Sa\u011fl\u0131k Bakanl\u0131\u011f\u0131 T\u00fcrkiye \u0130la\u00e7 ve T\u0131bbi Cihaz Kurumu (T\u0130TCK) taraf\u0131ndan haz\u0131rlanan y\u00f6netmelik de\u011fi\u015fikli\u011fi kapsam\u0131nda bundan b\u00f6yle ila\u00e7 kutular\u0131nda ila\u00e7lar\u0131n isimleri, g\u00f6rme engelliler i\u00e7in ayn\u0131 zamanda Braille format\u0131nda kabartma yaz\u0131 ile yaz\u0131lacak.<\/p>\n
“Be\u015feri T\u0131bbi \u00dcr\u00fcnlerin Ambalaj Bilgileri, Kullanma Talimat\u0131 ve Takibi Y\u00f6netmeli\u011fi”nde de\u011fi\u015fiklik yap\u0131lmas\u0131na ili\u015fkin y\u00f6netmelik, Resmi Gazete’de yay\u0131mland\u0131.<\/p>\n
Y\u00f6netmelikle a\u015f\u0131lar gibi sa\u011fl\u0131k mesle\u011fi mensuplar\u0131 taraf\u0131ndan uygulanmas\u0131 ama\u00e7lanan \u00fcr\u00fcnler hari\u00e7 t\u00fcm ila\u00e7lar\u0131n d\u0131\u015f ambalajlar\u0131nda, ila\u00e7lar\u0131n isminin g\u00f6rme engelliler i\u00e7in ayn\u0131 zamanda Braille format\u0131nda kabartma yaz\u0131 ile yaz\u0131lmas\u0131 zorunlulu\u011fu getirildi. G\u00f6rme engelliler i\u00e7in kullanma talimat\u0131, duyarak alg\u0131lanabilecek bir formatta sunulabilecek.<\/p>\n
\u0130lac\u0131n terkibindeki t\u00fcm maddeler i\u00e7in, hayvansal kaynak kullan\u0131ld\u0131\u011f\u0131 durumlarda, ilac\u0131n kullanma talimat\u0131nda bu kaynak a\u00e7\u0131k\u00e7a belirtilecek.<\/p>\n
Emniyet Genel M\u00fcd\u00fcrl\u00fc\u011f\u00fcn\u00fcn de \u00f6nerisiyle, Avrupa Birli\u011fi’ne \u00fcye baz\u0131 \u00fclkelerdeki uygulamaya benzer \u015fekilde ara\u00e7 s\u00fcrme veya makine kullanma becerisini azaltabilecek ya da engelleyebilecek \u00fcr\u00fcnlerde bu durum ila\u00e7 kutusunun \u00fczerinde bir sembol (uyar\u0131 \u00fc\u00e7geni) ile mutlaka belirtilecek.<\/p>\n
\u00d6l\u00e7ekle kullan\u0131lan ila\u00e7larda \u00f6l\u00e7\u00fc kab\u0131 hacminin \u00f6l\u00e7ekten farkl\u0131 olmas\u0131 durumunda kullan\u0131c\u0131 hatas\u0131na ba\u011fl\u0131 olarak hastan\u0131n eksik ya da fazla doz alma olas\u0131l\u0131\u011f\u0131n\u0131 ortadan kald\u0131racak bir d\u00fczenleme de yap\u0131ld\u0131. Yeni d\u00fczenlemeye g\u00f6re, ilac\u0131n i\u00e7 ve d\u0131\u015f ambalaj\u0131nda \u00f6l\u00e7\u00fc kab\u0131 hacminin \u00f6l\u00e7ekten farkl\u0131 olmas\u0131 durumunda \u00f6l\u00e7ek hacmi ve \u00f6l\u00e7\u00fc kab\u0131 hacmi ayr\u0131 ayr\u0131 belirtilerek kullan\u0131c\u0131 hatalar\u0131 \u00f6nlenecek.<\/p>\n
Y\u00f6netmelikle b\u00fcy\u00fck hacimli parenteraller (a\u011f\u0131z yoluyla de\u011fil damar yolu, kas i\u00e7i ve cilt alt\u0131 gibi yollarla al\u0131nan ila\u00e7lar), radyofarmas\u00f6tikler (radyoaktif madde i\u00e7eren ila\u00e7lar), ki\u015fiye \u00f6zel \u00fcretilmi\u015f ila\u00e7lar, tan\u0131t\u0131m numuneleri ve \u00f6zel t\u0131bbi ama\u00e7l\u0131 g\u0131dalar da \u0130la\u00e7 Takip Sistemi (\u0130TS) kapsam\u0131na al\u0131nd\u0131.<\/p>\n
Karekodda “g\u00fcn\/ay\/y\u0131l” \u015feklinde ifade edilen ilac\u0131n son kullanma tarihi, ambalaj bilgilerinde “ay\/y\u0131l” \u015feklinde ifade edildi\u011finde kar\u0131\u015f\u0131kl\u0131\u011fa yol a\u00e7abildi\u011finden, bu tarihlerin birbiri ile uyumlu olarak belirtilmesine y\u00f6nelik d\u00fczenleme de y\u00f6netmelikte yer ald\u0131<\/p>\n","protected":false},"excerpt":{"rendered":"
Sa\u011fl\u0131k Bakanl\u0131\u011f\u0131 T\u00fcrkiye \u0130la\u00e7 ve T\u0131bbi Cihaz Kurumu (T\u0130TCK) taraf\u0131ndan haz\u0131rlanan y\u00f6netmelik de\u011fi\u015fikli\u011fi kapsam\u0131nda bundan b\u00f6yle ila\u00e7 kutular\u0131nda ila\u00e7lar\u0131n isimleri,…<\/p>\n","protected":false},"author":2,"featured_media":3642,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[4595],"tags":[406,407,345],"yoast_head":"\n