Verify actual use
Separate prescribed directions from the patient’s real-world pattern, including missed, extra, delayed, or intermittent doses.
Metropolitan General Health System
PMHNP Clinical Learning Environment
Medication Safety Resource
Medication reconciliation establishes what a patient is actually taking, compares it with what is documented and intended, resolves discrepancies, and communicates a safe current plan. Monitoring asks whether treatment remains effective, tolerable, feasible, and appropriate as the patient and clinical situation change.
Separate prescribed directions from the patient’s real-world pattern, including missed, extra, delayed, or intermittent doses.
Normalize differences and barriers so the patient can describe use honestly without fear of being labeled difficult or noncompliant.
Every medication should have a current indication, treatment target, evidence of benefit, and plan for evaluating harm.
Resolve discrepancies, update the shared record, teach the current plan, coordinate changes, and define follow-up.
Best possible medication history
No single source is automatically complete. Start with the patient's account, then compare other evidence when accuracy, risk, a care transition, or conflicting information makes verification important.
Ask the patient to describe what they take in their own words—including doses taken differently, skipped, borrowed, shared, or stopped.
Review bottles, organizers, photos, discharge lists, after-visit summaries, and the patient’s personal list when available.
Use dispensing history, pharmacy clarification, and the applicable prescription drug monitoring program to identify fills, overlap, and discrepancies.
Compare prior notes, hospital records, laboratory results, medication administration records, and information from other clinicians or supports when appropriate.
For every medication
“Takes sertraline” is not a usable medication history. Clarify the product, intended directions, actual use, purpose, response, safety, access, and timeline.
Generic and brand name, formulation, route, and strength
Prescribed dose, frequency, timing, and PRN parameters
What is taken, how often, at what time, and in what pattern
Indication understood by the patient and intended treatment target
Benefit, residual symptoms, function, and time course
Adverse effects, allergies, prior reactions, and concerns
Last dose, supply, refills, cost, transportation, and pharmacy
Start date, prior changes, previous trials, and reasons stopped
The full exposure picture
Psychiatric and nonpsychiatric medications from every prescriber, including injections, patches, inhalers, topical products, and PRN use.
Pain, sleep, allergy, cold, gastrointestinal, weight-loss, and other nonprescription products that may add risk or alter symptoms.
Herbal products, vitamins, minerals, performance products, and products marketed for sleep, energy, mood, focus, or weight.
Coffee, tea, energy drinks, pre-workout products, vaping, cigarettes, nicotine pouches, and changes in usual exposure.
Amount, frequency, timing, route, reason for use, withdrawal risk, and overlap with prescribed medication.
Borrowed or shared medication, leftovers, online products, samples, compounded products, and medications obtained outside usual care.
Reconciliation workflow
Build the most accurate history possible from the patient and other available sources.
Compare reported use, documented orders, dispensing information, and the regimen intended for the current setting.
Assess indication, response, adverse effects, interactions, adherence, monitoring, and patient-specific risk.
Clarify whether each discrepancy is intentional, correct errors, and document unresolved uncertainty rather than guessing.
Give the patient and care team one understandable current plan, including what changed, why, and what happens next.
Discrepancy check
A discrepancy is not automatically an error. Determine whether it is intentional, clinically appropriate, accidental, or still unresolved.
A medication the patient uses is absent from the record or intended regimen.
The list contains an extra, discontinued, duplicate, or overlapping medication.
Prescribed directions, documented directions, and actual use do not match.
Use differs because of preference, effects, cost, supply, routine, stigma, understanding, or another barrier.
The treatment target is unclear, has changed, or benefit has not been established.
An allergy label, intolerance, side effect, or prior serious reaction is missing, vague, or misclassified.
A medication was started, held, changed, or stopped in another setting without a clear ongoing plan.
Patient report, pharmacy data, records, laboratory findings, or collateral do not agree.
Medication review
Confirm the current indication and treatment target. Do not carry a medication forward solely because it already appears on the list.
Assess symptom change, function, patient-defined benefit, time course, and whether an adequate trial actually occurred.
Look for adverse effects, toxicity, withdrawal, activation, sedation, falls, sexual effects, metabolic burden, cognitive effects, and safety concerns.
Consider age, pregnancy potential, medical and neurologic conditions, organ function, co-exposures, goals, and preferences.
Explore understanding, cost, access, complexity, beliefs, stigma, swallowing, memory, routine, and support without blame.
Identify missing records, collateral, examination findings, vitals, labs, ECG data, levels, scales, or specialist input.
Continue, adjust, taper, discontinue, defer, consult, or escalate only after the evidence, risks, alternatives, and follow-up plan are clear.
Prior trials
A prior medication cannot be interpreted without the dose, duration, adherence, target, response, adverse effects, reason for stopping, and what happened afterward. A brief exposure, unaffordable prescription, intolerable reaction, and adequate ineffective trial mean very different things.
Psychiatric medication monitoring
Monitoring begins before a change and continues after it. Use the current product label, evidence-based guidance, the patient's conditions and co-exposures, and the care setting to determine exact measures and timing. These are clinical prompts, not a complete protocol.
Track response, weight and metabolic health, blood pressure, movement symptoms, sedation, orthostasis, sexual or prolactin-related effects, and medication-specific risks. Use structured movement assessment when indicated.
Verify formulation, dose and level timing, renal and thyroid status, calcium, hydration and sodium changes, interacting medications, pregnancy considerations, and symptoms of toxicity.
Review medication-specific hepatic, hematologic, dermatologic, metabolic, reproductive, interaction, and serum-level considerations. Do not treat different agents as interchangeable.
Monitor target symptoms, suicide-related change when relevant, activation or emerging mania, anxiety, sleep, sexual effects, bleeding and sodium risks, discontinuation symptoms, and serotonin toxicity.
Review blood pressure, pulse, appetite, weight or growth, sleep, mood activation, cardiovascular history and symptoms, early refills, misuse, diversion, and substance exposure.
Assess sedation, cognition, falls, driving, respiratory risk, alcohol or opioid exposure, tolerance, dependence, withdrawal risk, duration, and controlled-substance history.
Escalation
A medication visit can become an urgent medical or psychiatric evaluation. Stabilization, consultation, testing, a higher level of care, or emergency response may take priority over the planned discussion.
Medications reviewed. Patient is noncompliant. Continue current regimen and monitor.
Patient reports taking sertraline 50 mg on approximately four mornings per week rather than daily because of nausea and an irregular work schedule; pharmacy history is consistent with delayed refills. Reports modest improvement in worry but persistent low mood and no clear activation. Also uses diphenhydramine most nights, two energy drinks daily, and cannabis on weekends for sleep. Discussed how inconsistent dosing and co-exposures limit interpretation of response. Plan addresses nausea and schedule barriers, sleep treatment, interaction concerns, an updated medication list, and reassessment after a defined interval.
Shared decisions and coordination
Explain what continues, changes, stops, or remains uncertain; why; how the medication should be used; which warning signs require action; what monitoring is needed; and when follow-up occurs. Use teach-back, provide an updated list, and communicate material changes to the care team as appropriate.