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Clonidine: Difference between revisions

From Pharmacopedia
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Assign pharmacological categories from List_of_CNS-active_medicines
Comprehensive categorization: +Alpha-2 Agonists (for ADHD), Alpha-2 agonists for withdrawal, Addiction Medicine
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[[Category:Stimulants & Wake-Promoting Agents]]
[[Category:Stimulants & Wake-Promoting Agents]]
[[Category:Psychostimulants]]
[[Category:Psychostimulants]]
[[Category:Alpha-2 Agonists (for ADHD)]]
[[Category:Alpha-2 agonists for withdrawal]]
[[Category:Addiction Medicine]]

Revision as of 18:42, 15 May 2026

Alpha-2 agonist, ADHD medicine
Clonidine
Kapvay

Experience

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Problems

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Titration strategies

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Effects

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Interactions

Pharmacogenomic + mechanism interactions2 edges
Pharmacokinetic mechanismSubstrate / metabolism relationships from primary literature
Transporter:SLC22A2 inhibitor Primary 70 / 100
FDA Drug Interactions Table: transporter inhibitor (SLC22A2).
Inferred from pharmacokinetic dataMaterialised by the inference engine; provenance shown per row
Metformin pk raises via SLC22A2 Inferred 49 / 100
Clonidine inhibits SLC22A2 (inhibitor, intensity 70); Metformin is a substrate of SLC22A2 (intensity 70). Derived: Metformin exposure raised.
Inferred via Enzyme:SLC22A2 (exposure raised)

Patient experience

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Summary
Classes
Alpha-2 agonist, ADHD medicine
Common uses
Pharmacy
Pharmacology
Purported mechanism
Alpha-2 adrenergic receptor agonist