Drug Legislation - Revision history

Bara: /* Introduction */

2013-08-15T13:17:55Z

Introduction

Raquel.gopal at 12:38, 14 August 2013

2013-08-14T12:38:45Z

Bara: /* Introduction */

2012-06-06T07:03:12Z

Introduction

Bara at 17:22, 9 December 2010

2010-12-09T17:22:54Z

Suzannah.stacey: /* Introduction */

2010-10-02T19:00:12Z

Introduction

Suzannah.stacey: /* Drug Classifications */

2010-09-15T19:33:35Z

Drug Classifications

Suzannah.stacey: /* Drug Classifications */

2010-09-15T18:48:38Z

Drug Classifications

Suzannah.stacey: /* Drug Classifications */

2010-09-15T18:42:40Z

Drug Classifications

Suzannah.stacey: /* The Drugs Cascade */

2010-08-31T21:13:59Z

The Drugs Cascade

Suzannah.stacey: /* The Drugs Cascade */

2010-08-31T21:13:15Z

The Drugs Cascade

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 The information below is mostly relevant to the United Kingdom.
-The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications occurring in the UK via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy.  Adverse events occurring in other European Union (EU) Member States, Norway, Iceland and Liechtenstein, should be reported to the relevant competent authority where the event occurred using the [http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/document_listing/document_listing_000176.jsp&mid=WC0b01ac058002ddcb/ EU reporting forms for veterinarians] which are available in each EU language on the [http://www.ema.europa.eu/ European Medicines Agency] website. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.
+The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications occurring in the UK via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy. [[Adverse Drug Reactions|Adverse events]] occurring in other European Union (EU) Member States, Norway, Iceland and Liechtenstein, should be reported to the relevant competent authority where the event occurred using the [http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/document_listing/document_listing_000176.jsp&mid=WC0b01ac058002ddcb/ EU reporting forms for veterinarians] which are available in each EU language on the [http://www.ema.europa.eu/ European Medicines Agency] website. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.
 In 2003 the Competition Commission investigated the supply of veterinary medicines, and an Order was drawn up by the Department of Trade and Industry to alter the way in which prescription only medicines (POMs) were supplied to the public in the UK. The aim of the order was to increase public awareness of the price of POMs, to encourage the use of prescriptions to give the public more choice of suppliers, and to increase the manufacturer’s supply of POMs to other outlets such as pharmacies. The Competition Commission’s involvement with veterinary medicines was to investigate potential monopolies; it has no interest in drug safety or efficacy.

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 The information below is mostly relevant to the United Kingdom.
-The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.
+The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications occurring in the UK via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy.  Adverse events occurring in other European Union (EU) Member States, Norway, Iceland and Liechtenstein, should be reported to the relevant competent authority where the event occurred using the [http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/document_listing/document_listing_000176.jsp&mid=WC0b01ac058002ddcb/ EU reporting forms for veterinarians] which are available in each EU language on the [http://www.ema.europa.eu/ European Medicines Agency] website. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.
 In 2003 the Competition Commission investigated the supply of veterinary medicines, and an Order was drawn up by the Department of Trade and Industry to alter the way in which prescription only medicines (POMs) were supplied to the public in the UK. The aim of the order was to increase public awareness of the price of POMs, to encourage the use of prescriptions to give the public more choice of suppliers, and to increase the manufacturer’s supply of POMs to other outlets such as pharmacies. The Competition Commission’s involvement with veterinary medicines was to investigate potential monopolies; it has no interest in drug safety or efficacy.

← Older revision		Revision as of 07:03, 6 June 2012
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	==Introduction==		==Introduction==
		+	The information below is mostly relevant to the United Kingdom.
		+
	The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.		The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.

← Older revision		Revision as of 17:22, 9 December 2010
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	<big>'''It is important to realise that failure to treat animals according to the cascade is a criminal offence.'''<big>		<big>'''It is important to realise that failure to treat animals according to the cascade is a criminal offence.'''<big>
		+
		+	[[Category:Pharmacology]]

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 ==Introduction==
-The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications via the 'yellow form' MLA252A - this can include incidents where treatments fail to show efficacy. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.
+The Veterinary Medicines Regulations, which are revised and updated on an annual basis, govern the supply and prescribing of veterinary drugs. The Veterinary Medicines Regulations replaced the Medicines Act 1968 in 2005. The Veterinary Medicines Directorate (VMD), which is a department of the Department for Environment, Food and Rural Affairs (DEFRA) check the safety and efficacy of veterinary drugs for owners, animals and the environment prior to a drug reaching the sales market. Once a drug is authorised, the VMD collect information from veterinary surgeons about suspected adverse reactions to medications via the [http://www.vmd.gov.uk/ 'yellow form' MLA252A] - this can include incidents where treatments fail to show efficacy. The VMD also inspect premises where veterinary drugs are manufactured, stocked or supplied to the general public and enforce the regulations where necessary.
 In 2003 the Competition Commission investigated the supply of veterinary medicines, and an Order was drawn up by the Department of Trade and Industry to alter the way in which prescription only medicines (POMs) were supplied to the public in the UK. The aim of the order was to increase public awareness of the price of POMs, to encourage the use of prescriptions to give the public more choice of suppliers, and to increase the manufacturer’s supply of POMs to other outlets such as pharmacies. The Competition Commission’s involvement with veterinary medicines was to investigate potential monopolies; it has no interest in drug safety or efficacy.

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 *'''POM-V'''  or prescription only medicine – veterinarian. Drugs in this class require a clinical assessment of the animal by a qualified vet; the animal must be under his or her care, and only the minimum amount of medication required for treatment should be dispensed. A prescription is always required but it need not be in writing if the vet who prescribed the medication also supplies it. Vets can delegate the handing over of a POM-V medicine to a ‘competent’ person proving that each transaction is individually authorised. The regulations do not define what competent means, but some evidence must be available for the vet to be able to justify delegating to the person concerned - such as attendance at a relevant Continued Professional Development (CPD) event, and a standard operating procedure for use by members of staff who give out POM-V drugs to clients is considered good practice under the regulations. Information must be given to the client on the safe use of the product, and the client must be assessed as intending to use the product in the authorised manner.
 *'''POM-VPS''' or prescription only medicine – veterinarian, pharmacist or [[SQPs|suitably qualified person (SQP)]]. Medicines in this category also require a prescription, but the animal does not have to be clinically assessed or be under the care of a vet. Prescriptions must consider the health and wellbeing of the animal concerned, and can also be written by a pharmacist or a SQP operating from premises registered with the VMD. The vet can delegate the handing over of these medicines to a competent person (see above) and prices of POM-V and POM-VPS medications can be advertised to the public, but not the medications themselves.
-*'''NFA-VPS''' or non food producing animal – veterinarian, pharmacist, SQP. Medicines in this category do not require a prescription, but must be supplied by a vet, pharmacist or SQP and the supplier must ascertain if the owner is likely to use the drug in the authorised manner. Information must be given on the safe use of the medication. NFA-VPS medication can be advertised to the general public.
+*'''NFA-VPS''' or non food producing animal – veterinarian, pharmacist, [[SQPs|SQP]]. Medicines in this category do not require a prescription, but must be supplied by a vet, pharmacist or SQP and the supplier must ascertain if the owner is likely to use the drug in the authorised manner. Information must be given on the safe use of the medication. NFA-VPS medication can be advertised to the general public.
 *'''AVM - GSL''' or authorized veterinary medicine – general sales list. Medicines in this category may be supplied to anyone by any retailer, but must be supplied responsibly by veterinary practices.

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 *'''POM-VPS''' or prescription only medicine – veterinarian, pharmacist or suitably qualified person (SQP). Medicines in this category also require a prescription, but the animal does not have to be clinically assessed or be under the care of a vet. Prescriptions must consider the health and wellbeing of the animal concerned, and can also be written by a pharmacist or a SQP operating from premises registered with the VMD. The vet can delegate the handing over of these medicines to a competent person (see above) and prices of POM-V and POM-VPS medications can be advertised to the public, but not the medications themselves.
 *'''NFA-VPS''' or non food producing animal – veterinarian, pharmacist, SQP. Medicines in this category do not require a prescription, but must be supplied by a vet, pharmacist or SQP and the supplier must ascertain if the owner is likely to use the drug in the authorised manner. Information must be given on the safe use of the medication. NFA-VPS medication can be advertised to the general public.
 ==RCVS Guidance on animals 'under the care of a vet'==

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 # authorised for the same condition but in another species, or
 # for another condition within the same species.
-As these medications have not been tested in the animal for the condition being treated, use of them requires the vet to inform the owner od this and the owner must give consent for the ('off label') use of the medication.
+As these medications have not been tested in the animal for the condition being treated, use of them requires the vet to inform the owner of this and the owner must give consent for the ('off label') use of the medication.
 If there is no suitable medication in these categories, then the vet can prescribe:

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 The VMR states that legally vets are required to treat animals with medications that have been:
-# safety tested in the species being treated
+# safety tested in the species being treated, and
 # have proven efficacy for the condition being treated, wherever possible. This precludes the use of generic drugs from the field of human medicine.