
VIZIMPRO is indicated for the first-line treatment of patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have epidermal growth factor receptor (EGFR) exon 19 deletion or exon 21 L858R substitution mutations, as detected by an FDA-approved test.
The recommended dosage is 45 mg taken orally once daily, with or without food. Treatment should continue until disease progression or unacceptable toxicity occurs. Dose reductions to 30 mg and then to 15 mg are recommended for management of specific adverse reactions. Avoid concomitant use with proton pump inhibitors (PPIs).
It is of great importance for both patients and doctors to understand the precautions before using dacomitinib...
Dacomitinib is an oral tyrosine kinase inhibitor primarily used as a first-line treatment for patients with...
Dacomitinib, with the English name Dacomitinib, is originally developed by Pfizer Inc. of the United States. It is a...
Dacomitinib is a second-generation, irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor...
Dacomitinib is a second-generation EGFR tyrosine kinase inhibitor, which has been approved in China for the...
Dacomitinib, also known by other names such as Vizimpro, Dacoplice, is mainly used for the treatment of metastatic...