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AvonoHealth
For men & womenODT

Microdose Tirzepatide ODT

Avono's lower-dose, needle-free compounded tirzepatide program in an oral-dissolving format.

Active ingredients: Tirzepatide

$239 per month

No membership fee · No clinician fee · Free shipping

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Compounded and not FDA-approved. Custom low dosing and a compounded ODT format both have less direct obesity-outcome evidence than standard FDA-approved injectable tirzepatide.

What it does

Tirzepatide is a dual GIP/GLP-1 receptor agonist. It acts on two incretin-hormone pathways involved in appetite and metabolism. It is not a sex hormone or steroid.

What's in it

Tirzepatide

What it is
Tirzepatide is a dual GIP/GLP-1 receptor agonist.
Hormone?
Acts on hormone signaling
Why it's here
It acts on two incretin-hormone pathways involved in appetite and metabolism.
What to know
It is not a sex hormone or steroid.

Why choose this one?

Why choose this one

For people prioritizing both injection avoidance and Avono's lower-dose tirzepatide program.

Why choose another option?

This combines a lower-dose strategy with a compounded oral-dissolving format. Do not borrow efficacy numbers from standard injectable tirzepatide trials.

Compare your options

Semaglutide vs tirzepatide

SemaglutideTirzepatide
Treatment typeGLP-1 receptor agonistDual GIP/GLP-1 receptor agonist
Who it's forMen & womenMen & women
FormatsInjection, oral capsule, microdose injection and ODTInjection, oral capsule, microdose injection and ODT
Why choose itLongest track record; a heart-outcomes trial (SELECT) in people with heart diseaseGreater average weight loss in the head-to-head SURMOUNT-5 trial
What to knowLess average weight loss than tirzepatide in SURMOUNT-5Shorter track record in weight management
Common side effectsNausea, diarrhea, vomiting, constipationNausea, diarrhea, vomiting, constipation
Evidence contextSTEP 1: 14.9% average weight loss over 68 weeks (semaglutide 2.4 mg)SURMOUNT-1: 15.0% to 20.9% over 72 weeks, by dose; SURMOUNT-5: 20.2% vs 13.7% for semaglutide
Price at AvonoFrom $159 per monthFrom $219 per month

Figures come from trials of FDA-approved products and doses, not compounded formulations.

Benefits and evidence

Evidence for Tirzepatide, not for this exact formula

SURMOUNT-1: tirzepatide 5, 10, 15 mg

What the study found
15.0% to 20.9%
Who was studied
2,539 adults with overweight or obesity, without diabetes
What it means
In SURMOUNT-1, studied tirzepatide doses produced average weight reductions of 15.0% to 20.9% over 72 weeks.
Important context
These findings apply to the formulations, doses and population studied and are not a prediction of results from an Avono compounded treatment. Once-weekly subcutaneous tirzepatide · 5 mg, 10 mg or 15 mg once weekly · 72 weeks
Source
Tirzepatide Once Weekly for the Treatment of Obesity N Engl J Med, 2022, PMID 35658024

Evidence for Tirzepatide, not for this exact formula

SURMOUNT-5: tirzepatide vs semaglutide

What the study found
20.2% vs 13.7%
Who was studied
751 adults with obesity, without diabetes
What it means
In the first head-to-head trial, adults taking tirzepatide lost more weight on average than those taking semaglutide over 72 weeks.
Important context
Compared the maximum tolerated doses of FDA-approved products in an open-label trial. It does not show that compounded versions produce the same results. Once-weekly subcutaneous tirzepatide vs semaglutide · Tirzepatide 10 or 15 mg; semaglutide 1.7 or 2.4 mg · 72 weeks
More about the evidence

Evidence for compounded ODT tirzepatide and custom low-dose strategies is limited compared with FDA-approved injectable tirzepatide.

Sources
  1. Zepbound (tirzepatide) prescribing information, DailyMed
  2. Jastreboff AM et al. Tirzepatide Once Weekly for the Treatment of Obesity (SURMOUNT-1). N Engl J Med. 2022
  3. Aronne LJ et al. Continued Treatment With Tirzepatide for Maintenance of Weight Reduction (SURMOUNT-4). JAMA. 2024
  4. Aronne LJ et al. Tirzepatide as Compared with Semaglutide for the Treatment of Obesity (SURMOUNT-5). N Engl J Med. 2025
  5. He L et al. GLP-1 receptor agonist use and risk of gallbladder and biliary diseases: systematic review and meta-analysis. JAMA Intern Med. 2022

Common side effects

Nausea, vomiting, diarrhea, constipation, abdominal discomfort and reflux are among the most common effects.

What may help

Stomach-related side effects are usually most noticeable when starting treatment or after a dose increase, and often ease over time. General measures that may help:

  • Eat smaller meals and stop when you first feel full.
  • Eat slowly, and avoid lying down right after eating.
  • Go easier on greasy, fried or very rich foods if they make symptoms worse.
  • Drink fluids steadily through the day, especially if you have vomiting or diarrhea.
  • For constipation, fluids and fiber-containing foods may help.
  • Include protein at meals and keep up regular activity, including strength exercise if it is appropriate for you, to help protect muscle during weight loss.

Do not change your dose or stop treatment on your own. If symptoms persist or get in the way of eating and drinking, your clinician can review your plan.

Important safety information

Pregnancy and fertility. Not for use during pregnancy. Tirzepatide can make birth-control pills less effective: the FDA label for Zepbound advises switching to a non-oral method, or adding a barrier method, for 4 weeks after starting and after each dose increase. Tell your clinician if you are pregnant, planning a pregnancy or breastfeeding.

Compounded and lower-dose use is not FDA-approved for weight management. Clinical review is required. Tirzepatide has important warnings and contraindications, including thyroid C-cell tumor risk language, MEN2/personal or family MTC history, pancreatitis, gallbladder disease, severe GI effects, dehydration/kidney risk and pregnancy considerations.

This is a compounded medication. Compounded medications are prepared by licensed pharmacies and are not FDA-approved.

Compounded semaglutide and tirzepatide are prepared by licensed pharmacies and are not FDA-approved. FDA does not review compounded drugs for safety, effectiveness or quality before they are marketed. Available by prescription only, following evaluation by a licensed clinician. Not appropriate for everyone and not available in all states. Individual results vary.

When to contact your clinician

Contact your clinician promptly if you have vomiting or diarrhea that does not settle, signs of dehydration (dizziness, very dark urine, passing little urine), or symptoms that stop you eating or drinking.

Before any surgery or procedure that uses sedation, tell the care team you take a GLP-1 medication.

When to seek urgent care

Seek urgent care for severe stomach pain that does not go away (with or without vomiting), pain in the upper right abdomen with fever or yellowing of the skin or eyes, a lump or swelling in the neck with trouble swallowing or persistent hoarseness, or signs of a serious allergic reaction such as swelling of the face, lips or throat or difficulty breathing.

What you may have heard about GLP-1s

Nausea, vomiting, diarrhea and constipation

What people hear. GLP-1s make everyone sick.

What the evidence shows. Stomach-related side effects are the most common. In the approved-product trials, nausea affected 44% of people on semaglutide 2.4 mg (16% on placebo) and 25% to 29% on tirzepatide (8% on placebo). Most cases were mild to moderate, happened during dose increases and often eased with time.

What may help. Smaller meals, eating slowly and stopping when you first feel full. Going easier on greasy or very rich foods. Steady fluids, and fiber with fluids for constipation. Clinicians may slow the pace of dose increases.

When to contact a clinician. Vomiting or diarrhea that does not settle, signs of dehydration such as dizziness or very dark urine, or being unable to keep fluids down.

Muscle and lean-mass loss

What people hear. You lose muscle, not fat.

What the evidence shows. Most weight lost in the trials was fat. In body-composition substudies of STEP 1 and SURMOUNT-1, lean mass fell by about 10% while fat mass fell more (about 19% and 34%), so the share of lean mass in the body went up. Scans count water and organ tissue as lean mass too, not only muscle. Some lean-mass loss happens with most significant weight loss, and how much it affects strength and function is still being studied.

What may help. Protein at every meal, regular strength training if it is appropriate for you, and staying active. Your clinician can suggest what fits your health.

When to contact a clinician. Noticeable weakness, falls, or trouble with everyday activities.

Bone density and fractures

What people hear. GLP-1s weaken your bones.

What the evidence shows. Significant weight loss by any method can be accompanied by some loss of bone density, partly because bones carry less load and partly because nutrition and body composition change. In one randomized trial, adults taking the GLP-1 medicine liraglutide alone lost some hip and spine bone density, while those who combined it with regular exercise did not. Bone-density changes are not the same as fractures, and evidence on fracture risk with GLP-1 treatment is limited and mixed.

What may help. Weight-bearing and strength exercise if appropriate, and enough protein, calcium and vitamin D from food or as your clinician recommends.

When to contact a clinician. A history of osteoporosis or fractures, a fall, or new bone pain.

Gallbladder problems

What people hear. GLP-1s cause gallstones.

What the evidence shows. Rapid weight loss itself raises gallstone risk. A 2022 analysis of 76 randomized trials found GLP-1 medicines were linked to a higher relative risk of gallbladder and bile-duct problems (about 37% higher overall), with more risk at higher doses, longer use and weight-loss doses. These events were still uncommon.

What may help. Knowing the warning signs matters most. Tell your clinician if you have had gallstones before.

When to contact a clinician. Pain in the upper right or middle of the abdomen, especially after eating, fever, or yellowing of the skin or eyes. Severe pain needs urgent care.

Pancreatitis

What people hear. GLP-1s cause pancreatitis.

What the evidence shows. Acute pancreatitis is listed as a warning on the labels. Large randomized trials have generally not shown a clear increase, while some observational studies have: a 2023 insurance-claims study of people using GLP-1 medicines for weight loss reported a higher rate than with another weight-loss medicine, though events were rare and the estimate was uncertain. The risk appears uncommon.

What may help. Tell your clinician about any history of pancreatitis, gallstones, heavy alcohol use or very high triglycerides.

When to contact a clinician. Severe, persistent pain in the upper abdomen that may spread to your back, with or without vomiting, needs urgent care.

Delayed stomach emptying and severe stomach symptoms

What people hear. GLP-1s paralyze your stomach.

What the evidence shows. Slowing stomach emptying is part of how these medicines reduce appetite. Severe or persistent symptoms are uncommon but have been reported, and the same 2023 claims study reported higher rates of gastroparesis and bowel obstruction diagnoses, based on small numbers. The labels warn about severe stomach reactions, and the medicines are not recommended for people with severe gastroparesis.

What may help. Small meals and stopping when full. Tell the care team before any surgery or procedure that uses sedation, because food may stay in the stomach longer.

When to contact a clinician. Vomiting that will not stop, being unable to keep food or fluids down, severe bloating or abdominal pain, or no bowel movement with pain.

Hair shedding

What people hear. GLP-1s make your hair fall out.

What the evidence shows. Hair loss was reported slightly more often than with placebo in the approved-product trials: about 3% vs 1% with semaglutide 2.4 mg, and 4% to 5% vs 1% with tirzepatide. Shedding after rapid or large weight loss (telogen effluvium) is a recognized pattern with weight loss of any cause and is usually temporary.

What may help. Enough protein and a balanced diet, gentle hair care, and patience: this kind of shedding usually settles within months.

When to contact a clinician. Heavy or patchy hair loss, or shedding that lasts more than about six months.

Stopping treatment and weight regain

What people hear. The weight all comes back when you stop.

What the evidence shows. Often a good part of it does. One year after stopping semaglutide in the STEP 1 extension, participants had regained about two-thirds of the weight they had lost. In SURMOUNT-4, people switched from tirzepatide to placebo regained about 14% of body weight over the next year, while those who continued kept losing. Obesity behaves like a long-term condition.

What may help. Planning with your clinician for what comes next, and building eating and activity habits during treatment that you can keep.

When to contact a clinician. Before stopping or changing treatment, or if cost or side effects make continuing hard.

The thyroid warning

What people hear. GLP-1s cause thyroid cancer.

What the evidence shows. Semaglutide and tirzepatide carry a boxed warning because they caused thyroid C-cell tumors in rodents. It is not known whether they cause these tumors in people. They are not used in anyone with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 (MEN 2).

What may help. Share your personal and family history during intake so the clinician can check.

When to contact a clinician. A lump or swelling in the neck, trouble swallowing, persistent hoarseness or shortness of breath.

Questions people ask

What is microdosing?

Microdosing uses the same molecule and receptor but follows a lower-dose strategy than standard evidence-based obesity regimens.

Does microdosing have the same evidence?

No. A lower custom dose should not be presented as proven to produce the same weight-loss outcomes as standard FDA-approved obesity dosing. Weight-loss effectiveness at custom microdoses is less established.

Why do I feel nauseated?

These medicines slow how quickly the stomach empties and act on appetite signals. Nausea was the most common side effect in the approved-product trials: 44% with semaglutide 2.4 mg versus 16% with placebo, and 25% to 29% with tirzepatide versus 8% with placebo. It is usually worst during dose increases and often improves. Smaller meals and eating slowly may help. Vomiting that does not settle needs medical review.

Will I lose muscle?

In body-composition substudies of the STEP 1 (semaglutide) and SURMOUNT-1 (tirzepatide) trials, most of the weight lost was fat, but lean mass also fell by about 10% from where participants started. Some lean-mass loss happens with most significant weight loss, whatever the method. Getting enough protein and doing regular strength exercise may help preserve muscle; ask your clinician what is appropriate for you.

Does weight come back after stopping a GLP-1?

Often, yes. One year after stopping semaglutide in the STEP 1 extension, participants had regained about two-thirds of the weight they had lost. In SURMOUNT-4, people who switched from tirzepatide to placebo regained about 14% of body weight over the next year, while those who continued kept losing. Obesity behaves like a long-term condition, so plans for staying on, tapering or stopping are worth discussing with your clinician.

Can GLP-1s cause hair loss?

Hair shedding was reported more often with the approved products than with placebo (about 3% vs 1% for semaglutide 2.4 mg, and 4% to 5% vs 1% for tirzepatide). Shedding after rapid or large weight loss (telogen effluvium) is a known pattern with weight loss generally and is usually temporary. Tell your clinician if shedding is heavy or lasts more than a few months.

Discuss Microdose Tirzepatide ODT with a licensed clinician

Your clinician reviews your health history and decides whether this option, or another, is appropriate.

$239 per month

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