Egrifta SV Dosing Schedule: 1.4 mg Daily Per the Label
[Dosing schedule · Egrifta SV]

Egrifta SV dosing schedule

tesamorelin · once-daily injection · Label checked

Short answer: The Egrifta SV label gives one dose: 1.4 mg injected under the skin of the abdomen once daily. There is no starting dose or step-up schedule. Each 2 mg vial is single-dose: the dose is given right after the vial is prepared and anything left is thrown away. Injection sites are rotated around the abdomen, avoiding scar tissue, bruises and the navel.

This is what the FDA label says. Follow your prescriber. Your prescriber may use a different dose or pace than the label's standard schedule.

What Egrifta SV is approved for: Egrifta SV is approved to reduce excess abdominal fat in adults with HIV who have lipodystrophy. The label says it is not for weight loss management, its long-term heart and blood vessel safety has not been established, and there are no data that it improves how well people take their HIV medicines (section 1).

Source
EGRIFTA SV (tesamorelin) for injection, prescribing information and Patient Information. Theratechnologies. DailyMed, version published July 31, 2026. DailyMed setid 3d783378-b02d-4f19-99dd-0fc91a042224

How is Egrifta SV taken?

Egrifta SV is injected under the skin (subcutaneously) into the abdomen once a day. The label says to rotate injection sites to different areas of the abdomen and not to inject into scar tissue, bruises or the navel (section 2.1).

It comes as a 2 mg single-dose vial with Sterile Water for Injection as the diluent (section 3). The dose is given immediately after the vial is prepared; any unused solution is thrown away, and prepared solution is never stored, frozen or refrigerated (section 2.2). The label points patients to the Instructions for Use in the Medication Box.

The Patient Information says never to share an Egrifta SV syringe or needles with anyone, even if the needle has been changed.

What is the Egrifta SV dosing schedule on the label?

The table below is the label's schedule, from the Dosage and Administration section. Numbers are copied exactly; the section is in brackets.

Built from the text of section 2.1 [Section 2.1]
ItemWhat the label says
Dose1.4 mg
How oftenOnce daily
RouteSubcutaneous (under the skin)
WhereAbdomen, rotating to different areas of the abdomen
AvoidScar tissue, bruises or the navel
Vial2 mg single-dose vial; given immediately after it is prepared, unused solution thrown away
TitrationNone given; the label lists a single dose

Other dosing rules on the label

  • Section 2.1

    The dose of Egrifta SV is 1.4 mg injected subcutaneously once daily. The label gives no other dose and no step-up schedule.

  • Section 2.1

    The label's dosing applies only to the 2 mg per vial formulation. It says the tesamorelin formulations and strengths differ in dosage, the number of vials needed for a dose, preparation and storage.

  • Section 5.2

    IGF-1 levels are monitored during treatment. Stopping is considered in people whose IGF-1 stays high (for example above 3 SDS), particularly if the response is not robust.

  • Section 5.4

    Glucose status is checked before starting and periodically during treatment. If glucose intolerance or diabetes develops, stopping is considered in people without a clear response. People with diabetes may need changes to their diabetes medicines (section 17).

  • Section 1

    Because long-term heart safety is not established, the label says to weigh the risk and benefit of continuing in people who have not had a reduction in visceral (deep belly) fat.

  • Section 5.7

    Stopping Egrifta SV is considered in critically ill patients.

  • Section 4

    Egrifta SV is not used during pregnancy; the label says to stop it if pregnancy occurs (section 17). Mothers on Egrifta SV are told not to breastfeed.

What does the label say about a missed dose?

  • No rule

    The label gives no missed-dose instruction.

What does the label say about switching?

  • Section 2.1

    The Egrifta SV dosing covers only the 2 mg per vial formulation. For the 1 mg per vial formulation, the label points to the EGRIFTA prescribing information, because the formulations differ in dosage, number of vials per dose, preparation and storage.

How can Dose Track follow this schedule?

In Dose Track you set up Egrifta SV as a protocol with the dose and schedule your prescriber gave you. A protocol can hold dose steps, each with its own dose and length in days or weeks, so a step-up plan like the one on the label can be entered once and the app moves to the next step on its own. Reminders follow the schedule, and every dose is logged with the date and time, so you can see which step you are on and when your last dose was. The app follows what you enter; it does not choose or change a dose.

This page is what the FDA label says, in plain words. It is not medical advice. Follow your prescriber, and ask them or your pharmacist about anything here.

Dosing schedules for similar medicines

Frequently asked questions

What is the dose of Egrifta SV?+
1.4 mg injected under the skin of the abdomen once daily (section 2.1). The label lists this single dose with no starting dose or titration steps.
Can an Egrifta SV vial be saved for the next day?+
No. Egrifta SV comes in a 2 mg single-dose vial. The label says to give the dose immediately after preparing it and throw away any unused solution, and not to freeze or refrigerate the prepared solution (sections 2.2 and 3).
How should Egrifta SV vials be stored?+
The Patient Information says to keep the 2 mg vials in their Medication Box at room temperature, 20°C to 25°C (68°F to 77°F), out of the light, and not to use them after the expiration date.
Where is Egrifta SV injected?+
Into the abdomen, rotating to different areas of the abdomen with each dose, and never into scar tissue, bruises or the navel (section 2.1). The label ties site rotation to fewer injection site reactions (section 5.6).