
The 2023 AGS Beers Criteria list medications that are potentially inappropriate for most adults 65 and older because the risk of harm usually exceeds the benefit, organized into drugs to avoid in general, drugs to avoid with specific diseases, drugs to use with caution, drug-drug interactions, and drugs that need renal dose adjustment. On the NP exam the criteria appear as a vignette in which one option is a Beers drug (an anticholinergic, a benzodiazepine, a sulfonylurea, a long-term NSAID, a sliding-scale insulin) and another option is the safer alternative or the non-drug approach. Knowing the class, the reason it is listed, and the substitute answers most of these items.
The American Geriatrics Society Beers Criteria, last updated in 2023, name the medications whose risks usually outweigh their benefits in adults 65 and older, and the exam tests them in one recurring shape: a vignette offers a Beers drug and a safer substitute, and the candidate must recognize both. The criteria are organized into five working tables: drugs to avoid for most older adults, drugs to avoid with specific diseases or syndromes, drugs to use with caution, drug-drug interactions to avoid, and drugs that need adjustment or avoidance by kidney function. A sixth table lists the drugs with strong anticholinergic properties, which is where most exam items come from.
The 2023 update applies to adults 65 and older in all settings except hospice and end-of-life care. Every entry carries a rationale, a recommendation (avoid, avoid in a defined situation, or use with caution), a quality-of-evidence rating, and a strength of recommendation. The panel removed 28 medications in 2023 because they are no longer marketed in the United States or are used by very few Medicare beneficiaries, which is why older study material still lists drugs that no longer appear.
Three framing rules apply. "Potentially inappropriate" means an alternative deserves consideration, not that the drug is contraindicated. The criteria do not replace a full medication review for duplications, omissions, and cascades. Continuing an established therapy differs from starting one: a long-term warfarin user with stable INRs may continue, while a new patient should usually receive a DOAC.
The table below groups the high-yield entries by class, with the reason the panel gives and the alternative that an exam answer usually points to. Doses are standard label doses; confirm any threshold in the current criteria before applying it to a patient.
| Class or drug | Why it is listed | What to use instead |
|---|---|---|
| First-generation antihistamines (diphenhydramine, hydroxyzine, chlorpheniramine, promethazine, meclizine) | Strongly anticholinergic: confusion, urinary retention, constipation, falls; tolerance to the sedative effect develops | Second-generation antihistamine (loratadine, cetirizine, fexofenadine) or intranasal corticosteroid for rhinitis; for insomnia, cognitive behavioral therapy for insomnia (CBT-I) |
| Antiparkinsonian anticholinergics (benztropine, trihexyphenidyl) | Not recommended for antipsychotic-induced extrapyramidal symptoms; more effective agents exist for Parkinson disease | Address the antipsychotic; dopaminergic therapy for Parkinson disease |
| Antispasmodics (dicyclomine, hyoscyamine, scopolamine) | Highly anticholinergic, uncertain effectiveness | Treat the underlying bowel disorder; peppermint oil or dietary measures for IBS symptoms |
| Peripheral alpha-1 blockers for hypertension (doxazosin, prazosin, terazosin) | Orthostatic hypotension; not first-line | Thiazide, calcium channel blocker, ACE inhibitor, or ARB |
| Central alpha agonists as first-line (clonidine) | Bradycardia, orthostasis, CNS effects | Same first-line antihypertensives |
| Nifedipine immediate release | Hypotension, precipitated myocardial ischemia | Amlodipine or another long-acting dihydropyridine |
| Amiodarone as first-line for atrial fibrillation | Toxicity exceeds other agents unless heart failure or substantial LV hypertrophy is present | Rate control with a beta blocker or non-dihydropyridine calcium channel blocker when ejection fraction allows |
| Digoxin as first-line for atrial fibrillation or heart failure; doses above 0.125 mg daily | Safer, more effective agents exist; toxicity rises with reduced clearance | Beta blocker for rate control; guideline-directed heart failure therapy |
| Warfarin as initial therapy for nonvalvular atrial fibrillation or VTE | DOACs have lower bleeding risk | Apixaban or another DOAC unless contraindicated; long-term warfarin users may continue |
| Rivaroxaban for long-term atrial fibrillation or VTE treatment | Higher major and GI bleeding than other DOACs in older adults | Apixaban; rivaroxaban only when once-daily dosing is essential |
| Aspirin for primary prevention | Bleeding risk outweighs benefit; aligns with the 2022 USPSTF statement | Do not start; consider deprescribing; secondary prevention is unaffected |
| Tricyclic antidepressants (amitriptyline, imipramine, doxepin above 6 mg) and paroxetine | Strongly anticholinergic, sedating, orthostatic | Sertraline, escitalopram, or an SNRI for depression; duloxetine or a gabapentinoid with caution for neuropathic pain |
| Antipsychotics (all) for behavioral symptoms of dementia or delirium | Increased stroke and mortality in dementia; limited benefit | Nonpharmacologic management first; antipsychotic only when the patient is a danger or has psychosis causing distress, with a deprescribing plan |
| Benzodiazepines (all) | Cognitive impairment, delirium, falls, fractures, motor vehicle crashes; dependence (FDA boxed warning 2020) | SSRI or SNRI and psychotherapy for anxiety; CBT-I for insomnia; taper existing users |
| Nonbenzodiazepine hypnotics (zolpidem, zaleplon, eszopiclone) | Same adverse-event profile as benzodiazepines with minimal improvement in sleep | CBT-I; sleep hygiene; treat the cause of insomnia |
| Skeletal muscle relaxants (carisoprodol, cyclobenzaprine, methocarbamol, metaxalone, chlorzoxazone, orphenadrine) | Anticholinergic, sedating, fracture risk; questionable efficacy at tolerated doses | Heat, physical therapy, acetaminophen, topical NSAID; baclofen and tizanidine for spasticity are exempt but still poorly tolerated |
| Meperidine | Neurotoxicity, delirium; other opioids safer | Morphine, hydromorphone, or oxycodone at reduced starting dose when an opioid is needed |
| Chronic oral NSAIDs, and short-term NSAIDs in the presence of an interacting drug; indomethacin and ketorolac at any duration | GI bleeding, kidney injury, blood pressure elevation, heart failure | Acetaminophen, topical diclofenac; if an NSAID is unavoidable, shortest course with a PPI |
| Sulfonylureas (now the whole class, including glipizide) | Prolonged hypoglycemia; 2023 added cardiovascular events and mortality | Metformin if eGFR allows; DPP-4 inhibitor; GLP-1 receptor agonist or SGLT2 inhibitor when indicated and tolerated |
| Sliding-scale insulin (short- or rapid-acting without basal) | Hypoglycemia without better glucose control | Basal insulin with scheduled correction if needed |
| Systemic estrogen with or without progestin | Breast and endometrial cancer, VTE, no cardioprotection; risks exceed benefits after 60 | Low-dose vaginal estrogen for genitourinary symptoms is acceptable |
| Megestrol | Thrombosis, death, minimal weight benefit | Address reversible causes of weight loss; dietary intervention |
| Desmopressin for nocturia | Hyponatremia | Evening fluid limits, timed diuretic, treat the cause |
| Metoclopramide (beyond 12 weeks) | Tardive dyskinesia | Limit to 12 weeks for gastroparesis; dietary measures |
| Proton pump inhibitors beyond 8 weeks without indication | C. difficile, pneumonia, fractures, B12 deficiency, GI malignancy added 2023 | Deprescribe, on-demand dosing, or H2 blocker; continue for Barrett esophagus, erosive esophagitis, hypersecretory states, or high-bleeding-risk NSAID users |
| Nitrofurantoin with CrCl below 30 mL/min or for long-term suppression | Pulmonary, hepatic, and neuropathic toxicity | Culture-directed alternative (fosfomycin, cephalexin, TMP-SMX if kidney function allows) |
These items read as "a patient with condition X is on drug Y; which should be stopped."
| Condition | Avoid | Reason | Preferred approach |
|---|---|---|---|
| Heart failure | NSAIDs, COX-2 inhibitors, non-dihydropyridine CCBs in HFrEF (diltiazem, verapamil), thiazolidinediones, dronedarone, cilostazol, dextromethorphan-quinidine (added 2023) | Fluid retention, negative inotropy, exacerbation | Guideline-directed HF therapy; acetaminophen for pain |
| Syncope | Cholinesterase inhibitors, nonselective peripheral alpha blockers, tertiary TCAs, antipsychotics | Bradycardia, orthostasis | Review need for the drug; treat the cause of syncope |
| Delirium | Anticholinergics, antipsychotics, benzodiazepines, Z-drugs, corticosteroids, H2 blockers, meperidine, opioids (added 2023) | Precipitate or worsen delirium | Nonpharmacologic delirium prevention; treat precipitants |
| Dementia or cognitive impairment | Anticholinergics, benzodiazepines, Z-drugs, antipsychotics | Worsen cognition; antipsychotics raise stroke and mortality | Behavioral interventions; cholinesterase inhibitor or memantine for the dementia itself |
| History of falls or fractures | Antiepileptics, antipsychotics, benzodiazepines, Z-drugs, antidepressants (TCAs, SSRIs, SNRIs), opioids, anticholinergics (added 2023) | Ataxia, sedation, orthostasis | Deprescribe where possible; strength and balance exercise |
| Parkinson disease | Antiemetics (metoclopramide, prochlorperazine, promethazine), most antipsychotics other than quetiapine, clozapine, and pimavanserin | Dopamine antagonism worsens parkinsonism | Ondansetron for nausea; quetiapine or pimavanserin for psychosis if needed |
| History of gastric or duodenal ulcer | Aspirin above 325 mg daily, non-COX-selective NSAIDs | Recurrent ulcer, bleeding | Acetaminophen; if unavoidable, add a PPI or misoprostol |
| CKD stage 4 or worse | NSAIDs | Acute kidney injury, progression | Acetaminophen, topical agents |
| Urinary incontinence in women | Oral or transdermal estrogen, peripheral alpha-1 blockers | Worsened incontinence | Pelvic floor training, bladder training, mirabegron or vibegron |
| Lower urinary tract symptoms or BPH | Strongly anticholinergic drugs | Urinary retention | Alpha-1 blocker for BPH; avoid anticholinergic add-ons |
Table 4 (use with caution) carries situational risks: dabigatran and prasugrel in patients 75 and older; antidepressants, antipsychotics, carbamazepine, diuretics, and tramadol for SIADH and hyponatremia, so check sodium after starting them; and, new in 2023, ticagrelor and SGLT2 inhibitors, the latter for euglycemic ketoacidosis and genitourinary infection.
Table 5 (drug-drug interactions) rewards memorization of a short list:
The exam often supplies an estimated creatinine clearance and expects action on it. Thresholds vary slightly by labeling; confirm in the current criteria before prescribing.
The exam tests the strongly anticholinergic table in two ways: naming the anticholinergic hiding in a list (paroxetine among SSRIs, oxybutynin among incontinence drugs, cyclobenzaprine among muscle relaxants, meclizine among vertigo treatments) and recognizing the syndrome it causes (new confusion, urinary retention, constipation, dry mouth, falls). Cumulative exposure matters more than any single agent; on the Anticholinergic Cognitive Burden scale, a total of 3 or more is a prompt for review, not a diagnostic cut-off.
Substitutes: oxybutynin to mirabegron or vibegron; diphenhydramine to a second-generation antihistamine or CBT-I; amitriptyline to duloxetine; paroxetine to sertraline or escitalopram; meclizine to vestibular rehabilitation.
Teach the patient and caregiver the reason, the substitute, and the symptom to report. A patient who hears that a sleep aid causes confusion and falls accepts a taper more readily than one told only that it is "on a list."
A 79-year-old woman with hypertension, osteoarthritis, and mild cognitive impairment presents for follow-up accompanied by her daughter, who reports that her mother has become more confused over the past month and had a near-fall in the bathroom at night. Medications: amlodipine 5 mg daily, acetaminophen 650 mg three times daily, and, started 6 weeks ago by another clinician, oxybutynin 5 mg twice daily for urinary urgency. She also takes diphenhydramine 25 mg nightly, bought over the counter, for sleep. Blood pressure is 128/74 mm Hg sitting and 122/70 mm Hg standing. Mini-Cog score is 2 of 5, down from 4 of 5 a year ago. Basic metabolic panel, TSH, and vitamin B12 are normal. Which of the following is the most appropriate next step?
Answer: B. The vignette describes a new cognitive decline and a near-fall after two strongly anticholinergic drugs were added to an older adult with baseline cognitive impairment, a Table 3 pairing (anticholinergics in dementia or cognitive impairment, and in patients with falls) and a Table 5 interaction (two anticholinergics together). The correct action is to remove both, offer a nonpharmacologic alternative for urgency, and reassess cognition after the drugs have cleared. Option A keeps the anticholinergic burden; a formulation change does not remove the central effect in a patient already showing harm. Option C treats a drug-induced decline as a neurodegenerative one before the reversible cause has been removed, and cholinesterase inhibitors are also listed to avoid in syncope. Option D swaps one Beers hypnotic for another; Z-drugs carry the same fall and cognitive risks and remain on the avoid list.
Common follow-up questions on Geriatrics & Prescribing (AGNP).
No. The criteria flag drugs that are potentially inappropriate for most older adults; they are a prompt for a risk-benefit discussion, not a prohibition. The 2023 panel is explicit that the criteria do not apply in hospice or end-of-life care and that clinical judgment and patient goals govern individual decisions.
Aspirin for primary prevention moved to avoid initiating; rivaroxaban moved to avoid for long-term atrial fibrillation or venous thromboembolism treatment because of bleeding risk; warfarin should not be started first-line when a DOAC is usable; all sulfonylureas, including glipizide, are now listed; opioids were added to drugs that worsen delirium; anticholinergics were added to drugs to avoid in patients with falls or fractures; baclofen was added to the renal table.
Not always. A short course of metoclopramide for gastroparesis, a cholinesterase inhibitor in a patient without syncope, or a continued long-term warfarin regimen with stable INRs can be correct. The exam tests whether you recognize the listed risk and whether the vignette contains the exception.
Beers is a US list built around drugs and drug-disease pairs to avoid, with a short caution table. STOPP/START version 3 (2023) is European, organized by physiologic system, and includes START criteria that flag omissions such as a missing statin, anticoagulant, or bone-protective therapy. Boards draw mostly on Beers, but omission items borrow the START logic.
FNP and AGNP board questions written as primary-care cases, with guideline-based explanations, for the AANP and ANCC exams. Create a free account and pick your track.
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