Release date: 2024-08-15 10:22:29 Article From: Lucius Laos Recommended: 133
Pemigatinib is the world's first targeted therapy for cholangiocarcinoma for the treatment of adult patients with advanced, metastatic or unresectable cholangiocarcinoma who have received at least one prior systemic therapy and have been tested to have FGFR2 fusion or rearrangement.
There is a potential risk of Pemigatinib during treatment, that is, it may cause retinal pigment epithelial detachment. When this eye disease occurs, it can further lead to visual disturbance symptoms such as blurred vision, floaters-like floaters in vision, or flashes of light in front of the eyes.
During the clinical trial phase of Pemigatinib, routine optical coherence tomography was not included in the monitoring process to proactively screen and detect those cases of RPED that did not yet show significant symptoms. This monitoring gap means that there is a lack of definitive data and a clear understanding of the actual incidence of asymptomatic RPED after Pemigatinib.
Patients who are receiving Pemigatinib and potential patient groups considering the use of the drug need to be extra aware of this potential risk and closely monitor their eye health under the guidance of a physician. As soon as any abnormal vision or uncomfortable symptoms occur, you should seek medical attention immediately and inform your doctor that you are taking Pemigatinib so that necessary tests and interventions can be taken in time.
The following is guidance on the use of Pemigatinib.
Typically, the recommended dose of Pemigatinib is 13.5 mg orally daily for 1 day for 14 days, followed by 7 days off in a 21-day cycle. Patients should strictly follow the doctor's guidance before taking the medication, and do not change the dose or stop the medication at will.
Tablets should be swallowed whole, not crushed, chewed, split, or dissolved. This helps to maintain the stability and effectiveness of the drug.
Pemigatinib can cause harm to the fetus, so pregnant and breastfeeding women should avoid using this drug. Women and men of childbearing age should use effective contraception during and for a certain period of time after treatment.
Older patients may need to adjust their dose or pay more attention to monitoring when taking Pemigatinib, as they may have decreased physical function.
【Warm tips】When patients buy generic drugs, they should choose formal channels to ensure the quality and safety of the drugs. Avoid purchasing counterfeit products from informal sources.
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:2012024-09-07
On November 14, 2024, the Committee for Medicinal Products for Human Use (CHMP) of the European Medi···【more】
Recommended:1582025-13-01
Recent advancements have reaffirmed the significance of liquid biopsy in the management of advanced ···【more】
Recommended:1562025-06-01
FDA Approves First Generic Version of Victoza (liraglutide injection)The U.S. Food and Drug Administ···【more】
Recommended:1712024-30-12
The new indication involves the treatment of adult patients with locally advanced, unresectable non-···【more】
Recommended:1612024-24-12
he U.S. Food and Drug Administration (FDA) has approved Crenessity (crinecerfont) for use in combina···【more】
Recommended:1462024-17-12
In the phase Ib/II multicenter pivotal FELIX study, the autologous 41BB-ζ anti-CD19 chimeric antigen···【more】
Recommended:1052024-13-12
On 25 July 2024, the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHM···【more】
Recommended:2482024-26-08
Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
Whatsapp: