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Drug Details
YUTOPAR
- Drug Class Description
b-agonists (beta-agonists, beta- adrenoceptor stimulants). - Generic Name
Ritodrine - Presentation
Yutopar Tablets: Ritodrine hydrochloride 10 mg . Yutopar: Ritodrine hydrochloride 10 mg /mL. - Description
Yutopar Tablets: yellow, scored tablet marked YUTOPAR. Yutopar: ampoule. - Indications
Yutopar Tablets: Follow-on to Yutopar
Tablets: Follow-on to parenteral therapy to maintain uterine quiescence.
Yutopar: Uncomplicated preterm labour between 24 - 33 weeks gestation. To delay delivery to enable glucocorticosteroids or other measures to be used.
- Adult Dosage
Yutopar Tablets: 1 approximately 30 minutes before termination of intravenous therapy. Maintenance: 1 two hourly for 24 hours, then 1 or 2 four to six hourly.
Yutopar: Initially 50 microgram/ minute intravenously in 5% dextrose solution, increase gradually until control. Usual range, 150 - 350 microgram/ minute. Continue infusion for 12 - 48 hours after contractions have stopped. Use a syringe pump to reduce fluid overload.
- Child Dosage
Not applicable. - Contra Indications
Antepartum haemorrhage, eclampsia, pre-eclampsia, cord compression, foetal death, chorioamnionitis, maternal cardiac disease. - Special Precautions
Avoid fluid overload; keep intravenous fluids to minimum and monitor maternal hydration. Multiple pregnancy, suspected cardiovascular disease, maternal infection, hyperthyroidism, hypertension, diabetes. Monitor maternal and foetal heart rate. - Interactions
MAOIs, tricyclic antidepressants, corticosteroids, sympathomimetics, anaesthetics, K+-depleting diuretics, b- blockers. - Adverse Drug Reactions
Maternal pulmonary oedema (withdraw drug immediately and institute diuretic therapy). Tachycardia, flushing, sweating, nausea, chest pain, arrhythmia, vomiting, rise in blood sugar, tremor, leucopenia and/or agranulocytosis, impaired liver function, raised liver transaminases, enlarged salivary glands, increased amylase