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Official bodies concerned with the use, quality and safety of medicines are the Commission on Human Medicines, the Medicines and Healthcare Products Regulatory Agency and the National Institute for Health and Clinical Excellence.
The medicinal products to which this exemption applies are shown below: в Any medicinal product for external use that is on the current general sale list в Any of the following medicinal products all of which are legally classified as Pharmacy Medicines, and are for external use: potassium permanganate crystals or solution, ointment of heparinoid and hyaluronidase в Any product which contains any of the following substances, providing the stated strength is not exceeded: в and recently added: в Any of the following medicinal products, a most of which are POM: co-dydramol does not exceed three days treatment amorolfine hydrochloride cream where the maximum concentration does not exceed amorolfine hydrochloride lacquer where the maximum concentration does not exceed topical hydrocortisone cream where the maximum concentration does not exceed ibuprofen, other than POM preparations, sufficient for three days treatment at a maximum single dose of pack size of в and recently added: silver sulfadiazine amoxicillin erythromycin flucloxacillin tioconazole Registered podiatrists who hold a certificate of competence in the use of analgesics approved by the HPC are allowed to administer parenteral analgesics (and some other injectable drugs) in the course of their professional practice.
These substances are POM and would otherwise only be available for use by appropriate medical practitioners.
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Fatalities have occurred and these drugs are still being monitored by the Medicines and Voltaren emulgel price Products Regulatory Agency. ( A monoclonal antibody against human epidermal growth factor receptors has been developed for use in metastatic breast cancer. This drug is trastuzumab and is also being monitored by the MHRA. Drugs that target known oncogenes are under development.
These drugs are known as antisense oligonucleotides, which are small synthetic pieces of DNA that are complementary to a segment of mRNA.
Discussions with those holding responsibility for creating the PGDs revealed that there was no mechanism for sharing paperwork between Trusts. It is not surprising, therefore, that PGDs for the same application can look remarkably different in different Trusts. A further consequence is that considerable time can be wasted by people repeating the same development work time and time again. While there is fairly widespread uptake of PGDs in diagnostic radiography, there is also a wide range of good and suboptimal practice.
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