Also called: teduglutide
Teduglutide is a man-made copy of a natural body chemical called GLP-2, a hormone made in the gut. It is a real medicine that has been approved for use in people.
It is given as a shot under the skin. It is used mostly by people with short bowel syndrome, a serious condition where a person has lost a large part of their intestine, often from surgery or disease.
These people often cannot get enough food and water on their own and need feeding through a vein, called parenteral nutrition.
Benefits
The benefits people report — backed by research.
You just read the research on Teduglutide. The cheat-sheet maps the most-used peptide stacks — doses, timing, and what to check before buying — on one page.
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1 reported routine — each line links to the source it came from.
Self-reported & vendor-suggested
Routines shared by users and sellers in forums and product pages — anecdotal, not tested in clinical trials. We show them for completeness, not as a recommendation.
SubQ
mg vs mcg: one milligram (mg) equals 1,000 micrograms (mcg) — multiply by 1,000 going from mg to mcg, divide by 1,000 going from mcg to mg. Mixing the two up is a thousand-fold dosing error: 1 mg taken instead of 1 mcg is a 1,000× overdose; 1 mcg instead of 1 mg is a 1,000× underdose. Always double-check the unit label and the decimal place.
Safety
Adverse effects reported in the research and by community use.
Reported in research and community sources — not exhaustive. Discontinue use and consult a healthcare professional if side effects occur.
Compare research-grade suppliers with third-party COAs and published purity data. For in-vitro and laboratory research use only — not for human consumption, diagnosis, or treatment.
Evidence
Every claim above traces back to a source you can check — here are 2 of them.
Randomised placebo-controlled trial of teduglutide in reducing parenteral nutrition and/or intravenous fluid requirements in patients with short bowel syndrome.
Teduglutide reduces need for parenteral support among patients with short bowel syndrome with intestinal failure
News
Dated, sourced reporting that mentions Teduglutide.
An updated review in Current Gastroenterology Reports (July 2016, Carroll and Benedetti) walks the complications and management ladder of short bowel syndrome - from diet and antisecretory drugs to growth factors - and places teduglutide as the enteral-trophic option for patients still dependent on IV nutrition.
The STEP trial (Gut, July 2011, Jeppesen et al.) randomized short-bowel patients to teduglutide - a GLP-2 analog - or placebo and showed a meaningful share of treated patients reduced or ended parenteral nutrition and fluid support, the result that underpinned the medicine's approvals (Gattex/Revestive) for intestinal failure.
This interim analysis of a 36-month post-marketing surveillance program reports real-world safety and effectiveness of teduglutide in 92 adults and children with short bowel syndrome in Japan (all patients who started treatment August 2021-August 2022). At 6 months, the overall mean change in parenteral nutrition dose was about -2402 mL/week, and 42.4% of patients (39/92) achieved at least a 20% reduction in parenteral-support volume. The paper notes teduglutide was approved in the USA and Europe in 2012 and in Japan in 2021 as the first GLP-2 analogue promoting intestinal adaptation.
Takeda announced that FDA approved extending the GATTEX (teduglutide) indication to pediatric patients 1 year of age and older with short bowel syndrome who depend on parenteral support. The approval was supported by a 24-week pediatric study (NCT02682381) in 59 patients aged 1-17. In the study, 69% (18/26) of patients on GATTEX 0.05 mg/kg/day reduced parenteral-support volume by 20% or more, and 3 of 26 (12%) weaned off parenteral support entirely.
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