In 1953, a new drug was made, and by 1957 it was on the market. In the six years that followed, over 10,000 children in 46 countries were born with congenital deformities[1]. The disaster was known as the thalidomide scandal, and led to serious reforms in drug regulation and monitoring worldwide.
Then, in 1961, two doctors independently called out statistically high numbers of congenital abnormalities in “thalidomide babies” – 20% where the normal rate is 1.5% (or a bit higher, depending on your source)[2].
What happened?
Thalidomide was prescribed for insomnia, anxiety, asthma, hypertension, migraine, and morning sickness. Doctors thought that it was very safe because taking an overdose simply cast the drinker into a prolonged sleep – and did not cause death. It was also non-addictive. Nobody tested it in pregnant women or animals.Then, in 1961, two doctors independently called out statistically high numbers of congenital abnormalities in “thalidomide babies” – 20% where the normal rate is 1.5% (or a bit higher, depending on your source)[2].
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Thalidomide babies. Image via Wikipedia Commons. |