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The end result is cell death by apoptosis. Although alkylating agents can act on cells at any stage of the cell cycle, they are most effective in the S phase of the cell cycle and are therefore most cytotoxic to rapidly dividing cells.
Nowadays all such contrast media are derivatives of tri-iodinated benzoic acid. Monomeric contrast agents contain one benzene ring and have been used orally for examination of the gall bladder.
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Oral antihistamines that have a sedative effect may be useful at night to reduce nocturnal itching, which can cause skin damage and secondary infection. In very severe eczema, topical corticosteroids may not be sufficient to relieve the inflammation. In these cases, specialist treatment with drugs that suppress the immune system may be required. These drugs are normally used to prevent transplant rejection. For severe eczema refractory to other treatment, ciclosporin is licensed for oral use and tacrolimus is licensed for topical use.
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In fact, penicillins are probably the least toxic drugs known. Hypersensitivity reactions to penicillins occur in up to from mild skin rashes to exfoliative dermatitis and Stevens-Johnson syndrome (immune vasculitis with arthritis, nephritis, central nervous system abnormalities and myocarditis) and from bronchoconstriction to life-threatening anaphylactic shock. Flucloxacillin and amoxicillin have recently been added to the list of drugs that can be accessed and supplied by podiatrists registered with the Health Professions Council ( of medicines by podiatrists). There are many drugs in the cephalosporin group.
After five years of treatment about half of patients will experience the drug becoming less effective and a gradual recurrence of symptoms, especially hypokinesia, occurs. Another type of deterioration is the shortening of action of each dose with time (end of dose deterioration) and unpredictable fluctuations in response to treatment, which can happen quite abruptly. It is not known why these effects occur, but they may be due to advance of the disease process. End of dose deterioration can be alleviated to a certain extent by the use of modified release preparations of levodopa or by the concurrent use of catechol-o-methyl transferase inhibitors, for example entacapone. COMT inhibitors prevent the peripheral breakdown of levodopa by an enzyme, COMT.
Authored by Dr. Tibor Moskovits, MD