• Dosing/administration guidelines. • Not to be given by IV push. • To be infused over at least 10 minutes. Maximum dose of 12.5mg. • No infusion in hand or wrist veins. • Autosubstitution to prochlorperazine unless ordered as “do not substitute.” • Pregnant patients will not be automatically substituted to prochlorperazine. • Stored in dispensing cabinet with warning alert “not for IV push” and reference to policy.
Per policy, use of these medications is restricted as noted below:
generic (Brand)
Restrictions
promethazine IV (Phenergan)
Intravenous promethazine is restricted to Obstetric patients with hyperemesis ONLY, where other treatments have failed.
Per policy, orders for these non-formulary agents will be changed to formulary equivalents.
Non-Formulary Agent
Formulary Equivalent
promethazine (Phenergan) 12.5 mg IV push
prochlorperazine (Compazine) 5 mg IV push Intravenous Promethazine is restricted to Obstetric patients with hyperemesis ONLY, where other treatments have failed.
promethazine (Phenergan) 25 mg IV push
prochlorperazine (Compazine) 10 mg IV push Intravenous Promethazine is restricted to Obstetric patients with hyperemesis ONLY, where other treatments have failed.
2023 American Geriatrics Society Beers Criteria® for potentially inappropriate medication use in older adults.
Medication:
promethazine (Phenadoz, Phenergan)
Criteria 1: Potentially inappropriate medication use in older adults. (Table 2)
Drug(s)
first-generation antihistamines
Rationale
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. Cumulative exposure to anticholinergic drugs is associated with an increased risk of falls, delirium, and dementia, even in younger adults. Consider total anticholinergic burden during regular medication reviews and be cautious in "young-old" as well as "old-old" adults.
Recommendation
Avoid
Quality of evidence: Moderate, Strength of Recommendation: Strong
Criteria 2: Potentially inappropriate medication use in older adults due to drug–disease or drug–syndrome interactions that may exacerbate the disease or syndrome. (Table 3)
Drug(s) ⇆ disease or syndrome
anticholinergics ⇄ Delirium
Rationale
Avoid in older adults with or at high risk of delirium because of the potential of inducing or worsening delirium.
Recommendation
Avoid
Quality of evidence: Moderate, Strength of Recommendation: Strong
Drug(s) ⇆ disease or syndrome
anticholinergics ⇄ Dementia or cognitive impairment
Rationale
Avoid because of adverse CNS effects. If used, periodic deprescribing attempts should be considered to assess ongoing need and/or the lowest effective dose.
Recommendation
Avoid
Quality of evidence: Moderate, Strength of Recommendation: Strong
Drug(s) ⇆ disease or syndrome
anticholinergics ⇄ History of falls or fractures
Rationale
May cause ataxia, impaired psychomotor function, syncope, or additional falls. If one of the drugs must be used, consider reducing the use of other CNS-active medications that increase the risk of falls and fractures. (i.e., anticholinergics, selected antidepressants, antiepileptics, antipsychotics, sedative/hypnotics including benzodiazepines and, Nonbenzodiazepine benzodiazepine receptor agonist hypnotics, opioids) and implement other strategies to reduce fall risk.
Recommendation
Avoid unless safer alternatives are not available.
Quality of evidence: High, Strength of Recommendation: Strong
Refrigerator item (suppository)
• Not to be given by IV push.
• To be infused over at least 10 minutes. Maximum dose of 12.5mg.
• No infusion in hand or wrist veins.
• Autosubstitution to prochlorperazine unless ordered as “do not substitute.”
• Pregnant patients will not be automatically substituted to prochlorperazine.
• Stored in dispensing cabinet with warning alert “not for IV push” and reference to policy.
Acute dystonic reactions (e.g., oculogyric crisis, torticollis)
Caution in 2-18 yr of age