Pirsue

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

pirlimycin

Available from:

Zoetis Belgium SA

ATC code:

QJ51FF90

INN (International Name):

pirlimycin

Therapeutic group:

Cattle

Therapeutic area:

Antibacterials for intramammary use

Therapeutic indications:

For the treatment of subclinical mastitis in lactating cows due to Gram-positive cocci susceptible to pirlimycin including staphylococcal organisms such as Staphylococcus aureus, both penicillinase-positive and penicillinase-negative, and coagulase-negative staphylococci; streptococcal organisms including Streptococcus agalactiae, Streptococcus dysgalactiae and Streptococcus uberis.

Product summary:

Revision: 15

Authorization status:

Authorised

Authorization date:

2001-01-29

Patient Information leaflet

                                14
B. PACKAGE LEAFLET
15
PACKAGE LEAFLET:
PIRSUE 5 MG/ML INTRAMAMMARY SOLUTION FOR CATTLE
1.
NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER AND OF
THE MANUFACTURING AUTHORISATION HOLDER RESPONSIBLE FOR BATCH
RELEASE, IF DIFFERENT
Marketing authorisation holder:
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
BELGIUM
Manufacturer responsible for batch release:
Norbrook Laboratories Limited
Station Works, Camlough Road,
Newry, County Down,
BT35 6JP
UNITED KINGDOM
or
Zoetis Belgium SA
Rue Laid Burniat 1
1348 Louvain-la-Neuve
BELGIUM
2.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Pirsue 5 mg/ml intramammary solution for cattle
3.
STATEMENT OF THE ACTIVE SUBSTANCE(S) AND OTHER INGREDIENT(S)
Pirlimycin (as Pirlimycin hydrochloride)
50 mg/10 ml
4.
INDICATION(S)
For the treatment of subclinical mastitis in lactating cows due to
Gram-positive cocci susceptible to
pirlimycin including staphylococcal organisms such as
_Staphylococcus aureus_
, both penicillinase-positive
and penicillinase-negative, and coagulase-negative staphylococci;
streptococcal organisms including
_Streptococcus agalactiae_
,
_Streptococcus dysgalactiae_
, and
_Streptococcus uberis. _
5.
CONTRAINDICATIONS
Resistance against pirlimycin.
Treatment of infections due to Gram-negative bacteria such as
_E. coli_
.
Do not treat cows with palpable udder changes due to chronic
subclinical mastitis.
16
6.
ADVERSE REACTIONS
None known.
If you notice any side effects, even those not already listed in this
package leaflet or you think that the
medicine has not worked, please inform your veterinary surgeon.
7.
TARGET SPECIES
Cattle (lactating dairy cows).
8.
DOSAGE FOR EACH SPECIES, ROUTE(S) AND METHOD OF ADMINISTRATION
Intramammary use.
Infuse one syringe (50 mg pirlimycin) into each infected quarter.
The treatment consists of eight infusions of one syringe every 24
hours.
9.
ADVICE ON CORRECT ADMINISTRATION
Care must be taken not to introduce pathogens into the teat in order
to reduce the risk of
_E. coli_
infections. Ensure adequate cleansing of t
                                
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Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE VETERINARY MEDICINAL PRODUCT
Pirsue 5 mg/ml intramammary solution for cattle
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
ACTIVE SUBSTANCE:
Pirlimycin (as Pirlimycin hydrochloride)
50 mg/10 ml
For the full list of excipients see Section 6.1
3.
PHARMACEUTICAL FORM
Intramammary solution.
4.
CLINICAL PARTICULARS
4.1
TARGET SPECIES
Cattle (lactating dairy cows).
4.2
INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment of subclinical mastitis in lactating cows due to
Gram-positive cocci susceptible to
pirlimycin including staphylococcal organisms such as
_Staphylococcus aureus_
, both penicillinase-positive
and penicillinase-negative, and coagulase-negative staphylococci;
streptococcal organisms including
_Streptococcus agalactiae_
,
_Streptococcus dysgalactiae_
and
_Streptococcus uberis._
4.3
CONTRAINDICATIONS
Resistance against pirlimycin.
Treatment of infections due to Gram-negative bacteria such as
_E. coli_
.
Do not treat cows with palpable udder changes due to chronic
subclinical mastitis.
4.4
SPECIAL WARNINGS FOR EACH TARGET SPECIES
None.
4.5
SPECIAL PRECAUTIONS FOR USE
Special precautions for use in animals
Susceptibility testing of the target bacteria should be carried out
prior to treatment.
_ _
Special precautions to be taken by the person administering the
veterinary medicinal product to
animals
Avoid contact with the solution. Wash hands and any exposed skin with
soap and water and remove
contaminated clothing immediately after use. Flush eyes with water for
15 minutes immediately after
exposure. Hold eyelids open to ensure complete contact with water.
3
4.6
ADVERSE REACTIONS (FREQUENCY AND SERIOUSNESS)
None known.
4.7
USE DURING PREGNANCY, LACTATION OR LAY
The product is indicated for use in lactating dairy cows and can be
used during pregnancy.
4.8
INTERACTION WITH OTHER MEDICINAL PRODUCTS AND OTHER FORMS OF
INTERACTION
Cross-resistance may occur between pirlimycin and other lincosamides
or macrolides.
4.9
AMOUNTS TO BE ADMINIS
                                
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Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 18-06-2021
Summary of Product characteristics Summary of Product characteristics Bulgarian 18-06-2021
Patient Information leaflet Patient Information leaflet Spanish 18-06-2021
Public Assessment Report Public Assessment Report Spanish 03-06-2013
Patient Information leaflet Patient Information leaflet Czech 18-06-2021
Public Assessment Report Public Assessment Report Czech 03-06-2013
Patient Information leaflet Patient Information leaflet Danish 18-06-2021
Public Assessment Report Public Assessment Report Danish 03-06-2013
Patient Information leaflet Patient Information leaflet German 18-06-2021
Public Assessment Report Public Assessment Report German 03-06-2013
Patient Information leaflet Patient Information leaflet Estonian 18-06-2021
Public Assessment Report Public Assessment Report Estonian 03-06-2013
Patient Information leaflet Patient Information leaflet Greek 18-06-2021
Public Assessment Report Public Assessment Report Greek 03-06-2013
Patient Information leaflet Patient Information leaflet French 18-06-2021
Public Assessment Report Public Assessment Report French 03-06-2013
Patient Information leaflet Patient Information leaflet Italian 18-06-2021
Public Assessment Report Public Assessment Report Italian 03-06-2013
Patient Information leaflet Patient Information leaflet Latvian 18-06-2021
Public Assessment Report Public Assessment Report Latvian 03-06-2013
Patient Information leaflet Patient Information leaflet Lithuanian 18-06-2021
Summary of Product characteristics Summary of Product characteristics Lithuanian 18-06-2021
Public Assessment Report Public Assessment Report Lithuanian 03-06-2013
Patient Information leaflet Patient Information leaflet Hungarian 18-06-2021
Summary of Product characteristics Summary of Product characteristics Hungarian 18-06-2021
Public Assessment Report Public Assessment Report Hungarian 03-06-2013
Patient Information leaflet Patient Information leaflet Maltese 18-06-2021
Patient Information leaflet Patient Information leaflet Dutch 18-06-2021
Public Assessment Report Public Assessment Report Dutch 03-06-2013
Patient Information leaflet Patient Information leaflet Polish 18-06-2021
Public Assessment Report Public Assessment Report Polish 03-06-2013
Patient Information leaflet Patient Information leaflet Portuguese 18-06-2021
Summary of Product characteristics Summary of Product characteristics Portuguese 18-06-2021
Public Assessment Report Public Assessment Report Portuguese 03-06-2013
Patient Information leaflet Patient Information leaflet Romanian 18-06-2021
Patient Information leaflet Patient Information leaflet Slovak 18-06-2021
Public Assessment Report Public Assessment Report Slovak 03-06-2013
Patient Information leaflet Patient Information leaflet Slovenian 18-06-2021
Summary of Product characteristics Summary of Product characteristics Slovenian 18-06-2021
Public Assessment Report Public Assessment Report Slovenian 03-06-2013
Patient Information leaflet Patient Information leaflet Finnish 18-06-2021
Public Assessment Report Public Assessment Report Finnish 03-06-2013
Patient Information leaflet Patient Information leaflet Swedish 18-06-2021
Public Assessment Report Public Assessment Report Swedish 03-06-2013
Patient Information leaflet Patient Information leaflet Norwegian 18-06-2021
Summary of Product characteristics Summary of Product characteristics Norwegian 18-06-2021
Patient Information leaflet Patient Information leaflet Icelandic 18-06-2021
Summary of Product characteristics Summary of Product characteristics Icelandic 18-06-2021
Patient Information leaflet Patient Information leaflet Croatian 18-06-2021

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