Stevia (steviol glycosides)
Also called steviol glycosides, stevioside, rebaudioside A, Reb A, Stevia rebaudiana, E960.
Best grade C across 18 graded outcomes Botanical Last checked
The short answer
From 28 sourcesStevia sweeteners are purified steviol glycosides with almost no calories. At sweetener amounts they did not change glucose or blood pressure in trials. Two Chinese trials found lower blood pressure with 750 to 1,500 mg of stevioside a day (grade C), at or above the acceptable daily intake for a 70 kg adult; pooled analyses show small, uncertain effects.
Every graded outcome on this page
18 rows · line = participants- CGrade CBlood glucose, insulin and HbA1c (pooled)Blood sugarn 1,439
- CGrade CFasting glucose and HbA1c in adults (pooled)Blood sugarn 871
- CGrade CBlood pressure, fasting glucose and lipids (pooled)Blood pressuren 756
- CGrade CDiabetes markers, blood pressure and lipids (pooled)Blood sugarn 462
- CGrade CAppetite scores (pooled)Appetiten 428
- CGrade CBlood pressure in mild hypertension (2 years)Blood pressuren 168
- CGrade CBody weight with sweetened drinks for 12 weeksWeightn 123
- CGrade CGlucose tolerance and gut microbes after 2 weeks of sweetener sachetsGut bacterian 120
- CGrade CBlood pressure in hypertension (1 year)Blood pressuren 106
- CGrade CGut microbiome and short-chain fatty acids vs a sucrose drinkGut bacterian 59
- DGrade DGlucose regulation and cardiometabolic markers after 14 days of sweetened drinksBlood sugarn 39
- DGrade DGlucose tolerance in type 2 diabetes the day after 3 gBlood sugarn 30
- DGrade DDaily energy intake and glucose after a sweetened drinkAppetiten 30
- DGrade DGlucose tolerance and weight with a daily stevia extractBlood sugarn 28
- DGrade DAppetite and total energy intake at lunch after a stevia drinkAppetiten 20
- DGrade DAfter-meal glucose in type 2 diabetes (one dose)Blood sugarn 12
- ∅No effectHbA1c and fasting glucose in type 2 diabetesBlood sugarn 122
- ∅No effectBlood pressure in people with normal or low-normal pressureBlood pressuren 100
- 15 more graded outcomes, in the evidence chapter
Key facts
- What it is
- Sweet glycosides (stevioside, rebaudioside A and others) from Stevia rebaudiana leaves, 200 to 400 times sweeter than table sugar12
- US status
- High-purity (95% minimum) steviol glycosides are used under GRAS notices FDA did not question; stevia leaf and crude extracts are not considered GRAS as sweeteners1
- Safe intake
- Acceptable daily intake 4 mg per kg of body weight as steviol equivalents (JECFA), which FDA gives as 12 mg/kg for rebaudioside A1
- How the body handles it
- Not digested or absorbed in the upper gut; gut bacteria release steviol, which is absorbed, turned into steviol glucuronide and excreted mainly in urine11413
- Blood pressure
- Two Chinese trials (106 and 174 people) found lower blood pressure with 750 to 1,500 mg a day of stevioside (C); rebaudioside A at 1,000 mg a day and a crude stevioside extract did not beat placebo, and shorter trials were negative5462625
- Blood sugar
- 1,000 mg a day of rebaudioside A for 16 weeks did not change HbA1c in type 2 diabetes (no effect); pooled trials show a small fall in fasting glucose of low certainty11910
- Weight
- In a 12-week trial, drinks sweetened with rebaudioside A did not change weight, while sucrose drinks added 1.85 kg15
What it is
Stevia sweeteners are purified steviol glycosides from the leaves of Stevia rebaudiana, 200 to 400 times sweeter than sugar.
How it works
EstablishedSteviol glycosides are diterpene glycosides that taste intensely sweet. In people they are not hydrolysed by digestive enzymes or absorbed in the upper gut; colon bacteria remove the sugars to release steviol, which is absorbed, conjugated to steviol glucuronide and excreted mainly in urine, while steviol itself appears in faeces. Rebaudioside A and stevioside follow the same pathway, with somewhat lower exposure from rebaudioside A. Glucose-lowering effects seen in mice have not been reproduced with rebaudioside A in people with type 2 diabetes; the mechanism behind the blood-pressure fall in the stevioside trials is not established.11314
Forms side by side: purified sweeteners, research capsules and leaf
4 forms named in our sources. The rest show what our data holds, and say plainly where it holds nothing yet.
Stevia (steviol glycosides) forms compared
4 forms| 4 forms | High-purity steviol glycosides (tabletop packets, drinks, foods) | Stevioside capsules (research doses) | Rebaudioside A (single purified glycoside) | Stevia leaf and crude extracts |
|---|---|---|---|---|
| Standardized toMarker compounds, share of extract weight | 95%1At least 95% steviol glycosides (rebaudioside A, stevioside, rebaudioside D or mixtures), the purity in the GRAS notices FDA did not question | Not applicable (stevioside, C38H60O18; about 40% steviol by weight)23 | Not applicable (rebaudioside A, C44H70O23; about 33% steviol by weight)243 | Not applicable (whole leaf or unpurified extract; glycoside content varies)1 |
| Absorption in people | Not absorbed in the upper gut; gut bacteria release steviol, which is absorbed and excreted as steviol glucuronide.114 | Steviol glucuronide peaks about 8 hours after a dose and has a half-life of about 14 hours.14 | Steviol glucuronide exposure about 10% to 22% lower than after stevioside; peak about 12 hours after a dose.14 | No head-to-head human data.1 |
| GI tolerance | No adverse effects on gut bacteria, glucose or lipids in a 4-week trial at 25% of the acceptable daily intake.16 | Adverse events did not differ from placebo over 2 years at 1,500 mg a day; reviews list abdominal fullness, stomach pain and dizziness.57 | 1,000 mg a day for 16 weeks was well tolerated in type 2 diabetes, with no excess of low blood sugar.11 | FDA does not consider stevia leaf or crude extracts GRAS, and their import as sweeteners is not permitted.1 |
| Studied for | Weight, appetite and gut-bacteria studies (C to D) | Blood pressure in hypertension (C, at 750 to 1,500 mg/day) | HbA1c in type 2 diabetes (no effect); blood pressure in normal pressure (no effect) | Not graded here (a crude stevioside trial up to 15 mg/kg/day found no blood-pressure effect beyond placebo) |
- High-purity steviol glycosides (tabletop packets, drinks, foods)
- Standardized to
- 95%1At least 95% steviol glycosides (rebaudioside A, stevioside, rebaudioside D or mixtures), the purity in the GRAS notices FDA did not question
- Absorption in people
- Not absorbed in the upper gut; gut bacteria release steviol, which is absorbed and excreted as steviol glucuronide.114
- GI tolerance
- No adverse effects on gut bacteria, glucose or lipids in a 4-week trial at 25% of the acceptable daily intake.16
- Studied for
- Weight, appetite and gut-bacteria studies (C to D)
- Stevioside capsules (research doses)
- Absorption in people
- Steviol glucuronide peaks about 8 hours after a dose and has a half-life of about 14 hours.14
- GI tolerance
- Adverse events did not differ from placebo over 2 years at 1,500 mg a day; reviews list abdominal fullness, stomach pain and dizziness.57
- Studied for
- Blood pressure in hypertension (C, at 750 to 1,500 mg/day)
- Rebaudioside A (single purified glycoside)
- Absorption in people
- Steviol glucuronide exposure about 10% to 22% lower than after stevioside; peak about 12 hours after a dose.14
- GI tolerance
- 1,000 mg a day for 16 weeks was well tolerated in type 2 diabetes, with no excess of low blood sugar.11
- Studied for
- HbA1c in type 2 diabetes (no effect); blood pressure in normal pressure (no effect)
- Stevia leaf and crude extracts
- Standardized to
- Not applicable (whole leaf or unpurified extract; glycoside content varies)1
- Absorption in people
- No head-to-head human data.1
- GI tolerance
- FDA does not consider stevia leaf or crude extracts GRAS, and their import as sweeteners is not permitted.1
- Studied for
- Not graded here (a crude stevioside trial up to 15 mg/kg/day found no blood-pressure effect beyond placebo)
What the human research says
Human trials only, one row per outcome. The form line shows what each trial actually tested. Grades follow our evidence-grading policy.
Trial map
18 graded outcomes, largest study first18 graded outcomes: 4 improved, 5 mixed, 9 no effect. The largest, a 2024 meta-analysis of 1,439 people on blood glucose, insulin and HbA1c (pooled), found mixed results.
1Blood glucose, insulin and HbA1c (pooled)
Mixed · Grade C · Meta-analysis, 1,439 people, 2024
Participants of 26 studies
Dose, result and source| Outcome | Found | People | Study | Who was studied |
|---|---|---|---|---|
| Blood glucose, insulin and HbA1c (pooled) | Mixed | 1,439 | Grade C · Meta-analysis, 2024 | Participants of 26 studies |
| Fasting glucose and HbA1c in adults (pooled) | Mixed | 871 | Grade C · Meta-analysis, 2024 | Adults in 12 randomized trials (48% women) |
| Blood pressure, fasting glucose and lipids (pooled) | Mixed | 756 | Grade C · Meta-analysis, 2015 | Participants of 9 randomized trials, most at high cardiovascular risk |
| Diabetes markers, blood pressure and lipids (pooled) | Mixed | 462 | Grade C · Meta-analysis, 2019 | Participants of 9 randomized trials (7 studies) |
| Appetite scores (pooled) | No effect | 428 | Grade C · Meta-analysis, 2025 | Adults in 11 clinical trials |
| Blood pressure in mild hypertension (2 years) | Improved | 168 | Grade C · RCT, 2003 | Chinese adults aged 20 to 75 with mild essential hypertension (174 enrolled, 87 men and 87 women) |
| Body weight with sweetened drinks for 12 weeks | No effect | 123 | Grade C · RCT, 2019 | Adults aged 18 to 60 with overweight or obesity (154 randomized to five drinks) |
| HbA1c and fasting glucose in type 2 diabetes | No effect | 122 | No-effect grade · RCT, 2008 | Men and women aged 33 to 75 with type 2 diabetes |
| Glucose tolerance and gut microbes after 2 weeks of sweetener sachets | Mixed | 120 | Grade C · RCT, 2022 | Healthy adults randomized to saccharin, sucralose, aspartame, stevia, glucose vehicle or no supplement |
| Blood pressure in hypertension (1 year) | Improved | 106 | Grade C · RCT, 2000 | Chinese adults aged 28 to 75 with diastolic pressure 95 to 110 mm Hg |
| Blood pressure in people with normal or low-normal pressure | No effect | 100 | No-effect grade · RCT, 2008 | Healthy adults aged 18 to 73, mostly women, with resting pressure around 110/70 mm Hg |
| Gut microbiome and short-chain fatty acids vs a sucrose drink | No effect | 59 | Grade C · RCT, 2024 | Healthy adults, mean age 31 (36 women, 23 men) |
| Glucose regulation and cardiometabolic markers after 14 days of sweetened drinks | No effect | 39 | Grade D · Crossover RCT, 2026 | Healthy, normal-weight adults (Sweden) |
| Glucose tolerance in type 2 diabetes the day after 3 g | No effect | 30 | Grade D · Crossover RCT, 2022 | Adults with type 2 diabetes on metformin or no treatment, University Hospitals Leuven (Belgium), 86.7% men |
| Daily energy intake and glucose after a sweetened drink | No effect | 30 | Grade D · Crossover RCT, 2017 | Healthy men |
| Glucose tolerance and weight with a daily stevia extract | No effect | 28 | Grade D · Open-label trial, 2020 | Healthy normal-weight adults, mean age 25 |
| Appetite and total energy intake at lunch after a stevia drink | Improved | 20 | Grade D · Crossover RCT, 2020 | Healthy adults, mean age 27, 55% women |
| After-meal glucose in type 2 diabetes (one dose) | Improved | 12 | Grade D · Crossover RCT, 2004 | People with type 2 diabetes |
Every graded row
18 rowsShowing 18 of 18 outcomes. Human trials only.
CGrade CBlood glucose, insulin and HbA1c (pooled)Blood sugar−3.84 mg/dL glucoseMeta-analysis · 26 studies
n 1,439 · 2024
Mixed Blood glucose fell slightly (−3.84 mg/dL, 95% CI −7.15 to −0.53; low certainty), mainly in people with higher BMI, diabetes or hypertension. Insulin and HbA1c did not change significantly.
- Design
- Meta-analysis, 26 studies, n = 1,439, 2024
- Population
- Participants of 26 studies
- Form
- Stevia
- Dose
- As given in each study; glucose fell at 3,342 mg/day or more in dose-response analysis
- Duration
- Varied by study
- Source
- Reference 10 · PubMed 39098209 (opens PubMed)
CGrade CFasting glucose and HbA1c in adults (pooled)Blood sugarFBG −4.10 mg/dL; HbA1c no changeMeta-analysis · 12 studies
n 871 · 2024
Mixed Fasting glucose was 4.10 mg/dL lower than control (95% CI −6.55 to −1.65); HbA1c did not differ (0.01%). The overall quality of evidence was rated low.
- Design
- Meta-analysis, 12 studies, n = 871, 2024
- Population
- Adults in 12 randomized trials (48% women)
- Form
- Steviol glycosides
- Dose
- As given in each included trial
- Duration
- Varied by trial
- Source
- Reference 9 · PubMed 38512280 (opens PubMed)
CGrade CBlood pressure, fasting glucose and lipids (pooled)Blood pressureSBP −2.98 mm Hg (n.s.)Meta-analysis · 9 studies
n 756 · 2015
Mixed Systolic pressure did not differ significantly from placebo (−2.98 mm Hg, 95% CI −6.23 to 0.27); diastolic pressure and fasting glucose fell significantly, with no effect on lipids. Rebaudioside A had no significant effect on blood pressure or other risk factors. Heterogeneity was significant.
- Design
- Meta-analysis, 9 studies, n = 756, 2015
- Population
- Participants of 9 randomized trials, most at high cardiovascular risk
- Form
- Stevioside or rebaudioside A
- Dose
- As given in each included trial
- Duration
- Varied by trial
- Source
- Reference 7 · PubMed 25412840 (opens PubMed)
CGrade CDiabetes markers, blood pressure and lipids (pooled)Blood sugarNo effect on HbA1cMeta-analysis · 9 studies
n 462 · 2019
Mixed The review reports a significant fall in systolic pressure (−6.32 mm Hg) and non-significant changes in BMI, diastolic pressure, fasting glucose and cholesterol, with no effect on HbA1c. Heterogeneity was significant.
- Design
- Meta-analysis, 9 studies, n = 462, 2019
- Population
- Participants of 9 randomized trials (7 studies)
- Form
- Steviol glycosides
- Dose
- As given in each included trial
- Duration
- Varied by trial
- Source
- Reference 8 · PubMed 31438580 (opens PubMed)
CGrade CAppetite scores (pooled)AppetiteNo change in appetiteMeta-analysis · 11 studies
n 428 · 2025
No effect Stevia had no significant effect on any appetite score (very low to moderate certainty); too few trials reported energy intake to pool.
- Design
- Meta-analysis, 11 studies, n = 428, 2025
- Population
- Adults in 11 clinical trials
- Form
- Stevia
- Dose
- As given in each trial
- Duration
- Varied by trial
- Source
- Reference 20 · PubMed 39887829 (opens PubMed)
CGrade CBlood pressure in mild hypertension (2 years)Blood pressure150/95 to 140/89 mm HgRCT
n 168 · 2003
Improved Systolic pressure fell from 150 to 140 mm Hg and diastolic from 95 to 89 mm Hg with stevioside, significantly more than placebo; the effect began about a week after starting. Body mass index, blood tests and adverse events did not differ from placebo.
- Design
- RCT, n = 168, 2003
- Population
- Chinese adults aged 20 to 75 with mild essential hypertension (174 enrolled, 87 men and 87 women)
- Form
- Stevioside powder capsules vs placebo
- Dose
- 500 mg three times a day (1,500 mg/day)
- Duration
- 2 years
- Source
- Reference 5 · PubMed 14693305 (opens PubMed)
CGrade CBody weight with sweetened drinks for 12 weeksWeightNo weight gain (sucrose +1.85 kg)RCT
n 123 · 2019
No effect Weight rose with sucrose (+1.85 kg) and saccharin (+1.18 kg) but did not change significantly with rebaudioside A. Glucose tolerance did not change with any sweetener.
- Design
- RCT, n = 123, 2019
- Population
- Adults aged 18 to 60 with overweight or obesity (154 randomized to five drinks)
- Form
- Drinks sweetened with rebaudioside A, aspartame, saccharin, sucralose or sucrose
- Dose
- 1.25 to 1.75 L of sweetened drink a day
- Duration
- 12 weeks
- Source
- Reference 15 · PubMed 30997499 (opens PubMed)
CGrade CGlucose tolerance and gut microbes after 2 weeks of sweetener sachetsGut bacteriaMicrobes changed; glucose not impairedRCT
n 120 · 2022
Mixed Each sweetener, stevia included, changed stool and oral microbes and plasma metabolites. Saccharin and sucralose significantly impaired glucose responses; stevia was not reported to.
- Design
- RCT, n = 120, 2022
- Population
- Healthy adults randomized to saccharin, sucralose, aspartame, stevia, glucose vehicle or no supplement
- Form
- Stevia sachets (below the acceptable daily intake)
- Dose
- Sachets daily, below the acceptable daily intake
- Duration
- 2 weeks
- Source
- Reference 17 · PubMed 35987213 (opens PubMed)
CGrade CBlood pressure in hypertension (1 year)Blood pressure166/105 to 153/90 mm HgRCT
n 106 · 2000
Improved After 3 months, systolic pressure fell from 166.0 to 152.6 mm Hg and diastolic from 104.7 to 90.3 mm Hg, and the effect persisted for the year. Lipids and glucose did not change and no significant adverse effects were seen.
- Design
- RCT, n = 106, 2000
- Population
- Chinese adults aged 28 to 75 with diastolic pressure 95 to 110 mm Hg
- Form
- Stevioside capsules vs placebo
- Dose
- 250 mg three times a day (750 mg/day)
- Duration
- 1 year
- Source
- Reference 4 · PubMed 10971305 (opens PubMed)
CGrade CGut microbiome and short-chain fatty acids vs a sucrose drinkGut bacteriaNo microbiome changeRCT
n 59 · 2024
No effect No differences in the gut microbiome at any level or in faecal short-chain fatty acids; fasting glucose, insulin, lipids and blood pressure did not differ. BMI rose 0.3 kg/m² with sucrose compared with stevia.
- Design
- RCT, n = 59, 2024
- Population
- Healthy adults, mean age 31 (36 women, 23 men)
- Form
- Drink with 25% of the acceptable daily intake of stevia vs drink with 30 g sucrose
- Dose
- 16 oz drink daily
- Duration
- 4 weeks, then 4-week washout
- Source
- Reference 16 · PubMed 38408729 (opens PubMed)
DGrade DGlucose regulation and cardiometabolic markers after 14 days of sweetened drinksBlood sugarNo difference vs sucrose or saccharinCrossover RCT
n 39 · 2026
No effect Glucose regulation did not differ between steviol glycosides, saccharin (220 mg/day) and sucrose (66 g/day). Fasting insulin rose from baseline after stevia, and all three drinks raised after-meal insulin. Triglycerides were higher after sucrose than saccharin; cholesterol, CRP and appetite did not differ.
- Design
- Crossover RCT, n = 39, 2026
- Population
- Healthy, normal-weight adults (Sweden)
- Form
- Steviol glycosides in drinks
- Dose
- 220 mg/day
- Duration
- 14 days per drink, with washouts
- Source
- Reference 27 · PubMed 42514406 (opens PubMed)
DGrade DGlucose tolerance in type 2 diabetes the day after 3 gBlood sugarNo change in glucose curveCrossover RCT
n 30 · 2022
No effect Rebaudioside A was absorbed and converted to steviol and steviol glucuronide, but did not lower the 2-hour glucose curve (−0.7 h·mg/dL, 95% CI −22.3 to 20.9) or change insulin or C-peptide.
- Design
- Crossover RCT, n = 30, 2022
- Population
- Adults with type 2 diabetes on metformin or no treatment, University Hospitals Leuven (Belgium), 86.7% men
- Form
- Rebaudioside A vs placebo (open-label crossover)
- Dose
- 3 g single dose
- Duration
- Glucose tolerance test 19 hours later
- Source
- Reference 13 · PubMed 36057030 (opens PubMed)
DGrade DDaily energy intake and glucose after a sweetened drinkAppetiteNo difference in daily energyCrossover RCT
n 30 · 2017
No effect People ate more at lunch after the no-calorie drinks, so the energy saved was fully made up and total daily intake did not differ. Total 3-hour glucose and insulin areas did not differ between the four drinks.
- Design
- Crossover RCT, n = 30, 2017
- Population
- Healthy men
- Form
- Stevia-, monk fruit-, aspartame- or sucrose-sweetened drink
- Dose
- One drink mid-morning
- Duration
- Single test days
- Source
- Reference 21 · PubMed 27956737 (opens PubMed)
DGrade DGlucose tolerance and weight with a daily stevia extractBlood sugarNo glucose change; −0.22 vs +0.89 kgOpen-label trial
n 28 · 2020
No effect Glucose and insulin responses to a glucose tolerance test did not change. Weight was stable with stevia (−0.22 kg) while the control group gained 0.89 kg, and energy intake fell in the stevia group.
- Design
- Open-label trial, n = 28, 2020
- Population
- Healthy normal-weight adults, mean age 25
- Form
- Daily stevia extract vs no stevia (randomized, open-label)
- Dose
- A stevia extract daily (amount not stated in the abstract)
- Duration
- 12 weeks
- Source
- Reference 18 · PubMed 33036155 (opens PubMed)
DGrade DAppetite and total energy intake at lunch after a stevia drinkAppetite727 vs 832 kcalCrossover RCT
n 20 · 2020
Improved Total energy (drink plus lunch) was lower after the stevia drink (727 kcal) than after water (832 kcal, P = 0.013). Blood glucose after stevia was similar to water and lower than after the caloric drinks.
- Design
- Crossover RCT, n = 20, 2020
- Population
- Healthy adults, mean age 27, 55% women
- Form
- 240 ppm stevia drink vs water, glucose, sucrose or maltodextrin drinks (330 mL)
- Dose
- One 330 mL drink before lunch
- Duration
- Single test visits
- Source
- Reference 19 · PubMed 32125421 (opens PubMed)
DGrade DAfter-meal glucose in type 2 diabetes (one dose)Blood sugar−18% glucose areaCrossover RCT
n 12 · 2004
Improved Stevioside cut the incremental glucose area under the curve by 18% (P = 0.013) and raised the insulinogenic index by about 40%; insulin, GLP-1 and GIP areas did not change significantly.
- Design
- Crossover RCT, n = 12, 2004
- Population
- People with type 2 diabetes
- Form
- 1 g stevioside vs 1 g maize starch added to a test meal
- Dose
- 1 g with one meal
- Duration
- Single test meals
- Source
- Reference 12 · PubMed 14681845 (opens PubMed)
∅No effectHbA1c and fasting glucose in type 2 diabetesBlood sugarHbA1c +0.11% vs +0.09%RCT
n 122 · 2008
No effect HbA1c changed by 0.11% with rebaudioside A and 0.09% with placebo (p = 0.355); fasting glucose, insulin, C-peptide, blood pressure, weight and lipids did not differ. Hypoglycaemic episodes were not more common.
- Design
- RCT, n = 122, 2008
- Population
- Men and women aged 33 to 75 with type 2 diabetes
- Form
- Rebaudioside A vs placebo
- Dose
- 1,000 mg/day
- Duration
- 16 weeks
- Source
- Reference 11 · PubMed 18555575 (opens PubMed)
∅No effectBlood pressure in people with normal or low-normal pressureBlood pressureNo change vs placeboRCT
n 100 · 2008
No effect Rebaudioside A did not change resting blood pressure, mean arterial pressure, heart rate or 24-hour ambulatory pressure compared with placebo.
- Design
- RCT, n = 100, 2008
- Population
- Healthy adults aged 18 to 73, mostly women, with resting pressure around 110/70 mm Hg
- Form
- Rebaudioside A vs placebo
- Dose
- 1,000 mg/day
- Duration
- 4 weeks
- Source
- Reference 6 · PubMed 18555574 (opens PubMed)
What the numbers add up to
Each point is worked out from the data and the sources numbered on this page, with the arithmetic shown under it. It adds no new data and is not medical advice.
The blood-pressure trials used about twice the daily limit
The daily limit in rebaudioside A
Sweetener use vs research use
The glucose fall in the 2024 dose-response analysis appeared at 3,342 mg of stevia a day or more, which is well above what sweetening food and drinks requires.10
Studied doses
Doses used in research, shown against the official limits. They describe the studies, not a recommendation for you.
Studied doses in research, not advice. These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.
Doses studied in human trials
Doses studied in human trials ranged from 250 mg of stevioside three times a day (750 mg/day) to 500 mg three times a day (1,500 mg/day) for 1 to 2 years in blood-pressure trials, 1,000 mg/day of rebaudioside A for 4 to 16 weeks, and single test doses of 1 g of stevioside with a meal and 3 g of rebaudioside A. Weight, appetite and microbiome studies used sweetener amounts in drinks and sachets. These are research amounts, not product directions.4561112131516
When trials measured an effect
3 outcomes| Outcome | Measured at | Basis |
|---|---|---|
| Blood pressure (stevioside, hypertension) | From about 1 week on home readings; significant by 3 months and sustained to 1 and 2 years | Two Chinese placebo-controlled trials54 |
| HbA1c (rebaudioside A, type 2 diabetes) | No change at 16 weeks | Placebo-controlled trial in 122 people11 |
| Blood steviol glucuronide after a dose | Peaks about 8 to 12 hours after a dose; half-life about 14 hours | Pharmacokinetic study in healthy men14 |
Interactions and safety
Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.
What Stevia meets
2 cited rowsMedicines 2
Supplements and foods 0
No supplement rows in our sources.
- Reference summary
Choose a medicine or supplement above to read its cited rows here.
Also cited:
Blood-pressure medicines
ReviewReference summary
Blood-pressure medicines, for example Verapamil: MSKCC: animal studies suggest stevia may add to the blood-pressure-lowering effect; clinical relevance has not been determined. Stevioside at 750 to 1,500 mg a day lowered blood pressure in two trials, far above sweetener amounts.
Source 28, Memorial Sloan Kettering Cancer Center (2022); Source 4, Br J Clin Pharmacol (2000); Source 5, Clin Ther (2003)
Glucose-lowering medicines
ReviewReference summary
Glucose-lowering medicines: MSKCC: animal studies suggest stevia may affect blood glucose; clinical relevance has not been determined. 1,000 mg a day of rebaudioside A did not change HbA1c in type 2 diabetes.
Source 28, Memorial Sloan Kettering Cancer Center (2022); Source 11, Food Chem Toxicol (2008)
Interactions
2 agents| Agent | What the source says | Evidence |
|---|---|---|
| Medicines2 | ||
| Blood-pressure medicinese.g. Verapamil | MSKCC: animal studies suggest stevia may add to the blood-pressure-lowering effect; clinical relevance has not been determined. Stevioside at 750 to 1,500 mg a day lowered blood pressure in two trials, far above sweetener amounts.2845 | Review |
| Glucose-lowering medicines | MSKCC: animal studies suggest stevia may affect blood glucose; clinical relevance has not been determined. 1,000 mg a day of rebaudioside A did not change HbA1c in type 2 diabetes.2811 | Review |
Check with what you take
Kept on this device onlyAdd what you take. We list every interaction our evidence profiles cite between Stevia and your picks, and between your picks.
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Add a supplement or medicine you take to check it against Stevia.
Starting from one medicine? The interaction checker rates how serious each pair is, on a curated list of 19 entries for 11 medicines. This cabinet has no severity rating: it lists every interaction row our supplement pages cite.
Who should be careful
3 groups- Pregnancy and breastfeeding
- Pregnancy: MSKCC advises against stevia in pregnancy because little is known about how non-nutritive sweeteners affect offspring. Breastfeeding: NIH's LactMed found no data on stevia in breast milk or in nursing infants; it notes the risk to a breastfed infant appears low and that a sweetener with more data may be preferred while nursing a newborn or preterm infant.2822
- People on blood-pressure medicines
- Stevioside at 750 to 1,500 mg a day lowered blood pressure in two trials. Sweetener amounts are far lower, but anyone using stevia extracts at research doses alongside blood-pressure treatment should tell their clinician.45
- Leaf and crude extracts
- FDA does not consider whole-leaf or crude stevia extracts GRAS as sweeteners; the safety data behind the acceptable daily intake are for purified steviol glycosides.1
How to read the label
What to check on the Supplement Facts panel.
How to read the label
3 checksWhich glycoside, and how pure
US stevia sweeteners use high-purity (95% minimum) steviol glycosides such as rebaudioside A, stevioside or rebaudioside D. Leaf and crude extracts are a different, non-GRAS category.1
What else is in the packet
Brand names
FDA lists Truvia, PureVia and Enliten as examples of steviol glycoside sweeteners.1
Frequently asked questions
Short answers to common questions; the numbers link to the sources below.
Common questions
8 answersDoes stevia raise blood sugar?
Does stevia lower blood pressure?
Two Chinese trials found lower blood pressure with 750 to 1,500 mg of stevioside a day for 1 to 2 years; the higher dose is about twice the acceptable daily intake. Rebaudioside A and a crude stevioside extract did not beat placebo, and a 2010 review found shorter 1- to 3-month studies negative. Grade C.4562625
Can stevia help with weight loss?
Is stevia safe?
High-purity steviol glycosides are used in the US under GRAS notices FDA did not question. The acceptable daily intake is 4 mg per kg of body weight as steviol equivalents (12 mg/kg as rebaudioside A, about 840 mg a day for a 70 kg adult), far above normal use. Trials found no change in glucose, blood pressure or gut bacteria at sweetener amounts.11611
Does stevia harm gut bacteria?
Is stevia safe in pregnancy or while breastfeeding?
Is stevia better than artificial sweeteners?
What is the difference between stevia leaf and stevia sweeteners?
Sweeteners use purified steviol glycosides (95% minimum purity in the US). FDA does not consider the leaf or crude extracts GRAS as sweeteners and does not permit their import for that use.1
Sources
28 sources: trial abstracts, NIH fact sheets and reference databases. Numbers in the text link here.
Sources cited on this page
28 sources- 1Aspartame and Other Sweeteners in Food (steviol glycosides, Luo Han Guo, acceptable daily intakes)Fact sheet U.S. Food and Drug Administration, 2025 · fda.gov
- 2PubChem compound summary: Stevioside (CID 442089)Database National Library of Medicine, 2026 · pubchem.ncbi.nlm.nih.gov
- 3PubChem compound summary: Steviol (CID 452967)Database National Library of Medicine, 2026 · pubchem.ncbi.nlm.nih.gov
- 4A double-blind placebo-controlled study of the effectiveness and tolerability of oral stevioside in human hypertension.RCT Br J Clin Pharmacol, 2000 · PMID 10971305
- 5Efficacy and tolerability of oral stevioside in patients with mild essential hypertension: a two-year, randomized, placebo-controlled study.RCT Clin Ther, 2003 · PMID 14693305
- 6The hemodynamic effects of rebaudioside A in healthy adults with normal and low-normal blood pressure.RCT Food Chem Toxicol, 2008 · PMID 18555574
- 7Effect of the natural sweetener, steviol glycoside, on cardiovascular risk factors: a systematic review and meta-analysis of randomised clinical trials.Meta-analysis Eur J Prev Cardiol, 2015 · PMID 25412840
- 8Effect of Steviol Glycosides on Human Health with Emphasis on Type 2 Diabetic Biomarkers: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.Meta-analysis Nutrients, 2019 · PMID 31438580
- 9Effect of steviol glycosides as natural sweeteners on glucose metabolism in adult participants.Meta-analysis Food Funct, 2024 · PMID 38512280
- 10Effect of stevia on blood glucose and HbA1C: A meta-analysis.Meta-analysis Diabetes Metab Syndr, 2024 · PMID 39098209
- 11Chronic consumption of rebaudioside A, a steviol glycoside, in men and women with type 2 diabetes mellitus.RCT Food Chem Toxicol, 2008 · PMID 18555575
- 12Antihyperglycemic effects of stevioside in type 2 diabetic subjects.Crossover RCT Metabolism, 2004 · PMID 14681845
- 13Pharmacokinetics of Oral Rebaudioside A in Patients with Type 2 Diabetes Mellitus and Its Effects on Glucose Homeostasis: A Placebo-Controlled Crossover Trial.Crossover RCT Eur J Drug Metab Pharmacokinet, 2022 · PMID 36057030
- 14Pharmacokinetics of rebaudioside A and stevioside after single oral doses in healthy men.PK study Food Chem Toxicol, 2008 · PMID 18555578
- 15A randomized controlled trial contrasting the effects of 4 low-calorie sweeteners and sucrose on body weight in adults with overweight or obesity.RCT Am J Clin Nutr, 2019 · PMID 30997499
- 16Comparison of a Daily Steviol Glycoside Beverage compared with a Sucrose Beverage for Four Weeks on Gut Microbiome in Healthy Adults.RCT J Nutr, 2024 · PMID 38408729
- 17Personalized microbiome-driven effects of non-nutritive sweeteners on human glucose tolerance.RCT Cell, 2022 · PMID 35987213
- 18Effects of the Daily Consumption of Stevia on Glucose Homeostasis, Body Weight, and Energy Intake: A Randomised Open-Label 12-Week Trial in Healthy Adults.Open-label trial Nutrients, 2020 · PMID 33036155
- 19Stevia Beverage Consumption prior to Lunch Reduces Appetite and Total Energy Intake without Affecting Glycemia or Attentional Bias to Food Cues: A Double-Blind Randomized Controlled Trial in Healthy Adults.Crossover RCT J Nutr, 2020 · PMID 32125421
- 20Effects of stevia consumption on appetite in adults: A systematic review and dose-response meta-analysis of randomized controlled trials.Meta-analysis Obes Rev, 2025 · PMID 39887829
- 21Effects of aspartame-, monk fruit-, stevia- and sucrose-sweetened beverages on postprandial glucose, insulin and energy intake.Crossover RCT Int J Obes (Lond), 2017 · PMID 27956737
- 22Stevia. Drugs and Lactation Database (LactMed).Database National Institute of Child Health and Human Development, 2024 · PMID 30000908
- 23A polyol-stevia blended sugar replacer exhibits low glycemic response among human subjects.RCT Clin Nutr ESPEN, 2019 · PMID 31451273
- 24PubChem compound summary: Rebaudioside A (CID 6918840)Database National Library of Medicine, 2026 · pubchem.ncbi.nlm.nih.gov
- 25An evidence-based systematic review of stevia by the Natural Standard Research Collaboration.Systematic review Cardiovasc Hematol Agents Med Chem, 2010 · PMID 20370653
- 26Investigation of the antihypertensive effect of oral crude stevioside in patients with mild essential hypertension.RCT Phytother Res, 2006 · PMID 16775813
- 27Effects of Short-Term (14-Day) Intake of Sucrose and Non-Caloric Sweeteners on Glucose Regulation, Blood Lipids, Gut Hormones, Inflammation Markers, and Appetite in Healthy Adults: A Randomized Controlled Trial.Crossover RCT Nutrients, 2026 · PMID 42514406
- 28Stevia (About Herbs)Database Memorial Sloan Kettering Cancer Center, 2022 · mskcc.org
What changed
Every dated change to this page: what changed, who made it and why.
Change log
2 entries| Date | Change | Who and why |
|---|---|---|
| evidence, interactions, who should be careful, FAQ | Added a 2026 crossover trial of steviol glycosides vs sucrose and saccharin (PMID 42514406, no difference in glucose regulation). Added blood-pressure and glucose-lowering medicine interactions and a pregnancy note from MSKCC About Herbs (Stevia); both interactions rest on animal data. FAQ trimmed to 8 by folding the daily-limit answer into the safety question; the pregnancy and breastfeeding answer now covers both. Fact-checked against the sources; corrected: the 2026 crossover trial result now notes triglycerides were higher after sucrose than saccharin (lipids did differ), and its grade lowered from C to D as a single small trial. | Writer: Kymata Health EditorialTrigger: A–Z page audit |
| all | New page. Every PMID checked with NCBI E-utilities (esummary title, year and journal) and its abstract read with efetch, including the LactMed record; FDA's sweetener page (GRAS status, acceptable daily intakes, sweetness) and PubChem molecular weights read on the date shown. The crude-stevioside trial (Ferri 2006) is cited but not graded because its abstract gives no participant count. | Writer: Kymata Health EditorialTrigger: new page |
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