Medication errors are a major cause of serious injury and death in the United States. In fact, it is estimated that at least 7,000 Americans die each year due to medication-related issues. Many of these are due to patients being provided the wrong drug or wrong dose by their pharmacist. Of course, the pharmaceutical industry and pharmacies themselves are strictly regulated by the United States government, but it is largely left to the individual pharmacist how they go about doing their job on a day-to-day basis. While some pharmacists certainly implement fail-safe protocols to ensure they are error-free, others are more fast and loose, creating an increased risk of a serious or fatal medication error.
The Food and Drug Administration (FDA) is the government body responsible for the oversight of pharmacies nationwide. According to one industry news source, the FDA has recently issued specific protocols for pharmacists and drug manufacturers to follow so that they can reduce the chance of causing a serious pharmacy error.
One of the issues the FDA sees as a major problem is the fact that many medications with vastly different purposes share similar names. This can lead to a situation in which a busy pharmacist inadvertently grabs the wrong medication and provides it to a patient. To help alleviate this, the FDA recommends that pharmacy staff should “write down the prescription and then read back the medication name, strength, dose, and frequency of administration for verification.”