Toggle menu
Toggle preferences menu
Toggle personal menu
Not logged in
Your IP address will be publicly visible if you make any edits.

Topiramate

From Pharmacopedia
Revision as of 06:44, 23 May 2026 by MDElliottMD (talk | contribs) (parser-claude: Topiramate MedTemplate refill, Top 300 stub upgrade)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Topiramate
Topamax (IR), Trokendi XR, Qudexy XR, Eprontia (oral solution); component of Qsymia (with phentermine)

Experience

👥 No personal reports yet
No clinical reports yet

Log in to add your own experience.

Problems

No problems yet. Be the first to suggest one.

+ Add a problem

Titration strategies

No titration strategies yet. Be the first to suggest one.

+ Add a titration strategy

Effects

No effects listed yet. Be the first to suggest one.

+ Add an effect

Relevant anecdote

No anecdotes yet. Share a relevant one.

+ Add an anecdote

Relevant Literature

No literature entries yet.

Log in to submit relevant literature.

Summary
Common uses
Partial-onset seizures (FDA, monotherapy and adjunct)0, Primary generalized tonic-clonic seizures (FDA, ages 2+)0, Lennox-Gastaut syndrome (FDA adjunct)0, Migraine prophylaxis (FDA, adult)0, Alcohol use disorder (off-label, evidence-supported)0, Binge-eating disorder and bulimia nervosa (off-label)0, Chronic weight management (Qsymia combination with phentermine, FDA)0
Pharmacy
Starting dose
Migraine: 25 mg PO at bedtime, titrate by 25 mg weekly to target 100 mg/day divided BID. Seizures: 25-50 mg/day, titrate weekly to 200-400 mg/day divided BID
Preparations
IR tablets 25, 50, 100, 200 mg; sprinkle capsules 15, 25 mg; Trokendi XR capsules 25, 50, 100, 200 mg; Qudexy XR capsules; Eprontia oral solution 25 mg/mL
US FDA Max
1600 mg/day (theoretical seizure dosing); practical use 400 mg/day for seizures, 100-200 mg/day for migraine prophylaxis
Pharmacology
Routes
Oral
Onset
Anticonvulsant effect within days at therapeutic level; migraine prophylaxis effect emerges over 2-3 months
Duration
12-24 hours (IR BID); 24 hours (ER once-daily)
Half-life
~21 hours[1]
Bioavailability
~80% (oral)[1]
Pregnancy
Substantial teratogenic risk including cleft lip/palate, hypospadias, and growth restriction (pregnancy registry data clear); effective contraception and pre-pregnancy counseling are required in reproductive-age patients[1]
Legal status
Rx-only in US. Not a controlled substance[1]
Purported mechanism
Multi-target anticonvulsant: voltage-gated sodium channel blocker in the inactivated state, GABA-A receptor potentiator at a non-benzodiazepine site, AMPA/kainate glutamate receptor antagonist, and weak carbonic anhydrase inhibitor. The carbonic anhydrase inhibition explains the characteristic adverse-effect cluster (paresthesias, metabolic acidosis, kidney stones, oligohidrosis with heat intolerance) and likely contributes to the cognitive slowing nicknamed "dopamax" in clinical lore.0 Weight loss is a class effect, the basis of the Qsymia combination with phentermine for chronic weight management. Carbonic-anhydrase-related acute angle-closure glaucoma is a rare but vision-threatening idiosyncratic reaction, typically within the first month[1].

References

  1. 1.0 1.1 1.2 1.3 1.4 FDA Prescribing Information, Topamax (topiramate), Janssen, current revision. https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/020844s050lbl.pdf