FLORIDA'S ONLY JOINT COMMISSION-ACCREDITED URGENT CARE
FLORIDA'S ONLY JOINT COMMISSION-ACCREDITED URGENT CARE · ONE OF JUST 8 NATIONWIDE
Tirzepatide and semaglutide are the two dominant incretin-based medications reshaping the management of type 2 diabetes and obesity. They share a mechanism—GLP-1 receptor agonism—but differ in molecular design, efficacy, and side-effect profile. Tirzepatide adds GIP receptor activity, producing greater average weight loss in head-to-head clinical trials. At TrufaMED in Surfside, these medications are prescribed only within a physician-led, fully evaluated medical weight management program—never as a retail product.
Glucagon-like peptide-1 (GLP-1) is a gut hormone released in response to food intake. It slows gastric emptying, stimulates glucose-dependent insulin secretion, suppresses glucagon, and signals satiety to the hypothalamus. Glucose-dependent insulinotropic polypeptide (GIP) is a related incretin with complementary effects on insulin release and adipose tissue biology.
Semaglutide (brand names Ozempic, Wegovy) is a long-acting GLP-1 receptor agonist. Tirzepatide (brand names Mounjaro, Zepbound) is a dual GIP/GLP-1 receptor agonist—engineered to activate both receptor families in a single molecule.
In the SURMOUNT-1 trial, tirzepatide at the highest maintenance dose produced mean weight loss of approximately 20–22% at 72 weeks in adults with obesity without diabetes. In the STEP trials, semaglutide 2.4 mg weekly produced mean weight loss of approximately 14–15% at 68 weeks. Head-to-head data from SURMOUNT-5 has shown tirzepatide produces greater average weight loss than semaglutide when compared directly. (See: Jastreboff AM et al., Tirzepatide Once Weekly for the Treatment of Obesity, NEJM 2022, and Wilding JPH et al., Once-Weekly Semaglutide in Adults with Overweight or Obesity, NEJM 2021.)
Both medications also improve glycemic control, blood pressure, triglycerides, and—in the SELECT trial for semaglutide—cardiovascular event rates in adults with established cardiovascular disease and obesity without diabetes.
Wegovy is titrated slowly to minimize gastrointestinal side effects. The standard escalation is:
Ozempic (same active ingredient, diabetes labeling) is titrated to 0.5, 1.0, or 2.0 mg weekly.
Zepbound follows a similar titration:
Dose selection is clinical. Higher doses produce greater weight loss on average but also greater rates of GI side effects. A skilled clinician titrates to the lowest dose that produces durable results.
The most common side effects of both tirzepatide and semaglutide are gastrointestinal:
Less common but clinically important:
Both medications carry a boxed warning regarding thyroid C-cell tumors observed in rodents. They are contraindicated in patients with a personal or family history of medullary thyroid carcinoma or MEN 2.
TrufaMED offers GLP-1 and dual-agonist therapy only within a supervised physician-led program. That means:
Medical weight management at TrufaMED is a concierge medicine service integrated with our broader preventive and metabolic programs.
Pricing for GLP-1 and tirzepatide therapy varies with insurance coverage, pharmacy source, and dose. At TrufaMED we provide transparent program pricing at consult and work with each patient to identify the most appropriate sourcing strategy. Program components include the physician consult, laboratory work, medication prescription, structured follow-up, and adjunctive IV support as indicated.
If you are evaluating tirzepatide or semaglutide, the first step is a proper medical workup—not a prescription. Call (305) 537-6396 or book online to schedule a physician consult at TrufaMED.
On average, tirzepatide produces greater weight loss than semaglutide in clinical trials. Individual response varies, and the most effective medication is the one a patient tolerates and can sustain under physician supervision.
Gastrointestinal: nausea, vomiting, diarrhea or constipation, and abdominal discomfort—most pronounced during titration. Slow titration and dietary adjustments reduce severity.
Wegovy titrates from 0.25 mg weekly at initiation through 0.5, 1.0, and 1.7 mg at four-week intervals, reaching 2.4 mg weekly maintenance by approximately week 17.
Duration is individualized. Some patients transition to a maintenance dose after reaching goal weight; others taper under supervision. Abrupt discontinuation frequently leads to weight regain, which is why a planned maintenance strategy is part of every TrufaMED program.
Rapid weight loss from any cause can reduce lean mass. Resistance training, adequate protein intake (1.2–1.6 g/kg/day for most patients), and appropriate micronutrient support mitigate this. TrufaMED builds these elements into every program.
Coverage for the medication itself depends on the patient’s plan and the indication. The TrufaMED concierge program components (consult, follow-up, IV support) are offered as elective services.