
How I Decide to Prescribe
Before I prescribe anything, I run one test: does this drug actually change the outcome? If yes, we pick the narrowest effective option, the lowest effective dose, and the shortest appropriate duration. If the answer is no, we leave the pad alone. The same lens runs across antibiotics, statins, GLP-1s, hormone therapy, sleep meds, and the controlled substances we do prescribe under structure. Deprescribing what no longer helps is the same conversation in reverse.
How I Decide to Prescribe: The Lens Before a Single Rx
The question I ask before writing anything
The lens I use before every prescription is simple: would this drug, in this person, at this dose, for this duration, change the outcome? If yes, we prescribe. If no, we do not. The test sounds obvious. It is also what most prescribing fails on. A prescription for a viral cold does not change the course of the cold. A statin for a 30-year-old with normal ApoB and zero family history does not change the cardiovascular trajectory. A daily benzodiazepine for chronic anxiety usually does not solve the anxiety; it builds tolerance and quietly creates a new problem. The question forces honesty about what we are doing with each prescription. Once the answer is yes, the next three are mechanical.The three knobs
Every prescription is a setting on three dials:- The right drug. Match the mechanism to the problem. The narrowest effective option for what is actually happening, not the most-marketed or most-prescribed one.
- The right dose. The lowest dose that produces the outcome. Many side effects are dose-dependent and reversible; many benefits are achievable at lower doses than people assume.
- The right duration. The shortest appropriate course. The default in too much of medicine is "until further notice." Most prescriptions deserve a planned endpoint and a check-in.
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Where I lean toward prescribing
A short list of the places medications usually earn their place when the clinical picture supports them:- Antibiotics for a confirmed bacterial infection where the cost of waiting is real (pyelonephritis, cellulitis, bacterial pneumonia, certain dental and skin infections). We pick the narrowest agent the culture or clinical picture allows, for the shortest duration the evidence supports. See Antibiotics and your gut for the detailed stewardship lens.
- Statins or PCSK9 inhibitors for elevated ApoB and Lp(a) when imaging or risk calculators support it. The cardiovascular benefit at meaningful baseline risk is one of the most well-supported preventive interventions in medicine. We pick the right intensity for the actual ApoB target, not the average target.
- GLP-1 medications for metabolic disease, obesity with metabolic risk, and selected cases where lifestyle work has not closed the gap. They are not a shortcut. They are a tool that, used alongside protein, training, and sleep, can change long trajectories. We monitor body composition, not just the number on the scale.
- Hormone optimization in symptomatic patients with clearly low values and a clean safety profile: TRT for genuine hypogonadism with monitoring; menopausal hormone therapy for patients within the right window and risk profile.
- Targeted mental health prescriptions alongside therapy, sleep, and lifestyle. SSRIs, SNRIs, and short-term anxiolytics in the right person, with a real plan for follow-up, can be the lever that lets everything else move.
- Controlled substances under clear structure when they fit. ADHD stimulants for properly diagnosed ADHD, short-term sleep aids in specific contexts, with the safeguards described in our controlled substances policy.
Where I lean against prescribing
The places a prescription often does more harm than good:- Antibiotics for a viral illness. Colds, flu, most sore throats, most sinus pressure in the first week. Antibiotics do nothing to viruses. They expose you to side effects, push resistance, and disrupt the microbiome.
- Sleep aids as a long-term plan. Benzodiazepines, "Z-drugs" like zolpidem, and even chronic over-the-counter antihistamine sleep aids have real downsides: tolerance, dependency, worsened sleep architecture, and (in older adults) falls and cognitive side effects. Short-term, situational use is one conversation. Daily, forever use is a different one.
- Statins for borderline risk without baseline imaging or advanced lipids. When ApoB, Lp(a), and risk modifiers (CAC or CCTA) are stable and reassuring, the case for a lifelong statin is weaker than the default. The decision should match the actual risk, not the prescriber's reflex.
- "Just-in-case" antibiotics, antifungals, or steroid bursts without a clear diagnosis. Often the symptom resolves on its own, and the prescription took credit for the resolution while adding side-effect risk.
- Stacked supplements and stacked medications without a defined endpoint. Polypharmacy is one of the strongest predictors of preventable adverse events, especially over 65. Every additional active prescription deserves a "still earning its place?" review.
- Controlled substances without structure. Early refills, missed follow-ups, no Prescription Drug Monitoring Program review. These are how a treatment becomes a problem.
Deprescribing: the other half of the conversation
A medication that earned its place last year may not earn it today. Bodies change, risks change, the evidence base changes. Deprescribing, the deliberate work of stopping a medication that has stopped helping, is part of the same lens.Fishtown Medicine
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How the order actually reaches you
Once a prescription is the right move, the goal is to make the rest of the path feel like one step, not five.- The Rx routes through Photon to the pharmacy you pick, so you see what was sent and where, and you can manage refills without a phone call.
- Prior authorizations for GLP-1s, PCSK9 inhibitors, biologics, and newer migraine medications are handled by our team. You should not have to chase your own insurer.
- For controlled substances, refills follow the structure laid out in our policy. No early refills, no chasing on weekends; the rhythm is built in advance so it actually works for both sides.
- For specialty injectables and titration-based meds, we set the cadence and check-ins in advance so the medication has a chance to do its job.
Guidance from the clinic
Actionable Steps
Before you start (or stay on) a medication.- Name the outcome. "Lower my ApoB to under 60." "Get my A1c below 5.7." "Sleep through the night without grogginess." A specific outcome lets us measure whether the drug is doing its job.
- Ask what changes if you do not take it. If the answer is "not much," the medication probably is not earning its place.
- Set a planned check-in. When will we look at whether this is working? Most prescriptions deserve a 4-to-12-week first check, not "see you next year."
- Bring the full list every visit. Every supplement, every over-the-counter, every leftover prescription from another clinician. Hidden interactions are responsible for a lot of preventable harm.
- Ask the deprescribing question once a year. "Is anything on my list still earning its place?" If the answer is unclear, that is the conversation to have.
Key Takeaways
- The deciding question for any prescription is whether the drug would change the outcome for this person at this dose for this duration. If not, do not write it.
- Every prescription has three knobs: right drug, right dose, right duration. Most medication harm comes from defaulting on one of them.
- Strong evidence cases (statins for elevated ApoB in real risk, GLP-1s for metabolic disease, antibiotics for confirmed bacterial infection, hormone optimization in the right patient) deserve a real plan, including monitoring.
- Polypharmacy is one of the strongest predictors of preventable adverse events. Deprescribing what no longer helps is hygiene, not failure.
- Logistics matter. Clear routing, clean follow-up, and structured monitoring are what make medications safe to use long term.
Scientific References
- Llor, C., & Bjerrum, L. (2014). Antimicrobial resistance: risk associated with antibiotic overuse and initiatives to reduce the problem. Therapeutic Advances in Drug Safety, 5(6), 229-241.
- Scott, I. A., et al. (2015). Reducing inappropriate polypharmacy: the process of deprescribing. JAMA Internal Medicine, 175(5), 827-834.
- Sabatine, M. S., et al. (2017). Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease (FOURIER). New England Journal of Medicine, 376(18), 1713-1722.
- Wilding, J. P. H., et al. (2021). Once-Weekly Semaglutide in Adults with Overweight or Obesity (STEP 1). New England Journal of Medicine, 384(11), 989-1002.
- Grundy, S. M., et al. (2018). 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol. Journal of the American College of Cardiology, 73(24), e285-e350.
- By the 2023 American Geriatrics Society Beers Criteria Update Expert Panel. (2023). American Geriatrics Society 2023 updated AGS Beers Criteria for potentially inappropriate medication use in older adults. Journal of the American Geriatrics Society, 71(7), 2052-2081.
- O'Mahony, D., et al. (2015). STOPP/START criteria for potentially inappropriate prescribing in older people: version 2. Age and Ageing, 44(2), 213-218.
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