WEANAVAC

Main information

  • Trade name:
  • WEANAVAC - E. COLI VACCINE FOR PIGS
  • Pharmaceutical form:
  • PARENTERAL LIQUID/SOLUTION/SUSPENSION
  • Units in package:
  • 2mL,250mL
  • Class:
  • Veterinary Medicine
  • Medicine domain:
  • Animals
  • Medicine type:
  • Allopathic drug
  • Manufactured by:
  • INTERVET AUSTRALIA

Documents

Localization

  • Available in:
  • WEANAVAC - E. COLI VACCINE FOR PIGS
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • PIG WEANER
  • Therapeutic area:
  • vaccine
  • Therapeutic indications:
  • ESCHERICHIA COLI SCOURS | VACCINE | EQUINE ROTAVIRUS | WHITE SCOURS
  • Product summary:
  • An aid in the control of post weaning E.coli scours in weaner pigs.Piglets may develop a mild lethargy for a short period.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 35780/0205
  • Authorization date:
  • 01-03-2005
  • Last update:
  • 15-06-2017

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

250 mL Pack

ACTIVE CONSTITUENTS:

Inactivated adjuvanted vaccine containing:

Whole cell E. coli including fimbrial antigens K88 and F107.

Preservatives: 0.1 mg/mL Thiomersal; <1.2 mg/mL Formaldehyde

An aid in the control of post-weaning E. coli scours in weaner pigs.

WEANAvac is a joint development of the Department of Primary

Industries and Intervet Australia Pty Limited.

E. coli Vaccine for Pigs.

DISPOSAL:

Dispose of empty container by wrapping with paper and

putting in garbage.

STORAGE:

Store between 2

C and 8

(Refrigerate. Do not freeze). Protect from light.

Discard if previously frozen.

250 mL

E. coli Vaccine for Pigs.

E. coli Vaccine for Pigs.

E. coli Vaccine for Pigs.

E. coli Vaccine for Pigs.

READ ENCLOSED LEAFLET

BEFORE USING THIS PRODUCT.

DIRECTIONS FOR USE:

SHAKE WELL TO MIX BEFORE USE

AND KEEP MIXED DURING USE.

FOR INTRAMUSCULAR

INJECTION ONLY

2 mL by intramuscular injection to

sucker pigs.

Vaccinate sucker pigs one week

before weaning.

WITHHOLDING PERIOD: NIL

FIRST AID:

If poisoning occurs contact a doctor

or Poisons Information Centre.

Phone Australia 131126.

EQUIPMENT:

The pack is designed for use with

an automatic vaccination gun.

For sterilisation of automatic

vaccinator see enclosed leaflet.

CONNECTING PACK TO

AUTOMATIC VACCINATOR:

Connect the tube firmly onto the

automatic vaccinator.

The pack may be suspended by

means of a carrying strap.

Eject air from the vaccinator and

tube by depressing plunger until

vaccine flows through needle.

RESEALING VACCINE PACK:

For best practice vaccine should

be used during one administration.

Unused vaccine must be kept

refrigerated and used within 24

hours of opening.

Remove tube from the vaccinator gun.

Store between 2ºC and 8ºC

(Refrigerate. Do not freeze).

Protect from light.

Discard if previously frozen.

FOR ANIMAL TREATMENT ONLY

FOR ANIMAL TREATMENT ONLY

APVMA Approval No.: 35780/250M/0205

9322839 02052 5

WEANAvac

WEANAvac

WEANAvac

WEANAvac

WEANAvac

INTERVET AUSTRALIA PTY LIMITED

91 - 105 Harpin Street

BENDIGO EAST VIC 3550

Phone: (03) 5440 9888

Fax.: (03) 5442 3162

CA3600B/03

Batch No.:

Expiry Date:

Info

pest

Verified

FOR ANIMAL TREATMENT ONLY

READ ENCLOSED LEAFLET BEFORE USING

THIS PRODUCT.

DIRECTIONS FOR USE:

SHAKE WELL TO MIX BEFORE USE AND

KEEP MIXED DURING USE.

FOR INTRAMUSCULAR INJECTION ONLY

DOSAGE: 2 mL

WITHHOLDING PERIOD: NIL

FIRST AID:

If poisoning occurs contact a doctor

or Poisons Information Centre.

Phone Australia 131126.

LA3600B/05

WEANAvac

E. coli Vaccine for Pigs.

ACTIVE CONSTITUENTS:

Inactivated adjuvanted vaccine containing:

Whole cell E. coli including fimbrial

antigens K88 and F107.

Preservatives: 0.1 mg/mL Thiomersal;

<1.2 mg/mL Formaldehyde

An aid in the control of post-weaning

E. coli scours in weaner pigs.

250 mL Pack

DISPOSAL: Dispose of empty container by

wrapping with paper and putting in garbage.

STORAGE: Store between 2

C and 8

(Refrigerate. Do not freeze).

Protect from light.

Discard if previously frozen.

APVMA Approval No.: 35780/250M/0205

Batch No.:

Expiry Date:

INTERVET AUSTRALIA PTY LIMITED

91-105 Harpin Street

BENDIGO EAST VIC 3550

Phone: (03) 5440 9888

Fax.: (03) 5442 3162

FOR ANIMAL TREATMENT ONLY

WEANAvac

E. coli Vaccine for Pigs.

ACTIVE CONSTITUENTS:

Inactivated adjuvanted vaccine containing:

Whole cell E. coli including fimbrial antigens K88 and F107.

Preservatives: 0.1 mg/mL Thiomersal; <1.2 mg/mL Formaldehyde

An aid in the control of post-weaning E. coli scours in weaner pigs.

DESCRIPTION:

WEANAvac‚ is a polyvalent, killed, whole cell vaccine

containing the important serotypes of E. coli. It is recommended

as an aid in the control of post-weaning scours in pigs. The

adjuvant (aluminium hydroxide) increases the level and duration

of immunity. Vaccination of sucker pigs stimulates a high level

of specific antibodies, which will protect pigs in the critical 2

weeks following weaning.

SAFETY:

WEANAvac has been shown to be safe when administered to

sucker pigs at the recommended dose rate.

INDICATIONS:

WEANAvac is effective as an aid in the control of scours in

weaner pigs caused by E. coli types 08, 0138, 0139, 0141, 0149

and 0157. If E. coli other than those in the vaccine are involved

in your piggery, consult your veterinarian.

DIRECTIONS FOR USE:

No side effects from vaccination have been noted in the vast majority

of cases. However, in some instances piglets may develop a mild

lethargy for a short period. These pigs regain normal habits

within 2-3 hours.

2 mL by intramuscular injection. The recommended site of injection

is that used for routine injection in pigs. i.e. behind and below

the ear. 2 mL to sucker pigs one week before weaning.

CAUTION: Avoid Carcase Damage

Sterilise all injection apparatus by boiling before use.

Avoid use of strong disinfectants on apparatus.

2. Maintain cleanliness at all times.

3. Keep needles sharp and clean. Replace frequently.

4. Use needles of appropriate gauge and length.

5. As far as possible avoid injection of animals during wet

weather or under dusty conditions.

6. This product must be injected only into muscle tissue.

If possible inject into muscle tissue on side of neck.

WITHHOLDING PERIOD: NIL

FIRST AID:

If poisoning occurs contact a doctor or Poisons Information

Centre. Phone Australia 131126.

CONNECTING PACK TO AUTOMATIC VACCINATOR:

Connect the tube firmly onto the automatic vaccinator.

The pack may be suspended by means of a carrying strap.

Eject air from the vaccinator and tube by depressing plunger

until vaccine flows through needle.

RESEALING VACCINE PACK:

For best practice vaccine should be used during one administration.

Unused vaccine must be kept refrigerated and used within

24 hours of opening.

Remove tube from the vaccinator gun.

Store between 2ºC and 8ºC (Refrigerate. Do not freeze).

Protect from light.

Discard if previously frozen.

USER SAFETY AND FIRST AID INFORMATION:

Wash and disinfect self injection injuries.

Seek medical advice if irritancy or an allergic response occurs.

PRESENTATION:

WEANAvac is available in a pack of 250 mL.

DISPOSAL:

Dispose of empty container by wrapping with paper and putting

in garbage.

STORAGE:

Store between 2ºC and 8ºC (Refrigerate. Do not freeze).

Protect from light.

Discard if previously frozen.

APVMA Approval No.: 35780/0205

INTERVET AUSTRALIA PTY LIMITED

91-105 Harpin Street

BENDIGO EAST VIC 3550

Phone: (03) 5440 9888

Fax.: (03) 5442 3162

LE3600/02

19-12-2018

Wegmans Issues Voluntary Recall of Fresh Cauliflower Rice, Veggie/Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower

Wegmans Issues Voluntary Recall of Fresh Cauliflower Rice, Veggie/Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower

Rochester, NY – Wegmans Food Markets, Inc. has issued a voluntary recall of fresh Cauliflower Rice, Veggie Cauliflower Rice Blend and Stir-Fry Mix with Cauliflower, sold in the produce department between 12/7/18 and 12/18/18, because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure called He...

FDA - U.S. Food and Drug Administration

18-12-2018

Adam Bros. Farming, Inc. Recalls Red and Green Leaf Lettuce and Cauliflower Because of Possible Health Risk

Adam Bros. Farming, Inc. Recalls Red and Green Leaf Lettuce and Cauliflower Because of Possible Health Risk

Adam Bros. Farming, Inc. of Santa Maria, California is recalling red leaf lettuce, green leaf lettuce and cauliflower harvested on November 27 through 30, 2018 out of an abundance of caution, because it may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7).

FDA - U.S. Food and Drug Administration

16-12-2018

Spokane Produce Voluntarily Recalls Northwest Cuisine Creations and Fresh&Local Sandwiches and Green Leaf Lettuce Filets

Spokane Produce Voluntarily Recalls Northwest Cuisine Creations and Fresh&Local Sandwiches and Green Leaf Lettuce Filets

Spokane Produce Inc. of Spokane, WA initiates a voluntary recall of sandwiches containing green leaf lettuce and foodservice lettuce filets following notice of a produce industry ingredient recall by Adam Bros. Farming Inc. Sandwich products bearing the Northwest Cuisine Creations and Fresh&Local labels. These prod- ucts are recalled because they may be contaminated with Escherichia coli O157:H7 bacteria (E. Coli O157:H7). E. coli O157:H7 causes a diarrheal illness often with bloody stools. Although most...

FDA - U.S. Food and Drug Administration

13-12-2018

Statement from FDA Commissioner Scott Gottlieb, M.D. and FDA Deputy Commissioner Frank Yiannas on new findings and updated consumer recommendations related to the romaine lettuce <i>E. coli</i> O157:H7 outbreak investigation

Statement from FDA Commissioner Scott Gottlieb, M.D. and FDA Deputy Commissioner Frank Yiannas on new findings and updated consumer recommendations related to the romaine lettuce <i>E. coli</i> O157:H7 outbreak investigation

Statement from FDA Commissioner Scott Gottlieb, M.D. and FDA Deputy Commissioner Frank Yiannas on new findings and updated consumer recommendations related to the romaine lettuce E. coli O157:H7 outbreak investigation

FDA - U.S. Food and Drug Administration

13-12-2018

The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2017

The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2017

Published on: Wed, 12 Dec 2018 This report of the European Food Safety Authority and the European Centre for Disease Prevention and Control presents the results of zoonoses monitoring activities carried out in 2017 in 37 European countries (28 Member States (MS) and nine non-MS). Campylobacteriosis was the commonest reported zoonosis and its EU trend for confirmed human cases increasing since 2008 stabilised during 2013–2017. The decreasing EU trend for confirmed human salmonellosis cases since 2008 end...

Europe - EFSA - European Food Safety Authority Publications

27-11-2018

INNUENDO: A cross‐sectoral platform for the integration of genomics in the surveillance of food‐borne pathogens

INNUENDO: A cross‐sectoral platform for the integration of genomics in the surveillance of food‐borne pathogens

Published on: Mon, 26 Nov 2018 Abstract In response to the EFSA call New approaches in identifying and characterizing microbial and chemical hazards, the project INNUENDO (https://sites.google.com/site/theinnuendoproject/) aimed to design an analytical platform and standard procedures for the use of whole‐genome sequencing in surveillance and outbreak investigation of food‐borne pathogens. The project firstly attempted to identify existing flaws and needs, and then to provide applicable cross‐sectorial ...

Europe - EFSA - European Food Safety Authority Publications

27-11-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on the current romaine lettuce <i>E. coli</i> O157:H7 outbreak investigation

Statement from FDA Commissioner Scott Gottlieb, M.D., on the current romaine lettuce <i>E. coli</i> O157:H7 outbreak investigation

Statement from FDA Commissioner Scott Gottlieb, M.D., on the current romaine lettuce E. coli O157:H7 outbreak investigation

FDA - U.S. Food and Drug Administration

17-11-2018

Evaluation of confirmatory data following the Article 12 MRL review for picolinafen

Evaluation of confirmatory data following the Article 12 MRL review for picolinafen

Published on: Fri, 16 Nov 2018 The applicant BASF Agro B.V. submitted a request to the competent national authority in Germany to evaluate the confirmatory data that were identified for picolinafen in the framework of the maximum residue level (MRL) review under Article 12 of Regulation (EC) No 396/2005 as not available. To address the data gaps, a new validated analytical method for enforcement of the residue in dry/high starch‐, high water content‐, high acid content‐ and high oil content commodities ...

Europe - EFSA - European Food Safety Authority Publications

16-11-2018

FDA approves new drug to treat travelers’ diarrhea

FDA approves new drug to treat travelers’ diarrhea

FDA approved Aemcolo (rifamycin), an antibacterial drug indicated for the treatment of adult patients with travelers’ diarrhea caused by noninvasive strains of Escherichia coli (E. coli), not complicated by fever or blood in the stool.

FDA - U.S. Food and Drug Administration

1-11-2018

Statement from FDA Commissioner Scott Gottlieb, M.D., on findings from the romaine lettuce E. coli O157:H7 outbreak investigation and FDA’s efforts to prevent future outbreaks

Statement from FDA Commissioner Scott Gottlieb, M.D., on findings from the romaine lettuce E. coli O157:H7 outbreak investigation and FDA’s efforts to prevent future outbreaks

Statement from FDA Commissioner Scott Gottlieb, M.D., on findings from the romaine lettuce E. coli O157:H7 outbreak investigation and FDA’s efforts to prevent future outbreaks

FDA - U.S. Food and Drug Administration

26-10-2018

Safety and efficacy of l‐threonine produced by fermentation using Escherichia coli CGMCC 7.232 for all animal species

Safety and efficacy of l‐threonine produced by fermentation using Escherichia coli CGMCC 7.232 for all animal species

Published on: Thu, 25 Oct 2018 00:00:00 +0200 The product subject of this assessment is l‐threonine produced by fermentation with a genetically modified strain of Escherichia coli (CGMCC 7.232). It is intended to be used in feed and water for drinking for all animal species and categories. The production strain and its recombinant DNA were not detected in the additive. The product l‐threonine, manufactured by fermentation with E. coli CGMCC 7.232, does not raise any safety concern with regard to the gen...

Europe - EFSA - European Food Safety Authority Publications

27-9-2018

Mauna Loa Macadamia Nut Corporation Voluntarily Recalls

Mauna Loa Macadamia Nut Corporation Voluntarily Recalls

Mauna Loa Macadamia Nut Corporation is voluntarily recalling all of its products produced at the Keaau facility between Sept. 6 - 21, 2018 due to a potential contamination of Escherichia coli (E. coli). The recall was initiated due to E. coli being detected in the well water and distribution system that supplies the firm's operations. No illnesses related to the water have been reported to the state.

FDA - U.S. Food and Drug Administration

6-7-2018

Radagast Pet Food, Inc. Voluntarily Recalls Three Lots of Rad Cat Raw Diet Free-Range Chicken Recipe and One Lot of Pasture-Raised Venison Recipe Because of Possible Health Risk

Radagast Pet Food, Inc. Voluntarily Recalls Three Lots of Rad Cat Raw Diet Free-Range Chicken Recipe and One Lot of Pasture-Raised Venison Recipe Because of Possible Health Risk

Radagast Pet Food, Inc. of Portland, OR is recalling three lots of Rad Cat Raw Diet Free-Range Chicken Recipe because testing results indicate they have the potential to be contaminated with Listeria monocytogenes. The Company is also recalling one lot of Rad Cat Raw Diet Pasture-Raised Venison Recipe because testing results indicate it has the potential to be contaminated with Shiga Toxin producing E. coli O121. This recall is being conducted out of an abundance of caution. Due to Radagast Pet Food’s ...

FDA - U.S. Food and Drug Administration

30-5-2018

FDA approves new treatment for moderately to severely active ulcerative colitis

FDA approves new treatment for moderately to severely active ulcerative colitis

FDA today expanded the approval of Xeljanz (tofacitinib) to include adults with moderately to severely active ulcerative colitis.

FDA - U.S. Food and Drug Administration

21-5-2018

Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir by MBI Distributing: Recall - Due to a Lack of Adequate Controls

Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir by MBI Distributing: Recall - Due to a Lack of Adequate Controls

Manufacturing products without proper process controls increases the probability that products will vary in strength, quality and purity

FDA - U.S. Food and Drug Administration

18-5-2018

MBI Distributing, Inc. Issues Voluntary Nationwide Recall of Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir Due to a Lack of Process Controls

MBI Distributing, Inc. Issues Voluntary Nationwide Recall of Homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir Due to a Lack of Process Controls

MBI Distributing, Inc. is voluntarily recalling all lots of homeopathic Teething Drops, Nausea Drops, Intestinal Colic Drops, Stomach Calm, Expectorant Cough Syrup, Silver-Zinc Throat Spray, and Argentum Elixir, within expiry, to the consumer level. The drug products have been found to be manufactured with a lack of adequate controls.

FDA - U.S. Food and Drug Administration

18-1-2019


Opinion/decision on a Paediatric investigation plan (PIP): Cell-free solution of lysed Escherichia coli culture, strain Laves, decision type: , therapeutic area: , PIP number: P/0328/2018

Opinion/decision on a Paediatric investigation plan (PIP): Cell-free solution of lysed Escherichia coli culture, strain Laves, decision type: , therapeutic area: , PIP number: P/0328/2018

Opinion/decision on a Paediatric investigation plan (PIP): Cell-free solution of lysed Escherichia coli culture, strain Laves, decision type: , therapeutic area: , PIP number: P/0328/2018

Europe - EMA - European Medicines Agency

11-7-2018

Coliprotec F4/F18 (Prevtec Microbia GmbH)

Coliprotec F4/F18 (Prevtec Microbia GmbH)

Coliprotec F4/F18 (Active substance: Porcine post-weaning diarrhoea vaccine (live)) - Centralised - Yearly update - Commission Decision (2018)4522 of Wed, 11 Jul 2018

Europe -DG Health and Food Safety