Pulmovet 250 mg/ml Solution for Use in Drinking Water/Milk for Cattle, Pigs, Chickens and Turkeys
Active ingredient: Tilmicosin
Form
Solution
Species
Manufacturer
Dopharma Research B.V.
VMD MA No.
28365/3003
What it's used for
susceptible to tilmicosin. Pigs: For the treatment and metaphylaxis of respiratory disease associated with Pasteurella multocidaActinobacillus pleuropneumo...
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Pulmovet 250 mg/ml Solution for Use in Drinking Water/Milk for Cattle, Pigs, Chickens and Turkeys — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Pigs: For the treatment and metaphylaxis of respiratory disease associated with
Pasteurella multocidaActinobacillus pleuropneumoniae and Mycoplasma hyopneumoniae
susceptible to tilmicosin.
Chickens: For the treatment and metaphylaxis of respiratory disease associated with
Mycoplasma gallisepticum and M. synoviae susceptible to tilmicosin.
Turkeys: For the treatment and metaphylaxis of respiratory disease associated with
Mycoplasma gallisepticum and M. synoviae susceptible to tilmicosin.
The presence of the disease in the group/flock must be established before the veterinary
medicinal product is used.
Calves: 12.5 mg tilmicosin/kg body weight (i.e.1 ml of veterinary medicinal product per 20
kg BW), twice daily, for 3-5 consecutive days.
Pigs: 15-20 mg tilmicosin/kg body weight/day (i.e. 6-8 ml of veterinary medicinal product
per 100 kg of BW per day), for 5 consecutive days, which may be achieved by the
inclusion of 200 mg of tilmicosin per litre (80 ml of veterinary medicinal product per 100
litres).
Chickens: 15-20 mg tilmicosin/kg body weight/day (i.e. 6-8 ml of veterinary medicinal
product per 100 kg of BW per day), for 3 consecutive days, which may be achieved by the
inclusion of 75 mg of tilmicosin per litre (30 ml of veterinary medicinal product per 100
litres).
Turkeys: 10-27 mg tilmicosin/kg body weight/day (i.e. 4-11 ml of veterinary medicinal
product per 100 kg of BW per day), for 3 consecutive days, which may be achieved by the
inclusion of 75 mg of tilmicosin per litre (30 ml of veterinary medicinal product per 100
litres).
Based on the recommended dose and the number and weight of animals to be treated, the
exact daily concentration of the veterinary medicinal product should be calculated
according to the following formula:
ml veterinary medicinal product per litre of drinking water = [ml veterinary medicinal
product per kg body weight per day x average body weight (kg) of animals to be treated] /
average daily water intake (l/animal).
One 960 ml bottle of veterinary medicinal product is sufficient to medicate 1200 litres of
drinking water for pigs or 3200 litres of drinking water for chickens or turkeys. One 5040 ml
can is sufficient to medicate 6300 litres of drinking water for pigs or 16800 litres of drinking
water for chickens or turkeys.
One 960 ml bottle and 5040 ml can of veterinary medicinal product are sufficient to
medicate in milk replacer respectively 48 to 80 and 252 to 420 veal calves each of 40 kg
body weight depending on the duration of treatment.
To ensure a correct dosage, body weight should be determined as accurately as possible.
The required dose should be measured using suitably calibrated measuring equipment.
Only sufficient medicated drinking water should be prepared to cover the daily
requirements.
The medicated water should be the only source of drinking water for the animals for the
entire duration of the treatment period.
Water intake should be monitored at frequent intervals during medication.
After the end of the medication period, the water supply system should be cleaned
appropriately to avoid intake of sub-therapeutic amounts of the active substance.
Medicated drinking water should be prepared fresh every 24 hours. Medicated milk
replacer should be prepared fresh every 6 hours.
The veterinary medicinal product should be diluted with water or milk replacer prior to its
use and the concentration of the prediluted solution should not exceed 200 ml of veterinary
medicinal product/litre (i.e. 1 in 5). The lowest concentrations of the veterinary medicinal
product at which stability can be assured are 0.3 ml veterinary medicinal product/litre
drinking water and 0.7 ml veterinary medicinal product/litre milk replacer.
The intake of medicated water/milk replacer depends on the clinical condition of the
animals. In order to obtain the correct dosage, the concentration of tilmicosin may need to
be adjusted accordingly.
Do not use in cases of hypersensitivity to the active substance or to any of the excipients.
Very rare
(<1 animal / 10,000 animals
treated, including isolated
reports):
Decreased drinking
Reporting adverse events is important. It allows continuous safety monitoring of a
veterinary medicinal product. Reports should be sent, preferably via a veterinarian, to
either the marketing authorisation holder or the national competent authority via the
national reporting system. See the label for respective contact details.
Pigs, chickens and turkeys: Water consumption should be monitored in order to guarantee
adequate dosing. In case water consumption does not match quantities for which
recommended concentrations were calculated, the concentration of the veterinary
medicinal product has to be adapted in a way that the recommended dosage will be taken
up by the animals or different medication should be considered.
The uptake of medication by animals can be altered as a consequence of illness. In case
of insufficient uptake of water or milk replacer, animals should be treated parenterally
using an appropriate injectable product.
Repeated use of the veterinary medicinal product should be avoided by improving
management practices and thorough cleansing and disinfection.
Use of the veterinary medicinal product deviating from the instructions given in the SPC
may increase the prevalence of bacteria resistant to tilmicosin and may decrease the
effectiveness of treatment with other macrolides, lincosamides and streptogramin B due to
the potential for cross-resistance.
Special precautions for safe use in the target species:
For oral use only. Contains disodium edetate; do not inject.
Use of the veterinary medicinal product should be based on susceptibility testing of the
bacteria isolated from the animal. If this is not possible, therapy should be based on local
(regional, farm level) epidemiological information about susceptibility of the target bacteria.
Official, national and regional antimicrobial policies should be taken into account when the
veterinary medicinal product is used.
Special precautions to be taken by the person administering the veterinary medicinal
product to animals:
Tilmicosin may induce irritation. Macrolides, such as tilmicosin, may also cause
hypersensitivity (allergy) following injection, inhalation, ingestion or contact with skin or
eye. Hypersensitivity to tilmicosin may lead to cross reactions to other macrolides and vice
versa. Allergic reactions to these substances may occasionally be serious and therefore
direct contact should be avoided.
To avoid exposure during preparation of the medicated drinking water or milk replacer,
wear overalls, safety glasses, and impervious gloves. Do not eat, drink or smoke when
handling this veterinary medicinal product. Wash hands after use.
In case of accidental ingestion, wash out mouth immediately with water, seek medical
advice and show the package leaflet or the label to the physician. In the event of
accidental skin contact, wash thoroughly with soap and water. In case of accidental eye
contact, flush the eyes with plenty of clean, running water.
Do not handle the veterinary medicinal product if you are allergic to ingredients in the
veterinary medicinal product.
If you develop symptoms following exposure, such as skin rash, you should seek medical
advice and show the physician this warning. Swelling of the face, lips and eyes or difficulty
in breathing are more serious symptoms and require urgent medical attention.
Special precautions for the protection of the environment:
Not applicable.
Do not use simultaneously with bacteriostatic antimicrobial agents.
Pigs: meat and offal: 14 days.
Chickens: meat and offal: 12 days.
Turkeys: meat and offal: 19 days.
Not authorised for use in animals producing milk for human consumption.
Not for use in birds producing eggs for human consumption. Do not use within 2 weeks
before the start of the laying period.
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 Tilmicosin
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Apotil 300 mg/ml Solution for Injection
POM-VNimrod Nederland B.V.
Apotil 300 mg/ml Solution for Injection
POM-VNimrod Nederland B.V.
Hymatil 300 mg/ml Solution for Injection for Cattle and Sheep
POM-VIndustrial Veterinaria SA
Micotil 300 mg/ml Solution for Injection
POM-VElanco Europe Ltd
Milbotyl 300 mg/ml Solution for Injection for Cattle and Sheep
POM-VChanelle Pharmaceuticals Manufacturing Ltd
Pulmotil AC 250 mg/ml Concentrate for Oral Solution for Use in Drinking Water or Milk Replacer
POM-VElanco Europe Ltd
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