Syntocinon Side Effects
Generic name: oxytocin
Medically reviewed by Drugs.com. Last updated on Jun 10, 2024.
Note: This document provides detailed information about Syntocinon.
Applies to oxytocin: parenteral injection Side Effects associated with oxytocin. Some dosage forms listed on this page may not apply specifically to the brand name Syntocinon.
Applies to oxytocin: parenteral injection.
Side effects include:
Adverse effects usually are dose related.
Uterine hyperstimulation and subsequent fetal heart rate deceleration most common. (See Uterine Hyperactivity under General Precautions.)
Maternal nausea, vomiting, sinus bradycardia, premature ventricular complexes; probably related to labor and not the drug.
Neonatal hyperbilirubinemia, jaundice, retinal hemorrhage, low Apgar scores at 5 minutes.
For healthcare professionals
Applies to oxytocin: compounding powder, injectable solution, intravenous solution.
General adverse events
The more commonly reported adverse effects have included headache, tachycardia, bradycardia, nausea and vomiting.[Ref]
Cardiovascular
- Common (1% to 10%): Tachycardia, bradycardia
- Frequency not reported: Premature ventricular contractions, hypertensive episodes, cardiac arrhythmia, bradycardia (neonate), premature ventricular contractions and other arrhythmias (neonate)
- Postmarketing reports: Myocardial ischemia, QTc prolongation, hypotension, flushing[Ref]
Bradycardia and premature ventricular contractions and other arrhythmias have been reported in the neonate due to induced uterine motility.[Ref]
Nervous system
- Common (1% to 10%): Headache
- Frequency not reported: Subarachnoid hemorrhage, permanent CNS or brain damage (neonate), neonatal seizures[Ref]
Permanent CNS or brain damage, and seizures have been reported in the neonate due to induced uterine motility.[Ref]
Metabolic
- Frequency not reported: Severe water intoxication with convulsions, coma, fatal water intoxication
- Postmarketing reports: Maternal hyponatremia, neonatal hyponatremia[Ref]
Hypersensitivity
- Frequency not reported: Anaphylactic reaction
- Postmarketing reports: Anaphylactic reaction and shock[Ref]
Genitourinary
- Frequency not reported: Uterine Rupture, pelvic hematoma, postpartum hemorrhage
- Postmarketing reports: Uterine hypertonicity, tetanic contractions, rupture of the uterus; fetal distress (neonate), amniotic fluid embolism[Ref]
Hematologic
- Frequency not reported: Fatal afibrinogenemia
- Postmarketing reports: Disseminated intravascular coagulation[Ref]
Hepatic
- Frequency not reported: Neonatal jaundice[Ref]
Neonatal jaundice has been reported in the neonate due to use of oxytocin in the mother.[Ref]
Gastrointestinal
- Common (1% to 10%): Nausea, vomiting[Ref]
Respiratory
- Postmarketing reports: Acute pulmonary edema, asphyxia (neonate)
Ocular
- Frequency not reported: Neonatal retinal hemorrhage[Ref]
Neonatal retinal hemorrhage has been reported in the neonate due to use of oxytocin in the mother.[Ref]
Other
- Frequency not reported: Fetal death, low Apgar scores at 5 minutes
Fetal death has been reported due to induced uterine motility; low Apgar scores at 5 minutes have been reported in the neonate due to oxytocin use in the mother.
Dermatologic
- Postmarketing reports: Angioedema
References
1. (2001) "Product Information. Syntocinon (oxytocin)." Sandoz Pharmaceuticals Corporation
2. Cerner Multum, Inc. "UK Summary of Product Characteristics."
3. Cerner Multum, Inc. "Australian Product Information."
4. (2004) "Product Information. Pitocin (oxytocin)." Pfizer U.S. Pharmaceuticals Group
More about Syntocinon (oxytocin)
- Check interactions
- Compare alternatives
- Dosage information
- During pregnancy
- Drug class: uterotonic agents
- Breastfeeding
Patient resources
Other brands
Professional resources
Other brands
Related treatment guides
Further information
Syntocinon side effects can vary depending on the individual. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
Note: Medication side effects may be underreported. If you are experiencing side effects that are not listed, submit a report to the FDA by following this guide.