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Reprod Toxicol ; 76: 103-108, 2018 03.
Article in English | MEDLINE | ID: mdl-29378258

ABSTRACT

OBJECTIVE: The 2014 report by European Medicines Agency (EMA) restricted the use of thiocolchicoside for all reproductive-age women. In this study, we aim to expand the systematically-collected human data and discuss it within the frame provided by this report. METHODS: We identified and evaluated the outcomes of 48 prospectively recorded pregnancies referred to Terafar (Teratology Information Service, Izmir, Turkey). RESULTS: Of 42 pregnancies with first-trimester exposure and known outcomes, 31 resulted in live births, four in miscarriage and seven ended with elective terminations. There were 26 normal outcomes, two major and three minor congenital malformations among the live births. CONCLUSIONS: Despite a number of limitations, our results and previous case series collectively strengthen the view that thiocolchicoside is unlikely to be a major teratogen. EMA's 2014 report should be revised to reflect this finding, while current restrictions on use should continue until more detailed safety information is available.


Subject(s)
Colchicine/analogs & derivatives , Maternal Exposure/adverse effects , Neuromuscular Agents/toxicity , Pregnancy Outcome , Prenatal Exposure Delayed Effects/chemically induced , Teratogens/toxicity , Colchicine/toxicity , Female , Humans , Pregnancy , Pregnancy Outcome/epidemiology , Prenatal Exposure Delayed Effects/epidemiology , Prospective Studies
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