Appendix C: Beers Criteria

TABLE C.1
2019 AMERICAN GERIATRICS SOCIETY BEERS CRITERIA FOR POTENTIALLY INAPPROPRIATE MEDICATION USE IN OLDER ADULTS
Organ System, Therapeutic Category, DrugsRationaleRecommendationQuality of EvidenceStrength of Recommendation
Anticholinergics
First-generation antihistamines

Brompheniramine

Carbinoxamine

Chlorpheniramine

Clemastine

Cyproheptadine

Dexbrompheniramine

Dexchlorpheniramine

Dimenhydrinate

Diphenhydramine (oral)

Doxylamine

Hydroxyzine

Meclizine

Promethazine

Pyrilamine

Triprolidine
Highly anticholinergic; clearance reduced with advanced age, and tolerance develops when used as hypnotic; risk of confusion, dry mouth, constipation, and other anticholinergic effects or toxicity.

Use of diphenhydramine in situations such as acute treatment of severe allergic reaction may be appropriate.
AvoidModerateStrong
Antiparkinsonian Agents
Benztropine (oral)

Trihexyphenidyl
Not recommended for prevention of extrapyramidal symptoms with antipsychotics; more effective agents available for treatment of Parkinson disease.AvoidModerateStrong
Antispasmodics

Atropine (excludes ophthalmic)

Belladonna alkaloids

Clidinium-chlordiazepoxide

Dicyclomine

Homatropine (excludes ophthalmic)

Hyoscyamine

Methscopolamine

Propantheline

Scopolamine
Highly anticholinergic, uncertain effectiveness.AvoidModerateStrong
Antithrombotics
Dipyridamole, oral short-acting (does not apply to the extended-release combination with aspirin)May cause orthostatic hypotension; more effective alternatives available; intravenous form acceptable for use in cardiac stress testing.AvoidModerateStrong
Anti-Infective
NitrofurantoinPotential for pulmonary toxicity, hepatotoxicity, and peripheral neuropathy, especially with long-term use; safer alternatives available.Avoid in individuals with creatinine clearance <30 mL/min or for long-term suppression.LowStrong
Cardiovascular
Peripheral alpha-1 blockers for treatment of hypertension

Doxazosin

Prazosin

Terazosin
High risk of orthostatic hypotension and associated harms, especially in older adults; not recommended as routine treatment for hypertension; alternative agents have superior risk–benefit profile.Avoid use as an antihypertensive.ModerateStrong
Central alpha agonists

Clonidine for first-line treatment of hypertension

Other CNS alpha-agonists

Guanabenz

Guanfacine

Methyldopa

Reserpine (>0.1 mg/d)
High risk of adverse CNS effects; may cause bradycardia and orthostatic hypotension; not recommended as routine treatment for hypertension.Avoid clonidine as first-line antihypertensive. Avoid others as listed.LowStrong
DisopyramideMay induce heart failure in older adults due to potent negative inotropic action; strongly anticholinergic; other antiarrhythmic drugs preferred.Avoid.LowStrong
DronedaroneWorse outcomes have been reported in clients taking dronedarone who have permanent atrial fibrillation or severe or recently decompensated heart failure.Avoid in individuals with permanent atrial fibrillation or severe or recently decompensated heart failure.HighStrong
DigoxinUse in atrial fibrillation: should not be used as a first-line agent in atrial fibrillation because there are safer and more effective alternatives for rate control supported by high-quality evidence.Avoid as first-line therapy for atrial fibrillation.Atrial fibrillation: lowAtrial fibrillation: strong
Use in heart failure: evidence for benefits and harms of digoxin is conflicting and of lower quality; most but not all of the evidence concerns use in HFrEF. There is strong evidence for other agents as first-line therapy to reduce hospitalizations and mortality in adults with HFrEF. In heart failure, higher dosages are not associated with additional benefit and may increase toxicity.Avoid as first-line therapy for heart failure.Heart failure: lowHeart failure: strong
Decreased renal clearance of digoxin may lead to increased risk of toxic effects; further dose reduction may be necessary in clients with stage 4 or 5 chronic kidney disease.If used for atrial fibrillation or heart failure dosage >0.125 mg/d.Dosage >0.125 mg/d: moderateDosage >0.125 mg/d: strong
Nifedipine, immediate–releasePotential for hypotension; risk of precipitating myocardial ischemia.Avoid.HighStrong
AmiodaroneEffective for maintaining sinus rhythm but has greater toxicities than other antiarrhythmics used in atrial fibrillation; may be reasonable first-line therapy in clients with concomitant heart failure or substantial left ventricular hypertrophy if rhythm control is preferred over rate control.Avoid amiodarone as first-line therapy for atrial fibrillation unless client has heart failure or substantial left ventricular hypertrophy.HighStrong
Central Nervous System
Antidepressants, alone or in combination

Amitriptyline

Amoxapine

Clomipramine

Desipramine

Doxepin >6 mg/d

Imipramine

Nortriptyline

Paroxetine

Protriptyline

Trimipramine
Highly anticholinergic, sedating, and cause orthostatic hypotension; safety profile of low-dose doxepin (≤6 mg/d) comparable with that of placebo.Avoid.HighStrong
Antipsychotics, first (conventional) and second (atypical) generationIncreased risk of cerebrovascular accident (stroke) and greater rate of cognitive decline and mortality in persons with dementia.

Avoid antipsychotics for behavioral problems of dementia or delirium unless nonpharmacologic options (e.g., behavioral interventions) have failed or are not possible and the older adult is threatening substantial harm to self or others.
Avoid, except for schizophrenia, bipolar disorder, or for short-term use as antiemetic during chemotherapy.ModerateStrong
Barbiturates

Amobarbital

Butabarbital

Butalbital

Mephobarbital

Pentobarbital

Phenobarbital

Secobarbital
High rate of physical dependence, tolerance to sleep benefits, greater risk of overdose at low dosages.Avoid.HighStrong
Benzodiazepines

Short- and intermediate-acting

Alprazolam

Estazolam

Lorazepam

Oxazepam

Temazepam

Triazolam
Older adults have increased sensitivity to benzodiazepines and decreased metabolism of long-acting agents; in general, all benzodiazepines increase risk of cognitive impairment, delirium, falls, fractures, and motor vehicle crashes in older adults.Avoid.ModerateStrong
Long-acting

Clorazepate

Chlordiazepoxide (alone or in combination with amitriptyline or clidinium)

Clonazepam

Clorazepate

Diazepam

Flurazepam

Quazepam
May be appropriate for seizure disorders, rapid eye movement sleep disorders, benzodiazepine withdrawal, ethanol withdrawal, severe generalized anxiety disorder, and periprocedural anesthesia.
MeprobamateHigh rate of physical dependence; sedating.Avoid.ModerateStrong
Nonbenzodiazepine, benzodiazepine receptor agonist hypnotics (i.e., “Z-drugs”)

Eszopiclone

Zaleplon

Zolpidem
Nonbenzodiazepine benzodiazepine receptor agonists (i.e., “Z drugs”) have adverse events similar to those of benzodiazepines in older adults (e.g., delirium, falls, fractures); increased ED visits and hospitalizations; motor vehicle crashes; minimal improvement in sleep latency and duration.Avoid.ModerateStrong
Ergoloid mesylates (dehydrogenated ergot alkaloids)

Isoxsuprine
Lack of efficacy.Avoid.HighStrong
Endocrine
Androgens

Methyltestosterone

Testosterone
Potential for cardiac problems; contraindicated in males with prostate cancer.Avoid unless indicated for confirmed hypogonadism with clinical symptoms.ModerateWeak
Desiccated thyroidConcerns about cardiac effects; safer alternatives available.Avoid.LowStrong
Estrogens with or without progestinsEvidence of carcinogenic potential (breast and endometrium); lack of cardioprotective effect and cognitive protection in older females.

Evidence indicates that vaginal estrogens for the treatment of vaginal dryness are safe and effective; females with a history of breast cancer who do not respond to nonhormonal therapies are advised to discuss the risk and benefits of low-dose vaginal estrogen (dosages of estradiol <25 mcg twice weekly) with their healthcare provider.
Avoid systemic estrogen (e.g., oral and topical patch). Vaginal cream or tablets: acceptable to use low-dose intravaginal estrogen for management of dyspareunia, lower urinary tract infections, and other vaginal symptoms.Oral and patch: high

Vaginal cream or tablets: moderate
Oral and patch: strong

Topical vaginal cream or tablets: weak
Growth hormoneImpact on body composition is small and associated with edema, arthralgia, carpal tunnel syndrome, gynecomastia, impaired fasting glucose.Avoid, except for clients rigorously diagnosed by evidence-based criteria with growth hormone deficiency due to an established etiology.HighStrong
Insulin, sliding scale (insulin regimens containing only short- or rapid-acting insulin dosed according to current blood glucose levels without concurrent use of basal or long-acting insulin)Higher risk of hypoglycemia without improvement in hyperglycemia management regardless of care setting; avoid insulin regimens that include only short- or rapid-acting insulin dosed according to current blood glucose levels without concurrent use of basal or long-acting insulin. This recommendation does not apply to regimens that contain basal insulin or long-acting insulin.Avoid.ModerateStrong
MegestrolMinimal effect on weight; increases risk of thrombotic events and possibly death in older adults.Avoid.ModerateStrong
Sulfonylureas, long-acting

Chlorpropamide

Glimepiride

Glyburide (also known as glibenclamide)
Chlorpropamide: prolonged half-life in older adults; can cause prolonged hypoglycemia; causes syndrome of inappropriate antidiuretic hormone secretion.

Glimepiride and glyburide: higher risk of severe prolonged hypoglycemia in older adults.
Avoid.ModerateStrong
Gastrointestinal
MetoclopramideCan cause extrapyramidal effects, including tardive dyskinesia; risk may be greater in frail older adults and with prolonged exposure.Avoid, unless for gastroparesis with duration of use not to exceed 12 weeks except in rare cases.ModerateStrong
Mineral oil, given orallyPotential for aspiration and adverse effects; safer alternatives available.Avoid.ModerateStrong
Proton pump inhibitorsRisk of Clostridium difficile infection and bone loss and fractures.Avoid scheduled use for >8 weeks unless for high-risk clients (e.g., oral corticosteroids or chronic NSAID use), erosive esophagitis, Barrett esophagitis, pathologic hypersecretory condition, or demonstrated need for maintenance treatment (e.g., due to failure of drug discontinuation trial or H2 receptor blockers).HighStrong
Pain Medications
MeperidineNot effective oral analgesic in dosages commonly used; may have higher risk of neurotoxicity, including delirium, than other opioids; safer alternatives available.Avoid.ModerateStrong
Non-Cyclooxygenase-Selective
Non-cyclooxygenase-selective NSAIDs, oral:

Aspirin >325 mg/d

Diclofenac

Diflunisal

Etodolac

Fenoprofen

Ibuprofen

Ketoprofen

Meclofenamate

Mefenamic acid

Meloxicam

Nabumetone

Naproxen

Oxaprozin

Piroxicam

Sulindac

Tolmetin
Increased risk of gastrointestinal bleeding or peptic ulcer disease in high-risk groups, including those aged >75 or taking oral or parenteral corticosteroids, anticoagulants, or antiplatelet agents; use of proton pump inhibitor reduces but does not eliminate risk. Upper gastrointestinal ulcers, gross bleeding, or perforation caused by NSAIDs occur in approximately 1% of clients treated for 3–6 months and in ~2%–4% of clients treated for 1 year; these trends continue with longer duration of use. Also can increase blood pressure and induce kidney injury. Risks are dose-related.Avoid chronic use, unless other alternatives are not effective and the client can take gastroprotective agent (proton pump inhibitor or misoprostol).ModerateStrong
Indomethacin

Ketorolac, includes parenteral
Increased risk of gastrointestinal bleeding, peptic ulcer disease, and acute kidney injury in other adults.

Indomethacin is more likely than other NSAIDs to have adverse CNS effects. Of all the NSAIDs, indomethacin has the most adverse effects.
Avoid.ModerateStrong
Skeletal muscle relaxants

Carisoprodol

Chlorzoxazone

Cyclobenzaprine

Metaxalone

Methocarbamol

Orphenadrine
Most muscle relaxants poorly tolerated by older adults because some have anticholinergic adverse effects, sedation, increased risk of fractures; effectiveness at dosages tolerated by older adults questionable.Avoid.ModerateStrong
Genitourinary
DesmopressinHigh risk of hyponatremia; safer alternative treatments.Avoid for treatment of nocturia or nocturnal polyuria.ModerateStrong

Note: The primary target audience is practicing clinicians. The intentions of the criteria are to improve the selection of prescription drugs by clinicians and clients; evaluate patterns of drug use within populations; educate clinicians and clients on proper drug usage; and evaluate health outcome, quality-of-care, cost, and utilization data.

CNS, central nervous system; HFrEF, heart failure with reduced ejection fraction; NSAIDs, nonsteroidal anti-inflammatory drugs.

Source: American Geriatrics Society Beers Criteria® Update Expert Panel. (2019). American Geriatrics Society 2019 Updated AGS Beers Criteria® for potentially inappropriate medication use in older adults. Journal of the American Geriatrics Society, 67, 674–694. https://doi.org/10.1111/jgs.15767.

TABLE C.2
2019 AMERICAN GERIATRICS SOCIETY BEERS CRITERIA FOR POTENTIALLY INAPPROPRIATE MEDICATION USE IN OLDER ADULTS DUE TO DRUG–DISEASE OR DRUG–SYNDROME INTERACTIONS THAT MAY EXACERBATE THE DISEASE OR SYNDROME
Disease or SyndromeDrug(s)RationaleRecommendationQuality of EvidenceStrength of Recommendation
Cardiovascular
Heart failureAvoid: cilostazol

Avoid in heart failure with reduced ejection fraction: non-dihydropyridine CCBs (diltiazem, verapamil)

Use with caution in clients with heart failure who are asymptomatic; avoid in clients with symptomatic heart failure;

NSAIDs and COX-2 inhibitors

Thiazolidinediones (pioglitazone, rosiglitazone)

Dronedarone
Potential to promote fluid retention and/or exacerbate heart failure (NSAIDs and COX-2 inhibitors, non-dihydropyridine CCBs, thiazolidinediones); potential to increase mortality in order adults with heart failure (cilostazol and dronedarone).Avoid or use with caution.NSAIDs: moderate

Non-dihydropyridine CCBs: moderate

Thiazolidinediones: high

Cilostazol: low

Dronedarone: high
Strong
SyncopeAChEIs

Nonselective peripheral alpha-1 blockers (e.g., doxazosin, prazosin, terazosin)

Tertiary TCAs

Antipsychotics:
  • Chlorpromazine

  • Thioridazine

  • Olanzapine

AChEIs cause bradycardia and should be avoided in older adults whose syncope may be due to bradycardia.

Nonselective peripheral alpha-1 blockers cause orthostatic blood pressure changes and should be avoided in older adults whose syncope may be due to orthostatic hypotension.

Tertiary TCAs and the antipsychotics listed increase the risk of orthostatic hypotension or bradycardia.
Avoid.AChEIs, TCAs, and antipsychotics: high

Nonselective peripheral alpha-1 blockers: high
AChEIs, TCAs: strong

Nonselective peripheral alpha-1 blockers, antipsychotics: weak
Central Nervous System
DeliriumAnticholinergicsa

Antipsychoticsb

Benzodiazepines

Corticosteroids (oral and parenteral)c

H2 receptor antagonists:
  • Cimetidine

  • Famotidine

  • Nizatidine

  • Ranitidine

  • Meperidine

Nonbenzodiazepine, benzodiazepine receptor agonist hypnotics: eszopiclone, zaleplon, zolpidem
Avoid in older adults with or at high risk of delirium because of the potential of inducing or worsening delirium.

Avoid antipsychotics for behavioral problems of dementia and/or delirium unless nonpharmacologic options (e.g., behavioral interventions) have failed or are not possible and the older adult is threatening substantial harm to self or others. Antipsychotics are associated with greater risk of cerebrovascular accident (stroke) and mortality in persons with dementia.
Avoid.H2 receptor antagonists: low

All others: moderate
Strong
Dementia or cognitive impairmentAnticholinergicsa

Benzodiazepines

Nonbenzodiazepine, benzodiazepine receptor agonist hypnotics:
  • Eszopiclone

  • Zolpidem

  • Zaleplon

Antipsychotics, chronic and as-needed useb
Avoid because of adverse CNS effects.

Avoid antipsychotics for behavioral problems of dementia or delirium unless nonpharmacologic options (e.g., behavioral interventions) have failed or are not possible and the older adult is threatening substantial harm to self or others. Antipsychotics are associated with greater risk of cerebrovascular accident (stroke) and mortality in persons with dementia.
Avoid.ModerateStrong
History of falls or fracturesAntiepileptics

Antipsychoticsb

Benzodiazepines

Nonbenzodiazepine, benzodiazepine receptor agonist hypnotics:
  • Eszopiclone

  • Zaleplon

  • Zolpidem

Antidepressants:
  • TCAs

  • SSRIs

  • SNRIs

  • Opioids

May cause ataxia, impaired psychomotor function, syncope, additional falls; shorter-acting benzodiazepines are not safer than long-acting ones.

If one of the drugs must be used, consider reducing use of other CNS-active medications that increase risk of falls and fractures (i.e., antiepileptics, opioid receptor agonists, antipsychotics, antidepressants, benzodiazepine receptor agonists, other sedatives and hypnotics) and implement other strategies to reduce fall risk. Data for antidepressants are mixed but no compelling evidence that certain antidepressants confer less fall risk than others.
Avoid unless safer alternatives are not available; avoid antiepileptics except for seizure and mood disorders

Opioids: Avoid except for pain management in the setting of severe acute pain (e.g., recent fractures or joint replacement).
Opioids: moderate

All others: high
Strong
Parkinson diseaseAntiemetics:
  • Metoclopramide

  • Prochlorperazine

  • Promethazine

All antipsychotics (except aripiprazole, quetiapine, clozapine)
Dopamine receptor antagonists with potential to worsen parkinsonian symptoms.

Exceptions: Pimavanserin and clozapine appear to be less likely to precipitate worsening of Parkinson disease.

Quetiapine has only been studied in low-quality clinical trials with efficacy comparable with that of placebo in five trials and to that of clozapine in two others.
Avoid.ModerateStrong
Gastrointestinal
History of gastric or duodenal ulcersAspirin (>325 mg/d)

Non-COX-2 selective NSAIDs
May exacerbate existing ulcers or cause new/additional ulcers.Avoid unless other alternatives are not effective and the client can take gastroprotective agent (e.g., proton pump inhibitor or misoprostol).ModerateStrong
Kidney/Urinary Tract
Chronic kidney disease stage IV or higher (creatinine clearance <30 mL/min)NSAIDs (non-COX and COX-selective, oral and parenteral, nonacetylated salicylates)May increase risk of acute kidney injury and further decline of renal function.Avoid.ModerateStrong
Urinary incontinence (all types) in femalesEstrogen oral and transdermal (excludes intravaginal estrogen)

Peripheral alpha-1 blockers: doxazosin, prazosin, terazosin
Lack of efficacy (oral estrogen) and aggravation of incontinence (alpha-1 blockers).Avoid in females.Estrogen: high

Peripheral alpha-1 blockers: moderate
Estrogen: strong

Peripheral alpha-1 blockers: strong
Lower urinary tract symptoms, benign prostatic hyperplasiaStrongly anticholinergic drugs, except antimuscarinics for urinary incontinenceaMay decrease urinary flow and cause urinary retention.Avoid in males.ModerateStrong

Note: The primary target audience is the practicing clinician. The intentions of the criteria are to improve selection of prescription drugs by clinicians and clients; evaluate patterns of drug use within populations; educate clinicians and clients on proper drug usage; and evaluate health outcome, quality-of-care, cost, and utilization data.

aSee Table 7 in full criteria available on geriatricscareonline.org.

bMay be required to treat concurrent schizophrenia, bipolar disorder, and other selected mental health conditions but should be prescribed in the lowest effective dose and shortest possible duration.

cExcludes inhaled and topical forms. Oral and parenteral corticosteroids may be required for conditions such as exacerbations of chronic obstructive pulmonary disease but should be prescribed in the lowest effective dose and for the shortest possible duration.

AChEI, acetylcholinesterase inhibitor; CCB, calcium channel blocker; CNS, central nervous system; COX, cyclooxygenase; NSAID, nonsteroidal anti-inflammatory drug; SNRIs, serotonin-norepinephrine reuptake inhibitor; SSRIs, selective serotonin reuptake inhibitors; TCA, tricyclic antidepressant.

Source: American Geriatrics Society Beers Criteria® Update Expert Panel. (2019). American Geriatrics Society 2019 Updated AGS Beers Criteria® for potentially inappropriate medication use in older adults. Journal of the American Geriatrics Society, 67, 674–694. https://doi.org/10.1111/jgs.15767.

TABLE C.3
2019 AMERICAN GERIATRICS SOCIETY BEERS CRITERIA FOR POTENTIALLY INAPPROPRIATE MEDICATIONS TO BE USED WITH CAUTION IN OLDER ADULTS
Drug(s)RationaleRecommendationQuality of EvidenceStrength of Recommendation
Aspirin for primary prevention of cardiovascular disease and colorectal cancerRisk of major bleeding from aspirin increases markedly in older age.

Several studies suggest lack of net benefit when used for primary prevention in older adults with cardiovascular risk factors, but evidence is not conclusive. Aspirin is generally indicated for secondary prevention in older adults with established cardiovascular disease.
Use with caution in adults aged ≥70 years old.ModerateStrong
Dabigatran

Rivaroxaban
Increased risk of gastrointestinal bleeding compared with warfarin and reported rates with other direct oral anticoagulants when used for long-term treatment of VTE or atrial fibrillation in adults aged ≥75 years.Use with caution for treatment of VTE or atrial fibrillation in adults aged ≥75 years old.ModerateStrong
PrasugrelIncreased risk of bleeding in older adults; benefit in highest risk older adults (e.g., those with prior myocardial infarction or diabetes mellitus) may offset risk when used for its approved indication of acute coronary syndrome to be managed with percutaneous coronary intervention.Use with caution in adults aged ≥75 years old.ModerateWeak
Antipsychotics

Carbamazepine

Diuretics

Mirtazapine

Oxcarbazepine

SNRIs

SSRIs

TCAs

Tramadol
May exacerbate or cause syndrome of inappropriate antidiuretic hormone secretion or hyponatremia; monitor sodium level closely when starting or changing dosages in older adults.Use with caution.ModerateStrong
Dextromethorphan/quinidineLimited efficacy in clients with behavioral symptoms of dementia (does not apply to treatment of PBA). May increase risk of falls and concerns with clinically significant drug interactions.Use with caution.ModerateStrong
Trimethoprim-sulfamethoxazoleIncreased risk of hyperkalemia when used concurrently with an ACEI or ARB in the presence of decreased creatinine clearance.Use with caution in clients on ACEI or ARB and decreased creatinine clearance.LowStrong

Note: The primary target audience is the practicing clinician. The intentions of the criteria are to improve selection of prescription drugs by clinicians and clients; evaluate patterns of drug use within populations; educate clinicians and clients on proper drug usage; and evaluate health outcome, quality-of-care, cost, and utilization data.

ACEI, angiotensin-converting enzyme inhibitor; ARB, angiotensin receptor blocker; PBA, pseudobulbar affect; SNRIs, serotonin-norepinephrine reuptake inhibitors; SSRIs, selective serotonin reuptake inhibitors; TCAs, tricyclic antidepressants; VTE, venous thromboembolism.

Source: American Geriatrics Society Beers Criteria® Update Expert Panel. (2019). American Geriatrics Society 2019 Updated AGS Beers Criteria® for potentially inappropriate medication use in older adults. Journal of the American Geriatrics Society, 67, 674–694. https://doi.org/10.1111/jgs.15767.

TABLE C.4
2019 AMERICAN GERIATRICS SOCIETY BEERS CRITERIA FOR POTENTIALLY CLINICALLY DRUG–DRUG INTERACTIONS THAT SHOULD BE AVOIDED IN OLDER ADULTS
Object Drug and ClassInteracting Drug and ClassRisk RationaleRecommendationQuality of EvidenceStrength of Recommendation
RAS inhibitor (ACEIs, ARBs, aliskiren) or potassium-sparing diuretics (amiloride, triamterene)Another RAS inhibitor (ACEIs, ARBs, aliskiren)Increased risk of hyperkalemiaAvoid routine use in those with chronic kidney disease stage 3a or higher.ModerateStrong
OpioidsBenzodiazepinesIncreased risk of overdoseAvoid.ModerateStrong
OpioidsGabapentin, pregabalinIncreased risk of severe sedation-related adverse events, including respiratory depression and deathAvoid; exceptions are when transitioning from opioid therapy to gabapentin or pregabalin, or when using gabapentinoids to reduce opioid dose, although caution should be used in all circumstances.ModerateStrong
AnticholinergicAnticholinergicIncreased risk of cognitive declineAvoid, minimize number of anticholinergic drugs.ModerateStrong
Antidepressants (i.e., TCAs and SSRIs)

Antipsychotics

Antiepileptics

Benzodiazepines and nonbenzodiazepines, benzodiazepine receptor agonist hypnotics (i.e., “Z-drugs”)

Opioids
Any combination of ≥3 of these CNS-active drugsaIncreased risk of falls (all) and of fracture (benzodiazepines and nonbenzodiazepine, benzodiazepine receptor agonist hypnotics)Avoid total of ≥3 CNS-active drugsa; minimize number of CNS-active drugs.Combinations including benzodiazepines and nonbenzodiazepine, benzodiazepine receptor agonist hypnotics or opioids: high

All other combinations: moderate
Strong
Corticosteroids, oral or parenteralNSAIDsIncreased risk of peptic ulcer disease or gastrointestinal bleedingAvoid; if not possible, provide gastrointestinal protection.ModerateStrong
LithiumACEIsIncreased risk of lithium toxicityAvoid, monitor lithium concentrations.ModerateStrong
LithiumLoop diureticsIncreased risk of lithium toxicityAvoid, monitor lithium concentrations.ModerateStrong
Peripheral alpha-1 blockersLoop diureticsIncreased risk of urinary incontinence in older femalesAvoid in older females, unless conditions warrant both drugs.ModerateStrong
PhenytoinTrimethoprim-sulfamethoxazoleIncreased risk of urinary incontinence in older femalesAvoid.ModerateStrong
TheophyllineCimetidine

Ciprofloxacin
Increased risk of theophylline toxicityAvoid.ModerateStrong
WarfarinAmiodaroneIncreased risk of bleedingAvoid when possible; if used together, monitor international normalized ratio closely.ModerateStrong
WarfarinCiprofloxacinIncreased risk of bleedingAvoid when possible; if used together, monitor international normalized ratio closely.ModerateStrong
WarfarinMacrolides (excluding azithromycin)Increased risk of bleedingAvoid when possible; if used together, monitor international normalized ratio closely.ModerateStrong
WarfarinTrimethoprim-sulfamethoxazoleIncreased risk of bleedingAvoid when possible; if used together, monitor INR closely.ModerateStrong
WarfarinNSAIDsIncreased risk of bleedingAvoid when possible; if used together, monitor for bleeding closely.HighStrong

aCNS-active drugs: antipsychotics; benzodiazepines; nonbenzodiazepines, benzodiazepine receptor agonist hypnotics; TCAs; SSRI; and opioids.

ACEI, angiotensin-converting enzyme inhibitor; ARB, angiotensin II receptor blocker; CNS, central nervous system; INR, international normalized ratio; NSAID, nonsteroidal anti-inflammatory drug; RAS, recurrent aphthous stomatitis; SSRI, selective serotonin reuptake inhibitor; TCA, tricyclic antidepressant.

Source: American Geriatrics Society Beers Criteria® Update Expert Panel. (2019). American Geriatrics Society 2019 Updated AGS Beers Criteria® for potentially inappropriate medication use in older adults. Journal of the American Geriatrics Society, 67, 674–694. https://doi.org/10.1111/jgs.15767.

TABLE C.5
2019 AMERICAN GERIATRICS SOCIETY BEERS CRITERIA FOR MEDICATIONS THAT SHOULD BE AVOIDED OR HAVE THEIR DOSAGE REDUCED WITH VARYING LEVELS OF KIDNEY FUNCTION IN OLDER ADULTS
Medication Class and MedicationCreatinine Clearance, mL/min, at Which Action RequiredRationaleRecommendationQuality of EvidenceStrength of Recommendation
Anti-Infective
Ciprofloxacin<30Increased risk of CNS effects (e.g., seizures, confusion) and tendon ruptureDoses used to treat common infections typically require reduction when CrCl <30 mL/min.ModerateStrong
Trimethoprim-sulfamethoxazole<30Increased risk of worsening renal function and hyperkalemiaCrCl 15–29 mL/min: Reduce dose.

<15 mL/min: Avoid.
ModerateStrong
Cardiovascular or Hemostasis
Amiloride<30Increased potassium, and decreased sodiumAvoid.ModerateStrong
Apixaban<25Lack of evidence for efficacy and safety in clients with a CrCl <25 mL/minAvoid.ModerateStrong
Dabigatran<30Lack of evidence for efficacy and safety in individuals with a CrCl <30 mL/min

Label dose for clients with a CrCl 15–30 mL/min based on pharmacokinetic data
Avoid; dose adjustment is advised when CrCl >30 mL/min in the presence of drug--drug interactions.ModerateStrong
Dofetilide<60QTc prolongation and torsades de pointesCrCl 20–59 mL/min: Reduce dose.

CrCl <20 mL/min: Avoid.
ModerateStrong
Edoxaban15–50

<15 or >95
Lack of evidence of efficacy or safety in clients with a CrCl <30 mL/minCrCl 15–50 mL/min: Reduce dose.

CrCl <15 or >95 mL/min: Avoid.
ModerateStrong
Enoxaparin<30Increased risk of bleedingReduce dose.ModerateStrong
Fondaparinux<30Increased risk of bleedingAvoid.ModerateStrong
Rivaroxaban<50Lack of efficacy or safety evidence in clients with a CrCl <30 mL/minNonvalvular atrial fibrillation: Reduce dose if CrCl 15–50 mL/min; avoid if CrCl <15 mL/min.

Venous thromboembolism treatment for VTE prophylaxis with hip or knee replacement: Avoid if CrCl <30 mL/min.
ModerateStrong
Spironolactone<30Increased potassiumAvoid.ModerateStrong
Triamterene<30Increased potassium and decreased sodiumAvoid.ModerateStrong
Central Nervous System and Analgesics
Duloxetine<30Increased gastrointestinal adverse effects (nausea, diarrhea)Avoid.ModerateWeak
Gabapentin<60CNS adverse effectsReduce dose.ModerateStrong
Levetiracetam≤80CNS adverse effectsReduce dose.ModerateStrong
Pregabalin<60CNS adverse effectsReduce dose.ModerateStrong
Tramadol<30CNS adverse effectsImmediate–release: Reduce dose.

Extended–release: Avoid.
LowWeak
Gastrointestinal
Cimetidine<50Mental status changesReduce dose.ModerateStrong
Famotidine<50Mental status changesReduce dose.ModerateStrong
Nizatidine<50Mental status changesReduce dose.ModerateStrong
Ranitidine<50Mental status changesReduce dose.ModerateStrong
Hyperuricemia
Colchicine<30Gastrointestinal, neuromuscular, bone marrow toxicityReduce dose; monitor for adverse effects.ModerateStrong
Probenecid<30Loss of effectivenessAvoid.ModerateStrong

CNS, central nervous system; CrCl, creatinine clearance; VTE, venous thromboembolism.

Source: American Geriatrics Society Beers Criteria® Update Expert Panel. (2019). American Geriatrics Society 2019 Updated AGS Beers Criteria® for potentially inappropriate medication use in older adults. Journal of the American Geriatrics Society, 67, 674–694. https://doi.org/10.1111/jgs.15767.