Standard Operating
Procedure (SOP)
Management of
High-Alert Medications – Hospital Pharmacy
1. Purpose
To minimize the risk of serious medication errors associated with high-alert medications by ensuring safe prescribing, storage, dispensing, administration, and monitoring within the hospital.
2. Scope
This SOP applies to all high-alert medications used in the hospital, including pharmacy, OPD, IPD, ICU, OT, Emergency, and wards.
3. Responsibility
- Hospital
Management: Support and enforcement of medication safety policies
- Pharmacy
Manager / Chief Pharmacist: Identification, implementation, and
monitoring of high-alert medication practices
- Pharmacists:
Safe dispensing, labeling, and counseling
- Medical
Officers: Safe prescribing and review
- Nursing
Staff: Safe administration and monitoring
- Quality / Patient Safety Team: Audit and incident review
4. Definitions
- High-Alert
Medications: Drugs that have a high risk of causing significant
patient harm when used in error
- Independent Double Check: Verification by two qualified healthcare professionals independently
5. Examples of High-Alert Medications
(Common examples; hospital-specific list should be
maintained)
- Insulin
(all types)
- Heparin
and Low Molecular Weight Heparin
- Potassium
chloride (concentrated)
- Magnesium
sulfate
- Chemotherapy
agents
- Narcotic
analgesics (e.g., morphine, fentanyl)
- Thrombolytics
- Neuromuscular blocking agents
Read About: What is hyperkalemia
6. Procedure
6.1 Identification and Listing
- A High-Alert
Medication List shall be:
- Prepared
by the Pharmacy Department
- Approved
by the Drugs & Therapeutics Committee (DTC)
- Reviewed
annually or as required
- High-alert medications shall be clearly identified with warning labels
6.2 Prescribing
- Prescriptions
for high-alert medications must be:
- Clear
and legible
- Include
patient weight (where applicable)
- Specify
dose, route, frequency, and duration
- Verbal
orders shall be discouraged and minimized
- Dose calculations must be double-checked
6.3 Storage
- High-alert
medications shall be:
- Stored
separately from routine medications
- Clearly
labeled “HIGH-ALERT MEDICATION.”
- Concentrated
electrolytes shall:
- Not
be stored in patient care areas (where possible)
- Access shall be restricted
6.4 Dispensing
- Dispensing
shall be done only by authorized pharmacists
- An independent double check shall be performed before dispensing
- Dispensed
medications shall be:
- Clearly
labeled
- Accompanied
by special handling instructions
- Look-Alike / Sound-Alike (LASA) precautions shall be followed
6.5 Administration
- Nursing
staff shall:
- Verify
patient identity using two identifiers
- Perform
an independent double check before administration
- Follow
the “Five Rights” of medication administration
- Infusion
pumps shall be used where required
- Administration shall be documented immediately
6.6 Monitoring
- Patients
receiving high-alert medications shall be:
- Closely
monitored for adverse effects
- Monitored
as per clinical guidelines
- Any abnormal findings shall be reported immediately
6.7 Error Reporting
- Medication
errors or near misses involving high-alert medications shall be:
- Reported
immediately
- Documented
in the medication error reporting system
- Root cause analysis shall be conducted
6.8 Education and Training
- All
healthcare staff shall receive:
- Initial
training on high-alert medications
- Periodic
refresher training
- Training records shall be maintained
7. Documentation
- High-Alert
Medication List
- Prescriptions
and medication charts
- Dispensing
and administration records
- Double-check
documentation
- Medication error reports
8. Audit and Quality Improvement
- Regular
audits shall be conducted to ensure compliance
- Audit findings shall be reviewed and corrective actions implemented
9. Review
This SOP shall be reviewed:
- Annually,
or
- When new high-alert medications are introduced
10. References
- NABH
Patient Safety Standards
- WHO
Patient Safety Guidelines
- Institute
for Safe Medication Practices (ISMP)
- Hospital Pharmacy Policy
11. Approval
- Prepared
by: __________________
- Reviewed
by: __________________
- Approved
by: __________________
- Effective
Date: ________________
- Review
Date: __________________
0 Comments