Hyland's Teething Tables
What evidence exists about the adverse events associated with Hyland's teething tablets?
According to investigations conducted by the U.S. Food and Drug Administration (FDA) regarding the Hyland's teething tablets in 2010, it was established that the drug does contain belladonna. Belladonna is a substance known to cause serious harm when consumed in huge doses. The FDA recognized whenever such a product was being used there should be careful controls in place to ensure that the amount being used is properly measured and controlled. According to the FDA laboratory results, it was established that Hyland's teething tablets contained inconsistent amounts of belladonna (Food and Drug Administration, 2016). This shows that the amounts specified by the company on its website is not true and each dosage of the drug could have too much or too little. Therefore, it would not be wise to use the drugs until there is a clear indication of how much belladonna is used. There have been reports of children developing seizures, excessive sleepiness, skin flushing, difficulty urinating, difficulty breathing, muscle weakness, constipation, or agitation after consuming the tablets (Anderson, 2004). These are just some of the symptoms reported by parents after giving their child the drug.
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