Oxytocin
Oxytocin Grindeks · ATC code H01BB02
Also known as: Oksitosin, Ossitocina, Ocytocine, Oxitocina · Brand names: Oxytocin Hexal, Oxytocin Panpharma, Oxytocin Grindeks, Oksitosel, Postuitrin Fort, Synpitan Forte, Uvera
- Key facts
- Active substance
- Oxytocin
- ATC code
- H01BB02
- Authorisation
- authorised nationally; no central EU authorisation
- Information as of
- 2026-11-06
Key facts
Oxytocin is a synthetic posterior pituitary hormone that stimulates uterine contractions. Per the US label it is used for medically indicated induction or stimulation of labour and to control postpartum bleeding; it is not for elective induction.
What it is used for
- Induction of labour with a medical indication (e.g. Rh problems, maternal diabetes, pre-eclampsia at or near term, prematurely ruptured membranes)
- Stimulation or reinforcement of labour in selected cases of uterine inertia
- Adjunct in incomplete or inevitable abortion
- Uterine contractions in the third stage of labour and control of postpartum bleeding
Dosing
- Labour: intravenous infusion only, with an infusion pump and monitoring of contractions and fetal heart rate
- Usual solution: 1 mL (10 units) in 1,000 mL of non-hydrating diluent (10 mU/mL)
- Start with no more than 1 to 2 mU/min; increase in increments of no more than 1 to 2 mU/min until a normal labour pattern is reached
- Postpartum bleeding: 10 to 40 units in 1,000 mL infused at the rate needed to control uterine atony, or 1 mL (10 units) intramuscularly after delivery of the placenta
- Incomplete or inevitable abortion: 10 units in 500 mL saline or dextrose-saline at 20 to 40 drops/minute
Contraindications
- Significant cephalopelvic disproportion; unfavourable fetal positions such as transverse lie
- Obstetric emergencies favouring surgery; fetal distress when delivery is not imminent
- Hypertonic uterine patterns; prolonged use in uterine inertia or severe toxaemia
- Vaginal delivery contraindicated (cord presentation or prolapse, total placenta previa, vasa previa)
- Hypersensitivity to the drug
Important warnings
- For labour only intravenously, in hospital, under continuous observation by trained staff
- Uterine overstimulation, tetanic contractions and rupture; stop the infusion at once in hyperactivity or fetal distress
- Avoid except in unusual circumstances: prematurity, previous Caesarean section or major uterine surgery, uterine overdistension, grand multiparity
- Antidiuretic effect: water intoxication, especially with continuous infusion and oral fluids
Side effects
- Mother: anaphylaxis, postpartum haemorrhage, arrhythmias, nausea, vomiting, pelvic haematoma, fatal afibrinogenaemia
- Severe water intoxication with convulsions and coma
- Fetus or infant: bradycardia, arrhythmias, brain damage, fetal death; neonatal retinal haemorrhage and jaundice
Interactions
- Severe hypertension when given three to four hours after a prophylactic vasoconstrictor with caudal block anaesthesia
- Cyclopropane anaesthesia: hypotension, maternal sinus bradycardia
Pregnancy and breastfeeding
- No known use in the first and second trimester other than in abortion; not expected to cause fetal abnormalities when used as indicated
- Excretion in human milk unknown; caution when breastfeeding
Summary of the official product information, written with AI on 2026-11-14. Every number was checked automatically against the original text. Not reviewed by a physician – the full official text is authoritative.
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For patients
Patient information (US)
This product has no separate US patient information.
Authorisation and brand names by country
Medicines with exactly this active-substance composition, as listed in the national registers – alphabetical and without ranking. Whether a product is currently available is not shown here.
Germany
- Oxytocin HexalHexal Ag · 1 register entry
- Oxytocin PanpharmaPanpharma Gmbh · 1 register entry
Source: EMA – Article 57 product data (EU/EEA), as of 2026-11-06
Austria
- Oxytocin GrindeksGrindeks · 1 register entry
Source: EMA – Article 57 product data (EU/EEA), as of 2026-11-06
Turkey
- OksitoselHAVER FARMA İLAÇ A.Ş. · 1 register entry
- Postuitrin FortMENARİNİ SAĞLIK VE İLAÇ SAN. TİC. A.Ş. · 1 register entry
- Synpitan ForteDEVA HOLDİNG A.Ş. · 3 register entries
- UveraVEM İLAÇ SAN. VE TİC. A.Ş. · 1 register entry
Source: TİTCK – Ruhsatlı Beşeri Tıbbi Ürünler Listesi, as of 2026-11-06
Brand names in 25 more European countries
- Belgium
- Oxytocin Grindeks, Syntocinon
- Bulgaria
- Окситоцин Pихtep
- Croatia
- Syntocinon
- Cyprus
- Syntocinon
- Czechia
- Ofost, Oxytocin Avmc
- Denmark
- Oxytocin Orifarm, Syntocinon
- Estonia
- Oxytocin Grindeks
- Finland
- Oxytocin Orifarm, Syntocinon
- France
- Oxytocine Ever Pharma, Oxytocine Grindeks, Oxytocine Medisol, Oxytocine Panpharma, Syntocinon
- Greece
- Oxytocin Gap
- Hungary
- Oxytocin Grindeks, Oxytocin Panpharma, Oxytocin Richter Gedeon
- Ireland
- Ofost, Oxytocin Pinewood Laboratories
- Italy
- Ossitocina Grindeks, Syntocinon
- Latvia
- Ofost, Oxytocin Grindeks
- Lithuania
- Ofost, Oxytocin Grindeks
- Malta
- Oxytocin Wockhardt, Syntocinon
- Netherlands
- Syntocinon
- Norway
- Oxytocin Cd Pharma, Oxytocin Orifarm
- Poland
- Oxytocin Grindeks, Oxytocin Grindex, Oxytocin Richter
- Portugal
- Oxitocina Generis, Oxitocina Grindeks, Oxitocina Hikma, Syntocinon
- Romania
- Ofost, Oxitocină Panpharma
- Slovakia
- Ofost, Oxygrindeks
- Slovenia
- Ofost, Syntocinon
- Spain
- Oxitocina Grindeks
- Sweden
- Oxytocin Cd Pharma, Oxytocin Grindeks, Oxytocin Pilum
EMA – Article 57 product data (EU/EEA), 2026-11-06
Medelix receives no money from pharmaceutical companies. Brand names are listed alphabetically and without ranking.
Another question about this substance?
Medelix answers clinical questions from guidelines, studies and product information – every claim with its source.
Sources
- U.S. Food and Drug Administration. Oxytocin (Fresenius Kabi USA, LLC) – Prescribing Information, 2026-01-12. DailyMed (NLM), 2026-11-06. https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c7fd585a-99b7-4309-b003-a6cbef05372c
- EMA – Article 57 product data (EU/EEA), 2026-11-06. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- EMA – Article 57 product data (EU/EEA), 2026-11-06. https://www.ema.europa.eu/en/human-regulatory-overview/post-authorisation/data-medicines-iso-idmp-standards-post-authorisation/public-data-article-57-database
- TİTCK – Ruhsatlı Beşeri Tıbbi Ürünler Listesi, 2026-11-06. https://www.titck.gov.tr/dinamikmodul/85
Editorial: Medelix editorial team · last updated 2026-11-06 · How these pages are made · Report an error
Source: U.S. Food and Drug Administration (FDA), prescribing information, via DailyMed (NLM); public domain. Not advertising, not a treatment recommendation. For questions about your own treatment, ask your doctor or pharmacist.