Adverse Effects of Atosiban
Atosiban has a favorable safety profile with minimal maternal-fetal side effects compared to other tocolytic agents, with the most common adverse effects being injection site reactions, nausea, vertigo, and transient flushing.
Common Adverse Effects
- Injection site reactions occur in 5-20% of patients receiving atosiban 1, 2
- Nausea, vertigo, and flushing may occur during initial bolus administration in approximately 20% of patients, typically lasting only 1-2 minutes 1
- Vomiting may occasionally occur during treatment 3
- Headache has been reported in some patients 4
Timing and Frequency of Adverse Effects
- Most adverse effects are observed during the initial bolus administration (20.2% of patients) 1
- During continuous infusion, drug-related side effects decrease significantly to approximately 6% of patients 1
- The majority of side effects are mild and transient, rarely requiring discontinuation of therapy 4
Comparison with Other Tocolytics
- Atosiban demonstrates significantly fewer maternal and fetal adverse events compared to beta-agonists and other tocolytic agents 5, 2
- Unlike beta-agonists such as hexoprenaline, atosiban rarely causes:
Rare Adverse Effects
- Dysguesia (altered taste) has been reported in rare cases 4
- Chest pain has been reported in isolated cases 4
- Diarrhea may occur in some patients 3
Special Considerations
- In patients treated before 24 weeks gestation, there have been reports of higher fetal-infant deaths compared to placebo, though data at this gestational age are inconclusive 6
- For gestational ages ≥28 weeks, infant morbidity and mortality rates with atosiban are similar to those with placebo-initiated standard care 6
Monitoring Recommendations
- Monitor for injection site reactions, particularly during initial administration 1, 2
- Observe for signs of nausea, vertigo, and flushing during bolus administration 1
- No specific laboratory monitoring is required during atosiban therapy 1, 5