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Tianjin Zhongsheng Glory Technology Co.,Ltd

Business Type:Manufacturer

Country/Region:China

Ddu Verified

HOT Rank

6/10

Product Information

Description

Ivermectin +Pirantel +Praziquantel Chewable Tablet

Composition:

Each chewable tablet contains 0.06 mg ivermectin,

144 mg pyrantel as pamoate salt and 50 mg praziquantel.

Indications:

For use in dogs to prevent canine heartworm disease by eliminating the tissue stage of heartworm larvae (Dirofilaria immitis) for a month (30 days) after infection and for the treatment and control of roundworms (Toxocara canis, Toxascaris leonina), hookworms (Ancylostoma caninum, Uncinaria stenocephala, Ancylostoma braziliense), and tapeworms (Dipylidium caninum, Taenia pisiformis).

Dosage:

(ivermectin/pyrantel pamoate/praziquantel) should be administered orally at monthly intervals at the recommended minimum dose level of 6 mcg of ivermectin per kilogram (2.72 mcg/lb), 5 mg of pyrantel (as pamoate salt) per kg (2.27 mg/lb) and 5 mg of praziquantel per kg (2.27 mg/lb) of body weight, as follows:

Dog Weight Lbs

Chewable Tablet per Month

Tablet Size

Ivermectin Content

Pyrantel Pamoate Content

Praziquantel Content

6.0 to 12

1

Toy

60 mcg

144mg

50 mg

12.1 to 25

1

Small

68 mcg

57 mg

57 mg

25.1 to 50

1

Medium

136 mcg

114 mg

114 mg

50.1 to 100

1

Large

272 mcg

228 mg

228 mg

 

Warning:

For use in dogs only. Keep this and all drugs out of reach of children.

Precaution:This product is recommended for dogs 8 weeks of age and older. For dogs over 100 lbs, use the appropriate combination of these chewable tablets.

Administration:

Remove only one tablet at a time from the foil-backed blister card. Return the remaining tablets to their box to protect the product from light. It can be offered to the dog by hand or be added intact to a small amount of dog food. Care should be taken that the dog consumes the complete dose, and the dog should be observed for a few minutes after administration to ensure that part of the dose is not lost or rejected. If it is suspected that any of the dose has been lost, redosing is recommended.

It should be given at monthly intervals during the period of the year when mosquitoes (vectors), potentially carrying infective heartworm larvae, are active. The initial dose must be given within a month (30 days) after the dog's first exposure to mosquitoes. The final dose must be given within a month (30 days) after the dog's last exposure to mosquitoes.

When replacing another heartworm preventive product in a heartworm disease prevention program, the first dose of this product must be given within a month (30 days) of the last dose of the former medication. A heartworm test should be performed prior to switching heartworm preventive products.

If the interval between doses exceeds a month (30 days), the efficacy of ivermectin can be reduced. Therefore, for optimal performance, the tablet must be given once a month on or about the same day of the month. If treatment is delayed, whether by a few days or many, immediate treatment with this product and resumption of the recommended dosing regimen will minimize the opportunity for the development of adult heartworms.

 

Use with caution in sick, debilitated, or underweight animals and dogs weighing less than 10 lbs .The safe use of this drug has not been evaluated in pregnant or lactating bitches.

All dogs should be tested for existing heartworm infection before starting treatment with this drug, which is not effective against adult D. immitis. Infected dogs should be treated to remove adult heartworms and microfilariae before initiating a heartworm prevention program.

While some microfilariae may be killed by the ivermectin in this drug at the recommended dose level, this drug is not effective for microfilariae clearance. A mild hypersensitivity-type reaction, presumably due to dead or dying microfilariae and particularly involving a transient diarrhea, has been observed in clinical trials with ivermectin alone after treatment of some dogs that have circulating microfilariae.

Adverse reaction:

Self-limiting adverse reactions including lethargy, limpness, salivation, shaking, diarrhea, decreased appetite, licking lips, and belching were reported between 20 minutes and 72 hours following treatment in a field study with this drug.

In clinical field trials with ivermectin/pyrantel pamoate, vomiting or diarrhea within 24 hours of dosing was rarely observed (1.1% of administered doses). The following adverse reactions have been reported following the use of ivermectin: depression/lethargy, vomiting, anorexia, diarrhea, mydriasis, ataxia, staggering, convulsions and hypersalivation.

Storage:

Store at 20°C-25°C (68°F-77°F), excursions permitted between 15°C-30°C (59°F-86°F). Protect product from light.

Package:  5 chewable tablets/blister, 10 blister/ box.

 


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