PLANIPART

Main information

  • Trade name:
  • PLANIPART TOCOLYTIC AGENT FOR FACILITATION & POSTPONEMENT OF PARTURITION
  • Pharmaceutical form:
  • PARENTERAL LIQUID/SOLUTION/SUSPENSION
  • Units in package:
  • 50mL
  • Class:
  • Veterinary Medicine
  • Medicine domain:
  • Animals
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • PLANIPART TOCOLYTIC AGENT FOR FACILITATION & POSTPONEMENT OF PARTURITION
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • COW | HEIFER (YOUNG FEMALE CATTLE) | SHEEP EWE (FEMALE) | BOVINE | COW YOUNG | FEMALE CATTLE | FEMALE SHEEP | OVINE
  • Therapeutic area:
  • bronchodilator
  • Therapeutic indications:
  • AGENT ACTING ON UTERUS | AGALACTIA | CONTRACTION | ENDOMETRITIS | HAEMORRHAGE POST-PARTUM | HEALING PROMOTANT | LABOUR | LET DOWN | OBSTETRICAL | PARTURITION | PLACENTA REMOVAL | POST-PARTUM HAEMORRHAGE | UTERINE
  • Product summary:
  • For abolition of contraction and postponement of parturition in cattle and sheep.Not to be used in conjunction with Atropine. Not to be used with general anaesthesia because of possible hypertensive effect. Antagonistic to the effects of prostaglandin FP alpha and oxytocin

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 35963/0405
  • Authorization date:
  • 20-10-2005
  • Last update:
  • 15-06-2017

Patient Information leaflet: composition, indications, side effects, dosage, interactions, adverse reactions, pregnancy, lactation

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PRESCRIPTION

ANIMAL

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FORAN

IMAL

TREATMENT

ONLY

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Date:

26.09.2005

Materfal number:

435531003

Product:

Planlpart

Country:

AUINZ

DimensIons:

45 x 85 mm

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PRESCRIPTION

ANIMAL

REMEDY

KEEP

OUTOF

REACH

CHILDREN

ANIMAL

TREATMENT

ONLY

Ptanlpart"

Tocolytic agent for facilitation and

po~ponementofparturition

26.09.2005

ff.i\

Boehringer

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Ingelheim

Pharmacology

Planipart" is a sympathomimetic

amine with a high degree

selectivity

for the

receptor sites in the body.

These sites are primarily found in the

lungs and uterus. Planipart" induces

relaxation

the uterine musculature

and thus dilation

ofthe

birth canal.

Following treatment

with

Planipart"

contractions are abolished,

the soft

birth canal continues to be prepared

for parturition. On recommencement

contractions the process of

parturi-

tion is noticeably easier, especially in

primaparae.

Tests have shown that depending on

the stage

labour, an interruption of

labour of two to eight hours duration

can be achieved. The further labour

has progressed, the shorter the period

of interruption of contractions.

Indications

For relaxation of the uterine muscula-

ture and abolition

contractions in

cattle and sheep to enable obstetric

intervention before, during and after

delivery.

For postponement

parturition espe-

cially overnight parturition and for

delay

parturition to allow for

improved dilation of the soft

birth

canal, particularly at first

parturition.

DIRECTIONS

Discard any unused

portion

within

days

first broaching bottle.

to be used in conjunction

with

atropine.

Not to be used

with

general

anaesthe-

sia because

possible hypotensive

effect.

Antagonistic to the effects

prosta-

glandin F2-alpha and oxytocin.

Planipart" is a beta-adrenergic stimu-

lant

and is therefore antagonised by

beta-adrenergic blocking agents. In

order to prevent additive effects,

product should

be given

with

other

sympathomimetics or vasodila-

tors.

Planipart° is administered during

labour, which has been induced by

corticoids, a shorter duration

action

must

be expected.

with

every biological

process, a

small

percentage

animals may be

expected

to respond to the toco-

lytic

agent.

Side effects were not observed in the

dam or offspring. No effect

on the

expulsion of the placenta, subsequent

fertility or

milk

yield was recorded.

43552/003 AU/NZ 124

8.5pt

26.09.2005

By single intravenous or intramuscular

injection.

Cows/Heifers

2 mL /100 kg bodyweight

Ewes

7 mL/lOO kg bodyweight

The onset of action occurs

within

approximately 20 minutes of intra-

muscular administration. The rapid

distribution after intravenous admin-

istration and the immediate onset

action may be beneficial

for obstetric

interventions.

an overnight postponement of

par-

turition is required, correct timing

administration is important.

abdominal

muscular contractions

are already visible and parts of the

foetus have entered the birth canal,

the preparation should be used only

for obstetric purposes, sinee at this

stage contractions can only be abol-

ished for a short

period.

WITHHOLDING PERIOD

Meat:

DO NOT

less than 6 days

before slaughter for human consump-

tion.

Milk:

Milk collected

within

6 days fol-

lowing treatment must

be used for

human consumption.

Disposal

Dispose of empty container by wrap-

ping

with

paper and putting in gar-

bage.

Storage Conditions

Store below 25°C (air conditioning)

Presentation

50 mL injectable solution, each mL

containing 0.03 mg Clenbuterol

hydrochloride.

Distributed by

Australia

Boehringer Ingelheim

Limited

Vetmedica Division

85 Waterloo Road

NORTH RYDE,N.S.W.2113

APVMA 35963/50/0405

New Zealand

Boehringer Ingelheim (N.Z.) Limited

Vetmedica Division

Levell,

Unit

49 Ormiston Road

EastTamaki

Auckland

Prescription Animal

Remedy

(P.A.R)

Class

For use only under the authority or

prescription of a veterinarian.

Registered pursuant to the ACVM

1997,No.A5382

Seewww.nzfsa.govt.nz/acvm for

registration conditions.

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Rezolsta (Janssen-Cilag International NV)

Rezolsta (Janssen-Cilag International NV)

Rezolsta (Active substance: Darunavir/Cobicistat) - Centralised - 2-Monthly update - Commission Decision (2018) 4239 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2819/WS/1312

Europe -DG Health and Food Safety

3-7-2018

Ristfor (Merck Sharp and Dohme B.V.)

Ristfor (Merck Sharp and Dohme B.V.)

Ristfor (Active substance: sitagliptin / metformin hydrochloride) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 4249 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1235/T/77

Europe -DG Health and Food Safety

3-7-2018

Velmetia (Merck Sharp and Dohme B.V.)

Velmetia (Merck Sharp and Dohme B.V.)

Velmetia (Active substance: sitagliptin / metformin hydrochloride) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 4252 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/862/T/93

Europe -DG Health and Food Safety

3-7-2018

Azomyr (Merck Sharp and Dohme B.V.)

Azomyr (Merck Sharp and Dohme B.V.)

Azomyr (Active substance: desloratadine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 4253 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/310/T/94

Europe -DG Health and Food Safety

3-7-2018

Janumet (Merck Sharp and Dohme B.V.)

Janumet (Merck Sharp and Dohme B.V.)

Janumet (Active substance: sitagliptin / metformin hydrochloride) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018) 4251 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/861/T/90

Europe -DG Health and Food Safety

3-7-2018

Trulicity (Eli Lilly Nederland B.V.)

Trulicity (Eli Lilly Nederland B.V.)

Trulicity (Active substance: dulaglutide) - PSUSA - Modification - Commission Decision (2018)4339 of Tue, 03 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2825/PSUSA/10311/201709

Europe -DG Health and Food Safety

27-6-2018

EU/3/02/124 (BioMarin International Limited)

EU/3/02/124 (BioMarin International Limited)

EU/3/02/124 (Active substance: 3,4-diaminopyridine phosphate) - Transfer of orphan designation - Commission Decision (2018)4095 of Wed, 27 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/050/02/T/03

Europe -DG Health and Food Safety

12-6-2018

EU/3/10/811 (Celgene Europe B.V.)

EU/3/10/811 (Celgene Europe B.V.)

EU/3/10/811 (Active substance: N-tert-butyl-3-[(5-methyl-2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}pyrimidin-4-yl)amino] benzenesulfonamide dihydrochloride monohydrate) - Transfer of orphan designation - Commission Decision (2018)3809 of Tue, 12 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/092/10/T/03

Europe -DG Health and Food Safety

12-6-2018

EU/3/10/810 (Celgene Europe B.V.)

EU/3/10/810 (Celgene Europe B.V.)

EU/3/10/810 (Active substance: N-tert-butyl-3-[(5-methyl-2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}pyrimidin-4-yl)amino] benzenesulfonamide dihydrochloride monohydrate) - Transfer of orphan designation - Commission Decision (2018)3808 of Tue, 12 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/084/10/T/03

Europe -DG Health and Food Safety

12-6-2018

EU/3/10/794 (Celgene Europe B.V.)

EU/3/10/794 (Celgene Europe B.V.)

EU/3/10/794 (Active substance: N-tert-butyl-3-[(5-methyl-2-{[4-(2-pyrrolidin-1-ylethoxy)phenyl]amino}pyrimidin-4-yl)amino] benzenesulfonamide dihydrochloride monohydrate) - Transfer of orphan designation - Commission Decision (2018)3803 of Tue, 12 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/069/10/T/03

Europe -DG Health and Food Safety

12-6-2018

EU/3/11/888 (Gilead Sciences Ireland UC)

EU/3/11/888 (Gilead Sciences Ireland UC)

EU/3/11/888 (Active substance: N-(cyanomethyl)-4-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzamide, dihydrochloride salt) - Transfer of orphan designation - Commission Decision (2018)3802 of Tue, 12 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/152/10/T/03

Europe -DG Health and Food Safety

12-6-2018

EU/3/11/887 (Gilead Sciences Ireland UC)

EU/3/11/887 (Gilead Sciences Ireland UC)

EU/3/11/887 (Active substance: N-(cyanomethyl)-4-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzamide, dihydrochloride salt) - Transfer of orphan designation - Commission Decision (2018)3801 of Tue, 12 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/020/11/T/03

Europe -DG Health and Food Safety

12-6-2018

EU/3/11/886 (Gilead Sciences Ireland UC)

EU/3/11/886 (Gilead Sciences Ireland UC)

EU/3/11/886 (Active substance: N-(cyanomethyl)-4-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzamide, dihydrochloride salt) - Transfer of orphan designation - Commission Decision (2018)3799 of Tue, 12 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/019/11/T/03

Europe -DG Health and Food Safety

4-6-2018

EU/3/05/334 (Florence Porte ThomE)

EU/3/05/334 (Florence Porte ThomE)

EU/3/05/334 (Active substance: Human immunoglobulin G1 constant region - human ectodysplasin-A1 receptor-binding domain fusion protein) - Transfer of orphan designation - Commission Decision (2018)3629 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMA/OD/064/05/T/03

Europe -DG Health and Food Safety

21-5-2018

EU/3/14/1353 (Lupin Europe GmbH)

EU/3/14/1353 (Lupin Europe GmbH)

EU/3/14/1353 (Active substance: Mexiletine hydrochloride) - Transfer of orphan designation - Commission Decision (2018)3134 of Mon, 21 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/074/14/T/03

Europe -DG Health and Food Safety

18-5-2018

EU/3/04/204 (Gilead Sciences Ireland UC)

EU/3/04/204 (Gilead Sciences Ireland UC)

EU/3/04/204 (Active substance: Aztreonam lysinate (inhalation use)) - Transfer of orphan designation - Commission Decision (2018)3131 of Fri, 18 May 2018 European Medicines Agency (EMA) procedure number: EMEA/OD/006/04/T/03

Europe -DG Health and Food Safety

16-5-2018

EU/3/06/391 (Novartis Europharm Limited)

EU/3/06/391 (Novartis Europharm Limited)

EU/3/06/391 (Active substance: Amphotericin B (for inhalation use)) - Transfer of orphan designation - Commission Decision (2018)3034 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMA/OD/027/06/T/03

Europe -DG Health and Food Safety

16-5-2018

EU/3/03/140 (Novartis Europharm Limited)

EU/3/03/140 (Novartis Europharm Limited)

EU/3/03/140 (Active substance: Tobramycin (inhalation powder)) - Transfer of orphan designation - Commission Decision (2018)3031 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMEA/OD/072/02/T/02

Europe -DG Health and Food Safety

3-5-2018

Perjeta (Roche Registration GmbH)

Perjeta (Roche Registration GmbH)

Perjeta (Active substance: pertuzumab) - Centralised - 2-Monthly update - Commission Decision (2018)2771 of Thu, 03 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2547/II/35

Europe -DG Health and Food Safety

3-5-2018

Avamys (Glaxo Group Ltd)

Avamys (Glaxo Group Ltd)

Avamys (Active substance: Fluticasone furoate) - Centralised - Yearly update - Commission Decision (2018)2773 of Thu, 03 May 2018

Europe -DG Health and Food Safety

3-5-2018

Pramipexole Teva (Teva B.V.)

Pramipexole Teva (Teva B.V.)

Pramipexole Teva (Active substance: pramipexole) - Centralised - Yearly update - Commission Decision (2018)2775 of Thu, 03 May 2018

Europe -DG Health and Food Safety

3-5-2018

Hemlibra (Roche Registration GmbH)

Hemlibra (Roche Registration GmbH)

Hemlibra (Active substance: emicizumab) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)2774 of Thu, 03 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4406/T/1

Europe -DG Health and Food Safety