BOMACILLIN

Main information

  • Trade name:
  • BOMACILLIN PENICILLIN INJECTION
  • Pharmaceutical form:
  • PARENTERAL LIQUID/SOLUTION/SUSPENSION
  • Units in package:
  • 100mL,250mL,500mL
  • Class:
  • Veterinary Medicine
  • Medicine domain:
  • Animals
  • Medicine type:
  • Allopathic drug
  • Manufactured by:
  • BAYER AUSTRALIA

Documents

Localization

  • Available in:
  • BOMACILLIN PENICILLIN INJECTION
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • CALF | CAT | CATTLE | DOG | HORSE | HORSE FOAL | PIGS | SHEEP | BEEF | BEEF CALF | BITCH | BOAR | BOS INDICUS | BOS TAURUS | BOV
  • Therapeutic area:
  • antibiotic
  • Therapeutic indications:
  • BACTERIAL INFECTION | AMOXYCILLIN SENSITIVE BACTERIA | ASSOCIATED WITH VIRAL DISEASE | GRAM NEGATIVE ORGANISMS | GRAM POSITIVE ORGANISMS | POST PARTURIENT BACTERIAL INFE | PRIMARY BACTERIAL INFECTION | SULFADIAZINE SENSITIVE BACTERI | TRIMETHOPRIM SENSITIVE BACTERI | TYLOSIN SENSITIVE BACTERIA
  • Product summary:
  • For the systemic treatment and control of infections caused by penicillin sensitive organisms in horses, cattle, sheep, dogs and cats.Anaphylactic reactions following administration may occur in young cattle and require prompt treatment with antihistamines.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered but not available
  • Authorization number:
  • 36023/0899
  • Authorization date:
  • 01-09-1999
  • Last update:
  • 15-06-2017

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

Version

Controlled

Dmf!

Label

Bomacillin

Penicillin InjEcton

Page 1 of 2

Printed on 13-08-99 10: 11

PRESCRIPTION ANIMAL REMEDY

KEEP OUT OF REACH OF CHILDREN

FOR ANIMAL TREATMENT ONLY

BOMACILLI-N

PENICILLIN

INJECTION

ACTIVE

CONSTITUENT

Each

contains

PROCAINE

PENICILLIN

300mg

For the systemic treatment

&

control of infections caused by penicillin

sensitive organisms in horses, cattle, sheep, pigs, dogs, and cats.

100 mL

[250

&

DIRECTIONS FOR USE

intramuscular

injection

only

Horses,

Cattle

. .. .. . .. .. . .. .. . .. . .. . . . .. . . .

.......

lo-20

Foals,

Calves

. .. .. . .. .. . .. .. . .. . .. . . . .. . . . .. . . . .. . . .

.5-10

Sheep, Pigs

. .. . .. .. . .. .. . .. .. . .. .

..................

.3-5

Dogs, Cats

.. .. . .. .. . .. .. . .. .. . .. . .. . . . .. .

..........

.l mLper 10 kg

Repeat daily as required.

WITHHOLDING

PERIODS:

MEAT: DO NOT USE less than 5 days before slaughter for human consumption.

MILK: Milk collected from cows

&

ewes within 72 hours (6 milkings) following

treatment MUST NOT BE USED for human consumption or processing. This milk

should not be fed to bobby calves.

Version

Controlled

Draft

Label

Bomadin

Peniciliin

Iq

jection

Page 2 of 2

WARNING

Printed on 13-08-99 10: 11

Anaphylactic reactions following administration may occur in young cattle

&

require

prompt

treatment

with

antihistamines.

Store below

25OC

(air conditioning).

Dispose of empty container by wrapping with paper and putting garbage.

NRANo.

36023/.eq

Manufactured in the UK

for:-

Bomac

Laboratories

Limited

Distributed by:-

-*Pharm

Tech Pty Limited

ACN 084 248 206

Apollo

West Pymble

l&W

2073

InfoLine: 1800 624

Batch

Exp.:

7-12-2018

Magnesium citrate malate as a source of magnesium added for nutritional purposes to food supplements

Magnesium citrate malate as a source of magnesium added for nutritional purposes to food supplements

Published on: Thu, 06 Dec 2018 The present scientific opinion deals with the assessment of the bioavailability of magnesium, from the proposed nutrient source, magnesium citrate malate (MgCM), when added for nutritional purposes to food supplements. MgCM is a mixed salt consisting of magnesium cations and citrate and malate anions, and with a magnesium content of 12–15%. MgCM is proposed to be used in food supplements that are intended to provide up to 300–540 mg/day magnesium. The data provided demonst...

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Safety evaluation of the food enzyme acetolactate decarboxylase from a genetically modified Bacillus licheniformis (strain NZYM‐JB)

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Published on: Wed, 14 Nov 2018 The food enzyme acetolactate decarboxylase (α‐acetolactate decarboxylase; EC 4.1.1.5) is produced with a genetically modified Bacillus licheniformis strain NZYM‐JB by Novozymes A/S. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and recombinant DNA. This acetolactate decarboxylase is intended to be used in distilled alcohol production and brewing processes. Residual amounts of total organi...

Europe - EFSA - European Food Safety Authority Publications

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“Vita-X Revitalizing Capsules” for men may pose serious health risks

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Health Canada is advising Canadians that two versions of “Vita-X Revitalizing Capsules” by Lanlay Healthmetic Inc., promoted for “long lasting vital energy for men,” may pose serious health risks. One version contains seven capsules and has “NPN 80053009,” a Natural Product Number (NPN) indicating Health Canada authorization, on the label. The second version contains one capsule, has no NPN on the label and is not authorized by Health Canada.

Health Canada

30-10-2018

Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP  75 Mg, 150 Mg, and 300 Mg Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in The Active Pharmaceutical Ingredient (API)

Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP 75 Mg, 150 Mg, and 300 Mg Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in The Active Pharmaceutical Ingredient (API)

ScieGen Pharmaceuticals, Inc. is voluntarily recalling listed lots, within expiry, of Irbesartan Tablets, USP 75 mg, 150 mg, and 300 mg dosage forms to the consumer level. These products are being recalled due to the presence of an impurity, N-nitrosodiethylamine (NDEA) contained in the API Irbesartan, USP manufactured by Aurobindo Pharma Limited. This impurity, which is a substance that occurs naturally in certain foods, drinking water, air pollution, and industrial processes, has been classified as a...

FDA - U.S. Food and Drug Administration

30-10-2018

Pest categorisation of Aleurocanthus spp.

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Europe - EFSA - European Food Safety Authority Publications

18-10-2018

Stewart’s Shops Issues Allergy Alert on Undeclared Milk in Cranberry Apple Refresher

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Saratoga Springs, NY - Stewart’s Shops Corp. is recalling units of Stewart’s Shops brand Cranberry Apple Refresher 16 fluid oz. because the product may contain undeclared milk. People who have an allergy to milk run the risk of serious or life-threatening allergic reaction if they consume this product. Approximately 2,300 units of affected product were distributed in upstate New York and Southern Vermont.

FDA - U.S. Food and Drug Administration

12-9-2018

FDA takes new steps to address epidemic of youth e-cigarette use, including a historic action against more than 1,300 retailers and 5 major manufacturers for their roles perpetuating youth access

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FDA - U.S. Food and Drug Administration

19-7-2018

Openfoodtox: over 300 substances added to EFSA chemical hazards database

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Europe - EFSA - European Food Safety Authority Press Releases & News Stories

17-5-2018

JAGUAR 30000 capsules

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Safety advisory

Therapeutic Goods Administration - Australia

27-4-2018

EpiPen 300 mcg adrenaline auto-injector

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Medicine shortages

Therapeutic Goods Administration - Australia

13-6-2017

Annual report 2016 - Clinical trials of medicines

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LLast year, the Danish Medicines Agency received 286 clinical trial applications. This is a small decline compared to 2015. However, the number of clinical trial applications has remained stable at around 300 applications per year since 2013.

Danish Medicines Agency

6-4-2017

More batches of EpiPen® are withdrawn

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Danish Medicines Agency

17-3-2017

Withdrawal of a batch of EpiPen® 300 micrograms

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Danish Medicines Agency

21-2-2017

Takeda Pharma A/S recalls batch of Pamol® in packs of 300 film-coated tablets

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Danish Medicines Agency

21-9-2018

Scientific guideline:  Reflection paper on the use of aminopenicillins and their beta-lactamase inhibitor combinations in animals in the European Union: development of resistance and impact on human and animal health, draft: consultation open

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Europe - EMA - European Medicines Agency

27-6-2018

Yondelis (Pharma Mar S.A.)

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Europe -DG Health and Food Safety

16-5-2018

Busulfan Fresenius Kabi (Fresenius Kabi Deutschland GmbH)

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Busulfan Fresenius Kabi (Active substance: busulfan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3005 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2806/T/8

Europe -DG Health and Food Safety

15-5-2018

Lonquex (UAB Sicor Biotech)

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Lonquex (Active substance: lipegfilgrastim) - Centralised - Renewal - Commission Decision (2018)3009 of Tue, 15 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2556/R/39

Europe -DG Health and Food Safety

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Izba (Novartis Europharm Limited)

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Europe -DG Health and Food Safety

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KEYTRUDA (Merck Sharp and Dohme B.V.)

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Europe -DG Health and Food Safety

15-5-2018

LIFMIOR (Pfizer Limited)

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Travatan (Novartis Europharm Limited)

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Europe -DG Health and Food Safety

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Imatinib Teva B.V. (Teva B.V.)

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Europe -DG Health and Food Safety

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Instanyl (Takeda Pharma A/S)

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Europe -DG Health and Food Safety

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PecFent (Kyowa Kirin Services Ltd)

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