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Medication Error Reporting Form

This document is a medication error report form for reporting errors without blame or punishment. It collects information about the date and time of an error, the diagnosis, drug name and details, where the error occurred, the type and stage of error, how it was discovered, whether the patient used the medication, the outcome, who made and reported the error, causes of the error, actions taken for resolution, recommendations to prevent recurrence. The goal is to learn from errors to improve safety.

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Ahmad Taramsy
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0% found this document useful (1 vote)
943 views2 pages

Medication Error Reporting Form

This document is a medication error report form for reporting errors without blame or punishment. It collects information about the date and time of an error, the diagnosis, drug name and details, where the error occurred, the type and stage of error, how it was discovered, whether the patient used the medication, the outcome, who made and reported the error, causes of the error, actions taken for resolution, recommendations to prevent recurrence. The goal is to learn from errors to improve safety.

Uploaded by

Ahmad Taramsy
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
  • Error Analysis: Analyzes the conditions under which the error was discovered and investigated to understand the context and contributing factors.
  • Report Information: Collects the fundamental details about the medication error occurrence, including dates and involved individuals.
  • Error Description: Requires specific information about the type and nature of the medication error, including affected medication and stage of error.
  • Error Resolution: Outlines actions taken to resolve the error and prevent its recurrence, documenting involved personnel and recommendations.

MEDICATION ERROR REPORT FORM

NO BLAME NO PUNISHMENT
(Please fill all application information)
1. Date when events occurred (Day/Month/Year):
2. Time of events:
3. Report date (Day/Month/Year):
4. Diagnosis
5. Brand and Generic name: ……………………………………………………………………………………………………………… Drug strength: ………………………………………………………………….……
Dosage form: ……………………………………………………………………………………………… Route of administration: ……………………………………………………………………………………….………
6. Where did the initial error occurred? ………………………………………………………………………………………………………………………………………………………………………………………………………
…………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………

7. Type of error (may select more than one):


 Omission error  Wrong dosage form
 Improper dose (over, under or extra dose)  Wrong time of administration
 Wrong patient  Deteriorated/Expired technique
 Wrong drug  Deteriorated/Expired medication
 Wrong strength/concentration  Monitoring errors – Clinical intervention or information
 Wrong route  Monitoring errors – Drug-Drug interaction
 Wrong frequency  Monitoring errors – Drug-Food interaction
 Wrong rate of infusion  Monitoring errors – Drug-Disease interaction
 Wrong dilution  Other, specify
8. Stage(s) involved: (may select more than one):
 Physician ordering  Dispensing and delivery  Monitoring (drug level/allergy/interaction/clinical)
 Transcription and entering process  Administration process
 Other …………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………
9. Description of error (circumstances relating to the event. All information from the beginning to the resolution of event) :
…………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………

…………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………

10. How event discovered?


…………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………

11. Used by patient:  Yes  No


12. Outcome (select only one)
 Circumstances/events with capacity to cause error
 Error occurred but did not reach the patient
 Error occurred but did not harm
 Error reached the patient & required monitoring
 Error reached the patient & result in temporary harm & required intervention
 Error reached the patient & result in permanent harm
 Error reached the patient & required intervention necessary to sustain life
 Error reached the patient & contributed to patient`s death
N.B (Index 4) immediately notify the sentinel event committee
13. Error made by (who initiated the error):
 MD/Physician  Dentist  Other …………………………………………….…
 Pharmacist  Patient / Caregiver
 Nurse  (Radiology, OR, RT, Lab, Pharmacy)

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14. Error reported by:
 MD/Physician  Dentist  Other …………………………………………….…
 Pharmacist  Patient / Caregiver
 Nurse  (Radiology, OR, RT, Lab, Pharmacy)
15. Was the error repeated?  Yes  No
(If Yes, explain) ……………………………………….………………………………………….………………………………………….………………………………………….…………………………………………
16. Cause(s) of error / contribution factor(s) (may select more than one):
 Clinical information missing (lab results or vital signs)
 Drug information missing
 Miscommunication of drug order (illegible, ambiguous, incomplete)
 Look-Alike and Sound-Alike medication problem
 Drug name, label, filling and package problem
 Drug storage or delivery problem
 Environmental, staffing deficiency and workload problem
 Lack of staff education and training problem
 Patient education problem
 Independent double check system
 Other, specify: ………….………………………………………….………………………………………….………………………………………….……………………………………………….………………
17. Action taken for resolution (For Pharmacist or Nurses):
 Call physician for verification for emergency order
 Clinical intervention
 Education & Training of medical staff
 Send pharmacists note to physician for clarification
 Change to correct dose
 Perform root cause analysis
 Discontinue one drug (improper combination)
 Return drugs to pharmacy
 Drug not dispensed to patient
 Memo sent to department
 Other, specify………….………………………………………….………………………………………….………………………………………….………………………………………….………………………
18. Intervention action taken for resolution (For physician) (IF NEEDED)
 Testing  Care escalated  Others ………………………………………………………………………….………
 Additional observation  Additional LOS ………………………………………………………………………….………………….……

 Give antidote  Change to correct drug, dose, frequency, duration


19. Recommendation (Suggestion on how to prevent recurrence of this error)
…….………………………………………….………………………………………….………………………………………….…………………………………….………………………………………….…………………………………
…….………………………………………….………………………………………….………………………………………….…………………………………….………………………………………….…………………………………
…….………………………………………….………………………………………….………………………………………….…………………………………….………………………………………….…………………………………

Please send complete form to Medication safety unit

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