COMPARISON

Octreotide vs Terlipressin

6 attributes held for at least one of the two. 6 differ. Each value carries the register it came from and the date that register was read.

Answer

Octreotide is authorised or registered in 10 and Terlipressin in 8 of the 10 registers read. Octreotide: highest phase Phase 4 (after approval). Terlipressin: highest phase Phase 3 (2 phase 3 trials, 0 with posted results). 10 registered trials include both.

States no view on which is preferable, safer or more effective. Not medical advice.

OctreotideTerlipressin
Registered trials
differs
344
clinicaltrials.gov · 2026-10-03
118
clinicaltrials.gov · 2026-10-03
FDA label
differs
FDA-approved: Octreotide Acetate
openfda · 2026-10-03T17:23:44.062Z
FDA-approved: Terlivaz
openfda · 2026-10-03T17:23:44.062Z
EU authorisation
differs
Authorised
ema · 2026-10-03
Nothing on record
ema read 2026-08-31
EU authorised on
differs
2025-06-30
ema · 2026-10-03
Not checked
no record of "authorisedOn" for terlipressin
EU withdrawn on
differs
2022-12-02
ema · 2026-10-03
Not checked
no record of "withdrawnOn" for terlipressin
ATC code
differs
H01CB02
ema · 2026-10-03
Not checked
no record of "atcCode" for terlipressin

SIDE EFFECTS

Most common side effects, each beside its own placebo

Side effectOctreotideplaceboTerlipressinplacebo
Diarrhoea46.2%31.7%16.4%5.7%
Nausea30.8%21.2%15.0%11.3%
Dyspnoea25.9%9.1%12.3%6.7%
Oedema peripheral34.9%19.6%--
Asthenia33.3%20.9%--
Fatigue29.8%27.7%--
Rash28.8%14.1%--
Decreased appetite28.5%15.2%--
Hypertension26.5%19.4%--
Anaemia24.3%9.1%--
Abdominal pain--21.8%13.4%
Hypotension--11.3%6.7%
Respiratory failure--10.5%3.0%
Vomiting--8.9%7.2%
Hypokalaemia--8.9%6.2%
Hepatic encephalopathy--8.5%11.3%
Fluid overload--8.2%4.1%

Trial register Octreotide: 5 placebo-controlled trials; Terlipressin: 2. Each peptide is compared with placebo in its own trials, not with the other: a dash means the event is not in that peptide's top list. Octreotide side effects · Terlipressin side effects

LEGAL STATUS

Approval in each country read

CountryOctreotideTerlipressinRegister
United StatesFDA-approvedFDA-approvedRegulator FDA
European UnionAuthorisedNot on the registerRegulator EMA
United KingdomAuthorisedAuthorisedRegulator MHRA
CanadaAuthorisedNot on the registerRegulator Health Canada
AustraliaRegisteredRegisteredRegulator TGA
SwitzerlandAuthorisedAuthorisedRegulator Swissmedic
BrazilRegistadoRegistadoRegulator ANVISA
SerbiaAuthorisedAuthorisedRegulator ALIMS
SingaporeRegisteredRegisteredRegulator HSA
TurkeyRuhsatliRuhsatliRegulator TITCK

HEAD TO HEAD

10 registered trials include both

NCT07460908Comparison of Terlipressin Versus Octreotide in Patients With Hepatorenal Syndrome
COMPLETED · updated 2026-03-10
NCT04028323Functional MRI-based Assessment of Terlipressin vs. Octreotide on Renal Function in Cirrhotic Patients With Acute Variceal Bleeding (CHESS1903)
UNKNOWN · updated 2021-08-17
NCT04353193Hemodynamic Profile of Terlipressin and Octreotide in Patients With Cirrhosis and Portal Hypertension. A Randomised, Single Blinded Clinical Trial.
UNKNOWN · updated 2020-04-20
NCT03846180Terlipressin on Effect of Renal Function in Cirrhotic Patients With Acute Gastrointestinal Hemorrhage
COMPLETED · updated 2019-07-05
NCT01370161Early TIPS With Polytetrafluoroethylene (PTFE) Covered Stents for Acute Variceal Bleeding in Patients With Advanced Cirrhosis
COMPLETED · updated 2019-01-17
NCT00966355Comparison of Terlipressin, Somatostatin, and Octreotide for Control of Variceal Bleeding
COMPLETED · updated 2018-03-19
NCT02119884Hemodynamic Effects of Terlipressin and High Dose Octreotide
COMPLETED · updated 2016-06-13
NCT02311608Effects of Terlipressin When Usual Somatostatin or Octreotide Dose Fails
UNKNOWN · updated 2014-12-08
NCT00742339Terlipressin + Albumin Versus Midodrine + Octreotide in the Treatment of Hepatorenal Syndrome
TERMINATED · updated 2014-10-15
NCT00534677The Safety & Efficacy of Terlipressin vs Octreotide for the Control of Variceal Bleed
COMPLETED · updated 2007-12-05

Values reproduce public registers on the dates shown. This comparison states no view on which compound is preferable, safer or more effective. Not medical, legal or regulatory advice.

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