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This interferes with the normal base pairing of guanine with cytosine and allows cross-linking of guanine with other guanine molecules in the same strand and opposite strand of DNA.

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These synthetic compounds resemble the natural nucleotides of viral DNA or RNA. They are phosphorylated in infected cells and then compete with the normal nucleotides for incorporation into viral DNA or RNA. This results in irreversible inhibition of viral polymerase. (Note: a nucleoside is a base [either purine or pyrimidine] plus a sugar molecule; a nucleotide is a base plus a phosphorylated sugar molecule. See Figure for a diagram of a nucleotide. ) Aciclovir is an analogue of guanosine nucleoside.

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As the same drug can be manufactured by several different companies, a drug can have multiple proprietary names and this can be confusing. Hence, proprietary names have been avoided in this book except where the proprietary name is in common usage. In the United Kingdom, the generic name is known as the British approved name. Following European Directive European Law requires the use of the recommended International Non-proprietary Name (rINN). This ensures that all countries, in Europe at least, recognize the same drug. In most cases, the BAN and the rINN were the same, but some British names have been changed. For example, amphetamine is now spelt amfetamine and lignocaine is now lidocaine. Where this has happened, both names are listed in the BNF. Wherever possible, drugs should be prescribed by their generic name; this allows any suitable product to be dispensed and in many cases, it saves the health service money.

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Gov. ukenPolicyAndGuidanceMedicinesPharmacyAndIndustry PrescriptionsTheNon-MedicalPrescribingProgrammeindex. htm Department of Health Non-medical Prescribing. http:www. mhra.

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From the gastrointestinal tract, a drug goes to the liver in the hepatic portal system where it is likely to be metabolized. Metabolism usually makes a buy valium online paypal more water soluble and less pharmacologically active. Distribution to the rest of the body depends on how well a drug can pass across cell membranes. Some drugs can be sequestered in certain tissues, particularly fat and muscle. Many drugs are bound to plasma proteins and this can limit their distribution and action because only the free drug can have an effect.

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Thalassaemia is found in people from countries around the Mediterranean. Pregnancy, infection and malnutrition all make these types of anaemias worse. There is no specific treatment for sickle cell disease or thalassaemia. Patients are usually given folic acid because there is a high turn over of erythrocytes and they are likely to become deficient in folic acid. In normal lipid metabolism, lipids in the diet are converted to triglycerides, which are used in muscle and adipose tissue. Cholesterol is used for the synthesis of steroid hormones and bile acids and by all cells as part of the cell membrane.

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An example is valsartan. This is a relatively new group of drugs and adverse effects appear to be rare. They provide an alternative for those who cannot tolerate ACE inhibitors because of a persistent dry cough, but should not be used in pregnancy either. Neither ACE inhibitors nor angiotensin II receptor inhibitors seem to benefit patients of African origin. Nitrates are used primarily to treat ischaemic heart disease. These drugs are potent coronary vasodilators and can increase blood flow to the myocardium.

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Treatment of hypertension is symptomatic, aiming to maintain blood pressure below life. Before treatment begins, it is important to weigh the benefits of blood pressure reduction against the possible consequences of drug treatment.

  • However, the majority of drugs are too large to diffuse in this way.
  • In many respects, supplementary prescribing is better than PGDs and the values of this mechanism with respect to toxicity management are indicated below: PGDs are inflexible, being restricted to specific medicines at specific doses.
  • Similarly, acidic drugs tend to bind to plasma albumin and therefore also remain in the blood stream and have a small volume of distribution.
  • The book is an introduction to pharmacology for health care professionals.
  • Both conditions result in increased risk of fracture and can be treated with calcitonin and bisphosphonates.

Cell membranes have LDL receptors to which LDLs attach prior to being taken into the cell. The LDLs are broken down in the cell, the lipids used and the receptors temporarily disappear.

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Plasmin is normally found circulating in the blood as its inactive precursor plasminogen. It is activated by tissue plasminogen activator as healing takes place.

An example is moclobemide. Nevertheless, MAOIs should be regarded as second line drugs and are indicated when the patient is resistant to other therapy, or is phobic, hysterical or has other atypical symptoms. All patients taking MAOIs should buy valium online paypal a warning card highlighting the potential dangers of interaction with other drugs and food substances. Lithium is used for the prophylactic control of mania and hypomania and bipolar depression. It also has a use in unipolar depression that is unresponsive to other antidepressants.

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This route can provide a rapid means of absorption of a drug. It is a route commonly used, for example, to treat attacks of angina with glyceryl trinitrate. Factors affecting absorption from the oral mucosal membranes include lipid solubility and molecular weight of the drug, pH of the saliva and the rate of removal by the blood as well as the application of the correct technique. Some drugs administered this way are intended to have a local effect, for example to treat oral or throat infections. The main disadvantage of this route of administration is that most drugs do not taste nice. Nasal administration is often intended to have a local effect, as in the use of nasal decongestants, although certain drugs are given this way to have a systemic effect.


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This results in a delay in electrical conduction in cardiac muscle, reduced contractility and reduction in the heart rate. Because of these effects, class I calcium channel blockers are used to treat ischaemic heart disease and atrial arrhythmia.

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