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Idealisierte Strukturdarstellung für Oxytocin

Aus der Sequenz aufgebautes idealisiertes Konformer; keine experimentell bestimmte oder vorhergesagte Struktur.

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ENTRY TYPE
approved drug
IDENTITY
Sequence verified

No structure asset recorded

TOP EVIDENCE
Grade A — Labour induction/augmentation
MAJOR STATUS
Jurisdiction-specific — see status table
SPORT
Prohibited — as of 2026-08-06
VERIFIED
2026-08-06

Bottom line

Oxytocin is an cyclic nonapeptide hormone and is approved in multiple named jurisdictions for product-specific pharmaceutical (Pitocin, Syntocinon) for obstetric use — labour induction/augmentation and control of postpartum haemorrhage. It is on the WHO Model List of Essential Medicines. In obstetric settings it carries important warnings about uterine hyperstimulation, water intoxication, and is not indicated for elective induction. Off-label use for neuropsychiatric conditions (social cognition, autism) has failed to show benefit in large .

Identity and composition

FieldVerified information
Preferred nameOxytocin
Key aliasesPitocin, Syntocinon, Ocytocin
Molecular/sequence identityCys-Tyr-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH₂ (cyclic nonapeptide; disulfide bridge Cys¹–Cys⁶)
Modifications/formC-terminal amide; disulfide bridge between residues 1 and 6
Stable identifiersCAS 50-56-6; 439302; DrugBank DB00107; UNII 1JQS135EYN; ATC H01BB02; ChEBI CHEBI:7872; KEGG D00089
Identity caveats hormone identical across most mammals; differs from vasopressin at positions 3 (Ile vs Phe) and 8 (Leu vs Arg)

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
FDA (US)Approved — labour induction/augmentation, postpartum haemorrhage, adjunct in incomplete/inevitable abortionPitocin (Par Pharmaceutical)1938+ (DESI)
EMA (EU)Approved — same obstetric indicationsSyntocinon (Novartis)Approved
MHRA (UK)Approved — sameSyntocinonApproved
WHOListed — Essential Medicine for postpartum haemorrhageVariousCurrent
Status is multi-axis
Oxytocin authorization and sport-status profileFour medicine-authorization axes reproduce only documented status rows; sport status is shown separately.UNITED STATESApproved — labourinduction/augmentation,SOURCE / AS OFROW 1 / 1938+ (DESI)EU/EEAApproved — same obstetricindicationsSOURCE / AS OFROW 2 / ApprovedUNITED KINGDOMApproved — sameSOURCE / AS OFROW 3 / ApprovedOTHER DOCUMENTEDListed — Essential Medicine forpostpartum haemorrhageSOURCE / AS OFROW 4 / CurrentSPORT STATUS — SEPARATE FROM MEDICINE AUTHORIZATIONWADA: not prohibited
Authorization belongs to the named product, use, place, and date; sport status is independent.
Textalternative
UNITED STATES
FDA (US): Approved — labour induction/augmentation, postpartum haemorrhage, adjunct in incomplete/inevitable abortion
EU/EEA
EMA (EU): Approved — same obstetric indications
UNITED KINGDOM
MHRA (UK): Approved — same
OTHER DOCUMENTED
WHO: Listed — Essential Medicine for postpartum haemorrhage

Sport status: WADA: not prohibited

Mechanism and pharmacology

Oxytocin is a full agonist at the oxytocin receptor (OTR), a rhodopsin-type GPCR. Activation triggers Gq/PLC → IP₃ → intracellular Ca²⁺ release from stores plus store-operated and voltage-operated Ca²⁺ entry, increasing sodium permeability of uterine myofibrils and causing smooth muscle contraction. Uterine sensitivity to oxytocin increases with gestational age. Oxytocin also triggers milk ejection by contracting mammary myoepithelial cells. The mechanism is well-characterised and high confidence.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
Labour induction/augmentationApproved (global)AMultiple ; FDA labelEffective for cervical ripening and uterine contractionRequires continuous monitoring; hospital setting only
Postpartum haemorrhage preventionApproved (global)AWHO recommendations; multiple RCTsFirst-line uterotonic; reduces PPH risk~10% PPH rate persists with oxytocin alone
Autism spectrum disorder (social function) (off-label)XSOARS-B (NIH RCT)No improvement in social functionNegative; large well-powered trial
Social cognition (healthy)Investigational (off-label)DMixed small studiesInconsistent effectsUnderpowered; varied tasks
Evidenzgrade
  • AKlasse A: Für eine bestimmte gekennzeichnete Anwendung nachgewiesen
  • BKlasse B: Mäßige Humanstudien
  • CKlasse C: Vorläufige Humanstudien
  • DKlasse D: Nur präklinisch
  • EKlasse E: Anekdotisch/Vermarktungsbehauptung
  • XKlasse X: Die Evidenz widerspricht der Behauptung oder stützt sie nicht
Mehr über die Evidenzbewertung erfahren
Claim-evidence profile
Oxytocin claim-evidence profileA: 2 claims; B: 0 claims; C: 0 claims; D: 1 claim; E: 0 claims; X: 1 claimCONTRADICTORY / 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.2 claimsLabour induction/augmentationPostpartum haemorrhage preventionB — Moderate human evidenceGrade B: Moderate human evidence — multiple controlled studies or a strong pivotal study, but no current approval for the claim.0 claimsC — 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.1 claimSocial cognition (healthy)E — 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.1 claimAutism spectrum disorder (social function)
This counts the page's claim rows; it does not average them into a score.
Textalternative

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

AEstablished for a specific labeled use
2 claims: Labour induction/augmentation; Postpartum haemorrhage prevention
BModerate human evidence
0 claims
CPreliminary human evidence
0 claims
DPreclinical only
1 claim: Social cognition (healthy)
EAnecdotal/marketing claim
0 claims
XEvidence contradicts or does not support the claim
1 claim: Autism spectrum disorder (social function)
United StatesApproved — labour induction/augmentation, postpartum haemorrhage, adjunct in incomplete/inevitable abortion
EU/EEAApproved — same obstetric indications
United KingdomApproved — same
OtherListed — Essential Medicine for postpartum haemorrhage

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
SOARS-B (NCT01944046) autism in children (n≈290)Intranasal oxytocin vs No improvement in social functioningDefinitive negative trial
WHO PPH guidelineSystematic reviewVarious oxytocin regimensRecommended as first-line uterotonicEvidence well-established
StatPearls (NCBI)Comprehensive reviewComplete safety/efficacy summaryReview; PMID 29939625

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.

FDA-approved regimens (Pitocin):

Studied regimens (not recommendations)

Intranasal oxytocin has been studied for off-label psychiatric indications at doses of 8–40 IU per dose, with no established efficacy.

What is not established

  • Safe or effective dose for any non-obstetric indication

  • Long-term safety of chronic intranasal use

  • Optimal regimen for postpartum haemorrhage in resource-limited settings

Safety

Established label risks

FDA boxed warning: Not indicated for elective induction of labour. Available data are inadequate to evaluate benefits-to-risks for elective induction.

Major warnings:

Contraindications: Significant cephalopelvic disproportion, unfavourable fetal positions, fetal distress, hyperactive uterus, conditions contraindicating vaginal delivery (invasive cervical carcinoma, active herpes genitalis, total placenta previa, vasa previa, cord prolapse), hypersensitivity.

Human-study signals

Well-characterised in obstetric populations. For intranasal off-label use in psychiatric conditions, the SOARS-B trial and other large have not shown safety concerns distinct from .

Unknowns and product-quality risks

  • Extemporaneously compounded intranasal oxytocin for non-obstetric use lacks standardisation

  • Chronic use effects on oxytocin system unknown

  • Reproductive safety in first-trimester non-obstetric use not evaluated

  • Research-chemical oxytocin products lack sterility and potency assurance

Interactions and special populations

  • Potentiated by prostaglandins; combination may cause uterine hyperstimulation

  • Cyclopropane anaesthesia: possible maternal bradycardia/hypotension

  • Caution in severe pre-eclampsia, cardiovascular disease, cervical surgery

  • Not for use in first trimester except for abortion

Regulatory, compounding, and sport notes

  • : not prohibited

  • US DEA: not scheduled

  • Reviewed obstetric products are prescription medicines in the cited jurisdictions; historical intranasal lactation-aid products and current scheduling vary by market and must be checked product by product

  • Compounded intranasal oxytocin for off-label psychiatric use is not FDA-reviewed

Evidence gaps

  • The obstetric evidence base is substantial but not “complete”; important product-, population-, and outcome-specific gaps remain. Off-label neuropsychiatric efficacy is a major unresolved area

  • Intranasal oxytocin dose-response and central penetration are poorly characterised after decades of study

  • Sex differences in response not systematically addressed

  • Long-term effects of synthetic oxytocin on oxytocin system unknown

  • Conflicting small studies on social cognition have not resolved whether meaningful effects exist in any subpopulation

Search notes

  • Databases and registries: PubMed, FDA Drugs@FDA, DailyMed, WHO EML, ClinicalTrials.gov

  • Search terms: Oxytocin, Pitocin, Syntocinon, 50-56-6, labour induction, SOARS-B, postpartum haemorrhage

  • Last searched: 2026-08-06

  • Inclusion emphasis: regulatory labels, large , systematic reviews

Sources

  1. FDA label: Pitocin (oxytocin injection). Drugs@FDA.

  2. PubChem CID 439302. https://pubchem.ncbi.nlm.nih.gov/compound/439302

  3. DrugBank DB00107. https://go.drugbank.com/drugs/DB00107

  4. SOARS-B Trial. NIH. ClinicalTrials.gov NCT01944046.

  5. WHO Model List of Essential Medicines. https://www.who.int/groups/expert-committee-on-selection-and-use-of-essential-medicines

  6. StatPearls (NCBI). Oxytocin. PMID 29939625

Expertenstimmen

Was Experten sagen

Kommentare sind Meinungen und nicht Teil der Evidenzprüfung; eine Aufnahme bedeutet keine Befürwortung.

Thousands of children with autism spectrum disorder were prescribed intranasal oxytocin before it was adequately tested

Jeremy Veenstra-VanderWeeleM.D.New York State Psychiatric Institute and Columbia UniversityDuke Department of Psychiatry & Behavioral SciencesAccessed 2026-08-09

Videos

Fragen

Is oxytocin FDA-approved?

Yes. Oxytocin (Pitocin) is FDA-approved for labour induction/augmentation, postpartum haemorrhage, and as an adjunct in incomplete/inevitable abortion. It is also EMA- and MHRA-approved for the same obstetric indications and is listed on the WHO Model List of Essential Medicines.

What does the evidence show for oxytocin and social cognition in autism?

The SOARS-B trial (NCT01944046, n≈290), a large well-powered RCT, found no improvement in social function with oxytocin nasal spray in children with autism. This is graded X (negative, well-powered trial). Other small studies on social cognition in healthy adults show inconsistent effects.

Is oxytocin the same as vasopressin?

No. Oxytocin and vasopressin are both cyclic nonapeptides but differ at positions 3 (Ile vs Phe) and 8 (Leu vs Arg). They act on different receptors and have distinct physiological roles: oxytocin in parturition and lactation, vasopressin in vasoconstriction and water reabsorption.

What are oxytocin's main safety signals?

Oxytocin carries an FDA boxed warning that it is not indicated for elective induction of labour. Major risks include uterine hyperstimulation leading to fetal distress, water intoxication during prolonged high exposure, and maternal hypotension when given too rapidly. Evidence for psychiatric uses remains off-label; see the monograph's safety and label summaries.

Is oxytocin prohibited in sport?

Oxytocin is not prohibited by WADA. It is not a controlled substance under US DEA scheduling. The reviewed obstetric products are prescription medicines in the cited jurisdictions.

How well does oxytocin reach the brain when given by nasal spray?

Oxytocin dose-response and central penetration by the nasal route are poorly characterised after decades of study. A safe or effective dose for any non-obstetric indication has not been established, and extemporaneously compounded nasal-spray products lack standardisation. Sex differences in response have not been systematically addressed. No approved product exists for any psychiatric or social indication.

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