About the Authors
Edwin G. Ortiz-Munoz is a 2026 PharmD candidate at the University of Puerto Rico School of Pharmacy.
Alejandro Rivera-Rodriguez, PharmD, BCGP, CPPS, DPLA, is pharmacy manager at Farmacia Caridad #41.
OTC “GLP-1 boosters” are marketed for weight loss, but pharmacists should help patients distinguish evidence-based care from supplement claims.
The rapid rise of glucagon-like peptide-1 (GLP-1) receptor agonists has transformed the treatment landscape for obesity and type 2 diabetes. GLP-1 is an incretin hormone secreted by intestinal L-cells in response to nutrient intake.1 It promotes glucose-dependent insulin secretion, suppresses glucagon release, slows gastric emptying, and contributes to appetite regulation through central nervous system pathways.1
GLP-1 receptor agonists are designed to directly activate this pathway in a durable and clinically measurable way.1 Medications such as semaglutide (Wegovy, Ozempic; Novo Nordisk) and tirzepatide (Zepbound; Eli Lilly) have demonstrated clinically significant weight reduction and cardiometabolic benefits in large clinical trials.2–5 Newer agents are also expanding the field, including orforglipron (Foundayo; Eli Lilly), an oral small-molecule GLP-1 receptor agonist, highlighting continued innovation in this therapeutic class.6,7
As public awareness of GLP-1 therapy has increased, so has consumer interest in OTC products marketed as “GLP-1 boosters.” These supplements are often promoted in pharmacies, online, and through social media as natural alternatives that can increase satiety, improve metabolism, or support weight loss. Compared with GLP-1 receptor agonists, these supplements generally do not directly activate GLP-1 receptors in a comparable manner. For community pharmacists, this creates an important counseling opportunity for patients asking about products that are similar to GLP-1 receptor agonists.
Common ingredients found in OTC products marketed as GLP-1 boosters include berberine, chromium picolinate, resveratrol, dietary fiber, green tea extract, and probiotics. Some may have modest metabolic effects, but none should be considered equivalent to GLP-1 receptor agonists. This distinction is especially important because the FDA has warned that many weight loss products marketed as supplements may contain hidden drug ingredients, may be falsely advertised as natural products, and can pose serious health risks.8 The National Institutes of Health Office of Dietary Supplements also emphasizes that weight-loss supplements vary widely in ingredients, mechanisms, evidence, and safety profiles.9
Berberine is one of the most promoted ingredients in so-called “natural Ozempic” messaging.10 Evidence suggests that berberine may improve lipid parameters, with 1 systematic review and meta-analysis finding reductions in total cholesterol, low-density lipoprotein cholesterol, and triglycerides.11,12 However, the authors noted high clinical heterogeneity and generally low methodological quality among included trials, meaning the findings should be interpreted cautiously.12 From a safety perspective, berberine was generally associated with mild adverse effects such as constipation, flatulence, nausea, headache, and transaminase elevation, with no serious adverse events reported in the reviewed trials.11,12 Pharmacists should still screen for gastrointestinal intolerance, pregnancy status, liver disease, and potential drug interactions.
Chromium picolinate is another common ingredient promoted for glucose metabolism and insulin sensitivity. A systematic review and meta-analysis in patients with diabetes found that chromium supplementation improved glycemic control and did not significantly increase adverse events compared with placebo.13 Reported adverse events included watery stool, dizziness, headache, nausea, constipation, and flatulence.14 However, this evidence is more relevant to glycemic outcomes in diabetes than to weight loss. Pharmacists should be cautious when patients use chromium alongside insulin or other glucose-lowering therapies because of the risk of additive glucose-lowering effects.
Resveratrol is a polyphenol marketed for metabolic health, antioxidant effects, and weight management.15 However, human evidence for weight loss remains inconsistent. A review of resveratrol obesity trials found substantial heterogeneity in study design, including differences in dose, duration, delivery method, participant characteristics, and outcomes measured.15 Additionally, a literature review reported that resveratrol may have dose-related adverse effects, possible cytochrome P450 interactions, and potential interaction with drugs such as warfarin, which could increase bleeding risk.16 High doses have also been associated with gastrointestinal symptoms such as diarrhea and nausea.16
Dietary fiber may be the most clinically reasonable ingredient to discuss as an adjunctive, nonprescription option, although not as a GLP-1 substitute. Fibers such as glucomannan, psyllium, and inulin may promote satiety, delay gastric emptying, and support modest weight reduction when combined with energy restriction.17 In a randomized controlled study of overweight or obese adults with traits of metabolic syndrome, fiber supplementation with energy restriction improved body weight, body mass index, fat mass, visceral fat, lipid profile, and inflammatory markers.17 Safety counseling should focus on bloating, flatulence, diarrhea, constipation, adequate water intake, and separation from other medications to reduce the risk of impaired absorption.17
Green tea extract is often marketed for thermogenesis and “fat burning.” A Cochrane review found that green tea preparations produced a small, statistically nonsignificant weight loss in overweight or obese adults and that the amount of weight loss was unlikely to be clinically meaningful.18 Safety concerns include gastrointestinal symptoms, caffeine-related effects such as insomnia or palpitations, and hepatotoxicity, particularly with concentrated extracts.18 The same review noted that reported adverse events were generally mild to moderate, although adverse event reporting was inconsistent across studies.18
Probiotics are increasingly included in weight-management supplements because of interest in the gut microbiome. A 2024 systematic review found that probiotics showed a trend toward preventing weight gain and reducing body weight in individuals with excess weight or obesity, with combinations of Lactobacillus and Bifidobacterium appearing most effective.19 Pharmacists should avoid generalizing the effects of a single probiotic strain or combination to all probiotic products. Although probiotics are generally well tolerated, caution is warranted in immunocompromised patients or those with significant underlying illness.
When counseling patients, pharmacists should clearly state that these products may have limited supportive metabolic data and do not replicate the pharmacologic action or clinical outcomes of GLP-1 receptor agonist therapies.
Community pharmacists are well positioned to respond to patient questions in a practical and nonjudgmental way. The first step is to identify the patient’s goal: weight loss, appetite control, glycemic improvement, or avoidance of prescription therapy due to cost, lack of access, or fear of injections. Pharmacists should then review current medications, pregnancy status, liver or kidney disease, diabetes history, anticoagulant use, immunocompromising conditions, and prior adverse reactions to medications.
Edwin G. Ortiz-Munoz is a 2026 PharmD candidate at the University of Puerto Rico School of Pharmacy.
Alejandro Rivera-Rodriguez, PharmD, BCGP, CPPS, DPLA, is pharmacy manager at Farmacia Caridad #41.
Pharmacists should also assess patient expectations regarding these products and clarify that OTC supplements do not produce effects comparable to semaglutide or tirzepatide. Counseling should include discussion of potential adverse effects, drug-supplement interactions, variability in supplement quality, and situations in which referral to a primary care clinician or specialist may be appropriate. This approach allows pharmacists to move beyond “Does it work?” and toward “Is it appropriate and safe for this patient?”
Clinical recommendations should emphasize evidence-based care. Patients with obesity, diabetes, cardiovascular risk, or obesity-related complications may benefit from referral to a primary care clinician, dietitian, or specialist. For patients interested in OTC options, fiber may be a reasonable adjunct when used appropriately, but it should be paired with nutrition, physical activity, and realistic expectations. Other supplements should be approached cautiously, especially when evidence is inconsistent or safety concerns exist.
OTC “GLP-1 boosters” reflect both the excitement surrounding modern obesity pharmacotherapy and the vulnerability of patients to marketing claims. While some ingredients may have varying degrees of metabolic evidence, none should be considered a substitute for FDA-approved GLP-1 receptor agonists. As demand for weight loss therapies grows, pharmacists play a critical role in separating evidence-based treatments from marketing-driven alternatives.