PlainMeds provides educational information only. This is not medical advice. Always consult your doctor or pharmacist.

tiagabine

Verify with FDA → · CMS NADAC pricing →

Brand names: Gabitril

Anticonvulsant (GABA Reuptake Inhibitor) Rx

Tiagabine is a medicine used with other medicines to treat partial seizures. It helps to control seizures by affecting certain chemicals in the brain.

Drug Pricing (NADAC)

Generic Price

$5.41/unit

Generic Available

Yes (2 manufacturers)

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

What it does

Tiagabine is used to treat partial seizures in adults and children 12 years and older.

Common side effects

Dizziness, Lack of energy, Sleepiness

Key warnings

This medicine may cause serious side effects.

How It Works

Tiagabine works by increasing the amount of a chemical called GABA in the brain. GABA helps to calm the brain and reduce seizures. Tiagabine blocks the reuptake of GABA, which means more GABA is available in the brain.

How to Take It

Take tiagabine with food. Do not take a large first dose. If you are already taking other seizure medicines, you may not need to change their dose. Your doctor will increase your dose of tiagabine slowly over time.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant or plan to become pregnant. It is not known if tiagabine will harm your unborn baby. Talk to your doctor about the risks and benefits of taking tiagabine during pregnancy.

Missed Dose

If you miss a dose, do not double the next dose. If you miss several doses, talk to your doctor.

Storage

Store tiagabine at room temperature (68° to 77°F) away from light and moisture.

Side Effects (from patient reports)

Based on 81 FDA adverse event reports.

Brain disorder
16
Muscle jerks
14
Using the medicine for something it is not approved for
13
The medicine is not working
10
Feeling dizzy
6
Feeling strange
5
Convulsion
5
Using the product for a condition it is not approved to treat
4
Too much serotonin in the body
4
Harm from different substances
4

FDA Adverse Event Report Analysis

Detailed analysis of 81 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

81

Death-Related Reports

7

Hospitalization Reports

32

Top Indication

Multiple Sclerosis

Gender Distribution

Female 55 (76%)
Male 17 (24%)

Age Distribution

0–17 1
18–44 17
45–64 26
65–74 8
75+ 1

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 ENCEPHALOPATHY 16
2 MYOCLONUS 14
3 OFF LABEL USE 13
4 DRUG INEFFECTIVE 10
5 DIZZINESS 6
6 FEELING ABNORMAL 5
7 SEIZURE 5
8 PRODUCT USE IN UNAPPROVED INDICATION 4
9 SEROTONIN SYNDROME 4
10 TOXICITY TO VARIOUS AGENTS 4
11 TREMOR 4
12 ABNORMAL BEHAVIOUR 3
13 COMPLETED SUICIDE 3
14 DRUG INTERACTION 3
15 DYSKINESIA 3

Reactions in Death Reports

COMPLETED SUICIDE 3
DEATH 2
CARDIAC ARREST 1
CONVULSION 1
OVERDOSE 1
RESPIRATORY ARREST 1
UNEVALUABLE EVENT 1
WEIGHT INCREASED 1

Reactions in Hospitalization Reports

ENCEPHALOPATHY 14
MYOCLONUS 14
OFF LABEL USE 11
DRUG INEFFECTIVE 7
FATIGUE 3
INSOMNIA 3
TOXICITY TO VARIOUS AGENTS 3
ANXIETY 2
DRUG INTERACTION 2
DYSARTHRIA 2

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

Serious Warnings

This medicine may cause serious side effects. Tell your doctor right away if you have any changes in mood or behavior, or any suicidal thoughts.

Known Drug Interactions

Carbamazepine, phenytoin, primidone, and phenobarbital are generally classified as enzyme inducers; valproate and gabapentin are not.

Mechanism: Gabapentin does not speed up or slow down the liver enzymes that process tiagabine. This means it is unlikely to change how much tiagabine stays in your body.

What to do: These drugs are generally safe to take together. Always follow the specific dosing instructions provided by your healthcare provider.

Warfarin: No significant differences were observed in the steady-state pharmacokinetics of R-warfarin or S-warfarin with the addition of tiagabine given as a single dose.

Mechanism: Studies show that tiagabine does not change the levels of warfarin in the blood. The two drugs do not seem to have a meaningful interaction.

What to do: No dose changes are typically needed for this combination. Continue to follow your regular schedule for blood monitoring.

Carbamazepine, phenytoin, primidone, and phenobarbital are generally classified as enzyme inducers; valproate and gabapentin are not. Valproate: Tiagabine causes a slight decrease (about 10%) in steady-state valproate concentrations. Valproate: The addition of tiagabine to patients taking valproate chronically had no effect on tiagabine pharmacokinetics, but valproate significantly decreased tiagabine binding in vitro from 96.3 to 94.8%, which resulted in an increase of approximately 40% in the free tiagabine concentration.

Mechanism: Valproate pushes tiagabine off blood proteins, which increases the amount of active tiagabine in the body. Tiagabine also slightly lowers the levels of valproate.

What to do: Your doctor may need to adjust your doses and monitor you for increased side effects.

minor digoxin

Digoxin: Concomitant administration of tiagabine did not affect the steady-state pharmacokinetics of digoxin or the mean daily trough serum level of digoxin.

Mechanism: These two drugs do not interfere with each other's levels or how the body uses them.

What to do: No dosage changes are usually necessary when taking these medicines together.

Theophylline: A single 10 mg dose of tiagabine did not affect the pharmacokinetics of theophylline at steady state.

Mechanism: Tiagabine does not change how the body breaks down or handles theophylline.

What to do: You can likely take these two drugs together without any special adjustments.

Check all your medications →

Common Questions

Can I stop taking tiagabine suddenly?
Do not stop taking tiagabine suddenly without talking to your doctor. Stopping suddenly can cause seizures.
Will tiagabine interact with my other medications?
Tiagabine can interact with other medications, especially other seizure medicines. Tell your doctor about all the medicines you take.
Can I drink alcohol while taking tiagabine?
Talk to your doctor about drinking alcohol while taking tiagabine. Alcohol can increase the risk of side effects.
How often will my dose be adjusted?
Your doctor may adjust your dose of tiagabine every week, depending on how well it is working and how you are tolerating it.
What should I do if I experience side effects?
Tell your doctor if you experience any side effects while taking tiagabine.
Is it safe to drive while taking tiagabine?
Tiagabine may cause drowsiness or dizziness. Do not drive or operate machinery until you know how tiagabine affects you.
Can children take tiagabine?
Tiagabine is approved for use in children 12 years and older.
What do I do if I accidentally take too much tiagabine?
Seek medical attention immediately.
Does food affect how tiagabine works?
Yes, you should take tiagabine with food.
How will I know if the medicine is working?
You should have fewer seizures.
What are the common side effects of tiagabine?
The most commonly reported side effects of tiagabine include Dizziness, Lack of energy, Sleepiness, Nausea, Nervousness or irritability. Based on 81 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does tiagabine interact with other medications?
Yes, tiagabine has 11 known drug interactions. Notable interactions include gabapentin, warfarin, valproate. Always inform your doctor about all medications you are taking.
What drug class is tiagabine?
tiagabine belongs to the Anticonvulsant (GABA Reuptake Inhibitor) drug class. It requires a prescription (Rx). Tiagabine is used to treat partial seizures in adults and children 12 years and older.
Is tiagabine safe during pregnancy?
Tell your doctor if you are pregnant or plan to become pregnant. It is not known if tiagabine will harm your unborn baby. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

Related Medications in Anticonvulsant (GABA Reuptake Inhibitor)

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

Compare tiagabine vs brivaracetam side-by-side →

Medication Guides

Related Health & Safety Data

Save on tiagabine

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 tiagabine

The FDA label for tiagabine (sold under brand names such as Gabitril) classifies it as a prescription-only medication in the Anticonvulsant (GABA Reuptake Inhibitor) class. Tiagabine is used to treat partial seizures in adults and children 12 years and older. Official labeling lists 8 commonly reported side effects, including Dizziness, Lack of energy, Sleepiness.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 81 voluntary reports. The database also lists 11 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 $5.41.

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 further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

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).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: March 1, 2021

All federal data sources used on this page