Petition · past parliament
Independent review of oxytocin doses and patient consent in labour induction
Closed
38 signatures
What the petition asks
Dosage practices with synthetic oxytocin (SO) in labour induction commonly exceed the licensed recommendations for dilution & safe increments (that should blend naturally with maternal oxytocin). As such, they risk foetal distress, postpartum haemorrhage, tetanic contractions, ruptured uterus etc.
These unlicensed dosage practices and whether women's consent for them was sought should be subject to an urgent review by experts independent of RCOG. They must investigate how SO is being used in and after labour and whether this is in accordance with the licensed instructions. They should make recommendations to re-introduce best practice in terms of previously proven effective administration and formalise the process of explaining risks, to seek valid, informed consent from pregnant women.
Timeline
| 30 Oct 2019 | Petition opened for signatures |
| 6 Nov 2019 | Closed to new signatures |
Key facts
Signatures
38
Status
Closed
Opened
30 Oct 2019
Closed
6 Nov 2019
Follow this petition
Sign in to get an email when the government responds, a debate is scheduled or held, or the petition closes.
Source: the official petition page. Last checked 15 Jul 2026.