Tesamorelin Tracker: Egrifta Daily Doses | Dose Track
[Tracker · Tesamorelin]

Tesamorelin tracker: daily Egrifta shots, vials and labs

Tesamorelin · daily injection (Egrifta) · Checked

Dose Track reminds you to inject tesamorelin each day, logs the shot with its spot on the abdomen, and counts your Egrifta vials. IGF-1 and glucose results, which the label says are checked during treatment, sit next to your doses.

What is the tesamorelin (Egrifta) schedule?

The Egrifta WR label gives one dose: 1.28 mg injected under the skin of the abdomen once daily. There is no starting dose or step-up schedule. Injection sites are rotated around the abdomen, avoiding scar tissue, bruises and the navel. One 11.6 mg vial covers daily doses for 7 days in a row. Egrifta WR and Egrifta SV are not substitutable.

From the FDA label for Egrifta WR, section 2.1.
ItemWhat the label says
Dose1.28 mg
How oftenOnce daily
RouteSubcutaneous (under the skin)
WhereAbdomen, rotating to different areas of the abdomen
AvoidScar tissue, bruises or the navel
Vial11.6 mg per vial; one vial provides daily doses for 7 consecutive days
TitrationNone given; the label lists a single recommended dosage

The label above is for Egrifta WR (11.6 mg vials). Egrifta SV is a different formulation: 1.4 mg once daily from a 2 mg single-dose vial. The label says the two are not substitutable, so add the one you actually have in Dose Track and log its dose.

What form does tesamorelin come in?

Both Egrifta products are powder vials you prepare before use. An Egrifta WR vial gives daily doses for 7 days in a row; an Egrifta SV vial is one dose. In Dose Track, add the vial with the date you prepared it and set its expiry, and each daily dose comes off it. The label instructions are below.

Egrifta WR 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 an 11.6 mg single-patient-use vial with a multiple-dose diluent. One prepared vial provides daily doses for 7 consecutive days, and any unused solution is thrown away 7 days later (sections 2.2 and 3). The label points patients to the Instructions for Use in the Injection Box.

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

What should you track on tesamorelin?

Each row is something worth writing down for tesamorelin, why it matters for this medicine, and what Dose Track does with it.

What to track on tesamorelin and how Dose Track handles it.
What to trackWhy it mattersIn Dose Track
Daily doseThe Egrifta WR label gives one dose of 1.28 mg once daily, with no step-up schedule (2.1).A daily reminder at your time; one tap to log.
Vial in useOne prepared WR vial covers 7 days in a row, and unused solution is thrown away after 7 days (2.2, 3).Each vial keeps its prepared date and expiry, and counts down as you log.
Abdominal siteThe label rotates sites around the abdomen and avoids scar tissue, bruises and the navel (2.1).Each shot is logged with its abdominal site; the app suggests the next one and warns on reuse.
Injection site reactionsInjection site reactions were the most common side effect in the label's trials (17% vs 6% on placebo).Record a reaction with each shot: redness, swelling, bruising, a lump or itching.
IGF-1The label says IGF-1 is monitored during treatment (5.2).Upload a lab report; IGF-1 is read out and shown next to your doses.
GlucoseThe label says glucose status is checked before starting and during treatment (5.4).Glucose and HbA1c from your labs are charted against your own target range.

Which side effects does the Egrifta WR label list?

In the label's 26-week placebo-controlled trials, the most common reactions were injection site reactions (17% vs 6% on placebo), joint pain (13% vs 11%), pain in the arms or legs (6% vs 5%), muscle pain (6% vs 2%) and swelling of the legs (6% vs 2%). The label also warns about higher IGF-1 levels, fluid retention, raised blood sugar and allergic reactions. There is no boxed warning.

In Dose Track you can log any of these with a severity, and use the quick picks for side effects people on peptides log most: injection-site reaction, tiredness, headache, nausea, flushing and water retention.

Egrifta WR side effects from the FDA label

What if you miss a tesamorelin dose?

The label gives no missed-dose instruction. Missed an Egrifta dose.

A day with no logged shot shows as missed in your history.

More about tesamorelin on Dose Track

Dose Track is a tracking app, not medical advice. It records what you and your prescriber decide; it does not recommend doses. Check any dose change with your prescriber.

Frequently asked questions

Is tesamorelin FDA approved?+
Yes, as Egrifta WR and Egrifta SV, to reduce excess abdominal fat in adults with HIV who have lipodystrophy. The label says it is not for weight loss management.
What is the difference between Egrifta WR and Egrifta SV?+
Egrifta WR is 1.28 mg once daily from an 11.6 mg vial that lasts 7 days. Egrifta SV is 1.4 mg once daily from a 2 mg single-dose vial used right away. The label says they are not substitutable.
Can Dose Track count my Egrifta WR vial over 7 days?+
Yes. Add the vial with the date you prepared it; each daily dose comes off it, and the expiry you set reminds you when it is time for a new one.
Can I see IGF-1 and glucose next to my tesamorelin doses?+
Yes. Upload a lab report as a photo or PDF and the values are added to your timeline next to your doses.

Other peptide trackers

Sources: the FDA label for Egrifta WR (tesamorelin), version of August 3, 2026. Read on DailyMed or the guides linked above; app features checked against the current app.

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