Post-synaptic receptors. Mirtazapine enhances both noradrenergic and serotonergic transmission through block of pre-synaptic α-adrenergic receptors and Due to the blockade of drug does not produce the nausea associated with other serotonergic drugs. Mirtazapine does cause sedation and weight gain. Trazodone antagonizes both pre-synaptic α-adrenergic and post-synaptic It has sedative properties and causes fewer anti-cholinergic side effects than the tricyclics. Monoamine oxidase inhibitors are drugs that irreversibly inhibit the action of the enzyme monoamine oxidase. Monoamine oxidase exists in two forms: MAO-A and MAO-B.

Disadvantages are that many drugs do not taste particularly nice; some can upset the stomach and cause nausea and vomiting or even ulcerate the stomach lining, while others may be destroyed by stomach acid or digestive enzymes or be extensively metabolized in the liver. The oral route requires a co-operative and conscious patient. Rectal administration avoids drug inactivation by stomach acid and digestive enzymes and about circulation. In some circumstances, it may be advantageous to administer a drug rectally, for example if a patient is unconscious or vomiting, or uncooperative in some way, but generally, it is considered an unpleasant method. Many of the general factors considered above that affect absorption from the gastrointestinal tract apply equally to this route of administration. Sublingual administration of a drug allows the drug to go directly into the systemic circulation without first passing through the liver.

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Osteoarthritis is primarily a degenerative disease of cartilage. With breakdown of cartilage inflammation of the synovium can occur. This is followed by more cartilage destruction and bone remodelling as an attempt at repair. Unlike rheumatoid arthritis, there is no systemic disease associated with osteoarthritis. Treatment of osteoarthritis is with NSAIDs for their analgesic and anti-inflammatory effects.

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It is diagnosed after persistent symmetrical multiple joint inflammation of more than six weeks duration. There is elevation of acute phase plasma proteins, which are released during inflammation and often vasculitis and damage to heart muscle. The serum of most patients contains rheumatoid factors, which are autoantibodies that induce complement and macrophage activation and contribute to inflammation. The disease progression varies in different individuals. Juvenile rheumatoid arthritis occurs before the age of and the disease can adversely affect growth in children. Ankylosing spondylitis particularly affects the iliosacral and vertebral joints which eventually become fused.

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Adverse effects of phenobarbital include sedation, which can occur at therapeutic doses and is a serious disadvantage in a drug that would have to be taken for many years. Other adverse effects include megaloblastic anaemia, mild hypersensitivity reactions and osteomalacia. Phenobarbital is dangerous in overdose, producing coma and respiratory and circulatory failure and consequently is not much used nowadays. Most benzodiazepines are not useful in treating epilepsy because of their sedative effects and exacerbation of seizures on withdrawal. However, intravenous diazepam is used to treat status epilepticus. Not all epileptic seizures can be controlled by conventional therapy, and so new drugs have and are being developed.

Flucytosine is used to treat some systemic fungal infections. It is an antimetabolite that is converted to an enzyme necessary for DNA synthesis. Adverse effects of flucytosine are gastrointestinal upset, anaemia, neutropenia, thrombocytopenia and alopecia, all mild and reversible. 1000 mg of acyclovir group of drugs inhibits an enzyme necessary for ergosterol synthesis. Some of these drugs are used orally to treat systemic fungal infections; others are used topically to treat skin and nail infection.

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Supplementary prescribing would be appropriate in these situations. Independent prescribing would grow out of supplementary prescribing for specific conditions and particular patient groups. Nuclear medicine is worthy of aturan minum acyclovir tablet 400mg mention for three reasons: Medicines for Human Use Miscellaneous Amendments Order, While working within nuclear medicine, technicians and radiographers often have similar responsibilities. This is particularly true for activities involving the scanning of patients where there is frequently a requirement to administer adjunct medicines, such as diuretics. For this activity, radiographers have been working within PGDs or in limited cases using PSDs.

The importance of this is that highly lipid-soluble drugs, for example benzodiazepines, tend to have prolonged duration of action. Plasma protein concentration also falls with age. This means that for extensively protein bound drugs there will be a greater concentration of free drug than expected. This could lead to increased incidence of side effects. This is the case with pethidine (an analgesic).

Premedication with corticosteroids is recommended for such patients. Cautious use of contrast agents is indicated in patients with epilepsy, hepato-renal syndrome, severe respiratory disease and diabetes. They should not be administered to patients who are taking metformin for Type agents can increase the risk of lactic acidosis. Adverse reactions to iodine contrast agents are rare, especially with the newer non-ionic dimers of low osmolality. Adverse reactions range from mild effects, such as nausea and vomiting, to moderate effects, such as erythema and chest pain.

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