The amount of biological molecules already in use in human therapy and the consistency of the promised new entries demand attention to clinicians, oncologists, rheumatologists, immunologists, allergologists, to health care professionals, and to public health surveillance. It is reasonable to assume that, together with the new entries and their massive therapeutic expansion, an increasing number of known adverse events and new reactions are to be expected, and will need to be observed, possibly prevented, and controlled.
KeywordsAdverse Drug Event Biological Response Modifier Public Health Surveillance Autoinflammatory Disease Adverse Event Follow Immunization
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