ReproCyc PRRS EU Lyophilisate and Solvent for Suspension for Injection for Pigs
Active ingredient: Porcine respiratory and reproductive syndrome virus
Form
Injection
Species
Manufacturer
Boehringer Ingelheim Vetmedica GmbH
VMD MA No.
61700/3018
What it's used for
Onset of immunity: 4 weeks. Duration of immunity: 17 weeks. Vaccination of breeding females according to the recommended schedule described in section 4.9...
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ReproCyc PRRS EU Lyophilisate and Solvent for Suspension for Injection for Pigs — SPC Details
Source: VMD Summary of Product Characteristics (SPC). Last updated 27 Mar 2026.
Duration of immunity: 17 weeks.
Vaccination of breeding females according to the recommended schedule
described in section 4.9 reduces the negative reproductive disorders associated
with PRRSV.
Under experimental challenge conditions a reduction in transplacental virus
transmission after challenge was additionally demonstrated. In piglets from
vaccinated sows, a reduction in the negative impact of PRRS virus infection
(mortality, clinical signs and weight gain) was also demonstrated during the
first 20 days of life.
For reconstitution, transfer the entire content of the solvent vial to the vial
containing the lyophilisate and reconstitute the lyophilisate as follows: 10 doses
in 20 ml, 50 doses in 100 ml and 100 doses in 200 ml of the solvent.
Ensure that the lyophilisate is completely reconstituted before use.
Visual appearance after reconstitution: clear, colourless suspension.
Avoid introduction of contamination during use.
Use sterile equipment.
Avoid multiple broaching, for example by using automatic injectors
Regime of vaccination:
Gilts: for protection against PRRSV during pregnancy vaccination is
recommended before integration into the sow herd between 2
and 5 weeks prior to breeding. Gilts can then be subjected to the
same vaccination programme as the sow herd.
Sows: it is recommended to vaccinate pregnant and non-pregnant sows
every 3 to 4 months.
Mixing with ReproCyc ParvoFLEX:
The full content of one vial of ReproCyc ParvoFLEX should be used to
reconstitute the lyophilisate of one vial of ReproCyc PRRS EUReproCyc
ParvoFLEX hereby replaces the solvent of ReproCyc PRRS EU.
Ensure that the lyophilisate is completely reconstituted before use.
Administer a single dose (2 ml) of the mixture intramuscularly.
The following corresponding presentations (doses) can be mixed:
ReproCyc PRRS EU (lyophilisate)ReproCyc ParvoFLEX10 doses10 doses (20 ml)50 doses50 doses (100 ml)100 doses100 doses (200 ml)
The package leaflet of ReproCyc ParvoFLEX should also be consulted before
the administration of the mixed product.
Do not use in boars producing semen for naïve herds, as PRRSV can be shed
in semen
Do not use in PRRS naïve herds in which the presence of PRRSV has not been
established using reliable diagnostic methods.
Common
(1 to 10 animals / 100 animals
treated):
Injection site reaction (injection site
swelling; injection site reddening)
Decreased appetite, elevated
temperature
Uncommon
(1 to 10 animals / 1 000 animals
treated):
Increased respiratory rate
,
Recumbency
1
Very minimal (up to 10.5 cm but typically < 2 cm in size), subside within a
short time (maximum of 5 days but typically less than 2 days) without treatment.
Increase up to 2°C above the physiological range up to 5 days post-
vaccination. Temperatures return to the normal range without additional
treatment 1 to 4 days after the maximum temperature increase is observed.
On the day of vaccination and disappears spontaneously without any
treatment.
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 package leaflet
for respective contact details.
Precautions should be taken to avoid the transfer of the vaccine virus within
the herd, e.g. from positive animals to naïve animals.
Special precautions for safe use in the target species:
The vaccine strain may spread up to 5 weeks after vaccination to unvaccinated
animals in contact but without any clinical consequence. Vaccinated animals
may excrete the vaccine strain by faecal excretion. The potential excretion of the
vaccine strain in the urine of vaccinated animals has not been investigated.
The vaccine strain has been detected in new-born piglets (blood, lung
samples) when vaccinating gilts during last third of gestation but without
any clinical consequence.
Care should be taken to avoid spread of vaccine virus from vaccinated animals
to unvaccinated animals that should remain free from PRRS virus.
Vaccination should aim to achieve a homogenous immunity in the target
population at farm level.
PRRS virus-naïve breeding animals (e.g. replacement gilts from PRRS virus-
negative herds) which are introduced into a PRRSV-infected herd should be
vaccinated prior to first insemination. Vaccination should preferably be done in
a separated quarantine unit. A transition period should be respected between
vaccination and moving the animals to the breeding unit. This transition period
should be longer than the shedding phase of the PRRS MLV vaccine following
vaccination.
Do not routinely rotate two or more commercial PRRS MLV vaccines based on
different strains in a herd. A PRRS vaccine based on the same strain (strain
94881) and authorised for the immunisation of pigs from 17 days of age until the
end of fattening and older can be used on the same farm.
In order to limit the potential risk of recombination between PRRS MLV vaccine
strains of the same genotype, do not use different PRRS MLV vaccines based
on different strains of the same genotype on the same farm at the same time.
In the case of transitioning from one PRRS MLV vaccine to another PRRS MLV
vaccine, a transition period should be respected between the last administration
of the current vaccine and the first administration of the new vaccine. This
transition period should be longer than the shedding period of the current
vaccine following vaccination.
Special precautions to be taken by the person administering the veterinary
medicinal product to animals:
In case of accidental self-injection, seek medical advice immediately and show
the package leaflet or the label to the physician.
Special precautions for the protection of the environment:
Not applicable.
be mixed with ReproCyc ParvoFLEX and administered at one injection site.
No information is available on the safety and efficacy of this vaccine when used
with any other veterinary medicinal product except the product mentioned above.
A decision to use this vaccine before or after any other veterinary medicinal
product therefore needs to be made on a case-by-case basis.
Protect from light.
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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Other Products Containing Porcine respiratory and reproductive syndrome virus
These products share the same active ingredient and may be suitable alternatives. Always consult your vet.
Ingelvac PRRSFLEX EU Lyophilisate and Solvent for Suspension for Injection for Pigs
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Ingelvac PRRSFLEX EU Lyophilisate and Solvent for Suspension for Injection for Pigs
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