Qsymia (phentermine + topiramate ER): the 2026 GLP-1 guide
Qsymia is a non-GLP-1 oral weight-loss combo. ~7-11% weight loss in EQUIP/CONQUER. REMS-restricted (teratogenicity). Not on the Medicare Bridge.
Overview
Qsymia is a fixed-dose oral combination of phentermine (a sympathomimetic appetite suppressant; Schedule IV controlled substance) and topiramate ER (an anticonvulsant that suppresses appetite as a secondary effect), FDA-approved on July 17, 2012 for chronic weight management.
It is NOT a GLP-1 agonist. Phentermine drives appetite suppression via norepinephrine/dopamine release; topiramate’s mechanism in weight loss is multifactorial (GABA modulation, kainate inhibition, carbonic anhydrase inhibition).
Clinical Efficacy
In EQUIP (severe obesity, BMI ≥ 35), Qsymia 15/92 mg produced 10.9% body weight loss at 56 weeks vs 1.6% placebo. In CONQUER (BMI 27–45 + ≥ 2 comorbidities), 15/92 mg produced 9.8% loss vs 1.2% placebo1.
Qsymia is the highest-efficacy non-GLP-1 oral weight-loss medication available in 2026, but still produces less weight loss than oral GLP-1s (~12-16%) on average.
Dosing & Titration
Four approved capsule strengths (phentermine / topiramate, mg):
- 3.75 / 23 — starting dose, 14 days only
- 7.5 / 46 — recommended maintenance dose
- 11.25 / 69 — escalation step (14 days)
- 15 / 92 — maximum approved dose
Schedule: start at 3.75/23 mg once daily for 14 days, then increase to 7.5/46 mg. After 12 weeks at 7.5/46 mg, if weight loss is < 3% body weight, escalate to 11.25/69 mg for 14 days, then 15/92 mg. Discontinue if weight loss is < 5% after 12 weeks at the maximum dose.
Take in the morning. Evening doses raise insomnia risk substantially.
Side Effects
REMS program — pregnancy contraindication
Qsymia is distributed only through certified pharmacies under the QSYMIA REMS because of teratogenic risk: topiramate is associated with oral cleft birth defects when taken during the first trimester. Patients capable of pregnancy must use effective contraception and complete monthly pregnancy testing1. The REMS website is qsymiarems.com.
Most common adverse reactions (Qsymia 15/92 mg vs placebo)
| Adverse reaction | Qsymia 15/92 mg | Placebo |
|---|---|---|
| Paraesthesia (tingling) | 20% | 2% |
| Dry mouth | 19% | 3% |
| Constipation | 16% | 6% |
| Upper respiratory tract infection | 14% | 13% |
| Headache | 11% | 9% |
| Dysgeusia (taste alteration) | 9% | 1% |
Contraindications
- Pregnancy (teratogenicity)
- Glaucoma
- Hyperthyroidism
- Use of MAOIs (or within 14 days of stopping one)
- Known hypersensitivity to phentermine, topiramate, or excipients; or idiosyncrasy to sympathomimetic amines
2026 Availability
Qsymia is on Part D Tier 3 with most plans but distribution is limited to REMS-certified pharmacies. Cash list price is approximately $230/month at the 15/92 mg dose.
Qsymia is NOT on the Medicare GLP-1 Bridge program — Bridge eligibility is restricted to GLP-1 receptor agonists.
For patients comparing oral weight-loss options: Qsymia at ~10% loss + REMS friction sits below Foundayo (~12-16%, no REMS, $25-149/mo) and Wegovy Tablets (~12-15%, $149/mo) but above Contrave (~5-9%) on efficacy. Qsymia is the right pick for patients who: (a) can’t access GLP-1s, (b) won’t risk GLP-1 GI side effects, and (c) can accept the REMS contraception/testing requirement.
Footnotes
-
Qsymia Prescribing Information — DailyMed (NIH), revised April 22, 2026. ↩ ↩2
Your monthly price for Qsymia
Qsymia: frequently asked questions
Is Qsymia a GLP-1?
Why is Qsymia in a REMS program?
How does Qsymia compare to oral GLP-1s?
Is Qsymia covered by Medicare?
Sources & citations
Every clinical claim on this page traces to one of the 1 sources below — primarily FDA-approved labels via DailyMed (NIH) and peer-reviewed trial papers. Last reviewed ; next review due .
- 1 QSYMIA (phentermine and topiramate extended-release) capsules — Prescribing InformationPrimary National Library of Medicine (DailyMed) Published Accessed