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Side effects of non-depolarizing neuromuscular blockers are mainly caused by histamine release and include flushing, increased heart rate, hypotension and bronchospasm. Suxamethonium is the only example of a depolarizing neuromuscular blocker in current clinical use.
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Adverse effects include bone marrow suppression, liver and kidney toxicity and central nervous system damage. Some RNA viruses are known as retroviruses.
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This was probably because the majority of viral infections are eliminated by the hosts immune system. With the advent of the HIV and acquired immunodeficiency syndrome that follows infection with HIV, many new antiviral drugs have been introduced since the end of the about how viruses replicate inside cells and how they affect cell function, then no doubt more antiviral drugs will be developed. Antiviral drugs have been developed that work by the following mechanisms: inhibition of the synthesis of viral DNA, RNA and proteins (for example, nucleoside analogues, reverse transcriptase inhibitors, protease inhibitors); reduction in release of viral genetic material once inside the host cell (for example, amantadine); interference with penetration of virus through the cell membrane (for example, neuraminidase inhibitors); interference with attachment of the virus to the host cell membrane (for example, vaccines, immunoglobulins and interferons). Resistance can occur through a number of consequences of viral mutation. There may be reduced phosphorylation of the drug, alteration of viral enzyme targets, or alteration of target channel protein. These synthetic compounds resemble the natural nucleotides of viral DNA or RNA.
Adverse effects of protease inhibitors are similar to those seen with reverse transcriptase inhibitors. In addition, this group of drugs causes metabolic disturbances, particularly insulin resistance and hyperglycaemia, and fat redistribution leading to raised plasma lipid levels, which increases the risk of heart disease. These effects are collectively known as lipodystrophy syndrome, which appears to be similar to what happens with long-term corticosteroid use. All drugs in this group inhibit liver enzymes and cause interactions with many other drugs. In particular, they increase the risk of myopathy with statins. Some antiviral drugs in this group act by blocking an ion channel that allows the release of genetic material from viruses once they are inside the host cell and which allows viral particles to leave the infected host cell to infect other cells.
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Corticosteroids are anti-inflammatory drugs that can be used in asthma to reduce airway hyper-responsiveness and to decrease bronchial oedema and mucus secretion. They are effective in the late phase reaction and reduce the intensity of allergic reactions.
26.10.2016
Albert
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Metoclopramide is a dopamine antagonist that stimulates gastric emptying and small intestine transit and is used to speed up transit time of barium follow-through examinations.
17.04.2016
Bettina
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Cytotoxic drugs affect normal dividing cells producing unwanted adverse effects on bone marrow and the cells produced there; reduced healing; loss of hair due to damage to hair producing cells in hair follicles; damage to the gastrointestinal lining; reduced growth in children; sterility; and damage to the foetus. Nausea and vomiting are common with most anti-cancer drugs and are caused by toxic effects on the chemotrigger zone of the central nervous system.
09.05.2016
Manfred
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Nutrients absorbed pass directly to the liver in the hepatic portal system before going to other parts of the body. The liver excretes some drugs into the intestine via bile.
08.11.2017
Agathe
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Hyperuricaemia can result from the kidneys being unable to excrete uric acid fast enough or from the body making too much uric acid.
27.06.2020
Theobald
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