Why Unknown Side Effects Lead to Maryland Defective Product Cases

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The Federal Food and Drug Administration requires pharmaceutical manufacturers to go through years of trials in order for drugs and medical devices to go onto the market. However, there are unintended consequences that can lead to thousands of injuries, if not deaths. There are numerous drugs that have been linked to problems, both known and unknown.

For example, sleeping medications have been linked to a higher risk for cancer. Selective serotonin re-uptake inhibitor (SSRI) antidepressant birth defect side effects are already leading to settlements for distraught families. Several of the new blood thinners have no antidote, which means that if someone starts to hemorrhage, they may only have a one-in-four chance of surviving.

Some of these were known when the products launched, like the anticoagulants. Maryland defective product attorneys note that others did not surface until later, as with antidepressant birth defect risks. The problem comes from two sources: one, the FDA can be slow to take adverse effect reports and turn them into actual warnings and two, the drug makers can sometimes use first adopters like guinea pigs just like computer makers.

However, it is not just medical devices like hip implants or vaginal mesh implants, nor prescription drugs. People who develop medical conditions without being able to discern the cause with the help of medical professionals may also be the victim of exposure to dangerous chemicals. It is what caused decades of litigation with asbestos and the resulting mesothelioma.

The key takeaway is that it can take years between when someone develops symptoms for a disorder or disease, or when a medical researcher performs a small-scale study, and when the media finally draws attention to these problems. It does not help that the FDA is faster to approve drugs and devices than it is to take them off the market.

In the example of the blood thinner, hundreds of people die in the United States each year, a fact that the FDA ignores when it says the drugs are safer than older options that have antidotes. Thousands of metal on metal hip implant lawsuits have been filed, yet in spite of early warnings, the agency quickly approved next-generation models while failures were happening.

Experienced Maryland defective product attorneys do not go after companies when the evidence is lacking. However, there are a number of products and devices sold to the public where problems are known to experts, but not the general public.

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