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dc.contributor.authorKARAYAĞMURLU, Ali
dc.contributor.authorKAAN, Hüsna
dc.date.accessioned2021-03-05T07:55:25Z
dc.date.available2021-03-05T07:55:25Z
dc.date.issued2020
dc.identifier.citationKAAN H., KARAYAĞMURLU A., "Successful management of methylphenidate related thrombocytopenia during ADHD treatment: a case report", ANADOLU PSIKIYATRI DERGISI-ANATOLIAN JOURNAL OF PSYCHIATRY, cilt.21, ss.557-560, 2020
dc.identifier.issn1302-6631
dc.identifier.otherav_964c0afc-8c74-42b4-aefc-8d5c922006fc
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/101173
dc.identifier.urihttps://doi.org/10.5455/apd.78877
dc.description.abstractMethylphenidate is an effective and well tolerated agent frequently used in the treatment of attention deficit hyperactivity disorder. Thrombocytopenia is defined as a blood platelet count less than 150,000/mm(3), and is an important hematological side-effect capable of causing mild symptoms or severe complications such as intracranial hemorrhage. Thrombocytopenia may develop in association with various causes, including drug use. There have been very few case reports of thrombocytopenia developing during methylphenidate use, and to the best of our knowledge there have been no reports concerning the management of this side-effect. This report describes the development of thrombocytopenia likely related to methylphenidate therapy in an adolescent with attention deficit hyperactivity disorder and successful management with a safety switch to atomoxetine.
dc.language.isoeng
dc.subjectPsikiyatri
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.titleSuccessful management of methylphenidate related thrombocytopenia during ADHD treatment: a case report
dc.typeMakale
dc.relation.journalANADOLU PSIKIYATRI DERGISI-ANATOLIAN JOURNAL OF PSYCHIATRY
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume21
dc.identifier.issue5
dc.identifier.startpage557
dc.identifier.endpage560
dc.contributor.firstauthorID2195848


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