The risk management plan identifies several high risk issues for the pharmacy:
1. Wrong drug dosages or products being given could critically endanger patients.
2. Unreadable prescriptions pose a high risk of misuse or giving the wrong product.
3. Issuing impossible or erroneous prescriptions risks patient confusion.
4. Improper storage of light-sensitive or biological drugs risks product deterioration and could critically impact patient health.
5. Occurrence of adverse drug reactions should be reported to prevent future issues.
The risk management plan identifies several high risk issues for the pharmacy:
1. Wrong drug dosages or products being given could critically endanger patients.
2. Unreadable prescriptions pose a high risk of misuse or giving the wrong product.
3. Issuing impossible or erroneous prescriptions risks patient confusion.
4. Improper storage of light-sensitive or biological drugs risks product deterioration and could critically impact patient health.
5. Occurrence of adverse drug reactions should be reported to prevent future issues.
The risk management plan identifies several high risk issues for the pharmacy:
1. Wrong drug dosages or products being given could critically endanger patients.
2. Unreadable prescriptions pose a high risk of misuse or giving the wrong product.
3. Issuing impossible or erroneous prescriptions risks patient confusion.
4. Improper storage of light-sensitive or biological drugs risks product deterioration and could critically impact patient health.
5. Occurrence of adverse drug reactions should be reported to prevent future issues.
The risk management plan identifies several high risk issues for the pharmacy:
1. Wrong drug dosages or products being given could critically endanger patients.
2. Unreadable prescriptions pose a high risk of misuse or giving the wrong product.
3. Issuing impossible or erroneous prescriptions risks patient confusion.
4. Improper storage of light-sensitive or biological drugs risks product deterioration and could critically impact patient health.
5. Occurrence of adverse drug reactions should be reported to prevent future issues.
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RISK MANAGEMENT PLAN
DESCRIPTION OF RISK RISK IMPACT IF RISK OCCURS RISK SEVERITY PREVENTIVE/CONTINGENCY
PROBABILITY (CRITICAL/MODERATE/ PLAN (HIGH/MEDIUM/L LOW) OW) Underdosage/Overdosage Pharmacist must always check the Wrong drug dosage or drug High Might trigger the patient’s Critical medicine before giving to the product given to the patient condition patient. Patient counseling must be done Unreadable instruction on when the patient cannot understand the patient’s prescription High Drug Misuse Critical the prescription given by the doctor from the Doctor or when the patient doesn’t know how to take/use the product. Call the Doctor and ask for the right Issuance of Impossible Patient Confusion/Wrong prescribed medicine. Report the High Critical prescriptions product given prescription to the nearest FDA office. Issuance of Keep the Prescription and report to Erroneous/Violative Medium Patient Confusion Moderate the nearest FDA office. Prescriptions Garbage waste disposal must be Untidy area of the properly established inside the Pharmacy; Emergence of Medium Quality of the Drug Critical Pharmacy. Pest control must be Pests done from time to time. Increased risk for Adverse Pharmacist should make an incident Complaint on deteriorated Medium Drug Reaction / Moderate report regarding the complaint and drug product address to the supplier. Mistreatment Pharmacist shall monitor the proper storage of medicines especially the Improper storage and light-sensitive and refrigerated handling of light-sensitive medicines to ensure the stability of drugs and Biologicals High Drug Product Deterioration Critical the product. Light-sensitive drugs (Ascorbic acid, insulin, must be in an amber-colored battle Suppositories, etc.) and away from the sunlight; biologicals must be stored between 2-8 C. Pharmacist shall assess the patient regarding his/her medication history before dispensing the medicine. Occurrence of Adverse Drug Emergence of new illness/ High Critical Occurrence of adverse drug Reaction Drug interaction reaction must be reported to the nearest FDA office for record and preventive purposes. Expired medicines should be kept Drug inefficiency/ and stored separated from other Expired Drug Products High Critical Poisoning products and proper disposal must be done. All FDA-initiated product recall must be kept in the warehouse. Product Recall Low Incompliance to FDA order Low Pharmacist/Branch Manager should be updated regarding the product recalls from FDA website.
Prepared by: Scheha R. Mamalangkas, RPh. Pharmacist-in-charge