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cyproheptadine

Piperidine (H1 Antagonist) · Antiallergic, Antiserotonin, Antipruritic

Piperidine (H1 Antagonist)Antiallergic, Antiserotonin, Antipruritic
CDSCO approved
EXCRETION
not curated
INTERACTIONS
11 major
SEVERE in our sources
PREGNANCY
not curated
Top interactionssee all 11
  • AlcoholSevereDatabase
  • Benzodiazepines (e.g., Alprazolam, Diazepam, Lorazepam)SevereDatabase
  • DextropropoxypheneSevereDatabaseDDInter
  • Monoamine Oxidase Inhibitors (maois) (e.g., Phenelzine, Selegiline)SevereDatabase

Mechanism

Not yet extracted

Indications

appetite stimulation (off label in anorectic/convalescent patients)idiopathic pruritus

Dosing

Adult
4 mg oral

Side effects

Common
sedationdiminished alertnesslight headednessmotor incoordinationfatiguetendency to fall asleepappetite stimulating effectdry mouthalteration of bowel movementurinary hesitancyblurring of vision

Drug interactions

Alcohol
Severe
Database

Increased sedation, dizziness, impaired psychomotor function, respiratory depression.

Advise patients to avoid alcohol consumption while taking cyproheptadine. Warn about impaired ability to drive or operate machinery.

Benzodiazepines (e.g., Alprazolam, Diazepam, Lorazepam)
Severe
Database

Increased sedation, dizziness, confusion, impaired coordination, respiratory depression.

Avoid concomitant use if possible. If co-administration is necessary, use the lowest effective doses of both drugs, monitor closely for CNS depression. Educate patients about potential for severe drowsiness and impaired activities.

Dextropropoxyphene
Severe
Database

Clinical effect not specified

Source: DDInter

Monoamine Oxidase Inhibitors (maois) (e.g., Phenelzine, Selegiline)
Severe
Database

Exaggerated anticholinergic effects (severe dry mouth, blurred vision, urinary retention, constipation, tachycardia, confusion, delirium), increased CNS depression.

CONTRAINDICATED. Do not use cyproheptadine in patients receiving MAOIs or within 14 days of discontinuing MAOI therapy.

Opioids (e.g., Codeine, Tramadol, Morphine)
Severe
Database

Profound sedation, respiratory depression, hypotension, coma. Increased risk of falls in elderly.

Avoid concomitant use if possible. If co-administration is necessary, use the lowest effective doses of both drugs, monitor closely for CNS depression and respiratory status. Educate patients and caregivers about symptoms of overdose.

Potassium Chloride
Severe
Database

.

Source: DDInter

Potassium Citrate
Severe
Database

Clinical effect not specified

Source: DDInter

Sodium Oxybate
Severe
Database

Clinical effect not specified

Source: DDInter

Topiramate
Severe
Database

Clinical effect not specified

Source: DDInter

Tricyclic Antidepressants (tcas) (e.g., Amitriptyline, Imipramine)
Severe
Database

Increased risk of severe anticholinergic effects (dry mouth, blurred vision, urinary retention, constipation, tachycardia, confusion, delirium) and profound sedation.

Avoid concomitant use if possible. If co-administration is necessary, monitor closely for anticholinergic toxicity and CNS depression. Consider alternative agents.

Zonisamide
Severe
Database

Clinical effect not specified

Source: DDInter

1 additional low-confidence interaction hidden — those rows lack a documented mechanism or management plan in our sources.

Other Piperidine (H1 Antagonist) drugs

Ask House about cyproheptadine

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e·Verified: 2026-05-10 · House clinical team