L and Moxidectin 25grams/L.
Given it appears to be the moxidectin that has the impact on mange mites, some
might consider it questionable to bother using moxidectin in combination with any other chemical. Following our scale of doing the least harm we would not advise
adding further chemicals to one which removed the mite unless some other benefit were conferred. In dogs, where target parasites are often in combination or not
responsive to moxidectin, a mixed product might be justified, however we note that the products containing moxidectin for dogs ( eg; ADVOCATE ) in combination with
IMIDACLOPRID do so to target the mange mite which imidacloprid (alone in Advantage) apparently does not.It means that ADVOCATE would rank lower on our
assessment scale because it combines moxidectin with another unnecessary chemical, imiprochloprid given the basis of this study is to target the sarcoptes mite
Advocate, spot on for dogs - 3,3,3,2,2 =13 low ranking primarily due to imidacloprid
We include information covering the mixed product, ADVOCATE and the
Imiproclorpid alone product, ADVANTAGE, so that readers can make their own judgement regarding available product information and adverse effects.
Advantage Product Information. Bayer Health Care. Bayer Australia Limited. Product Information.
Australian Veterinary Journal. Letters. Vol 80, No.5, May 2002. NRA ruling re
ProHeartSR-12 injectable.See also Aust.Vet.Journal 80, No.3 p.128.
MOXIDECTIN Summary Report 2 .The Committee for Veterinary Medicinal Products of the European Agency for the Evaluation of Medicinal Products. Veterinary
was petitioned for use as a
broad spectrum topically applied antiparasitic www.ams.usda.gov/nop/NationalList/MoxidectinFinalTAP.pdf
Toparlak,M., Tuzer,E., Gargili,A. and Gulanber,A. Therapy of Knemidocoptic Mange in Budgerigars with Spot on Application of Moxidectin. In Turkish Journal of Veterinary
and Animal Sciences. 23 (1999) 173-174.
Shipstone,M. Generalised demodicosis in dogs, clinical perspective. Australian
Veterinary Journal. Vol 78. No.4. April 2000.pp.240-242
Rendell,R.Dr. in New Zealand Veterinary journal. Ivermectin/ Moxidectin Resistances, quoted in
Veale,Pi. Resistance to Macrocyclic Lactones in Nematodes of goats. Australian
Veterinary journal. Vol.80, No.5 May 2002.
Wardhaugh,K.G. and Ridsdill-Smith,T.J. Antiparasitic drugs, the livestock industry and dung beetles- cause for concern.? Australian Veterinary journal. Vol 76. No.4,
Wood, Alan. Compendium of Peticide Common Names. Classified Lists of Peticides.
Wooster,M.J., Woodgate, R.G. and Chick B.F. Veterinary Health research Pty. Ltd. West Armidale N.S.W. Australian Veterinary Journal. Vol.79 No.12 Dec.2001
Imidacloprid is found in a variety of commercial crop insecticides including Admire, Confidor, Gaucho, Premier, Provado, Marathon, Merit, Pre-empt,Winner, Hachikusan
(Japan) and animal products such as Advantage and Advocate. It is the sole ingredient in Advantage and is combined with moxidectin in Advocate. To be
effective animals treated with Imididacloprid should not be washed using shampoo (see Wikipaedia,p.3) . Advantage is 100g/L of Imidacloprid alone and according to its
manufacturer, Bayer , it is for the treatment and prevention of fleas Ctenocephalides
spp on dogs, cats, rabbits and ferrets. One application on the skin lasts for a month
on dogs and up to a month on cats. Larval flea stages are killed in the surroundings of Advantage treated pets. For the control of lice Trichodectes canis, Lingognathus
setosus on dogs for up to 6 weeks. There are six types of Advantage including the
Blue pack for dogs weighing 25 to 50 kilos. This is applied by dividing the dose
between the shoulder blades, on the midline of the back between the hips and on one point between. .(Bayer product information).
Imidacloprid is a systemic , chloro-nicotinyl insecticide which works by interfering
with the transmission of stimuli in the insect nervous system. It causes a blockage in the nicotinergic neuronal pathway which “is more abundant in insects than in warm
blooded animals (making the chemical selectively more toxic to insects than warm blooded animals). This blockage leads to the accumulation of acetycholine, an
important neurotransmitter, resulting in the insect’s paralysis and eventually death.”(ETN).
It is effective on contact and via stomach action and is widely used as a crop
insecticide where it is available as dustable powder, granular, seed dressing, soluble concentrate, suspension concentrate and wettable powder where it is applied in
ranges from 0.05 to 0.125 pounds/acre.
It is considered moderately toxic, the lethal oral dose to half the tested animals (LD50) is 450mg/kg body weight(bw) in rats and 131mg/kg in mice and 24 hour
dermal LD50 is greater than 5000mg/kg in rats. It is considered non irritating to the eyes and skin- tested on rabbits and non sensitizing to skin- tested on guinea pigs.
The No observable effect level (NOEL) broke down with rats at 5.7mg/k/day in male rats ( this represents 100ppm) and 7.6mg/k/day in females. At 100ppm reproductive
effects of decreased pup weight are noted in baby rats. At 300ppm weight decreases were found in female rats, thyroid lesions in males and at 900ppm thyroid lesions in
females. (ETN) In dogs the NOEL was 1250ppm ( 41/mg/kg) and included increased blood choloesterol levels and liver stress measured by elevated liver cytochrome p-
Imidacloprid is considered weakly mutagenic testing positive for causing changes in human lymphocytes and Chinese Hamster Ovary Cells,(ETN) however PAN reports
that new techniques in DNA testing since registration with ADMIRE have shown an
increased frequency of adducts ( the binding of a chemical to DNA) and that these
were five times more common in calf thymus cells exposed to imidacloprid compared to unexposed cells.(Buffin,p.1).
It is considered to have minimum carcinogenic risk, however some of the inert
products used in combination with it such as crystalline quartz silica found in Merit 0.5G is carcinogenic to humans.(Buffin, p.1) and Napthalene contained in
Leverage2.7 causes nasal cancers, anemia, liver damage, cataracts and skin allergies. (Cox,2001,p.16)
It has a number of ecological impacts including toxicity to game birds where the
LD50 of 152/mg/kg for bobtail quail and 31/mg/kg in Japanese Quail has been shown. (ETN,p.2) These effects are mainly based on seed treated being eaten by
birds and studies have shown birds learn to avoid treated seed. It causes abnormal behaviour at below toxic levels- including the inability to fly and eggshell thinning at
Toxicity to fish is considered moderate with lethal concentration causing death of half the test animals (LC50)after 96 hours ranging from 211mg/l for rainbow trout to
280mg/l for carp. Aquatic invertebrates are also effected with the EC50 (effective concentration, death of 50% of test animals) 85mg/l for Daphnia leading to the
conclusion that it may be very toxic to aquatic invertebrates.(ETN,p.2).
It is highly toxic to bees (ETN,p3) . In a number of countries it has been banned from use on certain crops due to the impact on bees, including Gaucho suspended
from use on sunflowers in France, and beekeepers elsewhere report losses of 50-80%.(Buffin in PAN,p.3). It is acutely toxic to earthworms killing some at
concentrations as low as 2 and 4 ppm in soil (Cox,2001,p.18) .
Resistance in insects has been noted and of even more concern is cross resistance. Thrips selected for their resistance to the organophosphate insecticide diazinon were
also found to be resistant to imidacloprid.(Buffin,p.2).
Imidacloprid has a half life in soil ranging from 48 to 190 days abd is greater than 31 days in groundwater at phs above 5.(ETN,p.3) but “it can have a half life in soil
under aerobic conditions as long as 997 days, which is the cause of concern over possible water contamination as it gradually leaches out”…The manufacturer
maintains that, when applied according to instructions, such long term contamination is only found as the result of “repetitive application over several years”.(Wikipedia).
According to the Wikipedia 96% of the chemical is eliminate from the body within 48
hours but there are reports of it degrading into toxic, persistent, 2 chloropyridine.
Over exposure to agricultural products included reduced activity, incoordination, tremors,diarrhea and emaciation lasting up to 6 days after imidaclopriod exposuire
alone and 12 days after imidacloprid plus inerts. (Cox,2001,p.16).
Overdose (to flea control product) was characterized by reduced activity, convulsions and labored breathing and cats are effected by an unidentified inert
ingredient in Advantage spot on with kittens showing toxicity when Advantage is applied above recommended dose rates as a spot on. Death, coma and
incoordination were observed in kittens given five times the recommended dose of Advantage and when fed Advantage or its inert ingredients vomiting, salivation and
depression were noted in cats. (Cox,2001,p.16)
Advantage and other products containing imidacloprid 3,2,2,2,0=9
Buffin,D. Imidacloprid. PAN UK Journal of Peticides.
Wood, Alan. Compendium of Peticide Common Names. Classified Lists of Peticides.
Cox,C. Imidacloprid. Journal of Peticide Reform/ Spring 2001 Vol 21, No.1.pp.15-21.
ETN- Extoxnet Extension Toxicology Network- Peticide Information Profiles. Project of cornell University, Oregon State University, University of Idaho, University of
California and the Institute for Environmental toxicology.
PAN-Peticide A Network. Imidacloprid see Buffin,D.
Wikipedia entry Imidacloprid. March 2007.
Porcine products, poron, porect, phosmets, Novartis. Found and mentioned in Yahoo search for porect, Novartis product list, article on Mange authored by Clare Davis-
“Mange Update” reproduced from WildCry- newsletter of the Wildlife Care Network. On Wrin site. Additional input- correspondence with Clare Davis, Novartis , discussion
According to correspondence with Novartis, Poron is no longer available and has been withdrawn from sale. Porect has been used on wombats but according to Clare
Davis was a once only use due to potential liver toxicity. Correspondence with Novartis indicates Porect is not a current Novartis product in Australia, it is however
listed on the U.K. list of Veterinary Medicines containing Organophosphates as being registered in the U.K. as Young’s Poron 20 for Cattle with the active ingredient
Phosmet as is Porect for pigs ,again with Phosmet as the active ingredient. It would appear any supplies of either in Australia are out of date and the products longer
These product contained phosmet which according to the Wikipedia is a non systemic, organophosphate insecticide used on plants and animals. It is highly toxic
to bees. It is listed on the US Emergency Planning List of Extremely Hazardous Substances. A recent ( controversial) report by Mark Purdey suggests it may be
linked to spongiform encephalopatheies (eg BSE) .
According to Alan Wood it is used in acaricides ( organophosphate acaricide; phthalimide acaricide) and insecticides (isoindole organothiophosphate insectices;
phthalimide insecticides). It is called phthalophos in Russia and PMP in Japan.
World Health Organisation lists it as a class 11, moderately hazardous chemical. It is
a cholinesterase inhibitor. Signs of poisoning are similar to all organophosphates and include dizziness, sweating, laboured breathing, nausea, papillary constriction,
muscle cramp and excessive salivation. Can be absorbed through skin, eyes become red, ingestion leads to abdominal cramps, convulsions, diahorrhoea, unconciousness
and vomiting. PAN rates it as a “Bad Actor Chemical”, considers it possibly carcinogenic, it is a cholinesterase inhibitor and is considered by PAN to be a possible
Its’ effects on other living organisms include growth and mortality impact on amphibians, mortality of annelids, accumulates in and effects behaviour of and kills
crustaceans, effects fish biochemistry, accumulates in fish and causes mortality, insects are affected by accumulation, intoxication and mortality, molluscs behaviour
and morphology are affected, it leads to intoxication and mortality of molluscs and zooplankton, it accumulates in zooplankton and phytoplankton and effects the later’s
Advice re use on wombats was that it was good to use as a once only product on free wombats and should only be used monthly on captive wombats. (ref. Clare Davis).
Cautionary advice re liver toxicity was given but cannot be documented. Given it is no longer available in Australia, this information has been included due to previous
references to its use on wombats. Novartis information indicates any remaining product left in Australia would be out of date and it should not be used. As a result
this product receives a zero rating.
PAN Pesticide Data Base – Pesticide Action Network http:www.pesticideinfo.org 2006
Letter via E-mail to Wombat P.S.A. March 2007 Novartis
Yahoo Search Porect March 2007- Article 5 “mange” and 6 Products from Novartis
Phosmet Wikipedia Entry March 20Mange update by Clare Davis- reproduced from Wildcry-Newsletter of the Wildlife
Care Network on http://www.wombatechidna.id.au/mange.html
Wood, Alan. Compendium of Pesticide Common Names. Classified Lists of Peticides. 20
Main ingredient in Frontline Spot On for Dogs and Cats, Topspot, Frontline Plus, Chipco Choice, combat, Maxforce, Termidor
Marketing in Australia for fleas and Paralysis and Brown Dog ticks on Dogs.
Frontline Plus for dogs contains Fipronil 100g/L and S-Methoprene 90g/L and its
maufacturer Merial advises it is for use on dogs 8 weeks and older. Merial say it prevents the development of flea eggs and larvae and pupae( see Methoprene) for
up to 3 months after treatment. It is supplied in pre-dosed pipettes for 20-40kg dogs at 2.68mL and for 40-60kg dogs in 4.02mL pipette which are applied to a place the
animal won’t lick. In Australia the product is registered for the brown dog tick
Rhipicephalus sanguineus, biteing lice Trichodectes canis and the paralysis tick
Ixodes holocyclus Merial product information) but Fipronil controls mites (PAN
The N.P.T.N. fact sheet of the U.S. Environmental Protection Agency calls Fipronil a
phenylpyrazole insecticide, these act by disrupting normal nerve function. Fipronil acts by blocking the GABA- gate chloride channels of neuron in the central nervous
system. Neural excitation caused by contact causes the insect’s death.1997.p.1.
Information from PAN, the Pesticides Advisory Netwrok of the U.K. follows. Fipronil is
an insecticide discovered and developed by Rhône-Poulenc between 1985-87 and placed on the market in 1993. Although effective against a variety of pests, there are
concerns about its environmental and human health effects. Actively marketed in many industrialised and developing countries its, worldwide use is increasing. Fipronil
is a member of the phenyl pyrazole class of pesticides, which are principally chemicals with a herbicidal effect. Fipronil, however, acts as an insecticide with
contact and stomach action. It is sparingly soluble in water; is stable at normal temperatures for one year but not stable in the presence of metal ions and is
degraded by sunlight to produce a variety of metabolites one of which (fipronil-desulfinyl (MB 46513) is extremely stable and is more toxic than the parent
Fipronil under the trade name Frontline or Top Spot is also used to control fleas,
ticks and mites on domestic animals and as a pour-on or dip for cattle to control ticks. In the UK, provisional approval for five years has been granted for fipronil use
Fipronil is an extremely active molecule and is a potent disruptor of the insect central nervous system via the (-aminobutyric acid (GABA) regulated chloride channel.
Despite the fact that the GABA channel is important in nerve transmission in both vertebrate and invertebrate animals, and that fipronil does bind to the GABA receptor
in vertebrates, the binding is ‘less tight” which offers a degree of selectivity.
Field persistence is low-moderate in water and soil (half-life 10-130 hours (h) in water and 45-530 h in soil) with three major degradates formed in soil – RPA 20076
(amide), MB46513 (fipronil-desulfinyl), and RPA 104615 and two major metabolites in water, including MB 45950 (sulfide). Under aerobic conditions in soil several
metabolites have been identified, including RPA 200766 and MB 46136 (sulfone).
Fipronil residues tend to stay in the upper 15 cm of soil and exhibit low potential
to leach to groundwater.
In aquatic environments, fipronil residues rapidly move from the water to the
sediment with over 95% of the residues being found in or on the sediments within one week of application.
Acute toxicityFipronil is classed as a WHO Class II moderately hazardous pesticide and has a rat
acute oral LD50 (the dose required to kill half a population of lab animals) is 97
mg/kg(35). It is less toxic to mammals than to some birds, fish and most invertebrates.
Fipronil has moderate acute toxicity by the oral and inhalation routes in rats. Dermal absorption in rats is less than 1% after 24 h and toxicity is considered to be
low. In contrast, it is of moderate dermal toxicity to rabbits.
Fipronil is neurotoxic in both rats and dogs, there are indications of developmental neurotoxicity and chronic carcinogenicity in the rat and in two dog studies.
There has been a low incidence of severe skin reactions to Frontline Spray treatment, Top Spot for Cats and Top Spot for Dogs, mostly resulting in skin
irritation and/or hair loss at the site of application. There is some suggestion that dogs are more severely affected than cats.
Fipronil is carcinogenic to rats at doses of 300 ppm in males (12.68 mg/kg/day) and females (16.75 mg/kg/day), causing thyroid cancer related to disruption in the
thyroid-pituitary status. However fipronil was not carcinogenic to female mice when administered at doses of 30 ppm.
Fipronil is associated with reproductive effects in rats fed 95.4% fipronil continuously in the diet at 300 ppm based on clinical signs of toxicity, decreased
litter size, decreased body weights, decrease in the percentage of animals mating, reduction in fertility index, reduced post-implantation survival and offspring postnatal
survivability, and delay in physical development.
There have been very few studies undertaken with human subjects, although human cells have been used in some carcinogenicity studies in which no adverse effects
Fipronil has been classified as a Group C (Possible Human) Carcinogen based on
an increase in thyroid follicular cell tumours in both sexes of the rat. In contrast, thyroid tumours induced by fipronil in rats are not considered of relevance to human
health in the UK.
Two Top Spot products were determined by the New York State Department of
Environmental Conservation to pose no significant exposure risks to workers applying the product. However, concerns were raised about human exposure to
Frontline spray treatment in 1996 leading to a denial of registration for the spray product. Commercial pet groomers and veterinarians were considered to be at risk
from chronic exposure via inhalation and dermal absorption during the application of the spray, assuming that they may have to treat up to 20 large dogs per day.
Fipronil is highly toxic to certain groups of gallinaceous birds (Acute LD50 for Bobwhite quail = 11.3 mg/kg), while being relatively innocuous to passerines (LD50
for field sparrow = 1120 mg/kg) and wildfowl (LD50for Mallard duck > 2150 mg/kg)(49).
The LD50 of fipronil for the fringe-toed lizard (Acanthodactylus dumerili)
[Lacertidae] has been estimated at 30 µg a.i./g body weight in laboratory tests,
indicating that it is highly toxic. Mortality was delayed and lizards died during the four weeks after treatment. Locomotor activity, prey consumption and body weight
remained significantly lower in lizards fed fipronil treated prey than in the control group for 2-4 weeks after treatment.
Toxicity of fipronil to fish varies with species. It is very highly toxic to bluegill sunfish, highly toxic to rainbow trout and to European carp. It is very highly toxic to
one of the African tilapia (Oreochromis niloticus) . Fipronil affects larval growth in
rainbow trout at concentrations greater than 0.0066 ppm.
Fipronil is also toxic to a wide range of aquatic invertebrates, very highly toxic to shrimps and other crustacea and very highly toxic to oysters.
Fipronil is highly toxic to bees and termites. It had the highest acute toxicity for the parasitoid Bracon hebetor [Hymenoptera: Braconidae]. Fipronil was given the
highest hazard ranking for beneficial tenebrionid beetles of six insecticides tested in the Locustox study. It is virtually non-toxic to earthworms.
Frontline; The use of fipronil is in combination with methoprene (see next) in
products available in Australia 3,2,3,2,0 =10
PAN Fipronil http://www.pan.-uk.org/pestnews/actives/fipronil.htm
Frontline Plus Product Information from Merial Australia 2006
National Pesticide Telecommunications Network FIPRONIL Information Sheet Oregon State University and the U.S. Environmental and Protection Agency
Methoprene is the second ingredient in Frontline made by Merial Australia. It is also
contained in products that include Atosid, Apex, Diacan, Dianex, Kabat, Minex, Pharorid, Precor and ZR-515.
According to Extoxnet , “Methoprene is mimics the action of an insect growth regulation hormone. It is used as an insecticide because it interferes with the normal
maturation process. In a normal life cycle, an insect goes from egg to larva, to pupa, and eventually to adult. Methoprene artifically stunts the insects' development,
making it impossible for insects to mature to the adult stages, and thus preventing them from reproducing.” The Wikipedia describes methoprene as a juvenile hormone
which stops pupae from developing into adult insects. Hence it is not effective against adults, but is effective against larval forms of insects and mites. It is used
most widely as a mosquito larvacide Altosid which is used to prevent West Nile virus.
Extoxnet information includes; “To be effective, it is essential that this growth
inhibitor be administered at the proper stage of the target pest's life cycle. Methoprene is not toxic to the pupal or adult stages. Treated larvae will pupate but
adults do not hatch from the pupal stage. Methoprene is also considered a larvicide since it is effective in controlling the larval stage of insects. Methoprene is used in
the production of a number of foods including meat, milk, eggs, mushrooms, peanuts, rice, and cereals. It is also used in aquatic areas to control mosquitoes and
several types of ants, flies, lice, moths, beetles, and fleas. It is available in suspension, emulsifiable and soluble concentrate formulations, as well as in
briquette, aerosol, and bait form.” In Frontline it is a “spot on” product, coming in preprepared weight based doses to be applied at a point between the shoulders
according to Merial frontline’s Australian makers product information. It is registered for use on cats and dogs for flea control.
According to Extoxnet, Methoprene is practically nontoxic when ingested or inhaled
and slightly toxic by dermal absorption. The oral LD50 for methoprene in rats is greater than 34,600 mg/kg, and in dogs is greater than 5000 mg/kg .It is slightly
toxic by skin exposure, with reported dermal LD50 values of greater than 2000 to 3000 mg/kg in rabbits. Methoprene is not an eye or skin irritant, and it is not a skin
sensitizer . The inhalation LC50 for methoprene in rats is greater than 210 mg/L . No overt signs of poisoning have been reported in incidents involving
accidental human exposure to methoprene .
No methoprene-related effects were observed in 2-year feeding trials with rats
given doses of 250 mg/kg/day, nor in mice given 30 mg/kg/day . At higher ingested amounts over a longer period some liver changes were seen in mice. Experimental
data indicate that no reproductive hazards are associated with methoprene. There have been no teratogenic effects in animals dosed with methoprene .Methoprene
does not appear to be mutagenic. Experimental data suggest that methoprene is not carcinogenic.
In mammals, methoprene is rapidly and completely broken down and excreted, mostly in the urine and feces . Some evidence suggests that methoprene metabolites
are incorporated into natural body components. Methoprene is excreted unchanged in cattle feces in amounts that are sufficient to kill some larvae that breed in dung .
Methoprene is slightly toxic to birds. These effects appeared as soon as 2 hours after treatment and persisted for up to 2 days and included slowness, reluctance to
move, sitting, withdrawal, and incoordination . Methoprene is slightly to moderately toxic to fish. Methoprene is very highly toxic to some species of freshwater,
estuarine, and marine invertebrates, while the acute LC50 values are greater than 100 mg/L in freshwater shrimp, and it is greater than 0.1 mg/L in estuarine mud
crabs. Methorprene had very little effect, if any, on exposed non-target aquatic organisms including waterfleas, damselflies, snails, tadpoles, and mosquito fish .
Tests with earthworms showed little if any toxic effects on contact . It is nontoxic to bees . Methoprene is of low persistence in the soil environment. In soil, microbial
degradation is rapid and appears to be the major route of its disappearance from soil. Methoprene also readily undergoes degradation by sunlight and is rapidly and
tightly absorbed to most soils. It is slightly soluble in water . Methoprene degrades rapidly in water. Studies have demonstrated half-lives in pond water of about 30 and
40 hours at initial concentrations of 0.001 mg/L and 0.01 mg/L, respectively . At normal temperatures and levels of sunlight, technical Altosid is rapidly degraded,
mainly by aquatic microorganisms and sunlight . Altosid is biodegradable and nonpersistent, even in plants treated at very high rates.
Methoprene is not available on its own and is therefore not given a separate rating.
Frontline Plus Product Information from Merial Australia 2006
EXTOXNET Extension Toxicology Network Pesticide Information Profile Methoprene.
Amitraz is a topical parasite control agent, its action is apparently not fully
understood, but it is suspected to work by interfering with the nervous system of susceptible parasites. It is supplied as a topical solution (19.9%) and in tick collars
(9%). Veterinary formulations include Mitaban (Upjohn), Preventic (Allerderm/Virbac) and Taktic (Hoescht) and Ectodex (50g/L amitraz) as well as
The following information about Amitraz was written by Shipstone ,2000 referring to
Demodex , a mite that affects dogs. Three types , a follicular mite D canis, a short
bodies mite D cornei and a long bodied mite (unnamed) have been described.
Topical Amitraz, a monoamine oxidase inhibitor in a xylene base is registered for use
as a miticide in Australia. The dose and frequency of application of amitraz affects reported efficacy (80% at 600mg/L weekly, 67% at 300mg/L weekly and 25% at
600mg/L fortnightly. The registered use rate in Australia is 500mg/L applied 3-5 days. Long haired animals should be clipped to allow increased penetration of the
active ingredient to skin level and all crusts and exudates should be removed using an antimicrobial shampoo such as benzyl peroxide or chlorohexidine.
The animals needs to be totally dried before application and allowed to air dry
Ectodex contains 50g/L of Amitraz and is registered for mange mites and some specific ticks on dogs by Intervet New Zealand. It cautions against use in
Chihuahuas, puppies under three months and in animals affected by heat stress.
In a treatment regime worked out by Lee Skerratt and Clare Davis and published in WildCry the newsletter of Wildlife Care Network, Amitraz as Ectodex was suggested
for use on day two after bathing the wombat . This contradicts information provided by Shipstone re ensuring the animal is dry before applying Amitraz, but given the
Skerratt/Davis regime also involved other miticidal interventions and not Ectodex alone , this perhaps explains the variation.
Ectodex’s manufacturer also advises wearing full chemical contamination wear while
Toxicity includes transitory sedation, bradycardia, hypothermia, hypotension, bloat, polyuria, hyperglycaemia and vomiting have been noted, particularly in animals 5kg
and less. These symptoms can be treated using yohimbine ( Parnell Lab.Aus.) or atipamezole (Novartis).(Shipstone 2000) and effects can last up to 72 hours and
ingestion of flea collars can lead to poisoning.(Ruben,D)Amitraz is toxic to fish .
Rating; Miticide and Ectodex are washes needing repeated applications; 1,3,1,1,1=7
Davis,C and Skerratt,L. Mange Update.Reproduced from Wildcry-newsletter of the Wildlife Care Network. 1995.
Ectodex EC Acaricidal Dog Wash. Product Information.Intervet. 49 george Stree
Ruben,D. PetPlace Product Information.
Shipstone,M. Generalised demodicosis in dogs, clinical perspective. Australian
Veterinary Journal. Vol 78. No.4. April 2000.pp.240-242
There are many other products that have not been included within this list. If people
caring for wombats would like a particular product researched and evaluated by the criteria used in this report they are welcome to contact the Wombat Protection
Society of Australia and an analysis will be made. We recognize that other easily accessible products including malathion ( in Malawash) and benzyl benzoate , used in
many human scabies treatments as well as carbaryl and coal tar products are available . Due to their method of application or other factors already canvassed in
the report, these have not been examined individually as it was felt they would receive lower rankings than those already examined.
Precipitated sulphur in oil-self application method -23
Lemon juice/fermented- 21Moxidectin in Cydectin pour on for cattle - 18
Selamectin in Revolution spot on for dogs –18Precipitated sulphur in oil –applied by human-16
Eprinomectin as pour on in Ivomec-Eprinex-15Moxidectin combined with Imidacloprid in Advocate spot on for dogs-13
Ivermectin as Ivomec Pour on –11Fipronil alone or in combination with Methoprene in Frontline spot on for dogs-10
Imidacloprid alone in Advantage spot on for dogs -9Ivermectin as an injectable – 7
Amitraz in washes; mticide/ectodex-7Phospmets in poron or porect in any form -0
CQLC-2004-09 Avis sur l'utilisation de la capécitabine (Xeloda®) dans le traitement du cancer colorectal métastatique ou avancé QUESTION Quelle est la valeur thérapeutique de la capécitabine (Xeloda®) dans le traitement du cancer colorectal métastatique ou avancé ? INTRODUCTION En 2003, au Québec, l’Institut national du cancer du Canada estime que 4500 nouveaux
PDE5 Inhibitors for Treatment of Erectile Dysfunction Introduction Three selective phosphodiesterase type-5 (PDE5) inhibitors are licensed for the treatment of erectile dysfunction – sildenafil, tadalafil and vardenafil. They are all included in the joint formulary. These medications have proven efficacy and safety; the major difference between them is that sildenafil a