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Equimax® Ivermectin 1.87% & Praziquantel 14.03% Oral Paste Horse Wormer

$18.95

SKU: 6405 Manufacturer: Bimeda
Description
  •  (ivermectin 1.87%/praziquantel 14.03%) is a broad spectrum parasite, bot and tapeworm control. It is safe to use in foals as early as 4 weeks of age, pregnant and lactating mares, and breeding stallions.
  • Apple flavored
  • A smooth, quick-dissolving paste
  • Broad spectrum activity against a wide range of parasites
  • Proven safe in horses of all ages
  • A single syringe contains enough active ingredients to treat horses weighing up to 1,320 lb
  • Easy-to-use-and-handle syringe/applicator for more accurate dosing

WARNING! NOT APPROVED FOR HUMAN USE!

Warning from the Manufacturer

COVID-19 ALERT CONCERNING IVERMECTIN PRODUCTS: WARNING! A number of products including Duramectin Equine Dewormer, Ivermectin Equine Dewormer, Ivermax Equine Dewormer, Ivermectin Sheep Drench, Ivermectin Pour On, Vetrimec Injection, Ivermax Injection, Agri-Mectin Injection, Ivermectin Injection and Ivermectin Plus Injection contain the anti-parasite ingredient Ivermectin. Despite media reports that Ivermectin could potentially be used to treat people with COVID-19, these products are not safe or approved for human use, which could cause severe personal injury or death.

42 in stock

Description

Anthelmintic and Boticide
FOR ORAL USE IN HORSES ONLY
For the treatment and control of worms and bots in horses with a single dose.
Safe for horses 4 weeks of age and older. Contents will treat up to 1320 lb body weight.
Net Weight: 0.225 oz (6.42 g)

INDICATIONS: Consult your veterinarian for assistance in the diagnosis, treatment and control of parasitism. EQUIMAX (ivermectin/praziquantel) Oral Paste is indicated for the treatment and control of the following parasites:
Tapeworms
Anoplocephala perfoliata
Large Strongyles (adults)
Strongylus vulgaris (also early forms in blood vessels)
S. edentatus (also tissue stages)
S. equinus
Triodontophorus spp.
Small Strongyles (adults, including those resistant to some benzimidazole class compounds)
Cyathostomum spp.
Cylicocyclus spp.
Cylicostephanus spp.
Cylicodontophorus spp.
Small Strongyles (fourth-stage larvae)
Pinworms (adults and fourth-stage larvae)
Oxyuris equi
Ascarids (adults and third- and fourth-stage larvae)
Parascaris equorum
Hairworms (adults)
Trichostrongylus axei
Large-mouth Stomach Worms (adults)
Habronema muscae
Bots (oral and gastric stages)
Gasterophilus spp.
Lungworms (adults and fourth-stage larvae)
Dictyocaulus arnfieldi
Intestinal Threadworms (adults)
Strongyloides westeri
Summer Sores caused by Habronema and Draschia spp. cutaneous third-stage larvae
Dermatitis caused by Neck Threadworm microfilariae, Onchocerca sp.

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Ingredients / Material How to Use
  • Equimax contains 1.87% Ivermectin and 14.03% Praziquantel

DOSAGE AND ADMINISTRATION: This syringe contains sufficient paste to treat one 1320-lb horse at the recommended dose rate of 91 mcg ivermectin per lb (200 mcg/kg) and 0.68 mg praziquantel per lb (1.5 mg/kg) of body weight. Each weight marking on the syringe plunger delivers enough paste to treat 220 lb (100 kg) of body weight.

  1. While holding plunger, turn the knurled ring on the plunger 1/4 turn to the left and slide it so the side nearest the barrel is at the prescribed weight marking.
  2. Lock the ring in place by making a 1/4 turn to the right.
  3. Make sure that the horse’s mouth contains no feed.
  4. Remove the cover from the tip of the syringe.
  5. Insert the syringe tip into the horse’s mouth at the space between the teeth.
  6. Depress the plunger as far as it will go, depositing paste on the back of the tongue.
  7. Immediately raise the horse’s head for a few seconds after dosing.

Do not underdose. Ensure each animal receives a complete dose based on a current body weight. Underdosing may result in ineffective treatment, and encourage the development of parasite resistance.

SAFETY: EQUIMAX Oral Paste may be used in horses 4 weeks of age and older. Stallions and breeding, pregnant or lactating mares may be treated without adverse effects on fertility.

In a tolerance study in which 3- to 4-week-old foals were treated at 10X once, loose watery stools were observed on post-treatment days 1, 2, and 5-9 in one foal. These signs resolved without treatment by day 10, and no other foals were affected.

In a reproductive safety study, eleven mares were treated with a 3X dose of EQUIMAX Oral Paste every two weeks throughout breeding, pregnancy and lactation, up until the foal was three months of age. Ten mares served as controls and were treated with the vehicle paste in a similar manner. An increased incidence of colic was observed in treated mares as compared to control mares. In addition, elevations of GGT and AST were more frequent in the 3X treated mares, and in two mares these enzymes were elevated at the time of colic episodes.

One treated mare was dropped from the study because she did not conceive after three breeding attempts.

Two treated mares had abnormally short diestrous periods of two days and eight days on the first estrous cycle following the birth of the study foal. In addition, one of these two mares failed to ovulate in the second and third estrous cycles.

In the first few weeks of life, foals born to the 3X treated mares had a higher incidence of transient ocular discharge and gastrointestinal disturbances (loose stools, diarrhea) and depression requiring medical intervention as compared to foals born to control mares.

PRECAUTIONS: EQUIMAX Oral Paste has been formulated specifically for use in horses and ponies only. This product should not be used in other animal species as severe adverse reactions, including fatalities in dogs, may result.

WARNING: Do not use in horses intended for human consumption.

HUMAN WARNINGS: Not for use in humans. Keep this and all drugs out of the reach of children. Refrain from eating or smoking when handling. Wash hands after use. Avoid contact with eyes. The Safety Data Sheet (SDS) contains more detailed occupational safety information. To report adverse reactions in users, to obtain more information, or to obtain a SDS, contact Bimeda Inc. at 1-888-524-6332.

ENVIRONMENTAL WARNINGS: Ivermectin and excreted ivermectin residues may adversely affect aquatic organisms. Do not contaminate ground or surface water. Dispose of the syringe in an approved landfill or by incineration.

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