guanfacine hydrochloride
Mechanism
Selective alpha-2A adrenergic receptor agonist. Stimulates receptors in the prefrontal cortex, strengthening working memory, reducing distractibility, and improving impulse control. Also has calming effect by reducing sympathetic outflow.
Chemical Structure
Drug Identifiers (RxNorm)
Approvals by Region
Prescribing Information
1 Indications and Usage
Guanfacine extended-release (Intuniv) is a selective alpha2A-adrenergic receptor agonist indicated for the treatment of: - Attention Deficit Hyperactivity Disorder (ADHD) in patients 6-17 years of age as monotherapy or adjunctive therapy to stimulants Note: Immediate-release guanfacine (Tenex) is FDA-approved only for hypertension; ADHD use is off-label. Intuniv is specifically formulated for once-daily ADHD treatment.
2 Dosage and Administration
ADHD (INTUNIV): - Starting dose: 1 mg once daily - Titration: Increase by increments of no more than 1 mg/week - Target dose: 1-4 mg once daily - Maximum dose: 4 mg/day (children 6-12); 7 mg/day (adolescents 13-17) Weight-Based Dosing: - 25-33 kg: 2 mg/day recommended - 34-41 kg: 3 mg/day recommended - 42-49 kg: 4 mg/day recommended - 50-58 kg: 5 mg/day recommended - 59-91 kg: 6 mg/day recommended - ≥91 kg: 7 mg/day recommended ADJUNCTIVE THERAPY WITH STIMULANTS: - Same dosing as monotherapy - If discontinuing stimulant, maintain guanfacine dose General Instructions: - Take once daily in the morning or evening at same time each day - Do NOT crush, chew, or break tablets (compromises extended-release) - May be taken with or without food - Avoid high-fat meals (increases absorption) DISCONTINUATION: - Taper dose gradually over 3-7 days to avoid rebound hypertension - Do NOT stop abruptly
3 Dosage Forms and Strengths
Extended-Release Tablets (Intuniv): 1 mg, 2 mg, 3 mg, 4 mg Immediate-Release Tablets (Tenex): 1 mg, 2 mg (not FDA-approved for ADHD)
4 Contraindications
Guanfacine is contraindicated in patients with: - Known hypersensitivity to guanfacine or any ingredients in the formulation CAUTIONS: - Hypotension - Bradycardia - Syncope - Sedation
5 Warnings and Precautions
HYPOTENSION, BRADYCARDIA, AND SYNCOPE: - Can cause dose-dependent decreases in blood pressure and heart rate - Syncope has been reported - Use caution in patients at risk: dehydration, hypotension, heart block, bradycardia, cardiovascular disease, or taking antihypertensives - Monitor blood pressure and heart rate before and during treatment SEDATION AND SOMNOLENCE: - Common adverse reaction, especially early in treatment - More pronounced with higher doses - Caution patients about driving or operating machinery until effects are known - Sedation may decrease with continued treatment CARDIAC CONDUCTION ABNORMALITIES: - May increase risk of QT prolongation with other QT-prolonging drugs ABRUPT DISCONTINUATION: - Rebound hypertension may occur - Taper dose gradually (decrease by no more than 1 mg every 3-7 days)
6 Adverse Reactions
Most Common Adverse Reactions (≥5%): Monotherapy: - Somnolence (38%) - Headache (24%) - Fatigue (14%) - Upper abdominal pain (10%) - Nausea (6%) - Lethargy (6%) - Dizziness (6%) - Irritability (6%) - Hypotension/decreased blood pressure (6%) - Decreased appetite (5%) Adjunctive Therapy with Stimulants: - Headache - Insomnia - Somnolence - Fatigue - Dizziness - Abdominal pain
7 Drug Interactions
USE WITH CAUTION: - CYP3A4 Inhibitors (ketoconazole, ritonavir): Increase guanfacine plasma concentrations; consider dose reduction - CYP3A4 Inducers (rifampin): Decrease guanfacine plasma concentrations; consider dose increase - Antihypertensives: Additive effects on blood pressure and heart rate - CNS Depressants: Additive sedative effects - Alcohol: Additive sedation and CNS depression - Valproic acid: May increase valproic acid levels NO SIGNIFICANT INTERACTIONS: - No clinically significant interaction with methylphenidate or lisdexamfetamine when used as adjunctive therapy
8 Use in Specific Populations
PREGNANCY: - Category B (animal studies showed no risk; no adequate human studies) - Use only if clearly needed LACTATION: - Unknown if excreted in human milk - Consider benefits vs. risks before use during breastfeeding PEDIATRIC USE: - Safety and efficacy established for patients 6-17 years - Not studied in children under 6 years GERIATRIC USE: - Clinical studies did not include sufficient patients 65 and older RENAL IMPAIRMENT: - Consider dose reduction in patients with significant renal impairment HEPATIC IMPAIRMENT: - Consider dose reduction in patients with hepatic impairment
9 Overdosage
SIGNS AND SYMPTOMS: - Drowsiness, lethargy - Bradycardia - Hypotension - Initial hypertensive response possible TREATMENT: - Provide supportive care - Monitor vital signs - Gastric lavage if recent ingestion - Guanfacine is not dialyzable in clinically significant amounts
10 Clinical Pharmacology
MECHANISM OF ACTION: Guanfacine is a selective alpha2A-adrenergic receptor agonist. It is thought to work in ADHD by: - Strengthening prefrontal cortex function - Enhancing working memory - Reducing distractibility - Improving impulse control - Reducing sympathetic nervous system activity Unlike stimulants, guanfacine does not increase dopamine in the nucleus accumbens, which may explain its lack of abuse potential. PHARMACOKINETICS: - Absorption: Peak plasma concentration at 5 hours (extended-release) - Distribution: 70% protein bound; moderate volume of distribution - Metabolism: Hepatic via CYP3A4 - Half-life: 17 hours (extended-release); allows once-daily dosing - Excretion: 80% renal (50% unchanged)
11 How Supplied/Storage
STORAGE AND HANDLING: - Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F) - Protect from light and moisture Not a Controlled Substance - No DEA Schedule
12 Patient Counseling Information
IMPORTANT PATIENT INFORMATION: 1. DOSING: Take at the same time each day (morning or evening). Swallow tablets whole - do NOT crush, chew, or break. 2. DO NOT STOP SUDDENLY: This medication must be tapered gradually to avoid rebound high blood pressure. Talk to your doctor before stopping. 3. DROWSINESS: This medication commonly causes drowsiness, especially when starting. Avoid driving or operating machinery until you know how it affects you. 4. LOW BLOOD PRESSURE: You may feel dizzy when standing up quickly. Rise slowly from sitting or lying positions. 5. AVOID ALCOHOL: Alcohol increases drowsiness and can worsen side effects. 6. FOOD: May be taken with or without food. Avoid high-fat meals as they increase absorption. 7. HEART MONITORING: Blood pressure and heart rate will be checked regularly during treatment. 8. MISSED DOSE: If you miss a dose, skip it if more than 2 consecutive doses are missed; consult your doctor about restarting. 9. NOT A STIMULANT: This is a non-stimulant medication. It may take 2-3 weeks to see full effect. 10. ADJUNCTIVE USE: This medication can be used alone or with stimulant medications.
Side Effects
- somnolence/fatigue 30-40%
- headache 20-25%
- dizziness 10-15%
- decreased appetite 10-15%
- abdominal pain 10%
- dry mouth 10%
- nausea 5-10%
- constipation 5%
- hypotension Can cause significant drops in blood pressure
- bradycardia May slow heart rate
- syncope Fainting due to blood pressure drop
- rebound hypertension If stopped abruptly; must taper
- sedation Can be severe, especially initially
Show raw YAML data ARCHIVE +
id: guanfacine
brandNames:
US:
- Intuniv
- Tenex
CN: []
EU:
- Intuniv
JP:
- インチュニブ (Intuniv)
UK:
- Intuniv
AU:
- Intuniv
CA:
- Intuniv
genericName:
en: guanfacine hydrochloride
zh: 盐酸胍法辛
ja: グアンファシン塩酸塩
manufacturers:
- name: Takeda (formerly Shire)
region: US
product: Intuniv
- name: Shionogi
region: JP
product: インチュニブ
chemicalStructure:
smiles: NC(=N)NC(=O)CC1=C(Cl)C=CC=C1Cl
pubchemCid: 3519
molecularFormula: C9H9Cl2N3O
imageUrl: https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/cid/3519/PNG
wikipediaUrl: https://en.wikipedia.org/wiki/File:Guanfacine.svg
drugClass: non-stimulant
drugClassLabel:
en: Non-Stimulant
zh: 非兴奋剂
ja: 非中枢刺激薬
category: alpha-2 adrenergic agonist
categoryLabel:
en: Alpha-2 Adrenergic Agonist
zh: α-2肾上腺素能激动剂
ja: α2アドレナリン受容体作動薬
controlledSubstance: false
schedule:
US: Not scheduled
CN: Not approved
EU: Not scheduled
JP: Not scheduled
UK: Not scheduled
activeIngredient:
en: guanfacine hydrochloride
zh: 盐酸胍法辛
ja: グアンファシン塩酸塩
mechanismOfAction:
en: Selective alpha-2A adrenergic receptor agonist. Stimulates receptors in the prefrontal cortex, strengthening working memory, reducing distractibility, and improving impulse control. Also has calming effect by reducing sympathetic outflow.
zh: 选择性α-2A肾上腺素能受体激动剂。刺激前额叶皮层的受体,增强工作记忆,减少分心,改善冲动控制。还通过减少交感神经传出而具有镇静作用。
ja: 選択的α2Aアドレナリン受容体作動薬。前頭前皮質の受容体を刺激し、ワーキングメモリを強化し、気が散りやすさを軽減し、衝動制御を改善します。また、交感神経出力を減少させることで鎮静効果もあります。
neurotransmittersAffected:
- norepinephrine
forms:
- type: tablet
typeLabel:
en: Tablet
zh: 片剂
ja: 錠剤
releaseType: extended
releaseTypeLabel:
en: Extended Release
zh: 缓释
ja: 徐放性
brandName: Intuniv
strengths:
- 1mg
- 2mg
- 3mg
- 4mg
durationHours: 24
notes:
en: Extended-release for ADHD; must swallow whole
zh: ADHD缓释制剂;需整片吞服
ja: ADHD用徐放製剤;そのまま飲み込む必要あり
- type: tablet
typeLabel:
en: Tablet
zh: 片剂
ja: 錠剤
releaseType: immediate
releaseTypeLabel:
en: Immediate Release
zh: 速释
ja: 即放性
brandName: Tenex
strengths:
- 1mg
- 2mg
durationHours: 8-12
notes:
en: Immediate-release; originally for hypertension; not FDA-approved for ADHD
zh: 速释制剂;最初用于高血压;未获FDA批准用于ADHD
ja: 即放性製剤;元々は高血圧用;ADHDにはFDA未承認
onsetMinutes:
peakEffectHours: 5
durationHours: 24
sideEffects:
common:
- name:
en: somnolence/fatigue
zh: 嗜睡/疲劳
ja: 傾眠/疲労
frequency: 30-40%
- name:
en: headache
zh: 头痛
ja: 頭痛
frequency: 20-25%
- name:
en: dizziness
zh: 头晕
ja: めまい
frequency: 10-15%
- name:
en: decreased appetite
zh: 食欲下降
ja: 食欲減退
frequency: 10-15%
- name:
en: abdominal pain
zh: 腹痛
ja: 腹痛
frequency: 10%
- name:
en: dry mouth
zh: 口干
ja: 口渇
frequency: 10%
- name:
en: nausea
zh: 恶心
ja: 悪心
frequency: 5-10%
- name:
en: constipation
zh: 便秘
ja: 便秘
frequency: 5%
uncommon:
- name:
en: hypotension
zh: 低血压
ja: 低血圧
frequency: 5-10%
- name:
en: bradycardia
zh: 心动过缓
ja: 徐脈
frequency: 5%
- name:
en: irritability
zh: 易怒
ja: 易刺激性
frequency: 5%
- name:
en: insomnia
zh: 失眠
ja: 不眠
frequency: 5%
serious:
- name:
en: hypotension
zh: 低血压
ja: 低血圧
notes:
en: Can cause significant drops in blood pressure
zh: 可导致血压明显下降
ja: 血圧の著しい低下を引き起こす可能性
- name:
en: bradycardia
zh: 心动过缓
ja: 徐脈
notes:
en: May slow heart rate
zh: 可能减慢心率
ja: 心拍数を低下させる可能性
- name:
en: syncope
zh: 晕厥
ja: 失神
notes:
en: Fainting due to blood pressure drop
zh: 因血压下降导致昏厥
ja: 血圧低下による失神
- name:
en: rebound hypertension
zh: 反跳性高血压
ja: リバウンド高血圧
notes:
en: If stopped abruptly; must taper
zh: 突然停药时发生;需逐渐减量
ja: 急に中止した場合;漸減が必要
- name:
en: sedation
zh: 镇静
ja: 鎮静
notes:
en: Can be severe, especially initially
zh: 可能很严重,尤其是在初期
ja: 特に初期は重度になる可能性
contraindications:
en:
- Hypersensitivity to guanfacine
- Severe bradycardia
- Heart block
zh:
- 对胍法辛过敏
- 严重心动过缓
- 心脏传导阻滞
ja:
- グアンファシンに対する過敏症
- 重度の徐脈
- 心ブロック
drugInteractions:
- drug:
en: CYP3A4 inhibitors (ketoconazole)
zh: CYP3A4抑制剂(酮康唑)
ja: CYP3A4阻害剤(ケトコナゾール)
severity: moderate
effect:
en: Increased guanfacine levels
zh: 胍法辛血药浓度升高
ja: グアンファシン濃度の上昇
- drug:
en: CYP3A4 inducers (rifampin)
zh: CYP3A4诱导剂(利福平)
ja: CYP3A4誘導剤(リファンピン)
severity: moderate
effect:
en: Decreased guanfacine levels
zh: 胍法辛血药浓度降低
ja: グアンファシン濃度の低下
- drug:
en: Antihypertensives
zh: 降压药
ja: 降圧薬
severity: moderate
effect:
en: Additive hypotensive effect
zh: 降压作用叠加
ja: 降圧作用の相加
- drug:
en: CNS depressants
zh: 中枢神经抑制剂
ja: 中枢神経抑制剤
severity: moderate
effect:
en: Enhanced sedation
zh: 镇静作用增强
ja: 鎮静作用の増強
- drug:
en: Valproic acid
zh: 丙戊酸
ja: バルプロ酸
severity: moderate
effect:
en: Increased guanfacine exposure
zh: 胍法辛暴露量增加
ja: グアンファシン曝露量の増加
blackBoxWarnings:
en: []
zh: []
ja: []
pregnancyCategory: B
foodInteractions:
en: Avoid high-fat meals (increases absorption); avoid grapefruit juice
zh: 避免高脂肪餐(增加吸收);避免葡萄柚汁
ja: 高脂肪食を避ける(吸収が増加);グレープフルーツジュースを避ける
typicalDosing:
children:
startingDose: 1mg once daily
maxDose: 4mg/day (children 6-12) or 7mg/day (adolescents)
notes:
en: Increase by 1mg weekly; take at same time daily (morning or evening)
zh: 每周增加1mg;每天同一时间服用(早上或晚上)
ja: 毎週1mgずつ増量;毎日同じ時間に服用(朝または夕方)
adults:
startingDose: 1mg once daily
maxDose: 4mg/day (off-label for adults)
notes:
en: Not FDA-approved for adult ADHD but commonly used
zh: 未获FDA批准用于成人ADHD但常用
ja: 成人ADHDにはFDA未承認だが一般的に使用される
costEstimate:
US:
brand: $300-400/month
generic: $50-100/month
CN:
brand: Not available
generic: Not available
storageRequirements:
en: Room temperature (25°C), protect from light and moisture
zh: 室温保存(25°C),避光避湿
ja: 室温(25°C)で保存、光と湿気を避ける
approvals:
- region: US
agency: FDA
year: 2009
approvedAges:
en: 6-17 years
zh: 6-17岁
ja: 6〜17歳
indications:
en:
- ADHD
zh:
- 注意缺陷多动障碍
ja:
- ADHD
available: true
notes:
en: Approved for children/adolescents; off-label for adults; can be used alone or with stimulants
zh: 批准用于儿童/青少年;成人为超说明书使用;可单独使用或与兴奋剂联用
ja: 小児/青年に承認;成人は適応外使用;単独または刺激薬との併用が可能
- region: CN
agency: NMPA
year:
approvedAges:
en: ""
zh: ""
ja: ""
indications:
en: []
zh: []
ja: []
available: false
notes:
en: Not approved in China
zh: 中国未批准
ja: 中国では未承認
- region: EU
agency: EMA
year: 2015
approvedAges:
en: 6-17 years
zh: 6-17岁
ja: 6〜17歳
indications:
en:
- ADHD
zh:
- 注意缺陷多动障碍
ja:
- ADHD
available: true
notes:
en: First ADHD medication approved through EMA centralized procedure
zh: 首个通过EMA集中审批程序批准的ADHD药物
ja: EMA集中審査手続きを通じて承認された最初のADHD薬
- region: JP
agency: PMDA
year: 2017
approvedAges:
en: 6-17 years
zh: 6-17岁
ja: 6〜17歳
indications:
en:
- ADHD
zh:
- 注意缺陷多动障碍
ja:
- ADHD
available: true
notes:
en: No registration requirement (unlike stimulants)
zh: 无需登记(与兴奋剂不同)
ja: 登録要件なし(刺激薬とは異なる)
- region: UK
agency: MHRA
year: 2016
approvedAges:
en: 6-17 years
zh: 6-17岁
ja: 6〜17歳
indications:
en:
- ADHD
zh:
- 注意缺陷多动障碍
ja:
- ADHD
available: true
notes:
en: ""
zh: ""
ja: ""
- region: AU
agency: TGA
year: 2013
approvedAges:
en: 6-17 years
zh: 6-17岁
ja: 6〜17歳
indications:
en:
- ADHD
zh:
- 注意缺陷多动障碍
ja:
- ADHD
available: true
notes:
en: ""
zh: ""
ja: ""
- region: CA
agency: Health Canada
year: 2013
approvedAges:
en: 6-17 years
zh: 6-17岁
ja: 6〜17歳
indications:
en:
- ADHD
zh:
- 注意缺陷多动障碍
ja:
- ADHD
available: true
notes:
en: ""
zh: ""
ja: ""
specialConsiderations:
cardiacRisk:
en: Can lower blood pressure and heart rate; use caution with cardiac conditions
zh: 可降低血压和心率;有心脏病者需谨慎
ja: 血圧と心拍数を低下させる可能性;心臓疾患には注意
abuseRisk:
en: No abuse potential; not a controlled substance
zh: 无滥用风险;非管制药物
ja: 乱用の可能性なし;規制物質ではない
withdrawalNotes:
en: MUST TAPER - stopping abruptly can cause rebound hypertension
zh: 必须逐渐减量 - 突然停药可导致反跳性高血压
ja: 必ず漸減すること - 急な中止はリバウンド高血圧を引き起こす可能性
monitoringRequired:
en: Blood pressure, heart rate; especially when starting or changing dose
zh: 血压、心率;尤其是开始用药或调整剂量时
ja: 血圧、心拍数;特に開始時または用量変更時
travelRules:
generalAdvice:
en: Guanfacine is NOT a controlled substance, making travel straightforward. However, it's not available in all countries (notably China). Carry prescription documentation.
zh: 胍法辛不是管制药物,旅行较为简单。但并非所有国家都有供应(特别是中国)。请携带处方文件。
ja: グアンファシンは規制物質ではないため、旅行は簡単です。ただし、すべての国で入手できるわけではありません(特に中国)。処方書類を携帯してください。
requiredDocumentation:
- type: prescription
typeLabel:
en: Valid prescription
zh: 有效处方
ja: 有効な処方箋
notes:
en: Recommended for longer trips
zh: 长途旅行建议携带
ja: 長期旅行の場合は推奨
maxPersonalSupply:
default: 90 days
crossBorderRules:
- fromRegion: US
toRegion: JP
status: allowed
statusLabel:
en: Allowed
zh: 允许
ja: 許可
requirements:
en:
- Carry prescription copy
- Keep in original packaging
zh:
- 携带处方副本
- 保持原包装
ja:
- 処方箋のコピーを携帯
- 元のパッケージを維持
maxSupply: 90 days
notes:
en: Guanfacine is approved in Japan and is not a controlled substance. No special permit required.
zh: 胍法辛在日本已获批且不是管制药物。无需特别许可。
ja: グアンファシンは日本で承認されており、規制物質ではありません。特別な許可は不要です。
- fromRegion: US
toRegion: CN
status: restricted
statusLabel:
en: Restricted - Not Available
zh: 受限 - 不可用
ja: 制限あり - 入手不可
requirements:
en:
- Carry prescription and doctor's letter
- Keep in original packaging
zh:
- 携带处方和医生证明信
- 保持原包装
ja:
- 処方箋と医師の手紙を携帯
- 元のパッケージを維持
maxSupply: 90 days
notes:
en: Guanfacine is NOT approved in China. You may bring personal supply but cannot obtain refills locally.
zh: 胍法辛在中国未获批准。可以携带个人使用量,但无法在当地补充。
ja: グアンファシンは中国では未承認です。個人使用分は持ち込めますが、現地での補充はできません。
- fromRegion: US
toRegion: EU
status: allowed
statusLabel:
en: Allowed
zh: 允许
ja: 許可
requirements:
en:
- Carry prescription copy
zh:
- 携带处方副本
ja:
- 処方箋のコピーを携帯
maxSupply: 90 days
notes:
en: Guanfacine is approved in EU. No special import requirements.
zh: 胍法辛在欧盟已获批。无特殊进口要求。
ja: グアンファシンはEUで承認されています。特別な輸入要件はありません。
rxnormData:
ingredientRxcui: "40114"
ingredientName: guanfacine
rxcuiMappings:
- rxcui: "40114"
name: guanfacine
tty: IN
description: Base ingredient
- rxcui: "862007"
name: Intuniv
tty: BN
description: Brand name
- rxcui: "203142"
name: guanfacine hydrochloride
tty: PIN
description: Precise ingredient (includes salt form)
- rxcui: "862004"
name: guafacine hydrochloride
tty: PIN
description: Precise ingredient (includes salt form)
- rxcui: "862010"
name: 24 HR guanfacine 1 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
description: Branded drug (brand + strength + form)
- rxcui: "862015"
name: 24 HR guanfacine 2 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
description: Branded drug (brand + strength + form)
- rxcui: "862021"
name: 24 HR guanfacine 3 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
description: Branded drug (brand + strength + form)
- rxcui: "862027"
name: 24 HR guanfacine 4 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
description: Branded drug (brand + strength + form)
- rxcui: "862009"
name: guanfacine Extended Release Oral Tablet [Intuniv]
tty: SBDF
description: Branded ingredient + dose form
- rxcui: "197745"
name: guanfacine 1 MG Oral Tablet
tty: SCD
description: Clinical drug (ingredient + strength + form)
- rxcui: "197746"
name: guanfacine 2 MG Oral Tablet
tty: SCD
description: Clinical drug (ingredient + strength + form)
- rxcui: "862006"
name: 24 HR guanfacine 1 MG Extended Release Oral Tablet
tty: SCD
description: Clinical drug (ingredient + strength + form)
- rxcui: "862013"
name: 24 HR guanfacine 2 MG Extended Release Oral Tablet
tty: SCD
description: Clinical drug (ingredient + strength + form)
- rxcui: "862019"
name: 24 HR guanfacine 3 MG Extended Release Oral Tablet
tty: SCD
description: Clinical drug (ingredient + strength + form)
- rxcui: "862025"
name: 24 HR guanfacine 4 MG Extended Release Oral Tablet
tty: SCD
description: Clinical drug (ingredient + strength + form)
- rxcui: "372368"
name: guanfacine Oral Tablet
tty: SCDF
description: Ingredient + dose form
- rxcui: "862005"
name: guanfacine Extended Release Oral Tablet
tty: SCDF
description: Ingredient + dose form
brandMappings:
- brandName: Intuniv
rxcui: "862007"
region: US
- brandName: Tenex
rxcui: ""
region: US
synonyms:
- name: guanfacine hydrochloride
type: chemical
source: RxNorm
- name: guafacine hydrochloride
type: chemical
source: RxNorm
- name: Intuniv
type: brand
source: RxNorm
- name: guanfacine
type: generic
source: RxNorm
relatedDrugs:
- rxcui: "197745"
name: guanfacine 1 MG Oral Tablet
tty: SCD
relationship: clinical_drug
- rxcui: "197746"
name: guanfacine 2 MG Oral Tablet
tty: SCD
relationship: clinical_drug
- rxcui: "862006"
name: 24 HR guanfacine 1 MG Extended Release Oral Tablet
tty: SCD
relationship: clinical_drug
- rxcui: "862013"
name: 24 HR guanfacine 2 MG Extended Release Oral Tablet
tty: SCD
relationship: clinical_drug
- rxcui: "862019"
name: 24 HR guanfacine 3 MG Extended Release Oral Tablet
tty: SCD
relationship: clinical_drug
- rxcui: "862025"
name: 24 HR guanfacine 4 MG Extended Release Oral Tablet
tty: SCD
relationship: clinical_drug
- rxcui: "862010"
name: 24 HR guanfacine 1 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
relationship: branded_drug
- rxcui: "862015"
name: 24 HR guanfacine 2 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
relationship: branded_drug
- rxcui: "862021"
name: 24 HR guanfacine 3 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
relationship: branded_drug
- rxcui: "862027"
name: 24 HR guanfacine 4 MG Extended Release Oral Tablet [Intuniv]
tty: SBD
relationship: branded_drug
- rxcui: "372368"
name: guanfacine Oral Tablet
tty: SCDF
relationship: drug_form
- rxcui: "862005"
name: guanfacine Extended Release Oral Tablet
tty: SCDF
relationship: drug_form
lastUpdated: 2025-12-04
instructions:
indicationsAndUsage:
en: |
Guanfacine extended-release (Intuniv) is a selective alpha2A-adrenergic receptor agonist indicated for the treatment of:
- Attention Deficit Hyperactivity Disorder (ADHD) in patients 6-17 years of age as monotherapy or adjunctive therapy to stimulants
Note: Immediate-release guanfacine (Tenex) is FDA-approved only for hypertension; ADHD use is off-label. Intuniv is specifically formulated for once-daily ADHD treatment.
dosageAndAdministration:
en: |
ADHD (INTUNIV):
- Starting dose: 1 mg once daily
- Titration: Increase by increments of no more than 1 mg/week
- Target dose: 1-4 mg once daily
- Maximum dose: 4 mg/day (children 6-12); 7 mg/day (adolescents 13-17)
Weight-Based Dosing:
- 25-33 kg: 2 mg/day recommended
- 34-41 kg: 3 mg/day recommended
- 42-49 kg: 4 mg/day recommended
- 50-58 kg: 5 mg/day recommended
- 59-91 kg: 6 mg/day recommended
- ≥91 kg: 7 mg/day recommended
ADJUNCTIVE THERAPY WITH STIMULANTS:
- Same dosing as monotherapy
- If discontinuing stimulant, maintain guanfacine dose
General Instructions:
- Take once daily in the morning or evening at same time each day
- Do NOT crush, chew, or break tablets (compromises extended-release)
- May be taken with or without food
- Avoid high-fat meals (increases absorption)
DISCONTINUATION:
- Taper dose gradually over 3-7 days to avoid rebound hypertension
- Do NOT stop abruptly
dosageForms:
en: |
Extended-Release Tablets (Intuniv): 1 mg, 2 mg, 3 mg, 4 mg
Immediate-Release Tablets (Tenex): 1 mg, 2 mg (not FDA-approved for ADHD)
contraindications:
en: |
Guanfacine is contraindicated in patients with:
- Known hypersensitivity to guanfacine or any ingredients in the formulation
CAUTIONS:
- Hypotension
- Bradycardia
- Syncope
- Sedation
warningsAndPrecautions:
en: |
HYPOTENSION, BRADYCARDIA, AND SYNCOPE:
- Can cause dose-dependent decreases in blood pressure and heart rate
- Syncope has been reported
- Use caution in patients at risk: dehydration, hypotension, heart block, bradycardia, cardiovascular disease, or taking antihypertensives
- Monitor blood pressure and heart rate before and during treatment
SEDATION AND SOMNOLENCE:
- Common adverse reaction, especially early in treatment
- More pronounced with higher doses
- Caution patients about driving or operating machinery until effects are known
- Sedation may decrease with continued treatment
CARDIAC CONDUCTION ABNORMALITIES:
- May increase risk of QT prolongation with other QT-prolonging drugs
ABRUPT DISCONTINUATION:
- Rebound hypertension may occur
- Taper dose gradually (decrease by no more than 1 mg every 3-7 days)
adverseReactions:
en: |
Most Common Adverse Reactions (≥5%):
Monotherapy:
- Somnolence (38%)
- Headache (24%)
- Fatigue (14%)
- Upper abdominal pain (10%)
- Nausea (6%)
- Lethargy (6%)
- Dizziness (6%)
- Irritability (6%)
- Hypotension/decreased blood pressure (6%)
- Decreased appetite (5%)
Adjunctive Therapy with Stimulants:
- Headache
- Insomnia
- Somnolence
- Fatigue
- Dizziness
- Abdominal pain
drugInteractions:
en: |
USE WITH CAUTION:
- CYP3A4 Inhibitors (ketoconazole, ritonavir): Increase guanfacine plasma concentrations; consider dose reduction
- CYP3A4 Inducers (rifampin): Decrease guanfacine plasma concentrations; consider dose increase
- Antihypertensives: Additive effects on blood pressure and heart rate
- CNS Depressants: Additive sedative effects
- Alcohol: Additive sedation and CNS depression
- Valproic acid: May increase valproic acid levels
NO SIGNIFICANT INTERACTIONS:
- No clinically significant interaction with methylphenidate or lisdexamfetamine when used as adjunctive therapy
useInSpecificPopulations:
en: |
PREGNANCY:
- Category B (animal studies showed no risk; no adequate human studies)
- Use only if clearly needed
LACTATION:
- Unknown if excreted in human milk
- Consider benefits vs. risks before use during breastfeeding
PEDIATRIC USE:
- Safety and efficacy established for patients 6-17 years
- Not studied in children under 6 years
GERIATRIC USE:
- Clinical studies did not include sufficient patients 65 and older
RENAL IMPAIRMENT:
- Consider dose reduction in patients with significant renal impairment
HEPATIC IMPAIRMENT:
- Consider dose reduction in patients with hepatic impairment
overdosage:
en: |
SIGNS AND SYMPTOMS:
- Drowsiness, lethargy
- Bradycardia
- Hypotension
- Initial hypertensive response possible
TREATMENT:
- Provide supportive care
- Monitor vital signs
- Gastric lavage if recent ingestion
- Guanfacine is not dialyzable in clinically significant amounts
clinicalPharmacology:
en: |
MECHANISM OF ACTION:
Guanfacine is a selective alpha2A-adrenergic receptor agonist. It is thought to work in ADHD by:
- Strengthening prefrontal cortex function
- Enhancing working memory
- Reducing distractibility
- Improving impulse control
- Reducing sympathetic nervous system activity
Unlike stimulants, guanfacine does not increase dopamine in the nucleus accumbens, which may explain its lack of abuse potential.
PHARMACOKINETICS:
- Absorption: Peak plasma concentration at 5 hours (extended-release)
- Distribution: 70% protein bound; moderate volume of distribution
- Metabolism: Hepatic via CYP3A4
- Half-life: 17 hours (extended-release); allows once-daily dosing
- Excretion: 80% renal (50% unchanged)
howSupplied:
en: |
STORAGE AND HANDLING:
- Store at 25°C (77°F); excursions permitted to 15-30°C (59-86°F)
- Protect from light and moisture
Not a Controlled Substance - No DEA Schedule
patientCounselingInfo:
en: |
IMPORTANT PATIENT INFORMATION:
1. DOSING: Take at the same time each day (morning or evening). Swallow tablets whole - do NOT crush, chew, or break.
2. DO NOT STOP SUDDENLY: This medication must be tapered gradually to avoid rebound high blood pressure. Talk to your doctor before stopping.
3. DROWSINESS: This medication commonly causes drowsiness, especially when starting. Avoid driving or operating machinery until you know how it affects you.
4. LOW BLOOD PRESSURE: You may feel dizzy when standing up quickly. Rise slowly from sitting or lying positions.
5. AVOID ALCOHOL: Alcohol increases drowsiness and can worsen side effects.
6. FOOD: May be taken with or without food. Avoid high-fat meals as they increase absorption.
7. HEART MONITORING: Blood pressure and heart rate will be checked regularly during treatment.
8. MISSED DOSE: If you miss a dose, skip it if more than 2 consecutive doses are missed; consult your doctor about restarting.
9. NOT A STIMULANT: This is a non-stimulant medication. It may take 2-3 weeks to see full effect.
10. ADJUNCTIVE USE: This medication can be used alone or with stimulant medications.
lastUpdated: 2025-12-04
sources:
- https://www.goodrx.com/conditions/adhd/non-stimulant-adhd-meds
- https://www.ema.europa.eu/en/news/ema-recommends-approval-treatment-attention-deficit-hyperactivity-disorder
- https://h-navi.jp/column/article/35028853
notes:
en: Good option for hyperactivity/impulsivity symptoms or when stimulants cause anxiety. Particularly helpful for emotional dysregulation. Can be combined with stimulants. Must taper when discontinuing. Not approved for adult ADHD but commonly used off-label.
zh: 适用于多动/冲动症状或兴奋剂引起焦虑时。对情绪失调特别有帮助。可与兴奋剂联用。停药时必须逐渐减量。未批准用于成人ADHD但常用于超说明书使用。
ja: 多動性/衝動性の症状、または刺激薬が不安を引き起こす場合に良い選択肢。感情調節障害に特に有用。刺激薬と併用可能。中止時は漸減が必要。成人ADHDには未承認だが適応外使用が一般的。
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