The 1982 Tylenol crisis influenced changes in medication safety rules in the United States through the creation of tamper-proof pill and bottle designs. Many people are afraid to take over-the-counter drugs because of the problem. People of all ages, from children to the elderly, were terrified. People who had just taken Tylenol were terrified. They had no faith in Tylenol or Johnson & Johnson. This incident taught us how to handle a similar circumstance and increase the consumer safety of medicines. September 29, 1982 saw the onset of the Tylenol Crisis of 1982. The first victim was a 12 year old Mary Kelleman who had a cold and to treat Mary's cold, her dad gave her tylenol and he witnessed Mary going to the bathroom which he hears a loud thud and goes to the bathroom to discover Mary on the bathroom door, motionless and convulsing. He immediately dialed 911 and hurried to the hospital, where physicians …show more content…
It enhanced Johnson & Johnson's quality. It caused individuals to identify Tylenol and John & Johnson with positive ethnicity. To safeguard future purchasers of the goods, new measures of product protection were created as a result of the recall. Johnson & Johnson collaborated with FDA officials to build innovative tamper-proof packaging that encompasses foil seals and other attributes that would be evident to a buyer if foul play had occurred, resulting in the packaging safeguards quickly becoming the industry standard for all over-the-counter medications. Tylenol's sales returned to normal after a year and a $100 million investment, transforming it into the nation's favorite over-the-counter pain reliever. The Tylenol Crisis of 1982 also resulted in a modification to the law. The Federal Anti-Tampering Act, also known as the Tylenol Act, made trying to interfere with medicines a felony and decided to make it an FDA requirement that medicines be encased with tamper-resistant