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GET A QSYMIA® PRESCRIPTION FOR WEIGHT MANAGEMENT

Meet Qsymia®

Prescription medication for weight loss
10% average reduction in weight after a year
A pill prescribed as part of a personalized care plan
Insurance accepted
Telehealth available
FDA-approved

Get bias-free weight management with knownwell

Experts in obesity medicine

Comprehensive, empathetic care from clinicians who specialize in weight management

In-network with insurance

We work with major insurance plans to help make your care and prescription as affordable as possible

Prior authorization support

Our dedicated team helps get your Qsymia® prescription covered — so you're not navigating coverage alone

Prior authorization support

Available via telehealth nationwide, with in-person clinics in select cities

What you need to know about Qsymia®

WHAT’S ON THIS PAGE

ABOUT QSYMIA®

What is Qsymia®?

Qsymia® is a prescription medication FDA-approved for chronic weight management in adults and pediatric patients aged 12 years and older with obesity, or in adults with overweight who have at least one weight-related health condition, like high blood pressure, type 2 diabetes, or high cholesterol.

It combines two well-studied medications, phentermine and topiramate extended-release, each of which works through a different pathway to help reduce appetite and support weight management. Together, the combination has been shown to produce greater weight reduction than either component alone.

Unlike injectable GLP-1 medications, Qsymia® is taken as a once-daily oral capsule, making it a convenient option for people who prefer not to use injections.

Qsymia® is available in multiple dose strengths and is started at a low dose, then gradually increased. Your care team will help determine whether it's the right fit based on your health history, goals, and treatment needs.

How Qsymia® works

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What it does in the body

Qsymia® works through two active ingredients that each target appetite through a different pathway.

Phentermine acts on the central nervous system to reduce appetite. It triggers the release of a chemical messenger in the brain that activates the body's natural appetite-suppressing signals, reducing the drive to eat.

Topiramate extended-release is a medication traditionally used to treat epilepsy and migraines, but it was also found to reduce appetite and support weight reduction. Exactly how it does this isn't fully understood, but it's thought to work through several brain pathways that influence feelings of fullness and the desire to eat.

How this leads to results

By working through two distinct pathways simultaneously, Qsymia® helps reduce hunger, increase feelings of fullness, and lower overall caloric intake, making it easier to maintain dietary changes as part of a broader care plan.

The extended-release formulation of topiramate is specifically designed to deliver a steady, gradual level of the medication throughout the day, supporting consistent appetite control.

Many people may notice
  • Reduced hunger throughout the day
  • Feeling full sooner and for longer after eating
  • Fewer cravings between meals
  • Gradual, sustained weight reduction over time

COST & COVERAGE

Is Qsymia® covered by insurance?

Qsymia® can be covered by insurance, but it depends on your plan.

Insurance coverage for Qsymia® varies by plan, employer, and whether weight management medications are included in your benefits. Coverage is typically most common when prescribed for obesity or overweight with a related health condition, which are FDA-approved indications for the medication.

Prior authorization may be required. Plans may ask for documentation of a qualifying diagnosis, BMI, and any previous medications tried.

knownwell helps patients navigate this process. Our dedicated authorization team can assist with prior benefit verification and next steps, so you understand your coverage options before moving forward.

How much does Qsymia® cost?

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Insurance accepted

With commercial insurance coverage, Qsymia® can cost as little as $2.33 per day ($70 per month) using the Qsymia® Savings Card. Actual costs vary based on your plan, benefits, pharmacy, and prescribed dose.

knownwell's care team helps review your coverage and navigate any required approvals, so you understand your options before starting treatment.

Self-pay option available

For patients paying without insurance, Qsymia® is available through the Qsymia® home delivery pharmacy at:

  • $2.33 per day ($70 per month) for a 90-day supply
  • $2.97 per day ($89 per month) for a 30-day supply

Your knownwell care team can help you explore your options and review costs with you as part of your plan.
It is also available generically for $60/mo with GoodRx coupon.

As low as $60 per month

Commercially insured patients may pay as little as $60 per month with the Qsymia® Savings Card. Terms and conditions apply.

Prescribed as part of a personalized medication plan with ongoing support from your knownwell care team.

Get started with knownwell

WHAT TO EXPECT

What results can you expect?

Clinical studies show that Qsymia® can support meaningful, sustained weight reduction for many people when used consistently as part of a broader care plan that includes a reduced-calorie diet and increased physical activity.

Reduction in body weight

The CONQUER study, a 56-week phase 3 clinical trial of nearly 2,500 adults with overweight or obesity and at least two weight-related health conditions, showed participants lost an average of 7.8% of their body weight on the recommended dose (7.5 mg / 46 mg) and 9.8% on the top dose (15 mg / 92 mg), compared to 1.2% with placebo.

Almost half of participants saw 10% or more weight reduction

The EQUIP study, a 56-week phase 3 trial of nearly 1,300 adults with overweight, showed participants taking the top dose (15 mg / 92 mg) lost an average of 10.9% of their body weight, and 47% of participants achieved 10% or more weight reduction, compared to 7% with placebo.

Improvements in cardiometabolic markers

The SEQUEL study, a 108-week extension of the CONQUER trial, showed Qsymia® demonstrated significant, sustained weight reduction through two years of treatment, along with improvements in cardiometabolic markers, including blood sugar, cholesterol, and blood pressure.

After 1 year...

83%
of knownwell patients lost ≥10% of body weight and 74% of patients lost ≥ 20% of their body weight
97%
of knownwell patients have sustained weight loss
15%
average reduction in body mass

How to get Qsymia® with knownwell

STEP 1

Complete a short questionnaire

Share your health history, goals, and preferences online or in person.

Start knownwell’s questionnaire.
STEP 2

Meet with a healthcare clinician

A knownwell care team member reviews your information and discusses treatment options with you.
STEP 3

Receive a prescription, if appropriate

If Ozempic® is a good fit, your care team will prescribe the medication and outline next steps.
STEP 4

Get your medication

Qysmia® is provided through knownwell, with guidance on how and when to start, plus ongoing support along the way.

A CLOSER LOOK AT Qysmia®

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Frequently asked questions

What side effects should I know about?

Common Qsymia® side effects in adults include tingling or numbness in the hands or feet (paraesthesia), dizziness, changes in taste (dysgeusia), trouble sleeping, constipation, and dry mouth, especially when starting or increasing the dose.

These things typically improve as your body adjusts.

Who should not take Qsymia®?

Qsymia® is not appropriate for people who are pregnant or planning to become pregnant, have glaucoma, have an overactive thyroid (hyperthyroidism), are taking monoamine oxidase inhibitors (MAOIs), or have a known allergy or sensitivity to phentermine, topiramate, or any inactive ingredient in Qsymia®.

People who can become pregnant must use effective birth control while taking Qsymia® due to the risk of birth defects. Qsymia® is available only through certified pharmacies as part of a Risk Evaluation and Mitigation Strategy (REMS) program.

Your knownwell care team will review your full health history to determine whether Qsymia® is a safe option for you.

How is Qsymia® taken?

Qsymia® is taken as a once-daily oral capsule, in the morning, with or without food. It shouldn’t be taken in the evening, as it may cause difficulty sleeping.

How is Qsymia® stored?

Qsymia® should be stored at room temperature, away from heat and moisture. Your knownwell care team will review proper storage and handling instructions for your prescription.

What should I know about Qsymia® dosing?

Qsymia® is started at the lowest available dose (3.75 mg / 23 mg) for the first two weeks, then increased to the recommended dose (7.5 mg / 46 mg). If additional weight management is needed after 12 weeks, the dose may be increased to 11.25 mg / 69 mg for two weeks before reaching the maximum dose (15 mg / 92 mg). 

The highest dose (15 mg / 92 mg) must be tapered gradually before stopping. It shouldn’t be discontinued abruptly, as this may increase the risk of seizure. 

Your knownwell care team will review your specific dosing plan and make adjustments based on how your body responds.

Does Qsymia® require any special monitoring?

Yes, Qsymia® does require special monitoring. Before starting and during treatment, your provider will recommend blood tests to check kidney function, electrolyte levels, and blood sugar (if you have diabetes).

People who can become pregnant will need a monthly pregnancy test while taking Qsymia®.

For adolescent patients, your provider will also monitor height and bone development during treatment, as Qsymia® may affect bone mineral density and growth rate in younger patients.

Nutrition tips while taking Qsymia®

Studies show that Qsymia® can support meaningful weight reduction over time for many people, when used consistently as part of a broader weight management plan.
Prioritize protein and fiber at every meal.
Protein and fiber-rich foods like lean meats, legumes, eggs, vegetables, and whole grains help preserve muscle and keep you feeling full longer. Fiber also supports digestive health, which matters because constipation is a common side effect of Qsymia®.
Drink plenty of water throughout the day.
Staying well hydrated is especially important with Qsymia®. Topiramate, one of its active ingredients, can increase the risk of kidney stones, and adequate fluid intake is one of the most important ways to reduce that risk.
Aim for a moderate, consistent calorie reduction.
Qsymia® is designed to be used alongside a reduced-calorie diet and increased physical activity to support weight reduction and help maintain it long term.
These general patterns fit with how Qsymia® works in the body and can help support your treatment goals alongside your care team's guidance.

Explore medication options

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Zepbound® A dual GLP-1/GIP receptor agonist that targets two appetite-related pathways, with clinical outcomes of 15–23% weight loss.
Wegovy® can be used as a daily oral medication or weekly injection. It has strong clinical evidence supporting weight loss outcomes of 15–20%.
Foundayo® is a daily oral GLP-1 medication that has shown 12.4% average reduction in weight in clinical trails.
Explore other medication options.

Ready to see if Qsymia® is right for you?

Meet with a knownwell provider to review your options, discuss whether Qsymia® fits your needs, and get guidance on next steps.

knownwell knows that long-term weight management support is critical. That's why our patients meet with the same clinician throughout their entire time at knownwell.

SEE CLINIC LOCATIONS

The science of Qsymia®

A closer look at GLP-1 receptor biology, peptide engineering, and metabolic effects

Qsymia® is a precision-formulated dual-mechanism combination pill

Qsymia® is a carefully engineered combination of two FDA-approved medications: phentermine and topiramate extended-release.

Each ingredient works through a different biological pathway. Together, they produce greater weight reduction than either medication alone, at doses lower than those used when either drug is prescribed by itself.

Phentermine is a sympathomimetic amine anorectic: a class of compounds that stimulate the central nervous system. It promotes the release of norepinephrine in the brain, which activates appetite-suppressing pathways and reduces the drive to eat. The result is reduced appetite and decreased food intake.

Topiramate extended-release was originally developed to treat epilepsy and migraines. Its weight-reducing effects were observed in clinical use and have since been studied extensively.

The precise mechanism behind its weight-management effects is unknown but thought to involve multiple pathways: augmentation of GABA activity, modulation of voltage-gated ion channels, inhibition of AMPA/kainate glutamate receptors, and carbonic anhydrase inhibition, all of which may influence food reward, satiety signaling, and caloric intake.

The extended-release formulation of topiramate is specifically designed to deliver the medication gradually and steadily, helping to minimize side effects associated with higher peak concentrations.

Central nervous system effects: Appetite regulation at the source

Both phentermine and topiramate act primarily in the central nervous system, targeting the brain pathways responsible for appetite, hunger, and reward-driven eating.

Phentermine stimulates the release of norepinephrine, activating appetite-suppressing pathways. It reduces the desire to eat and reduces overall food intake.

Topiramate is thought to act across multiple brain pathways involved in appetite and satiety. There, it modulates neurotransmitter activity to reduce food reward signaling and supports longer-lasting feelings of fullness.

Together, these complementary central mechanisms create a more comprehensive effect on appetite than either ingredient alone.

Metabolic and cardiometabolic effects

In clinical trials, Qsymia® has been associated with improvements in cardiometabolic markers beyond weight management alone, including:

  • Reductions in waist circumference, a measure of central (abdominal) fat
  • Improvements in blood sugar levels and insulin resistance in people with type 2 diabetes or pre-diabetes
  • Potential reductions in blood pressure and triglycerides
  • Improvements in HDL (good) cholesterol levels

The SEQUEL study (a 108-week extension of the CONQUER trial) showed maintained cardiometabolic improvements alongside sustained weight reduction over two years of treatment.

The history of GLP-1 medications

1950s–1970s

The first appetite-suppressing medications

Phentermine was first approved by the FDA in 1959 as a short-term treatment for obesity.

As one of the earliest appetite-suppressing medications, it worked by stimulating the release of norepinephrine in the brain, signaling the body to reduce hunger and increase energy.
 1990s–2000s

Discovering the weight effects of topiramate

Topiramate was approved by the FDA in 1996 for epilepsy. During clinical use, physicians and researchers noticed that patients taking it consistently lost weight. This observation prompted dedicated research into topiramate as a weight management agent and raised the question: could combining it with phentermine produce greater results at lower doses of each?
 2010s

The CONQUER and EQUIP trials

Phase 3 clinical trials evaluated the combination of phentermine and topiramate extended-release in adults with overweight and obesity. The CONQUER and EQUIP trials demonstrated that the combination produced significantly greater weight reduction than placebo.

Critically, combining the two medications at lower individual doses allowed for meaningful weight reduction while reducing the side effects associated with higher doses of either drug alone.
2021 - Present

FDA approval and expanding use of Qsymia®

In 2012, the FDA approved Qsymia® as a prescription treatment for weight management in adults, combining two previously approved agents into a single once-daily oral capsule at doses lower than either drug used alone. It became the first combination oral medication specifically formulated and approved for this indication.

In 2022, the FDA approved Qsymia® for use in adolescents aged 12 years and older with obesity, expanding its use beyond adults.

Important safety information

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Qsymia® is a prescription medication FDA-approved for chronic weight management in adults and pediatric patients aged 12 years and older with obesity, or in adults with overweight who have at least one weight-related health condition such as high blood pressure, type 2 diabetes, or high cholesterol.
You should not take Qsymia® if you
  • Are pregnant, breastfeeding, or planning to become pregnant (Qsymia® can cause birth defects and can pass through breast milk)
  • Have glaucoma
  • Have hyperthyroidism (overactive thyroid)
  • Are currently taking or have taken MAOIs within the past 14 days
  • Have a known hypersensitivity or idiosyncrasy to sympathomimetic amines, topiramate, or any inactive ingredient in Qsymia®

Important note about pregnancy: Because of the risk of birth defects, Qsymia® is only available through certified pharmacies under a REMS program. People who can become pregnant must have a negative pregnancy test before starting Qsymia® and monthly during treatment, and must use effective birth control while taking it.

Talk with your provider if you have a history of:

  • Depression, anxiety, or other mood disorders
  • Suicidal thoughts or behavior
  • Kidney stones
  • Other kidney or liver problems or disease
  • Too much acid in the blood (metabolic acidosis), or conditions that may increase that risk, like chronic diarrhea, surgery, a ketogenic diet, or weak, soft, or brittle bones
  • Seizures
What to watch for

Some side effects require prompt medical attention, including:

  • Sudden vision changes or eye pain (possible sign of acute angle-closure glaucoma) — stop Qsymia® immediately and contact your care team
  • Mood changes, depression, or thoughts of self-harm
  • A rapid or irregular heartbeat
  • Severe or unusual skin rash

Your knownwell care team will review your health history, medications, and safety considerations before prescribing Qsymia® and will continue to support you throughout treatment.

DISCLAIMERS & SOURCES

Disclaimers

In the SUSTAIN 7 clinical trial, those taking semaglutide 1 mg once weekly reduced their HbA1c by an average of 1.8%, compared to 1.4% with dulaglutide 1.5 mg. Individual results vary.

Sources

1.
Allison, D. B., Gadde, K. M., Garvey, W. T., et al. (2012). Controlled-release phentermine/topiramate in severely obese adults: A randomized controlled trial (EQUIP). Obesity (Silver Spring), 20(2), 330-342. doi:10.1038/oby.2011.330. Retrieved from https://pmc.ncbi.nlm.nih.gov/articles/PMC3270297/
2.
Aronne, L. J., Wadden, T. A., Peterson, C., et al. (2013). Evaluation of phentermine and topiramate versus phentermine/topiramate extended-release in obese adults. Obesity (Silver Spring), 21(11), 2163-2171. doi:10.1002/oby.20584. Retrieved from https://onlinelibrary.wiley.com/doi/10.1002/oby.20584
3.
Bays, H. E., Lazarus, E., Primack, C., et al. (2022). Obesity pillars roundtable: Phentermine - Past, present, and future. Obesity Pillars, 3, 100024. doi:10.1016/j.obpill.2022.100024. Retrieved from https://pmc.ncbi.nlm.nih.gov/articles/PMC10661986/
See all
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Gadde, K. M., Allison, D. B., Ryan, D. H., et al. (2011). Effects of low-dose, controlled-release, phentermine plus topiramate combination on weight and associated comorbidities in overweight and obese adults (CONQUER): a randomised, placebo-controlled, phase 3 trial. The Lancet, 377(9774), 1341-1352. doi:10.1016/S0140-6736(11)60205-5. Retrieved from https://pubmed.ncbi.nlm.nih.gov/21481449/
5.
Garvey, W. T., Frias, J. P., Jastreboff, A. M., et al. (2023). Tirzepatide once weekly for the treatment of obesity in people with type 2 diabetes (SURMOUNT-2): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial. The Lancet, 402(10402), 613-626. doi:10.1016/S0140-6736(23)01200-X. Retrieved from https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(23)01200-X/fulltext
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Garvey, W. T., Ryan, D. H., Look, M., et al. (2012). Two-year sustained weight loss and metabolic benefits with controlled-release phentermine/topiramate in obese and overweight adults (SEQUEL): a randomized, placebo-controlled, phase 3 extension study. The American Journal of Clinical Nutrition, 95(2), 297-308. doi:10.3945/ajcn.111.024927. Retrieved from https://pmc.ncbi.nlm.nih.gov/articles/PMC3260065/
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Guarneiri, L. L., Kirkpatrick, C. F., Maki, K. C. (2025). Protein, fiber, and exercise: A narrative review of their roles in weight management and cardiometabolic health. Lipids in Health and Disease, 24, 237. doi:10.1186/s12944-025-02659-7. Retrieved from https://pmc.ncbi.nlm.nih.gov/articles/PMC12255039/
8.
Jastreboff, A. M., Aronne, L. J., Ahmad, N. N., et al. (2022). Tirzepatide once weekly for the treatment of obesity. New England Journal of Medicine, 387(3), 205-216. doi:10.1056/NEJMoa2206038. Retrieved from https://www.nejm.org/doi/full/10.1056/NEJMoa2206038
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Johnson, D. B. & Quick, J. (2023). Topiramate and phentermine. StatPearls. Retrieved on Mar. 5, 2026, from https://www.ncbi.nlm.nih.gov/books/NBK482165/
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Qsymia. (n.d.). Multiple ways to save on Qsymia®. Retrieved from https://qsymia.com/patient/multiple-ways-to-save
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Qsymia. (n.d.). Qsymia® retail pharmacy savings card. Retrieved from https://qsymia.com/patient/multiple-ways-to-save/savings-card-landing
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U.S. Food and Drug Administration. (2022). FDA approves treatment for chronic weight management in pediatric patients aged 12 years and older. Retrieved from https://www.fda.gov/drugs/news-events-human-drugs/fda-approves-treatment-chronic-weight-management-pediatric-patients-aged-12-years-and-older
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U.S. Food and Drug Administration. (2025). OZEMPIC (semaglutide) injection, for subcutaneous use: Highlights of prescribing information. Retrieved from https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/209637s035,209637s037lbl.pdf
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U.S. Food and Drug Administration. (2024). QSYMIA® (phentermine and topiramate extended-release) capsules: Highlights of prescribing information. Retrieved from https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/022580s026lbl.pdf
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Wadden, T. A., Foreyt, J. P., Foster, G. D., et al. (2011). Weight loss with naltrexone SR/bupropion SR combination therapy as an adjunct to behavior modification: The COR-BMOD trial. Obesity, 19(1), 110-120. doi:10.1038/oby.2010.147. Retrieved from https://pubmed.ncbi.nlm.nih.gov/20559296/
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Wajid, I., Vega, A., Thornhill, K., et al. (2023). Topiramate (Topamax): Evolving role in weight reduction management: A narrative review. Life (Basel), 13(9), 1845. doi:10.3390/life13091845. Retrieved from https://pmc.ncbi.nlm.nih.gov/articles/PMC10532729/
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Wharton, S., Lingvay, I., Bogdanski, P., et al. (2025). Oral semaglutide at a dose of 25 mg in adults with overweight or obesity. New England Journal of Medicine, 393(11), 1077–1087. doi:10.1056/NEJMoa2500969. Retrieved from https://www.nejm.org/doi/10.1056/NEJMoa2500969
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Wilding, J. P. H., Batterham, R. L., Calanna, S., et al. (2021). Once-weekly semaglutide in adults with overweight or obesity. New England Journal of Medicine, 384(11), 989–1002. doi:10.1056/NEJMoa2032183. Retrieved from https://www.nejm.org/doi/full/10.1056/NEJMoa2032183
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