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It has been estimated that up to up to Many adverse reactions are well known. Information about them can be found in patient information leaflets supplied with medicines, in the Monthly Index of Medical Specialties (MIMS) or in the British National Formulary. However, not all patients will suffer all possible adverse reactions. Knowledge of family history can help predict who will suffer from adverse reactions.
It is therefore good practice when taking a patients history to ask about incidents of adverse reactions to drugs or allergies in the family.
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There are other metabolic affects associated with chronic corticosteroid use including: redistribution of fat giving the typical moon face and buffalo hump; hyperglycaemia and possible diabetes; protein loss from skeletal muscles with wasting and weakness; increased bone metabolism leading to osteoporosis; and growth inhibition in children due to early closure of the epiphyseal plates in long bones.
Adverse reactions to anti-inflammatory corticosteroids are summarized This is a diverse group of drugs that do not inhibit COX; neither do they have analgesic or direct anti-inflammatory activity. They appear to suppress the disease process in rheumatoid arthritis and other chronic inflammatory conditions and may cause remission of disease.
These are the disease-modifying antirheumatic drugs. Unlike NSAIDs and corticosteroids, they do not produce an immediate therapeutic effect but require four to six months of treatment for a full response. However, if one drug produces no objective benefit within six months, then it should be discontinued and replaced with an alternative.
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PΒ-blockers also show receptors in the peripheral staff vessels, kidney and ventricles.
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It is a drug that interacts with alcohol and generally increases the effects of central nervous system depressants and can produce hypertension.
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They are toxic drugs capable of causing skin reactions ranging from erythema to exfoliating dermatitis, inflammation of mucous membranes and blood dyscrasias. Penicillamine may inhibit production of inflammatory mediators and can delay the progress of disease.
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