Neomectin

Description

Neomectin

Composition: 1 ml solution for injection contains:

Ivermectin 10 mg

Indications: Treatment and control of parasitic infections of cattle, sheep and pigs,

caused by larval and adult forms of endo and ectoparasites sensitive to ivermectin:

Cattle: gastrointestinal nematodes adult and L4 stages of – Ostertagia ostertagi,

Ostertagia lyrata, Haemonchus placei, Trichostrongylus axei, Trichostrongylus

colubriformis, Cooperia oncofora, Cooperia punctata, Bunostomum phlebotomum,

Oesophagostomum radiatum, and asult forms of Strongyloides papillosus, Nematodirus

helvetianus, Nematodirus spathiger and Trichuris spp. Pulmonal nematodes:

Dictyocaulus viviparus(adult and L4 stages), a parasite of the eye-Thelazia spp.,parasite

of the skin – Hypoderma bovis and H.lineatum, mites – Psoroptes bovis and Sarcoptes

scabiei var.bovis, lice -Linognathus vituli, Haematopinus euyzsternus.

Sheep: gastrointestinal nematodes , adult and L4 stages- Ostertagia circumcinata,

Haemonchus contortus, Trichostrongylus axei, Trichostrongylus colubriformis, Trichuris

vitrinus, Cooperia curticei, Oesophagostomum venulosum, O.columbiatum, Nematodirus

filicollis, Chabertia ovina, Trichuris ovis, pulmonal nematodes – Dyctiocaulus filaria (adult

and L4 stages) Protostrongylus rufescens (only adult forms), mites -Psoroptes ovis and

warble Oestrus ovis (all larval stages).

Swine: gastrointestinal nematodes, adult and 4L stages- Ascaris suum, Hyostrongylus

rubidus, Oesophagostomum spp., larval and somatic stages Strongyoides ransomi,

pulmonal nematodes -Metastrongylus spp. (adult), mites- Haematopinus suis, lice-

Sarcoptes scabiei var.suis.

Contraindications: The product is not given to cows and sheep during lactation whose

milk is used for human consumption, or 60 days before calving and lambing. Do not give

to animals that are hypersensitive to the active drug component.

It is not given to animals that are hypersensitive to the active ingredient of the drug. It is

not given to sick and cachectic animals.

The product must not be administered intravenously and intramuscularly.

The product is not administered to animal species for which it is not indicated because it

can cause serious disorders and even death

Side effects: The application site may be transient pain and swelling.

If you notice any serious or any other side effects not listed in this leaflet, notify your

veterinarian.

Target species: Cattle, sheep, and pigs.

Dosage and method of administration:

For subcutaneous use.

The drug is administered once (or below the specified protocol in cows and sheep),

subcutaneously at a dose of cattle and sheep is 0.2 mg ivermectin / kg bw, and pigs 0.3

mg ivermectin / kg bw

Medicine applie in the following volumes:

Cattle: 1 ml / 50 kg TM

Sheep: 0.5 mL / 25 kg T.M.

Pigs: 1 mL / 33 kg T.M.

In order to properly dose the medicine, it is important to more accurately determine body

mass of animals.

If the animals are treated in groups, rather than individually, it is necessary to form

groups according to their body weight, to avoid their potentially subdosage or overdose

of the drug.

In the treatment of young pigs and lambs, especially those whose body weight exceeds

16 kg, especially pay attention to the precise dosage.It is advisable to use syringes

smaller volume with increments of 0.1 mL. At pigs with body weight below 16 kg given

0.1 ml of drug / kg body weight 3 or lambs 0.1 mL of drug / 5 kg bw

Herds do not give more than 10 ml of the drug per injection site.

In order to optimally protect cattle out to pasture, the treatment of this preparation should

be done 3, 8 and 13 weeks after release the stall.

For effective control of the itch induced by sheep Psoroptes ovis, on two occasions it is

necessary to treat an interval of 7 days. It is necessary to be treated all the sheep that

have been in contact with infected sheep. At least 7 days after treatment must prevent

contact between the treated and untreated infected herds due to the possibility of

infection transmission.

Instructions for proper use of drugs:

Do not give the drug intravenously and intramuscularly.The drug should not be used in

animals for which is not indicated. The more accurately determine the weight of the

animal before calculating the dosage. In young pigs, especially those whose weight not

exceeds 16 kg, pay attention to the precise dosage. It is preferable to use syringes,

small volume, with tick marks of 0.1 ml.

Cattle should not be given more than 10 ml of drug per injection site.

Withdrawal period: Cattle (meat and intestines): 49 days

Cattle (milk): Not to be used in laktciji cows whose milk is used in human nutrition. Do

not use in pregnant cows and heifers for at least 60 days prior to calving.

 

Sheep (meat and intestines): 42 days

Sheep (milk): Do not use in lactating sheep whose milk is used in human nutrition. Do

not use in pregnant sheep at least 60 days prior to lambing.

Pigs (meat and intestines): 28 days

Special considerations:

For use in animals.

Use during pregnancy and lactation

The drug is in all the target species can be used during pregnancy and lactation, with

restrictions applying to animals whose milk is used in human consumption listed in

Chapter 10. Waiting period.

Special warnings for persons administering veterinary medicinal product to

animals

In applying the drug should avoid direct contact with skin or mucous membranes, or

eyes. Do not eat, drink or smoke while handling the drug. After each administration to

wash your hands. Take into account to avoid accidental self-injection of the drug.

Special precautions for disposal and destruction of drug

Unused drug or drug residues shall be destroyed in accordance with applicable

regulations.

Special considerations for storing drugs: Store in original container below 25 ° C, out

of reach of children.

Shelf life: 2 years in original packaging.

Shelf life after opening: 28 days

Method of issuance: On prescription of veterinarian.

ATCvet code: QP54AA01

Packaging: Bottle of 20 mL, 50 mL, 100 mL and 250 mL.

Number and date of registration:

20ml 323-01-00579-14 date 04.08.2015.

50 ml 323-01-00580-14 date 04.08.2015.

100ml 323-01-00581-14 date 04.08.2015.

250ml 323-01-00582-14 date 04.08.2015.

Producer: “FM Pharm”, Subotica, 024/548-130