
The FDA has taken an industry-friendly approach toward companies using unproven cell cocktails to treat people desperate for relief from aging or damaged joints
Quick ReadThe FDA has taken an industry-friendly approach toward companies using unproven cell cocktails to treat people desperate for relief from aging or damaged joints
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Will Gene-Edited Food Be Government Regulated?May 10, 2019 |
If you take genes from another kind of plant, or bacteria, and insert them into a crop like soybeans, the result is considered a GMO. You need government approval to sell a new GMO. If you just take a snippet out of a gene without inserting anything new, though, the product falls into a gray area
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The Birth-Tissue ProfiteersMay 7, 2019 |
How well-meaning donations end up fueling an unproven, virtually unregulated $2 billion stem cell industry
Quick ReadThe agency ruled that Dengvaxia, can only be used in individuals aged 9 to 16 living in parts of the United States where the dengue virus is endemic. Furthermore, the vaccine can only be given to children and teens who have had one previous laboratory-confirmed case of dengue
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People Are Clamoring to Buy Old Insulin PumpsApril 29, 2019 |
How an obsolete medical device with a security flaw became a must-have for some patients with type 1 diabetes. In 2014, a few hackers realized that the security flaw in certain Medtronic pumps could be exploited for a DIY revolution.
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OverprescribedApril 3, 2019 |
High cost isn’t America’s only drug problem. The pharmaceutical industry has followed a brilliant two-pronged strategy to maximize its profits: raise prices and increase consumption of medications
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Drug Shortages Jeopardize the Lives of Children with CancerMarch 19, 2019 |
Our Yoram Unguru writes, “Having cancer is hard enough without unnecessary and preventable impediments such as drug shortages, which represent a particularly vexing challenge. In the United States, shortages of drugs for cancer and other diseases over the past decade have become the new normal and the problem is getting worse.”
Quick ReadThe Food and Drug Administration has let medical device companies file reports of injuries and malfunctions outside a widely scrutinized public database, which leave doctors and medical sleuths in the dark
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