Our study has demonstrated a wide range of prescription errors associated with 2000 prescriptions from faculty and non-faculty physicians in Shiraz, Iran. We documented 14764 errors from 2000 prescriptions. All prescriptions (100%) had at least one error. The maximum prescription error was 26 errors in one prescription. The total MEs in our study were greater than previous studies in Iran. In a study by Vazin
et al. 68.5% of prescription had an error (
12), Abbasinazari
et al. (
11) detected 262 errors in 132 patients (1.98 per each patients) and in Malaysia Kuan Mon Ni
et al. (
26) only 13 out of the 397 prescriptions screened complied with all the legal requirements. T. Khoja
et al. (
27) found that 18.7% of their prescriptions (5299) contained an error. Perwitasari
et al. (
28) reported 98.69% error in their study which was similar to our result. This indicates a need for the physicians to further emphasize the necessity of writing prescriptions clearly, and completely. Several causes of the high rate of prescription errors in our study compared to other studies were handwritten prescriptions, difference in references used for identify prescription errors and different populations studied.
The mean ± SD errors in prescriptions written by faculty members was significantly lower than the non-faculty members (6.93 ± 3.88 Vs 7.83 ± 4.2, P-value < 0.001). Faculty members practice in the academic area and have more complicated patients daily. They have the responsibility to educate the medical students and therefore need to keep themselves up to date.
The mean number of drugs prescribed per prescription in our study was 3.21 ± 1.71. This was similar to previous reports (3.0-4.5) from Nigeria (
29,
30) and higher than a study in Urmia (
31). (
N = 2.54 ± 0.58; 2.26 ± 0.43 for faculty vs. 2.65 ± 0.59 for non-faculty,
P-value < 0.001). This finding may be related to the greater awareness of faculty members about the existence of Rational Use of Drugs (RUD) committee in the university as an official authority for evaluation of physicians (
31). Based on the latest available annual repoort of Iranian RUD committee in 2011, the mean number of drugs per prescription for all prescriber in Iran was 3.05 (
31). Developing countries with programs promoting rational drug use as well as standards have described lower drug prescription errors rates, such as primary health care center in Jordan (2.3%), primary health care center in Tanzania (2.9%) and private hospitals in Uzbekistan (2.9%) (
32,
33). Poly pharmacy has been reported as one of the causes of prescription errors (such as increasing drug-drug interactions and combination error), increasing costs for patients and confusing patients (
34).
In our study average patientsꞌ age was 37.91 ± 21.10 years. About 7.45% of our prescriptions didnꞌt have any information about age or date of birth. In our study, we had a lower rate of lack of patient’s age data compared to a research conducted at Government Hospitalian Yogyakarta Indonesia in 2010 (52.4% of 229) registered outpatients (
28). One study in Oman reported that patientꞌs age is one of the most common omission errors and itꞌs frequency of occurrence was more than 72% (
35). The age has a great impact on the prescription and it is a very important variable in terms of dose and dosage form. The omission of age in prescriptions could be a reflection of the fact that some physicians does not appreciate the legal status of a prescription order (
28).
The mean ± SD spelling error was 1.95 ± 0.03 (11% in 2000 prescriptions) in our study which is higher than research done by Kuan Mun Ni
et al. (
26) who screened the prescriptions and were unable to read about 7% of prescriptions in their sample. In this study, 6.11% in 229 prescriptions contained spelling errors.
In our study, the mean ± SD strength error was 1.42 ± 0.03 (9.20% in 2000 prescriptions) and dosage form errors were 0.68 ± 0.02 (4.85% in 2000 prescriptions). Kuan Mon Ni
et alꞌs study (
26) 56.26% (485/862) of drugs were prescribed without strength specifications. Our study indicated lower errors than the mentioned study in Indonesia. Kuan Mon Ni
et al. (
26) reported that among 391 studied prescriptions, 27out of 862 drugs had wrong written dosage forms and 314 out of 862 drugs didn’t have dosage forms.
| Characteristics of physicians | Faculty prescription(N = 1000) | Non-faculty prescription(N = 1000) | Total prescription(N = 2000) |
|---|
| Sex | Male | 840 (84%) | 703 (70.3%) | 1543 (77.15%) |
| Female | 160 (16%) | 297 (29.7%) | 457 (22.85%) |
| Field ofPractice | General-physician | - | 292 (29.2%) | 292 (14.6%) |
| Specialist | 446 (44.6%) | 534 (53.4%) | 980 (49%) |
| Fellowship | 554 (55.4%) | 174 (17.4%) | 728 (36.4%) |
| AcademicalsGrade | Associate professor | 461 (46.1%) | - | 461 (23.05%) |
| Assistant professor | 360 (36%) | - | 360 (18%) |
| Full-professor | 179 (17.9%) | - | 179 (8.95%) |
| Errors | Faculty prescriptions(N = 1000) | Non-faculty prescriptions(N = 1000) | Total prescriptions (N = 2000) | P-value |
|---|
| Total numbers of prescribed drugs mean ± SD(N) | 3.02 ± 1.72(3023) | 3.39 ± 1.69(3388) | 3.21 ± 1.71(6411) | 0.00 |
| Spelling error mean ± SD(N) | 1.66 ± 0.04(1661) | 2.24 ± 0.04(2238) | 1.95 ± 0.03(3899) | 0.00 |
| Instruction error mean ± SD(N) | 1.44 ± 0.04(1444) | 1.66 ± 0.03(1662) | 1.55 ± 0.03(3106) | 0.00 |
| Strength error mean ± SD(N) | 1.21 ± 0.03(1208) | 1.62 ± 0.045(1624) | 1.42 ± 0.03(2832) | 0.00 |
| Dosage error mean ± SD(N) | 0.80 ± 0.04(799) | 0.56 ± 0.031(563) | 0.68 ± 0.02(1362) | 0.00 |
| Quantity error mean ± SD(N) | 0.47 ± 0.02(472) | 0.43 ± 0.026(429) | 0.45 ± 0.01(901) | 0.22 |
| Combination errorMean ± SD(N) | 0.21 ± 0.01(208) | 0.22 ± 0.01(225) | 0.22 ± 0.00(433) | 0.356 |
| Contraindication mean ± SD(N) | 0.03 ± 0.00(34) | 0.02 ± 0.00(18) | 0.03 ± 0.00(52) | 0.02 |
| Drug-drug interaction mean ± SD(N) | 0.12 ± 0.01(124) | 0.08 ± 0.01(76) | 0.1 ± 0.00(200) | 0.00 |
| Total prescription errors mean ± SD(N) | 6.93 ± 3.88(6232) | 7.83 ± 4.2(7832) | 7.38 ± 4.06(14764) | 0.00 |
| Total numbers of drugs per prescription | The Mean ± SD prescription errors based on total numbers of drugs per prescription
|
|---|
| Spelling error | Dosage form error | Strength error | Instruction error | Quantity error | Total errors |
|---|
| 1-2 | 1.39 ± 0.49 | 0.39 ± 0.02 | 0.72 ± 0.03 | 0.86 ± 0.03 | 0.22 ± 0.01 | 2444 |
| 3-4 | 2.35 ± 0.93 | 0.67 ± 0.03 | 1.70 ± 0.04 | 1.65 ± 0.03 | 0.52 ± 0.02 | 6202 |
| ≥5 | 3.66 ± 1.56 | 1.41 ± 0.11 | 2.4 ± 0.09 | 2.91 ± 0.10 | 0.75 ± 0.06 | 4139 |
| P-value | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | - |
Amount of omission and commission errors were 39.55 % (
26). If the strength of a drug is incorrect, it may lead to more serious consequences compared to when the strength is not written at all. If the drug is only available in a fixed dosage form, this type of error could be easily identified and rectified. An incorrect dosage form does not lead to serious consequences unless the strength or the frequency of use of that dosage form is also incorrect (
26).
In our survey, the mean ± SD instruction error was 1.55 ± 0.03 (10.64% in 2000 prescriptions), which is lower than the results of previous studies by Nadiya
et al. (
35) and Perwitasari
et al. (
28) who reported the instruction errors to be 46.33% and 26.43%, respectively. Based on a survey conducted in a general practice in USA, the highest frequency of errors was due to incomplete or missing instruction (
36). Instructions should be clear, complete and should provide careful instructions for pharmacists about the patient’s situation (
35).
Our results showed that pediatric patients had 2421 (17.69%) errors in 2000 prescriptions. Pediatrics pose a unique set of risks of prescription errors, predominantly because of the need to make dosage calculations, which are individually based on patientꞌs weight. Therefore, lack of patientꞌs weight, may result in overdose or under dose and patients would not benefit from treatment (
37,
38). Lack of appropriate information such as patientꞌs weight makes it difficult for pharmacists to carry out a prescription (
37). In our study, none of the prescriptions stated patient’s weight. It is possible that the physicians consider the patientꞌs weight (especially pediatrics) before prescribing and calculate the dose, therefore this may not lead to an error. In the study by Perwitasari
et al., Only 3 prescriptions included patient’s weight and 98.69% of the prescriptions lacked this variable (
28).
The mean ± SD quantity errors were 0.45 ± 0.01 (4.17% in 2000 prescriptions). In a study by Kuan Mun Ni
et al. (
26), they reported that 50 out of 862 (5.8%) drugs had quantity errors. Prescriptions should state the quantity of each drug. Although some drugs may be given on “as required” basis, the physician is still the best judge on the total quantity to be supplied based on the patient medical requirement. Even for dermatological, eye, ear, and nasal preparations, documentation of the amount to be supplied is still necessary (
26). In this study, quantity was considered as an indicator for treatment duration. If the quantity of drug/drugs is not enough the duration of treatment would not be completed which can increase the probable risk of treatment failure. On the other hand, excess amount of drugs may cause adverse effects, increase patient’s cost and drug waste (
34).
Combination therapy is considered to increase the efficacy of drug therapy. However, if co-prescribed drugs have the same mechanism of action or they antagonize each other, a combination error is observed. In our study, 433 (2.93%) in 2000 prescriptions had combination errors. We could not find any published study about these types of errors.
In the present study 52 (2.60%) in 2000 prescriptions had contraindication error. Our rate was higher than the reported rates by Teixeira
et al. in Brazil (0.4% of the prescriptions contained contraindications) (
39) and Guedon
et al. in France (0.4% contraindication in outpatient prescriptions) (
40). Describing “chief complain” and “diagnosis” help us identify contraindication but our physicians did not include these data. Thus we reported contraindication error only based on sex and age of patients. Therefore, our findings may be underestimated.
In this study 1090 (40.7%) drugs were prescribed by trade names. The rate of drugs prescribed by trade names was lower than rate of using generic names (7-7.3%) in other studies (
30,
33). Generic prescribing makes is possible to dispense various brands of drugs that are cheaper than or are as effective as proprietary brands (
4). The several suggestions for this type of prescription error in our study are as follows: 1-physicians are not certain enough about quality of generic drugs. 2-Trade names are used because physicians are more familiar with trade names than generic names. 3-when some drugs are launched in Iranꞌs market for the first time, they often are introduced by their trade names and prescribing drugs using trade name has become a routine.
Overall, the rate of occurrence of prescription errors in this study was higher than others (
26-
28). Some reasons for this difference may be: 1) Differences in prescribing systems between our country and other countries; 2) Use of different references to identify errors, 3) differences in sample size and design of studies such as different ways of selecting prescriptions.
Our study had some limitations: 1) Prescriptions were limited to handwritten prescriptions. Verbal instructions of physicians to patients remain unknown. 2) This study covered Shiraz city. Since certain types of drugs are available in a specific city, it’s possible that our study is restricted to certain types of drugs. Our results canꞌt be generalized to another university of Iran. For example in some therapeutic centers in Iran, the prescription control committee can be very strict making physicians to write prescriptions more carefully. 3) Our study’s focus was mainly on prescription errors and was not designed to detect adverse drug events or other complications of medication errors. 4) Vast majority of physicians did not state chief complain and diagnosis on their prescriptions, therefore it was not possible to make accurate judgments on all prescriptions especially regarding combination and contraindication errors. 5) One of the reasons for diversity in our results may be due to the fact that various types of physicians were included in our study. Prescriptions were selected using random sampling and there was no criteria or limits on the number of physicians in this study. 6) Because our study was retrospective, some contraindication errors, combination errors and quantity errors may not have a true error.