
Release date: 2026-06-05 11:57:25 Article From: Lucius Laos Recommended: 16
The safety of Repotrectinib was evaluated in 426 patients in the TRIDENT-1 study. Overall, most adverse reactions were Grade 1 or 2, but some patients experienced Grade 3 or 4 serious events. The most common adverse reactions (incidence ≥20%) included dizziness, dysgeusia, peripheral neuropathy, constipation, dyspnea, fatigue, ataxia, cognitive impairment, myasthenia, and nausea. These adverse reactions cover the nervous system, digestive system, respiratory system, and systemic symptoms. Among them, nervous system-related reactions (dizziness, dysgeusia, peripheral neuropathy, ataxia, cognitive impairment) were the most prominent.
Dizziness was the most frequently reported adverse reaction, with an incidence of 65%, including vertigo. Dysgeusia (taste abnormality or loss) also occurred at a high rate and may affect patient appetite and quality of life. Peripheral neuropathy manifested as paresthesia, numbness, burning sensation, etc., with incidence not specifically listed but among the most common. Constipation and nausea were common gastrointestinal reactions. Dyspnea (including exertional dyspnea) and fatigue significantly impacted daily activities. Ataxia often presented as gait and balance disorders. Cognitive impairment included memory decline and attention deficits. Myasthenia may manifest as limb weakness. Most of these reactions are manageable but require close monitoring.
For the above adverse reactions, physicians should adopt individualized management strategies. For dizziness and ataxia, patients are advised to avoid driving and hazardous activities, and fall prevention measures should be considered. For dysgeusia, dietary flavor adjustments may be helpful. For peripheral neuropathy, neurotrophic drugs or dose adjustment can be considered. For constipation, laxatives or dietary modification may be used. For dyspnea, interstitial lung disease should be ruled out. For fatigue, adequate rest and nutritional support are encouraged. For cognitive impairment, cognitive training may be performed. For myasthenia, creatine phosphokinase levels should be monitored. The general principle is to withhold, reduce, then resume dosing or permanently discontinue based on severity. Patient education is crucial; patients should be advised to promptly report any new or worsening symptoms.
On November 21, 2025, the U.S. Food and Drug Administration (FDA) approved the regimen of pembrolizu···【more】
Recommended:4092025-17-12
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:6012024-09-07
On May 28, 2026, AstraZeneca announced that its immunotherapy drug Imfinzi (durvalumab) in combinati···【more】
Recommended:522026-01-06
On December 12, 2025, the U.S. Food and Drug Administration (FDA) approved niraparib in combination ···【more】
Recommended:3802025-15-12
The U.S. Food and Drug Administration (FDA) announced today that it has approved Omisirge (omidubice···【more】
Recommended:3962025-10-12
On December 4, 2025, the U.S. Food and Drug Administration (FDA) approved lisocabtagene maraleucel (···【more】
Recommended:3782025-08-12
On December 3, 2025, the U.S. Food and Drug Administration (FDA) granted full approval to pirtobruti···【more】
Recommended:4462025-04-12
Primary analysis data from the randomized, double-blind, placebo-controlled phase III HER2CLIMB-02 s···【more】
Recommended:3622025-01-12

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

Name: Lucius

Telegram name: Vira
No.:0085253923643
Telegram name: Vira
No.:0085253923643