Prescription medication · Central Alpha-2 Agonist

guanfacine

Also sold as Intuniv, Tenex. Guanfacine extended-release tablets are used to treat Attention Deficit Hyperactivity Disorder (ADHD).

Data updated 2026-05-15

7,386
FDA reportsLightly reported
5
InteractionsFew interactions
In shortage
FDA status

What the data shows

guanfacine (Intuniv) is a prescription Central Alpha-2 Agonist, reported less often than most tracked drugs (7,386 FDA reports), with 5 documented drug interactions.

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

guanfacine (Intuniv) is a prescription Central Alpha-2 Agonist. Guanfacine extended-release tablets are used to treat Attention Deficit Hyperactivity Disorder (ADHD).

Guanfacine extended-release tablets can help treat ADHD. It can be used alone or with stimulant medicines.

Drug Shortage Alert

guanfacine is currently listed as to be discontinued by the FDA. Affected manufacturer: Actavis Pharma, Inc..

View all drug shortages →

Drug Pricing (NADAC)

Generic Price

$0.17/unit

Generic Available

Yes (19 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Guanfacine extended-release tablets are used to treat Attention Deficit Hyperactivity Disorder (ADHD).

Common side effects

Feeling sleepy or tired, Low blood pressure, Dizziness

Key warnings

Guanfacine can cause low blood pressure, slow heart rate, and fainting.

The sections below are summarized in plain English from guanfacine's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

How It Works

Guanfacine is a central alpha 2A-adrenergic receptor agonist. This means it works by stimulating specific receptors in the brain. By stimulating these receptors, guanfacine helps to improve attention and reduce impulsivity and hyperactivity in people with ADHD.

Side Effects (from patient reports)

Based on 7,386 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for guanfacine, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for guanfacine each year to the FDA Adverse Event Reporting System (FAERS).

0200400600800 20042007201020132016201920222025 622

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where guanfacine sits

guanfacine has more FDA adverse-event reports than 32% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is guanfacine; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 7,386 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

7,386

Reports Mentioning Death

228

3.1% of reports — not proof of cause

Hospitalization Reports

1,757

Top Indication

Attention Deficit/Hyperactivity Disorder

Gender Distribution

Female 2,210 (36%)
Male 3,811 (62%)

Age Distribution

0–17 3,034
18–44 884
45–64 338
65–74 90
75+ 89

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
3 SOMNOLENCE 455
4 AGGRESSION 376
5 FATIGUE 329
6 HYPOTENSION 289
7 DIZZINESS 270
8 HEADACHE 268
9 INSOMNIA 264
10 SUICIDAL IDEATION 259
11 ANXIETY 250
12 BRADYCARDIA 249
13 NAUSEA 245
14 ABNORMAL BEHAVIOUR 215
15 TOXICITY TO VARIOUS AGENTS 213
16 INTENTIONAL OVERDOSE 212
17 ELECTROCARDIOGRAM QT PROLONGED 211

Reactions in Death Reports

COMPLETED SUICIDE 68
DEATH 51
TOXICITY TO VARIOUS AGENTS 31
HYPOTENSION 16
COMA 13
GASTROINTESTINAL HAEMORRHAGE 13
TACHYCARDIA 13
RESPIRATORY DEPRESSION 12
DEPRESSED LEVEL OF CONSCIOUSNESS 11
ELECTROCARDIOGRAM QT PROLONGED 11

Reactions in Hospitalization Reports

INTENTIONAL OVERDOSE 181
BRADYCARDIA 175
TOXICITY TO VARIOUS AGENTS 169
HYPOTENSION 164
SOMNOLENCE 123
OVERDOSE 106
DRUG INTERACTION 99
VOMITING 92
SUICIDE ATTEMPT 89
AGGRESSION 84

Source: FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

Guanfacine can cause low blood pressure, slow heart rate, and fainting. Tell your doctor if you have heart problems. This medicine can also cause sleepiness, so be careful driving or using heavy machinery. Stopping guanfacine suddenly can cause high blood pressure. Your doctor will slowly lower your dose when you stop taking it.

Known Drug Interactions

Table 14: Clinically Important Drug Interactions: Effect of other Drugs on Guanfacine Concomitant Drug Name or Drug Class Clinical Rationale and Magnitude of Drug Interaction Clinical Recommendation Strong and moderate CYP3A4 inhibitors, e.g., ketoconazole, fluconazole Guanfacine is primarily metabolized by CYP3A4 and its plasma concentrations can be significantly affected resulting in an increase in exposure Consider dose reduction [see Dosage and administration (2.7)] Strong and moderate CYP3A4 inducers, e.g., rifampin, efavirenz Guanfacine is primarily metabolized by CYP3A4 and its...

Mechanism: Ketoconazole stops the body from breaking down guanfacine, which can cause the drug to build up to high levels.

Table 14: Clinically Important Drug Interactions: Effect of other Drugs on Guanfacine Concomitant Drug Name or Drug Class Clinical Rationale and Magnitude of Drug Interaction Clinical Recommendation Strong and moderate CYP3A4 inhibitors, e.g., ketoconazole, fluconazole Guanfacine is primarily metabolized by CYP3A4 and its plasma concentrations can be significantly affected resulting in an increase in exposure Consider dose reduction [see Dosage and administration (2.7)] Strong and moderate CYP3A4 inducers, e.g., rifampin, efavirenz Guanfacine is primarily metabolized by CYP3A4 and its...

Mechanism: Fluconazole slows down how fast your body processes guanfacine, leading to higher amounts of the drug in your system.

Table 14: Clinically Important Drug Interactions: Effect of other Drugs on Guanfacine Concomitant Drug Name or Drug Class Clinical Rationale and Magnitude of Drug Interaction Clinical Recommendation Strong and moderate CYP3A4 inhibitors, e.g., ketoconazole, fluconazole Guanfacine is primarily metabolized by CYP3A4 and its plasma concentrations can be significantly affected resulting in an increase in exposure Consider dose reduction [see Dosage and administration (2.7)] Strong and moderate CYP3A4 inducers, e.g., rifampin, efavirenz Guanfacine is primarily metabolized by CYP3A4 and its...

Mechanism: Rifampin causes your body to break down guanfacine much faster than normal, which can make the drug less effective.

Bosentan Guanfacine Monitor for adverse reactions.

Mechanism: Itraconazole blocks the process that clears guanfacine from your system. This leads to higher levels of the drug in your body.

7.2 Drugs Having No Clinically Important Interactions with Lisdexamfetamine Dimesylate Capsules From a pharmacokinetic perspective, no dose adjustment of lisdexamfetamine dimesylate capsules is necessary when lisdexamfetamine dimesylate capsules is co-administered with guanfacine, venlafaxine, or omeprazole. In addition, no dose adjustment of guanfacine or venlafaxine is needed when lisdexamfetamine dimesylate capsules is co-administered [see Clinical Pharmacology (12.3) ] .

Mechanism: These two drugs do not change how the body processes each other. They can be used together without affecting the amount of medicine in your blood.

This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

Common Questions

Can I crush the tablet?
No, swallow the tablet whole. Do not crush, chew, or break it.
Can I take this with food?
Do not take guanfacine with high-fat meals.
What should I do if I feel dizzy?
Be careful when standing up quickly, as guanfacine can lower your blood pressure.
Can I drive while taking this medicine?
Guanfacine can cause sleepiness, so be careful driving or using heavy machinery until you know how it affects you.
What happens if I stop taking it suddenly?
Stopping guanfacine suddenly can cause high blood pressure. Talk to your doctor before stopping.
How often should my blood pressure be checked?
Your doctor will check your heart rate and blood pressure before you start taking guanfacine, after dose increases, and regularly while you are taking it.
What if I am taking other medications?
Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
Can this medication cause heart problems?
Guanfacine can cause low blood pressure and slow heart rate. Tell your doctor if you have any heart problems.
What is the starting dose?
The usual starting dose is 1 mg per day.
How will my dose be adjusted?
Your doctor may increase your dose by 1 mg each week, depending on how well the medicine is working and how you tolerate it.
What are the common side effects of guanfacine?
The registry lists Feeling sleepy or tired, Low blood pressure, Dizziness, Upset stomach, Dry mouth among the most-reported FAERS reaction terms for guanfacine. The compiled record contains 7,386 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does guanfacine interact with other medications?
The registry has 5 documented interaction rows for guanfacine. Notable source-record pairings include ketoconazole, fluconazole, rifampin. These rows are not a complete medication review.
What drug class is guanfacine?
guanfacine belongs to the Central Alpha-2 Agonist drug class. It requires a prescription (Rx). Guanfacine extended-release tablets are used to treat Attention Deficit Hyperactivity Disorder (ADHD).
What pregnancy or breastfeeding source fields are listed for guanfacine?
The FDA label for guanfacine contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
Is guanfacine currently in shortage?
Yes, guanfacine is currently listed as to be discontinued by the FDA. Affected manufacturer: Actavis Pharma, Inc.. Visit the FDA Drug Shortages database for the latest updates.

Other drugs grouped near guanfacine - same-class peers and common alternatives.

Compare guanfacine vs acamprosate side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for guanfacine: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

Medication Guides

Save on guanfacine

Compare prices and find discounts at pharmacies near you. Free coupons can save up to 80% on prescriptions.

Disclosure: This link may earn us a commission at no extra cost to you. See our terms.

What the FDA Data Shows for guanfacine

The FDA label for guanfacine (sold under brand names such as Intuniv, Tenex) classifies it as a prescription-only medication in the Central Alpha-2 Agonist class. Guanfacine extended-release tablets are used to treat Attention Deficit Hyperactivity Disorder (ADHD). Official labeling lists 6 commonly reported side effects, including Feeling sleepy or tired, Low blood pressure, Dizziness.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 7,386 voluntary reports. The database also lists 5 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated minor severity. NADAC pricing from CMS shows a generic unit cost of $0.17.

Report counts do not establish causation, a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC). Shortage status: FDA Drug Shortages Database.

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. This registry does not provide medication decisions.

Last updated: January 23, 2025

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page