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If a drug is water soluble it is likely to remain in the blood stream and its volume of distribution will be relatively small and equal blood volume. Similarly, acidic drugs tend to bind to plasma albumin and therefore also remain in the blood stream and have a small volume of distribution. If a drug is highly lipid soluble, then it will be distributed to many parts of the body and have a large volume of distribution. In addition, basic drugs tend to bind to tissue proteins and as a result have a large volume of distribution. On entering the body, drugs are treated as if they are toxic substances, which need to be detoxified, if a mechanism exists, and eliminated as soon as possible. This means that most drugs are subjected to some kind of metabolism and then excreted. Metabolism involves changes to the molecular structure of a substance and these changes are produced by the action of enzymes. This has two important effects on drug molecules: kidneys; This is not always the case. A drug metabolite may have a new and completely different pharmacological activity, or it may be as active as or more active than the original drug. Some drugs have to be metabolized in order to become active.

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Cardiac output is the volume of blood pumped out of the left ventricle every minute and is a function of the stroke volume and heart rate. Stroke volume is the amount of blood ejected by the left ventricle during one contraction and the heart rate is the number of beats per minute. For an average person at rest, stroke volume is around rate is about or about in the bodys demand for oxygen, for example during exercise. Normally, the force of contraction of cardiac muscle depends on its resting length. End diastolic volume is the volume of blood in the ventricles just before they contract. If EDV increases, cardiac muscle is stretched and this produces an increase in the force of contraction.


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The effect of acarbose is to reduce the postprandial online ordering phentermine in blood glucose levels. Adverse effects of acarbose are abdominal discomfort and flatulence. Prandial glucose regulators are relatively new oral hypoglycaemics. Examples are nateglinide and repaglinide. They stimulate insulin release from β-cells in the pancreas.


A disadvantage of propofol is that it is painful on injection. Ketamine produces a different effect to other intravenous anaesthetics; analgesia, sensory loss, amnesia and muscle paralysis are produced without loss of consciousness, so-called dissociative anaesthesia, and with minimal respiratory depression. The site of action of ketamine is thought to be through inhibition at glutamate receptors. Ketamine is a phencyclidine derivative and as such has abuse potential. Phencyclidine was developed in the hallucinations and delirium.


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A number of drugs are used as adjuncts to radiography. They can be administered by qualified, registered and trained radiographers under patient group directions. Analgesia may be necessary for the after-effects of venepuncture or following therapeutic radiographic procedures. Peripherally acting analgesics, for example paracetamol, aspirin or ibuprofen should be sufficient. For pain that is more severe codeine may be necessary. Topical anaesthesia prior to venepuncture may be necessary.


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Mr Lewis also has type Mr Lewis is on a complex regime of drug therapy (and you may need to consult the BNF): Metformin Prednisolone Asasantin one capsule twice daily Omeprazole Sertraline Temazepam Salbutamol Glyceryl trinitrate Amlodipine Perindopril Acetazolamide Erythromycin Discuss the treatment of this patient using the questions below as a guide. They are intended to stimulate discussion not limit debate.

  • Initial referral from GPs of these high-risk patients includes the drawing up of pre-arranged CMPs, with the patients consent, before consultation with the podiatrist.
  • All NSAIDs are contraindicated in patients with active peptic ulceration and in those who have a history of hypersensitivity to any NSAID.
  • Finally, the chapters are finished off with review questions to test the readers understanding of key concepts.
  • Where does liability rest.

Resistance to antimalarial drugs is common. Toxoplasma infection is common in the United Kingdom and normally causes a mild illness that can go unnoticed.


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The mouth is where food is chewed and mixed with saliva before being swallowed. The oesophagus conveys food to the stomach.

They bind to tubulin and prevent its polymerization into microtubules. Microtubules form the spindle during mitosis, so vinca alkaloids halt mitosis at a certain stage. Examples of vinca alkaloids are vinblastine, vincristine and vindesine. These drugs are used to treat leukaemia, lymphoma, testicular cancer and lung cancer. Adverse reactions of vinca alkaloids are relatively mild.


In hospitals, coal tar is often combined with ultraviolet B (UVB) radiation. There are many proprietary preparations, which are more refined and therefore more acceptable to patients, but they are less effective. They are used as a creams, lotions, ointments and bath oils in concentrations from Coal tar preparations are less irritating to normal skin than dithranol, but can cause folliculitis. Keratolytics break down keratin and soften skin, which improves penetration of other treatments. Salicylic acid ointment is most frequently used either on its own or in combination with coal tar or dithranol. Phototherapy is the use of ultraviolet light, which produces improvement in most patients with psoriasis but should only be done under supervision of a dermatologist.

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