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Teduglutide

Also called Gattex, Revestive, ALX-0600

Subcutaneous (under the skin)Product label

Research reference

Product label

Gattex short-bowel schedule

0.05 mg/kg once daily; 0.025 mg/kg for specified kidney impairment

Long-term specialist monitoring, not a fixed repair cycle

Gattex product label ↗

When results may show

When change was measured
Parenteral support, fluid balance, GI examinations and bilirubin/pancreatic laboratory checks require a clinical team.
When to assess
Long-term specialist monitoring, not a fixed repair cycle
Conditions and limitations
Adults and children age ≥1 with short bowel syndrome requiring parenteral support. Exact kit preparation and baseline screening are necessary. No body-weight-to-fixed-dose conversion or generic mixing instructions are supplied.
When to stop
Use the exact product's clinical monitoring and stopping instructions. A supply interval is not a stop date; severe or persistent reactions need prompt clinical review.

Research timing is descriptive, not a promise or personal instruction. A severe or persistent reaction needs prompt clinical review. This is not medical advice.

Vial arithmetic

Published research contexts for Teduglutide describe 3–4 mg per administration. Descriptive only, not a recommendation.

Modelled level — every day

1× is the peak after a single dose.

Steady-state peak
1.00× single dose

Read off the modelled curve, not an even-interval formula

Time to steady state
10hours

About five half-lives

Administrations
7/ week

Where these numbers come from

  • Gattex product labelExact kit preparation and baseline screening are necessary. No body-weight-to-fixed-dose conversion or generic mixing instructions are supplied.

Next steps

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