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SHAHSWAR
Infectious disease may be an unavoidable fact of life, but there are many strategies available to
help us protect ourselves from infection and to treat a disease once it has developed.
Some are simple steps that individuals can take; others are national or global methods of
detection, prevention, and treatment. All are critical to keeping communities, nations, and global
populations healthy and secure.
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Vaccines and Medicines
Medicines have existed in human society probably as long as sickness itself. However, with the
advent of the modern pharmaceutical industry, biochemical approaches to preventing and
treating disease have acquired a new level of prominence in the evolving relationship between
microbes and their human hosts.
Vaccines
In the past, thimerosal, a preservative that contains mercury, was used in some vaccines and
other products. Use of this product became the subject of controversy, with some arguing that
the substance caused autism in children. Extensive, independent research has presented no
convincing evidence of harm associated with the low levels of thimerosal present in vaccines.
Since 2001, thimerosal has not been routinely used as a preservative in recommended
childhood vaccines.
Antibiotics don’t work against viral infections such as colds or the flu. In those cases, antiviral
drugs, which fight infection either by inhibiting a virus’s ability to reproduce or by strengthening
the body’s immune response to the infection, are used. There are several different classes of
drugs in the antiviral family, and each is used for specific kinds of viral infections. (Unlike
antibacterial drugs, which may cover a wide spectrum of pathogens, antiviral medications are
used to treat a narrower range of organisms.) Antiviral drugs are now available to treat a
number of viruses, including influenza, HIV, herpes, and hepatitis B. Like bacteria, viruses
mutate over time and develop resistance to antiviral drugs.
New Treatments
Modern medicine needs new kinds of antibiotics and antivirals to treat drug-resistant infections.
But the pipeline of new drugs is drying up. For example, nearly 40 years elapsed between
introduction of the two newest molecular classes of antibiotics: fluoroquinolones (such as Cipro)
in 1962 and the oxazolidinones (such as Zyvox) in 2000.
Major pharmaceutical companies have limited interest in dedicating resources to the antibiotics
market because these short-course drugs are not as profitable as drugs that treat chronic
conditions and lifestyle-related ailments, such as high blood pressure or high cholesterol.
Antibiotic research and development is also expensive, risky, and time consuming. Return on
that investment can be unpredictable, considering that resistance to antibiotics develops over
time, eventually making them less effective.