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- Uterine relaxant
- Threatened premature labour (preferably use nifedipine for this indication)
Forms and strengths, route of administration
- 0.5 mg in 1 ml ampoule (0.5 mg/ml) for IV infusion
- Dilute 5 mg (10 ampoules of 0.5 mg) in 500 ml of 5% glucose or 0.9% sodium chloride to obtain a solution of 10 micrograms/ml.
- Start infusion at the rate of 15 to 20 micrograms/minute (30 to 40 drops/minute).
- If contractions persist, increase the rate by 10 to 20 drops/minute every 30 minutes until uterine contractions cease. Do not exceed 45 micrograms/minute (90 drops/minute).
- Continue for one hour after contractions have ceased, then reduce the rate by half every 6 hours.
- 48 hours maximum
Contra-indications, adverse effects, precautions
- Do not administer to patients with pre-eclampsia, eclampsia, uterine haemorrhage, intra-uterine infection, intra-uterine foetal death, placenta praevia, placental abruption, rupture of membranes, multiple pregnancy, severe cardiopathy.
- Administer with caution to patients with diabetes, hyperthyroidism.
- Do not combine with nifedipine.
- May cause: pulmonary oedema, myocardial ischemia, foetal and maternal tachycardia, hypotension, tremor, headache, hypokalaemia, hyperglycaemia.
- Monitor maternal pulse regularly. Reduce the infusion rate in the event of maternal tachycardia (> 120/minute).
- Pregnancy: no contra-indication
- Breast-feeding: avoid
- Use salbutamol within 24 hours of mixing with infusion fluid.
- Do not mix with other drugs in the same infusion fluid.
- Also comes in 5 ml ampoule containing 0.25 mg (0.05 mg/ml).
– Below 25 °C