Tesamorelin
Visceral-fat treatment with a narrow approved indication.
The short version
- Why people discuss it
- Egrifta WR is approved to reduce excess abdominal fat in adults with HIV-associated lipodystrophy. Community discussion also focuses on abdominal fat and body recomposition outside that indication; those uses are not established by the label.
- What it is
- A growth hormone-releasing factor analog. Egrifta WR and Egrifta SV have different doses and preparation instructions and are not substitutable.
- Biggest caution
- Contraindications include active cancer, pregnancy, relevant pituitary-axis disruption and hypersensitivity. Long-term cardiovascular safety is not established; the full label covers monitoring and other risks.
- Stack context
- The approved indication does not establish a general fat-loss stack. No community combination is verified in this entry.
Dose and frequency reference
Reference only — not a recommendation. Amounts describe source-specific community examples, selected study regimens or the named product label. They do not establish safety, effectiveness, product identity, or a suitable dose for any person. Never convert mg, mcg, or IU into syringe “units” without the exact product concentration.
Sources report different amounts or schedules; the reference below is a named example, not a consensus.
Egrifta WR subcutaneous injection
Approved label · Product-specific- Amount
- 1.28 mg
- Frequency
- Once daily
- Duration / phase
- Ongoing with response review
Egrifta WR only, for HIV-associated lipodystrophy. WR 1.28 mg, SV 1.4 mg and the original 2 mg formulation are not interchangeable dose entries. General weight-loss or community cycling claims do not change the product label. Reference only; this does not establish safety, effectiveness or individual suitability.
Reference source · reviewed 2026-09-27Compare reported schedules
Saved source material reviewed 2026-09-27. Multiple pages from one publisher count as one source family; agreement does not establish what most people use. SC means subcutaneous; IM intramuscular; IP intraperitoneal.
- PeptideDosages — saved source reviewed September 27, 2026
Protocol 1 mg week 1 then 2 mg daily, 12–26 weeks; overview also names SV 1.4 mg and WR 1.28 mg.
- Peptidepedia — saved source reviewed September 27, 2026
SV 1.4 mg daily; off-label 1–1.4 mg; continuous treatment versus discretionary cycles.
Evidence & sources · Approved product label
Community references document claims and reported practices. They are not clinical evidence. Some references contain supplier promotions or market treatment; their commercial context is identified in the source label.
- Current Egrifta WR prescribing informationProduct label · Checked 2026-09-27
- Egrifta WR manufacturer dosing informationManufacturer update · Checked 2026-09-12
- PeptideDosages — saved source reviewed September 27, 2026Community reference · Checked 2026-09-27
- Peptidepedia — saved source reviewed September 27, 2026Community reference · Checked 2026-09-27