O conteúdo das evidências é mantido em inglês.

Representação de estrutura idealizada para Carbetocin

Conformador idealizado construído a partir de sequência; não é uma estrutura experimental ou prevista.

Visão rápida

ENTRY TYPE
approved drug
IDENTITY
Sequence verified

No structure asset recorded

TOP EVIDENCE
Grade A — PPH prevention after cesarean section
MAJOR STATUS
Jurisdiction-specific — see status table
SPORT
Prohibited — as of 2026-08-06
VERIFIED
2026-08-06

Bottom line

Carbetocin is a synthetic long-acting oxytocin receptor agonist approved in the EU, UK, Canada, Australia, and many other countries for prevention of postpartum hemorrhage (PPH) after cesarean section or vaginal delivery. Not FDA approved in the United States. Its longer allows a single dose compared to oxytocin continuous infusion. Route varies by jurisdiction and delivery mode: only after cesarean section under spinal/epidural anesthesia (UK Pabal SmPC); IV or after vaginal delivery.

Identity and composition

FieldVerified information
Preferred nameCarbetocin
Key aliasesDurato, Pabal, 1-deamino-1-monocarba-2-(O-methyltyrosine)-oxytocin, long-acting oxytocin analog
Molecular/sequence identity1-deamino-1-monocarba-2-(O-methyltyrosine)-oxytocin: N-(4-mercapto-1-oxobutyl)-Tyr(OMe)-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2. The nonreducible thioether joins the position-1 monocarba group to Cys6 in oxytocin numbering (the FDA GSRS systematic acyl-residue name reports the same closure as cyclic (1→5)-thioether).
Modifications/formOxytocin analog in which the native Cys1 amino group is removed, the Cys1-Cys6 disulfide is replaced by a nonreducible monocarba thioether, and Tyr2 is O-methylated; marketed as an injectable solution. Its formula, C45H69N11O12S, contains one sulfur atom: the molecule has a thioether, not a disulfide.
Stable identifiersUNII: 88TWF8015Y; : 16681432; CAS: 37025-55-1 (base); DrugBank: DB01282
Identity caveatsStructurally distinct from oxytocin — desamino and O-methyl modifications confer longer and enhanced metabolic stability.

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
US (FDA)Not approved2026
EU/EEA (EMA)Approved: PPH prevention after cesarean section under spinal/epidural anesthesiaPabal (Ferring)2007
UK (MHRA)Approved: PPH prevention (cesarean section)Pabal2007
Canada (Health Canada)Approved: PPH prevention after cesarean/vaginal deliveryDurato
Australia (TGA)Approved: PPH preventionPabal
Status is multi-axis
Carbetocin authorization and sport-status profileFour medicine-authorization axes reproduce only documented status rows; sport status is shown separately.UNITED STATESNot approvedSOURCE / AS OFROW 1 / 2026EU/EEAApproved: PPH prevention aftercesarean section underSOURCE / AS OFROW 2 / 2007UNITED KINGDOMApproved: PPH prevention(cesarean section)SOURCE / AS OFROW 3 / 2007OTHER DOCUMENTED2 status rows — see tableApproved: PPH prevention afterSOURCE / AS OFROW 4 / —SPORT STATUS — SEPARATE FROM MEDICINE AUTHORIZATIONWADA: carbetocin was not identified by exact name in the 2026 Prohibited List, and thisreview did not identify a matching prohibited class. Therapeutic purpose does not itself
Authorization belongs to the named product, use, place, and date; sport status is independent.
Alternativa em texto
UNITED STATES
US (FDA): Not approved
EU/EEA
EU/EEA (EMA): Approved: PPH prevention after cesarean section under spinal/epidural anesthesia
UNITED KINGDOM
UK (MHRA): Approved: PPH prevention (cesarean section)
OTHER DOCUMENTED
Canada (Health Canada): Approved: PPH prevention after cesarean/vaginal delivery; Australia (TGA): Approved: PPH prevention

Sport status: WADA: carbetocin was not identified by exact name in the 2026 Prohibited List, and this review did not identify a matching prohibited class. Therapeutic purpose does not itself create an exemption from a prohibition; athletes should verify the exact product and current status.

Mechanism and pharmacology

Oxytocin receptor agonist. Binds to uterine oxytocin receptors, stimulating rhythmic contractions of the uterine smooth muscle. The desamino and O-methyl modifications increase metabolic stability compared to oxytocin, providing a longer duration of action. Single-dose therapy sufficient for PPH prevention.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
PPH prevention after cesarean sectionApproved (EU, CN, AU)A and meta-analyses (Su LL, et al. BJOG. 2012;119:5–12. PMID: 22017979)Single dose carbetocin non-inferior or superior to oxytocin infusion for PPH (need for additional uterotonics reduced)Distinguished in specific settings; effect size modest
PPH prevention after vaginal deliveryApproved (Canada, AU)BRCTsComparable to oxytocin; possibly fewer additional uterotonicsLess studied for vaginal delivery
Graus de evidência
  • AGrau A: Estabelecido para um uso rotulado específico
  • BGrau B: Evidência humana moderada
  • CGrau C: Evidência humana preliminar
  • DGrau D: Apenas pré-clínico
  • EGrau E: Alegação anedótica/de marketing
  • XGrau X: A evidência contradiz ou não apoia a alegação
Saiba mais sobre a classificação de evidências
Claim-evidence profile
Carbetocin claim-evidence profileA: 1 claim; B: 1 claim; C: 0 claims; D: 0 claims; E: 0 claims; X: 0 claimsCONTRADICTORY / NON-SUPPORTIVEA — Established for a specific labeled useGrade A: Established for a specific labeled use — current approval plus adequate controlled trials and post-market context.1 claimPPH prevention after cesarean sectionB — Moderate human evidenceGrade B: Moderate human evidence — multiple controlled studies or a strong pivotal study, but no current approval for the claim.1 claimPPH prevention after vaginal deliveryC — Preliminary human evidenceGrade C: Preliminary human evidence — small, uncontrolled, surrogate-endpoint, or early-phase studies.0 claimsD — Preclinical onlyGrade D: Preclinical only — in vitro or animal evidence with no adequate human efficacy evidence.0 claimsE — Anecdotal/marketing claimGrade E: Anecdotal/marketing claim — testimonials, extrapolation, or vendor claims without adequate scientific support.0 claimsX — Evidence contradicts or does not support the claimGrade X: Evidence contradicts or does not support the claim — adequate negative evidence, failed program, or claim inconsistent with the studied material.0 claims
This counts the page's claim rows; it does not average them into a score.
Alternativa em texto

Text alternative for the claim-evidence diagram. Each grade is defined below:

AEstablished for a specific labeled use
1 claim: PPH prevention after cesarean section
BModerate human evidence
1 claim: PPH prevention after vaginal delivery
CPreliminary human evidence
0 claims
DPreclinical only
0 claims
EAnecdotal/marketing claim
0 claims
XEvidence contradicts or does not support the claim
0 claims
United StatesNot approved
EU/EEAApproved: PPH prevention after cesarean section under spinal/epidural anesthesia
United KingdomApproved: PPH prevention (cesarean section)
OtherApproved: PPH prevention after cesarean/vaginal deliveryApproved: PPH prevention

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
CHAMPION (Widmer M, et al. Lancet. 2018;392:1361–9. PMID: 30322456), N=29,645, vaginal delivery (heat-stable carbetocin, 10 countries)Heat-stable carbetocin 100 mcg vs oxytocin 10 IU IMBlood loss ≥500 mL: 14.5% vs 14.4% (non-inferior)Heat-stable formulation; resource-variable settings

Dose and administration evidence

Approved labeled regimen

The label summary below is product-, indication-, and jurisdiction-specific; consult the full current label and a licensed clinician/pharmacist.

PPH prevention after cesarean section (UK Pabal SmPC): 100 mcg (1 mL) only, as single dose after delivery of the infant, under spinal/epidural anesthesia. Administer slowly IV over 1 minute. PPH prevention after vaginal delivery: 100 mcg (1 mL) IV or as single dose.

Studied regimens (not recommendations)

  • CHAMPION: 100 mcg IM heat-stable carbetocin after vaginal delivery.

  • Standard carbetocin: 100 mcg IV/IM single dose.

What is not established

  • Treatment of established PPH (only prevention is labeled).

  • Repeat dosing (not studied for continued hemorrhage).

  • No established or recommended human dose for unapproved indications.

Safety

Established label risks

  • Uterine hyperstimulation: Transient; similar to oxytocin.

  • Cardiovascular: Hypotension, tachycardia, flushing (less than oxytocin).

  • GI: Nausea, vomiting, abdominal pain.

  • Water intoxication: Less risk than oxytocin (less antidiuretic effect).

  • Hypersensitivity: Rare.

Human-study signals

  • CHAMPION: similar safety profile to oxytocin; no new signals.

Unknowns and product-quality risks

  • No data on use in third trimester of pregnancy before delivery.

  • Research-grade vials not equivalent to pharmaceutical carbetocin.

Interactions and special populations

  • Prostaglandins: additive uterotonic effect (monitor).

  • Vasopressors: additive pressor effect.

  • Contraindicated in hepatic disease, renal disease, and serious cardiovascular disorders (per UK Pabal SmPC).

  • Caution in preeclampsia, cardiovascular disease.

Regulatory, compounding, and sport notes

  • : carbetocin was not identified by exact name in the 2026 Prohibited List, and this review did not identify a matching prohibited class. Therapeutic purpose does not itself create an exemption from a prohibition; athletes should verify the exact product and current status.

  • Not scheduled under US CSA.

  • Not FDA approved; any US-sourced vial is unapproved.

Evidence gaps

  • Comparative efficacy vs oxytocin for PPH treatment (not prevention).

  • Optimal storage conditions for non-heat-stable formulations.

  • Efficacy in high-risk PPH populations.

Search notes

  • Databases and registries: EMA, TGA, PubMed, ClinicalTrials.gov

  • Search terms: carbetocin, Durato, Pabal, postpartum hemorrhage, oxytocin analog

  • Last searched: 2026-08-06

  • Inclusion emphasis: Regulatory status, pivotal trials, meta-analyses

Sources

  1. UK electronic Medicines Compendium. Pabal 100 micrograms in 1ml solution for injection (SmPC). https://www.medicines.org.uk/emc/product/172/smpc

  2. Widmer M, et al. Heat-stable carbetocin vs oxytocin for PPH prevention (CHAMPION). Lancet. 2018;392(10152):1361–9. PMID: 30322456.

  3. Su LL, et al. Carbetocin for preventing PPH (meta-analysis). BJOG. 2012;119(1):5–12. PMID: 22017979.

  4. DrugBank. Carbetocin. https://go.drugbank.com/drugs/DB01282

  5. PubChem. Carbetocin. https://pubchem.ncbi.nlm.nih.gov/compound/16681432

  6. World Anti-Doping Agency. 2026 Prohibited List. https://www.wada-ama.org/sites/default/files/2025-09/2026list_en_final_clean_september_2025.pdf

  7. FDA GSRS. Carbetocin (UNII 88TWF8015Y): the systematic acyl-residue name reports cyclic (1→5)-thioether, corresponding to the position-1-to-Cys6 closure in oxytocin numbering; the formula contains one sulfur atom. https://precision.fda.gov/uniisearch/srs?search=88TWF8015Y

Vozes de especialistas

O que dizem os especialistas

Os comentários são opiniões e não fazem parte da revisão de evidências; a inclusão não significa endosso.

Nenhum comentário de especialista verificado foi encontrado para este composto nas fontes que este atlas aceita — literatura revisada por pares, comunicações universitárias, hospitalares e de sociedades médicas, reguladores e jornalismo científico com autoria nominal.

A ausência de comentários não é evidência a favor ou contra o composto.

Alegações de fornecedores, clínicas e redes sociais são excluídas por política e não são contabilizadas como comentários.

Nenhum vídeo de especialista verificado foi encontrado para este composto nas fontes deste atlas.

A ausência de vídeos não é evidência a favor ou contra o composto.

Vídeos de fornecedores e redes sociais são excluídos por política e não são contabilizados.

Questões

Is carbetocin FDA-approved?

No. Carbetocin (Pabal or Durato) is not FDA-approved in the United States. It is approved in the EU, UK, Canada, and Australia for prevention of postpartum hemorrhage in specified obstetric settings. Its longer half-life allows a single administration compared to oxytocin continuous administration.

What evidence supports carbetocin for PPH prevention?

For cesarean section, a cited meta-analysis reported carbetocin as non-inferior or superior to oxytocin for the studied outcomes. The CHAMPION trial (PMID: 30322456) found heat-stable carbetocin non-inferior to oxytocin for prevention of postpartum hemorrhage after vaginal birth.

What are carbetocin's main safety signals?

Risks include transient uterine hyperstimulation, hypotension, tachycardia, flushing, nausea, vomiting, and abdominal pain. Water intoxication risk is lower than with oxytocin. Per the UK Pabal SmPC, it is contraindicated in hepatic disease, renal disease, and serious cardiovascular disorders. The monograph says carbetocin was not identified by exact name in the 2026 WADA list and that its review found no matching prohibited class.

Why does the exact product and formulation matter when reading carbetocin evidence?

Carbetocin is structurally distinct from oxytocin — the native Cys1 amino group is removed, the disulfide bridge is replaced by a nonreducible thioether, and Tyr2 is O-methylated. These modifications confer a longer half-life and enhanced metabolic stability. Research-grade vials are not equivalent to pharmaceutical carbetocin.

Does the strongest evidence grade on this page establish approval for every carbetocin use?

No. The strongest claim (PPH prevention after cesarean section, Grade A) reflects approved use in the EU, UK, Canada, and Australia. The evidence table also records a Grade B claim for vaginal delivery, approved in Canada and Australia but less studied. Carbetocin is not FDA-approved and has no established dose for unapproved indications.

What remains unknown about carbetocin?

Comparative efficacy versus oxytocin for treatment of established PPH remains an evidence gap; only prevention is labeled. Optimal storage conditions for non-heat-stable formulations and efficacy in high-risk PPH populations also remain evidence gaps. The monograph reports no data on use in the third trimester before delivery.

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