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In US and European field studies, no dogs experienced seizures when dosed with COMFORTIS chewable tablets at the therapeutic dose range of 13.5-27.3 mg/lb (30-60 mg/kg), including 4 dogs with pre-existing epilepsy. Four epileptic dogs that received higher than the maximum recommended dose of 27.3 mg/lb (60 mg/kg) experienced at least one seizure within the week following the second dose of COMFORTIS chewable tablets, but no seizures following the first and third doses. The cause of the seizures observed in the field studies could not be determined. Chewable Tablets
Post Approval Experience (June 2009):
The following adverse reactions are based on post-approval adverse drug event reporting. The adverse reactions
are listed in decreasing order of frequency: vomiting, depression/lethargy, anorexia, ataxia, diarrhea, pruritus,
trembling, hypersalivation and seizures.
Caution: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.
Following concomitant extra label use of ivermectin with COMFORTIS, some dogs have experienced the following Description:
clinical signs: trembling/twitching, salivation/drooling, seizures, ataxia, mydriasis, blindness and disorientation. COMFORTIS chewable tablets (spinosad) are available in five chewable flavored tablet sizes for oral administration to dogs and puppies according to their weight. Each chewable tablet is formulated to provide a Post approval experience continues to support the safety of COMFORTIS when used concurrently with heartworm minimum spinosad dosage of 13.5 mg/lb (30 mg/kg). Spinosad is a member of the spinosyns class of insecticides, preventatives according to label directions. which are non-antibacterial tetracyclic macrolides. Spinosad contains two major factors, spinosyn A and spinosyn For technical assistance or to report an adverse drug reaction, call 1-888-545-5973. Additional information can be D, derived from the naturally occurring bacterium, Saccharopolyspora spinosa. Spinosyn A and spinosyn D have found at www.comfortis4dogs.com. For a complete listing of adverse reactions for spinosad reported to the CVM the chemical compositions 2-[(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyl)oxy]-13-[[5-dimethylamino)- see http://www.fda.gov/AnimalVeterinary/SafetyHealth/ProductSafetyInformation/ucm055394.htm tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl -1H-as-Indaceno[3,2-d]oxacyclododecin-7, 15-dione and 2-[(6-deoxy-2,3,4-tri-O-methyl-α-L-mannopyranosyl)oxy]- Mode of Action:
13-[[5-dimethylamino)-tetrahydro-6-methyl-2H-pyran-2-yl] oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b- The primary target of action of COMFORTIS chewable tablets in insects is an activation of nicotinic acetylcholine tetradecahydro-4,14-dimethyl-1H-as-Indaceno[3,2-d] oxacyclododecin-7,15-dione, respectively.
receptors (nAChRs). Spinosad does not interact with known insecticidal binding sites of other nicotinic or GABAergic insecticides such as neonicotinoids, fiproles, milbemycins, avermectins, and cyclodienes. Insects treated with spinosad show involuntary muscle contractions and tremors resulting from activation of motor neurons. Prolonged spinosad-induced hyperexcitation results in prostration, paralysis, and flea death. The selective toxicity of spinosad between insects and vertebrates may be conferred by the differential sensitivity of the Effectiveness:
In a well-controlled laboratory study, COMFORTIS chewable tablets began to kill fleas 30 minutes after
administration and demonstrated 100% effectiveness within 4 hours. COMFORTIS chewable tablets kill fleas before they can lay eggs. If a severe environmental infestation exists, fleas may persist for a period of time after dose administration due to the emergence of adult fleas from pupae already in the environment. In field studies conducted in households with existing flea infestations of varying severity, flea reductions of 98.0% to 99.8% were observed over the course of 3 monthly treatments with COMFORTIS chewable tablets. Dogs with signs of flea allergy dermatitis showed improvement in erythema, papules, scaling, alopecia, dermatitis/pyodermatitis and pruritus as a direct result of eliminating the fleas.
Animal Safety:
Indications:
COMFORTIS chewable tablets were tested in pure and mixed breeds of healthy dogs in well-controlled clinical COMFORTIS chewable tablets kill fleas and are indicated for the prevention and treatment of flea infestations and laboratory studies. No dogs were withdrawn from the field studies due to treatment-related adverse reactions.
(Ctenocephalides felis) on dogs for one month. In a dose tolerance study, COMFORTIS chewable tablets were administered orally to adult Beagle dogs at Dosage and Administration:
average doses of up to 100 mg/kg once daily for 10 consecutive days (16.7 times the maximum recommended COMFORTIS chewable tablets are given orally once a month, at the recommended minimum dosage of 13.5 mg/lb monthly dose). Vomiting was seen in 5 of 6 treated dogs during the first 6 days of treatment, usually within 2.5 hours of dosing. Treated females lost weight early in the treatment period, but their weights were similar to control dogs by the end of the 24-day study. COMFORTIS chewable tablets were not associated with any clinically significant changes in hematology, blood coagulation or urinalysis parameters; however, mild elevations in ALT occurred in all dogs treated with COMFORTIS chewable tablets. By day 24, ALT values had returned to near baseline levels. Phospholipidosis (vacuolation) of the lymphoid tissue was seen in all dogs treated with COMFORTIS chewable tablets, the long-term effects of which are unknown. In a margin of safety study, COMFORTIS chewable tablets were administered orally to 6-week-old Beagle puppies at average doses of 1.5, 4.4, and 7.4 times the maximum recommended dose at 28-day intervals over a 6-month period. Vomiting was observed across all groups, including the control. Increased vomiting was observed at elevated doses, usually within 1 hour following administration. Vomiting at all doses decreased over time and stabilized when puppies were 14 weeks of age. The average daily and total weight gains of treated dogs were smaller than control dogs and were dose dependent. COMFORTIS chewable tablets were not associated with clinically significant changes in hematology, clinical chemistry, coagulation or urinalysis parameters. * Dogs over 120 lbs should be administered the appropriate combination of tablets.
Phospholipidosis (vacuolation) of the lymphoid tissue was seen in some dogs in the 4.4X group and all dogs in the 7.4X group. The long term effects of phospholipidosis are unknown. Treatment with COMFORTIS chewable Administer COMFORTIS chewable tablets with food for maximum effectiveness.
tablets was not associated with any other clinically significant adverse clinical observations, gross necropsy or histopathological changes.
COMFORTIS is a chewable tablet and is readily consumed by dogs when offered by the owner just prior to feeding. Alternatively, COMFORTIS chewable tablets may be offered in food or administered like other tablet In a reproductive safety study, COMFORTIS chewable tablets were administered orally to female Beagles at 1.3 medications. COMFORTIS chewable tablets should be administered at monthly intervals. and 4.4 times the maximum recommended therapeutic dose every 28 days prior to mating, during gestation, and during a six-week lactation period. No treatment-related adverse effects were noted for conception rates in the If vomiting occurs within an hour of administration, redose with another full dose. If a dose is missed, administer dams, or for mortality, body temperature, necropsy, or histopathology findings for the dams or puppies. One dam COMFORTIS chewable tablets with food and resume a monthly dosing schedule. from each treatment group experienced early pregnancy loss and one additional high dose dam aborted late term. Treatment with COMFORTIS chewable tablets may begin at any time of the year, preferably starting one month The treated dams experienced more vomiting, especially at one hour post-dose, than the control dams. Puppies before fleas become active and continuing monthly through the end of flea season. In areas where fleas are from dams treated at 1.3 times the maximum recommended therapeutic dose had lower body weights than common year-round, monthly treatment with COMFORTIS chewable tablets should continue the entire year puppies from control dams. Although puppy mortality between treated and control dams was not different, the puppies from the treated dams experienced more lethargy (4.4X group only), dehydration, weakness and felt cold To minimize the likelihood of flea reinfestation, it is important to treat all animals within a household with an to the touch (4.4X group only) than puppies from control dams.
A pilot study without a control group was conducted to analyze milk from three lactating dogs treated with an Contraindications:
experimental formulation of spinosad at 1.5 times the maximum recommended dose administered at day 28 of There are no known contraindications for the use of COMFORTIS chewable tablets.
gestation and 24 hours prior to parturition. The data demonstrated that spinosyns were excreted in the milk of Warnings:
these dogs. Mortality and morbidity were greatest in puppies from the dam with the highest spinosyns level in milk. Not for human use. Keep this and all drugs out of the reach of children.
The spinosad milk: reference plasma exposure ratio calculated from this study ranged from 2.2 to 3.5.
Serious adverse reactions have been reported following concomitant extra label use of ivermectin with In well-controlled field studies, COMFORTIS chewable tablets were administered safely in conjunction with other COMFORTIS (see POST APPROVAL EXPERIENCE).
frequently used veterinary products, such as vaccines, anthelmintics, antibiotics, steroids, flea and tick control products, anesthetics, NSAIDs, antihistamines, alternative/herbal remedies, shampoos, and prescription diets. Precautions:
Changes in hematology, clinical chemistry and urinalysis values were compared pre-and post-study and were COMFORTIS chewable tablets are for use in dogs and puppies 14 weeks of age and older (see ANIMAL SAFETY).
Use with caution in breeding females (see ANIMAL SAFETY). Use with caution in dogs with pre-existing epilepsy
Storage Information:
(see ADVERSE REACTIONS). The safe use of COMFORTIS chewable tablets in breeding males has not been
Store at 20-25°C (68 -77°F), excursions permitted between 15 to 30°C (59 to 86°F).
evaluated.
Adverse Reactions:
How Supplied:
In a well-controlled US field study, which included a total of 470 dogs (330 dogs treated with COMFORTIS COMFORTIS chewable tablets are available in five flavored tablet sizes: 140, 270, 560, 810 or 1620 mg. chewable tablets and 140 dogs treated with an active control), no serious adverse reactions were observed with Each tablet size is available in color-coded packages of 6 tablets.
COMFORTIS chewable tablets. All reactions were regarded as mild and did not result in any dog being removed Over the 90-day study period, all observations of potential adverse reactions were recorded. Reactions that occurred at an incidence > 1% within any of the 3 months of observation are presented in the following table. The Lilly Corporate Center, Indianapolis, IN 46285 most frequently reported adverse reaction in dogs in the COMFORTIS chewable tablets and active control groups was vomiting. The occurrence of vomiting, most commonly within 48 hours after treatment, decreased with repeated doses of COMFORTIS chewable tablets. NDC 0986-4222-06NDC 0986-4223-06NDC 0986-4224-06 Percentage of Dogs (%) with Adverse Reactions COMFORTIS
COMFORTIS
COMFORTIS
Chewable
Chewable
Chewable
(N=139a)
a This number (n=139) is less than the total number of dogs in the safety population for the active control group (n=140) because one dog joined the study late and was only dosed at Month 3.

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