Chloromed 150 mg/g Premix for Medicated Feeding Stuff for Calves
Active ingredient: Chlortetracycline Hydrochloride
Form
Premix
Species
Manufacturer
Univet Limited
VMD MA No.
05150/4000
What it's used for
Calves The product is indicated in the treatment of respiratory disease in calves caused by Pasteurella spp., sensitive to chlortetracycline.
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Prescription required
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Chloromed 150 mg/g Premix for Medicated Feeding Stuff for Calves — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 26 Mar 2026.
The product is indicated in the treatment of respiratory disease in calves caused by
Pasteurella spp., sensitive to chlortetracycline.
medicate feed.
Administration:
The recommended therapeutic dose is 20 mg per kg bodyweight daily i.e. 20 grams
of Chloromed 150 mg/g Premix per 150 kg bodyweight.
For the preparation of the medicated feed the body weight of the animals to be
treated and their actual intake of feed should be taken into account. To ensure the
correct dosage and to avoid under-dosing, the body weight should be determined as
accurately as possible. The required dose should be measured by suitably calibrated
weighing equipment. During the treatment period, only feed medicated with the
product should be supplied. To provide the required amount of active substance per
kg medicated feed the premix has to be incorporated into the feed according to the
following formula:
feedofkgChloromed/mg...
)(kg/animalintakefeeddaily Average
treatedbe toanimalsof(kg)bwAveragebw/day x kgChloromed/mg...
Treatment should be continued for a period of seven days. If animals don’t recover
within 3 days after oral medication, diagnosis should be reconsidered and treatment
should be changed, if necessary.
Revised: September 2014
AN: 01768/2013Page 4 of 6
The uptake of medicated feed depends on the clinical condition of the animals. In
order to achieve the correct dosage the chlortetracycline inclusion rate in feed should
be adjusted for feed intake.
Pelleting should not be conducted at temperatures in excess of 70°C.
Do not use in animals with known hypersensitivity to tetracycline.
Do not use in animals with severe liver and renal disorders.
be discontinued.
On rare occasions the following adverse reactions may occur: allergic reactions and
photosensitivity; gastrointestinal disorders; disorders of the liver and the kidneys. If
suspected adverse reactions occur, treatment should be discontinued.
Due to the possible incorporation of chlortetracycline, treatment of pregnant and
newborn animals can lead to dysfunctional development of the skeleton and teeth in
foetal and growing animals.
In case of insufficient uptake of feed, animals should be treated parenterally.
Revised: September 2014
AN: 01768/2013Page 2 of 6
Special precautions for use in animals
Use of the product should be based on susceptibility testing and take into account
official and local antimicrobial policies.
Inappropriate use of the product may increase the prevalence of bacteria resistant to
chlortetracycline and may decrease the effectiveness of treatment with related
substances, due to the potential for cross-resistance.
Long term use of this product is not recommended as it may lead to the development
of bacterial resistance.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals
Handle this product with care to avoid exposure when incorporating into feed and
administering medicated feed to the animals.
Take adequate measures to avoid dust formation when incorporating the veterinary
medicinal product into feed.
Persons handling the product should do so in a mechanically ventilated area.
Wear either a disposable half-mask respirator conforming to European Standard
EN149 or a non-disposable respirator to European Standard EN 140 with a filter to
EN 143.
Wear protective gloves, overalls and approved safety glasses.
Direct contact of the veterinary medicinal product with the skin, the eyes and the
mucous membranes should be avoided. In case of accidental exposure rinse
abundantly with water.
Do not smoke, eat or drink when handling the veterinary medicinal product
Other precautions
None.
medication.
Do not incorporate the product in feed overloaded with polyvalent cations such as
Ca
2+
and Fe
3+
because the formation of chlortetracycline complexes with these
cations is possible.
Do not administer together with antacids, kaolin and iron preparations and in
conjunction with bactericidal antibiotics like beta-lactams.
The product should not be used in case of known resistance to other tetracyclines.
Store in a dry place.
Store in the original container.
Protect from light.
Meat and offal: 35 days.
Milk: The product is contraindicated for use in adult ruminants and dairy cows and
should therefore not be used in animals producing milk for human consumption.
5.
This information is sourced from the official Summary of Product Characteristics (SPC) published by the Veterinary Medicines Directorate (VMD). It is provided for informational purposes only and does not replace professional veterinary advice. Always consult your vet before administering any medication.
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Related Conditions
Other Products Containing Chlortetracycline Hydrochloride
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Animedazon Spray, 2.45 % w/w Cutaneous Spray Suspension for Cattle, Sheep and Pigs
POM-VaniMedica GmbH
Animedazon Spray, 2.45 % w/w Cutaneous Spray Suspension for Cattle, Sheep and Pigs
POM-VaniMedica GmbH
Aurofac Granular 100 mg/g Premix for Medicated Feeding Stuff
POM-VPhibro Animal Health (Poland) Sp z.o.o.
Aurofac Granular 100 mg/g Premix for Medicated Feeding Stuff
POM-VPhibro Animal Health (Poland) Sp z.o.o.
Aurofac Granular 250 mg/g Premix for Medicated Feeding Stuff
POM-VPhibro Animal Health (Poland) Sp z.o.o.
Aurofac Granular 250 mg/g Premix for Medicated Feeding Stuff
POM-VPhibro Animal Health (Poland) Sp z.o.o.
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