Topiramate

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Topiramate
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Pratik Bahekar, MBBS [2]

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Overview

Topiramate is a Mood Stabilizer that is FDA approved for the {{{indicationType}}} of Lennox-Gastaut syndrome (adjunct), migraine (prophylaxis), partial seizure (initial monotherapy), partial seizure(adjunct), tonic-clonic seizure, primary generalized (adjunct), tonic-clonic seizure, primary generalized (initial monotherapy). Common adverse reactions include flushing, serum bicarbonate level abnormal, loss of appetite, weight decreased, infectious disease, confusion, dizziness, impaired cognition, impaired, psychomotor performance, memory impairment, paresthesia, reduced concentration span, somnolence, feeling nervous, mood disorder, fatigue, fever.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

  • Lennox-Gastaut syndrome
  • Migraine prophylaxis
  • Partial seizure, initial monotherapy
  • Partial seizure; adjunct
  • Tonic-clonic seizure, primary generalized (adjunct)
  • Tonic-clonic seizure, primary generalized (initial monotherapy)

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

There is limited information about Off-Label Guideline-Supported Use of Topiramate in adult patients.

Non–Guideline-Supported Use

  • Alcoholism
  • Diabetes mellitus type 2 in obese (adjunct)
  • Eating disorder.
  • Essential tremor
  • Obesity

There is limited information about Off-Label Non–Guideline-Supported Use of Topiramate in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

  • Lennox-Gastaut syndrome
  • 2 years or older for opamax(R) and Qudexy(TM) XR,
  • 6 years or older for Trokendi XR(TM)
  • Migraine prophylaxis
  • 12 years or older for Topamax(R) only
  • Partial seizure, initial monotherapy
  • 2 years or older for Qudexy XR (TM)
  • 10 years or older for Trokendi XR(TM),
  • Partial seizure; adjunct
  • 2 years or older for Topamax(R) and Qudexy(TM) XR,
  • 6 years or older Trokendi XR(TM)
  • Tonic-clonic seizure, primary generalized (adjunct)
  • 2 years or older for Topamax(R) and Qudexy(TM) XR
  • 6 years or older for Trokendi XR(TM)
  • Tonic-clonic seizure, primary generalized (initial monotherapy)
  • 2 years or older for Topamax(R)
  • 10 years or older for Trokendi XR(TM) and Qudexy(TM) XR

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

There is limited information about Off-Label Guideline-Supported Use of Topiramate in pediatric patients.

Non–Guideline-Supported Use

  • Alcoholism
  • Diabetes mellitus type 2 in obese (adjunct)
  • Eating disorder.
  • Essential tremor
  • Obesity

There is limited information about Off-Label Non–Guideline-Supported Use of Topiramate in adult patients.

There is limited information about Off-Label Non–Guideline-Supported Use of Topiramate in pediatric patients.

Contraindications

There is limited information regarding Topiramate Contraindications in the drug label.

Warnings

There is limited information regarding Topiramate Warnings' in the drug label.

Adverse Reactions

Clinical Trials Experience

There is limited information regarding Topiramate Clinical Trials Experience in the drug label.

Postmarketing Experience

There is limited information regarding Topiramate Postmarketing Experience in the drug label.

Drug Interactions

There is limited information regarding Topiramate Drug Interactions in the drug label.

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA): There is no FDA guidance on usage of Topiramate in women who are pregnant.
Pregnancy Category (AUS): There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Topiramate in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Topiramate during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Topiramate in women who are nursing.

Pediatric Use

There is no FDA guidance on the use of Topiramate in pediatric settings.

Geriatic Use

There is no FDA guidance on the use of Topiramate in geriatric settings.

Gender

There is no FDA guidance on the use of Topiramate with respect to specific gender populations.

Race

There is no FDA guidance on the use of Topiramate with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Topiramate in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Topiramate in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Topiramate in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Topiramate in patients who are immunocompromised.

Administration and Monitoring

Administration

There is limited information regarding Topiramate Administration in the drug label.

Monitoring

There is limited information regarding Topiramate Monitoring in the drug label.

IV Compatibility

There is limited information regarding the compatibility of Topiramate and IV administrations.

Overdosage

There is limited information regarding Topiramate overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.

Pharmacology

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Topiramate
Systematic (IUPAC) name
2,3:4,5-Bis-O-(1-methylethylidene)-beta-D-fructopyranose sulfamate
Identifiers
CAS number 97240-79-4
ATC code N03AX11
PubChem 5284627
DrugBank DB00273
Chemical data
Formula Template:OrganicBox atomTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBox atomTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBoxTemplate:OrganicBox 
Mol. mass 339.363 g/mol
SMILES eMolecules & PubChem
Pharmacokinetic data
Bioavailability 80%
Protein binding 13-17%; 15-41%
Metabolism Hepatic (20-30%)
Half life 19-25 hours
Excretion Urine (70-80%)
Therapeutic considerations
Licence data

US

Pregnancy cat.

D(AU) D(US)

Legal status

Prescription Only (S4)(AU) ?(CA) POM(UK) [[Prescription drug|Template:Unicode-only]](US)

Routes Oral

Mechanism of Action

There is limited information regarding Topiramate Mechanism of Action in the drug label.

Structure

There is limited information regarding Topiramate Structure in the drug label.

Pharmacodynamics

There is limited information regarding Topiramate Pharmacodynamics in the drug label.

Pharmacokinetics

There is limited information regarding Topiramate Pharmacokinetics in the drug label.

Nonclinical Toxicology

There is limited information regarding Topiramate Nonclinical Toxicology in the drug label.

Clinical Studies

There is limited information regarding Topiramate Clinical Studies in the drug label.

How Supplied

There is limited information regarding Topiramate How Supplied in the drug label.

Storage

There is limited information regarding Topiramate Storage in the drug label.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Topiramate Patient Counseling Information in the drug label.

Precautions with Alcohol

Alcohol-Topiramate interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

There is limited information regarding Topiramate Brand Names in the drug label.

Look-Alike Drug Names

There is limited information regarding Topiramate Look-Alike Drug Names in the drug label.

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.