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India JIPMER Medication Error Reporting Form free printable template

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How to report Please fill in the medication error reporting form completely details of reporter is optional and send it by email to JIPMER Quality Council E-mail mereports gmail.com. Jawaharlal Institute of Postgraduate Medical Education and Research JIPMER Medication Error Reporting Form A blame free reporting tool Please tick the appropriate box. All fields must be filled except details of reporter which is optional* he appropriate box. All fields are mandatory. 2. Location of event 1. Date...
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How to fill out India JIPMER Medication Error Reporting Form

01
Obtain a copy of the JIPMER Medication Error Reporting Form from the JIPMER hospital or its website.
02
Fill in the date and time of the medication error incident.
03
Provide the patient’s details, including their name, age, and any relevant identification number.
04
Describe the medication involved, including the name, dosage, and route of administration.
05
Clearly explain the nature of the medication error (e.g., wrong medication, incorrect dosage).
06
Document the circumstances surrounding the error, including any contributing factors.
07
Include details on the actions taken following the error, such as notifying medical staff or administering corrective treatment.
08
Note any patient outcomes or complications resulting from the medication error.
09
Sign and date the completed form, ensuring accuracy before submission.
10
Submit the form to the designated hospital authority for review and analysis.

Who needs India JIPMER Medication Error Reporting Form?

01
Healthcare professionals involved in patient care at JIPMER who encounter medication errors.
02
Pharmacists managing medication records and safety.
03
Quality assurance and safety officers responsible for medication error monitoring.
04
Administrative personnel who compile and analyze medication error reports.
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someone else has made a medication error, you must IMMEDIATELY REPORT THE ERROR TO THE RN CM/DN AND APPROPRIATELY DOCUMENT THE ERROR. ing to your agency's policy, your supervisor should also be notified.
An example is choosing the incorrect diluent to reconstitute. Incorrect strength may potentially occur at many points in the medication process. It usually occurs due to human error when similar bottles or syringes with the incorrect strength is selected.
A Medication Error Report Form is a document used when reporting a medication error incident from health care settings like hospitals or clinics. This type of form helps to improve the way the medications are being administered and ensure the safety of the patient.
Types of Medication Errors Prescribing. Omission. Wrong time. Unauthorized drug. Improper dose. Wrong dose prescription/wrong dose preparation. Administration errors include the incorrect route of administration, giving the drug to the wrong patient, extra dose, or wrong rate.
Write a note in the medical record documenting what happened, the impact on the patient, treatment provided, and results. You can include who was told about it, what they were told, and when. The clinical record is the wrong place to guess what happened or to blame others.

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The India JIPMER Medication Error Reporting Form is a standardized document used to report medication errors encountered in clinical settings at JIPMER (Jawaharlal Institute of Postgraduate Medical Education and Research) in India.
Any healthcare professional, including doctors, nurses, and pharmacists, who encounters a medication error during patient care is required to file the India JIPMER Medication Error Reporting Form.
To fill out the form, one must provide detailed information about the medication error, including the date and time of the incident, the patient's details, the medication involved, the nature of the error, and any corrective actions taken.
The purpose of the India JIPMER Medication Error Reporting Form is to document and analyze medication errors in order to improve patient safety, enhance healthcare practices, and prevent future incidents.
The form must report information such as the patient's demographics, details of the medication involved, description of the error, potential consequences, actions taken to rectify the error, and recommendations for preventing similar errors in the future.
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