All Creatures Great and Small: Properly Medicate Them All
By Linda Kim-Jung, PharmD, Safety Reviewer, Division of Pharmacovigilance and Surveillance, Office of Surveillance & Compliance
Unclear Abbreviations
Other Problematic Abbreviations
Trailing and Leading Zeros
FDA's Initiative
Reporting ADEs
People make mistakes. Fortunately, most mistakes do not physically harm others. But if a person makes a mistake that causes a medication error, there may be serious, even fatal, consequences.
A medication error can occur anywhere in the medication use process, from a practitioner writing a prescription, to a pharmacist filling the prescription, to a nurse giving the drug to a person in the hospital, or to a person taking the drug at home. In an effort to prevent medication errors, FDA looks at the areas of the medication use process where mistakes are most likely to occur.
Unclear Abbreviations
Unclear medical abbreviations are one cause of medication errors. There are different reasons why practitioners use abbreviations, including what they were taught in school and training. Using abbreviations is also a way to save time when writing prescriptions and documenting what was prescribed in patient records. However, experience with marketed drugs shows medication errors occur because abbreviations are misinterpreted. Not all practitioners interpret abbreviations in the same way. Abbreviations can be vague and unfamiliar, causing the intended meaning to be improperly conveyed. Poor penmanship is not the only culprit – abbreviations are prone to misinterpretation even when prescriptions are typed.
In June 2006, FDA and the Institute for Safe Medication Practices (ISMP) launched a nationwide education campaign aimed at reducing medication errors caused by unclear abbreviations. Although the campaign targeted human drugs, a review of ISMP’s list of error-prone abbreviations shows that the same mistakes may easily cross over to animal drugs.1 In fact, FDA’s CVM is learning that medication errors caused by unclear medical abbreviations do occur with animal drugs.
After reviewing reports of problems with animal drugs, CVM found that the abbreviation “SID” (once daily) in prescriptions was misinterpreted as “BID” (twice daily) and “QID” (four times daily), resulting in drug overdoses for the patients. For a drug where there is a strong correlation between the dose and the severity of side effects, an overdose can be serious.
Medication errors in animals occur not only in veterinary clinics, but also in pharmacies where pharmacists and pharmacy technicians may be unfamiliar with veterinary abbreviations.
Other Problematic Abbreviations
Some drugs, such as insulin, are measured in units, abbreviated “U.” There have been cases where people have died from tenfold insulin overdoses when the abbreviation “U” (for units) was misread as a zero in a prescription, especially when the “U” closely followed a number. For example, “1U” for 1 unit can easily be misread as “10" units, resulting in a patient receiving ten times the intended dose. Also, the abbreviations “mcg” or “µg” (for microgram, or 1/1000 of a milligram) can be mistaken for “mg” (for milligram), creating a 1000-fold overdose.
Similar mistakes could also occur in veterinary medicine.
Commonly Misinterpreted Abbreviations
| Abbreviation Used | Intended as | Misread as |
|---|---|---|
| U | Units | 0 (Zero) |
| IU | International Units | IV (intravenously) |
| mcg or µg | Microgram | mg (milligram) |
| SID | Once Daily | BID (twice daily) and QID (four times daily) |
| TIW | Three times a week | Three times daily |
| Qhs | At bedtime | Every hour |
Trailing and Leading Zeros
Medication errors are also caused by using trailing zeros and not using leading zeros when writing out doses. FDA has received adverse drug event reports involving tenfold drug overdoses occurring in people due to a written prescription either using a trailing zero or not using a leading zero. Similar errors in animals could occur.
For example, a “5 mg” dose written with the trailing zero as “5.0 mg” can be misread as “50 mg,” resulting in a tenfold overdose. Similarly, a “0.5 mg” dose written without the leading zero as “.5 mg” can easily be mistaken for “5 mg,” also resulting in a tenfold overdose.
FDA’s Initiative
FDA has reviewed many cases of medication errors in people in an effort to prevent these mistakes. CVM’s Office of Surveillance and Compliance has identified reports of medication errors in animals that are similar to the medication errors in people. Fortunately, medication errors are preventable. By applying the lessons learned from human medicine to veterinary medicine, veterinarians can avoid making similar mistakes in animals.
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Reporting ADEs
An adverse drug event, also called an adverse drug experience or ADE, is an undesired side effect associated with the use of a drug, or a lack of a desired effect (the drug does not do what it is supposed to do). A medication error may result in an ADE. Veterinarians and pet owners are encouraged to report to CVM all ADEs, including those caused by medication errors. ADE reports help CVM determine the frequency and severity of medication errors in animals. The information collected from ADE reports can also help CVM develop education outreach programs aimed at preventing medication mistakes in animals.
Instructions on how to report an ADE can be found on CVM’s website at: How to Report Animal Drug and Device Side Effects and Product Problems.
1For ISMP’s complete list of error-prone abbreviations, see http://www.ismp.org/Tools/errorproneabbreviations.pdf