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▼Bu ilaç ek izlemeye tabidir. Bu üçgen yeni güvenlilik bilgisinin hızlı olarak belirlenmesini sağlayacaktır. Sağlık mesleği mensuplarının şüpheli advers reaksiyonlarını bildirmeleri beklenmektedir. Raporlama yapılması, ilacın yarar/risk dengesinin sürekli olarak izlenmesine olanak sağlamaktadır. Herhangi bir şüpheli advers reaksiyonu Türkiye Farmakovijilans Merkezi’ne \(TÜFAM\) \(www.titck.gov.tr; e-posta: tufam@titck.gov.tr; tel: 0800 314 00 08; faks: 0312 218 35 99\) aracılığı ile bildirmeniz gerekmektedir.
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