Pigzin Premix, 100% W/W Premix For Medicated Feeding Stuff
Revised: May 2013
AN: 00905/2012
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SUMMARY OF PRODUCT CHARACTERISTICS |
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1. |
NAME OF THE VETERINARY MEDICINAL PRODUCT |
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Pigzin Premix, 100%w/w Premix for medicated feeding stuff |
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2. |
QUALITATIVE AND QUANTITATIVE COMPOSITION |
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Qualitative composition Zinc Oxide For full list of excipients see section 6.1 |
Quantitative composition 100% w/w |
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3. |
PHARMACEUTICAL FORM |
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Premix for medicated feeding stuff A soft, white or faintly yellowish white amorphous powder. |
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4. |
CLINICAL PARTICULARS |
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4.1 |
Target species |
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Pigs up to 10 weeks of age |
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4.2 |
Indications for use, specifying the target species |
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For the treatment and control of diarrhoea in pigs |
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4.3 |
Contraindications |
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None known |
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4.4 |
Special warnings for each target species |
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None known |
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4.5 |
Special precautions for use |
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i. |
Special precautions for use in animals |
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None known |
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ii. |
Special precautions for the person administering the veterinary medicinal product to animals |
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Wear either a disposable half-mask respirator conforming to European Standard EN 149 or a non-disposable respirator to European Standard EN 140 with a filter to EN143 when mixing or handling the feed. Avoid contact with the skin by wearing protective clothing, including impermeable gloves. In case of accidental skin contact, wash the exposed skin with soap and water. Avoid contact with the eyes by wearing protective goggles or safety glasses. In case of accidental eye contact irrigate thoroughly with large quantities of water. Contaminated clothing should be removed and washed before being reused. In case of accidental ingestion, drink plenty of water and seek medical attention. Wash hands after use. |
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iii. |
Other precautions |
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None known |
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4.6 |
Adverse reactions (frequency and seriousness) |
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None known |
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4.7 |
Use during pregnancy, lactation or lay |
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Not applicable |
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4.8 |
Interaction with other medicinal products and other forms of interaction |
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None known |
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4.9 |
Amount(s) to be administered and administration route |
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For oral administration only For incorporation into dry feed at a registered/licensed mill. For more information:
Administer 2900-3100 mg/kg Pigzin Premix (which provides 2320 - 2489 mg/kg elemental zinc) so that the amount of zinc already present in the feed (naturally occurring zinc plus added nutritional zinc) is taken account of to ensure that the final feed contains 2500 mg/kg of elemental zinc. To ensure adequate distribution of the product in the final feed it is recommended that it be premixed with a suitable quantity of feed ingredients before blending into the final feed. The final feed should be fed as the only feed for up to 14 days. |
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4.10 |
Overdose (symptoms, emergency procedures, antidotes), if necessary |
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No known problems. |
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4.11 |
Withdrawal period(s) |
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Animals must not be slaughtered for human consumption during treatment. Animals may be slaughtered for human consumption only after 28 days after the end of treatment. |
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5. |
PHARMACOLOGICAL PROPERTIES |
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Pharmacotherapeutic group: |
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Anti-diarrhoeal |
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ATC Vet Code: QA07XA91 |
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5.1 |
Pharmacodynamic properties |
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The mode of action of zinc oxide in the treatment and control of diarrhoea has not been determined. It has been shown to have a favourable effect on the gut microflora by helping to prevent the reduction in diversity of microflora that occurred in the intestines of control pigs during the second week after weaning. |
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5.2 |
Pharmacokinetic properties |
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Absorption – Zinc is an essential trace element for livestock required for the maintenance of daily bodily function. Zinc oxide is known to be relatively poorly absorbed and therapeutic levels have increased blood levels by a factor of two. Distribution – Therapeutic levels of zinc oxide fed for four weeks after weaning have been shown to increase zinc levels in the liver and kidney of pigs by a factor of approximately five and two respectively. No increases in muscle levels were noted. Biotransformation – Zinc is a trace element essential for daily metabolism in the body. Since therapeutic levels are poorly absorbed, it is believed that most is voided unchanged in the faeces. Elimination – Most zinc from zinc oxide is excreted without absorption. |
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6. |
PHARMACEUTICAL PARTICULARS |
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6.1 |
List of excipients |
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None |
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6.2 |
Incompatibilities |
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None known |
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6.3 |
Shelf life |
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Shelf life of the veterinary medicinal product as packaged for sale: 2 Years. Shelf life after incorporation into meal or pelleted feed: 3 Months |
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6.4 |
Special precautions for storage |
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6.5 |
Nature and composition of immediate packaging |
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Three-ply paper sacks containing 25kg of a soft, white or yellowish white amorphous powder. Sacks are filled via a side valve, which is tucked in and glued to form a closure. |
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6.6 |
Special precautions for the disposal of unused veterinary medicinal product or waste materials derived from the use of such products, if appropriate |
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Any unused veterinary medicinal product or waste materials derived from such veterinary medicinal products should be disposed of in accordance with local requirements. |
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7. |
MARKETING AUTHORISATION HOLDER |
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DSM Nutritional Products (UK) Limited Delves Road Heanor Gate Industrial Estate Heanor Derbyshire DE75 7SG |
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8. |
MARKETING AUTHORISATION NUMBER |
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Vm 19108/4000 |
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9. |
DATE OF FIRST AUTHORISATION |
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05 May 2000 |
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10. |
DATE OF REVISION OF THE TEXT |
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May 2013 |
Approved: 17/05/2013
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