How many pills does a box of Cabozantinib contain?

After Cabozantinib is launched on the market, it is mainly used for the treatment of renal cell carcinoma (RCC), hepatocellular carcinoma (HCC), differentiated thyroid cancer (DTC), pancreatic neuroendocrine tumors (pNET) and other diseases. It is mainly sold in the overseas and Hong Kong markets in the form of tablets or capsules. Its packaging specifications are designed to take into account the clinical dosing cycle and the convenience of long-term medication for patients. Judging from the current public and actual circulation situation, cabozantinib tablets are usually packaged on the basis of "30 tablets per box", and this specification remains relatively uniform in different dosage strengths.

In the Hong Kong market, common cabozantinib tablet specifications include20 mg × 30 tablets, 40 mg × 30 tablets and 60 mg × 30 tablets. Although the dosage of a single tablet is different, the number of tablets in each box remains the same. This design helps doctors flexibly adjust the daily dosage according to the patient's condition and tolerance without the need to frequently change packaging specifications.

From the perspective of clinical use, each box of 30 tablets usually corresponds to a treatment cycle of about one month, which matches the prescription rhythm of most targeted anti-tumor drugs. During the patient's use, the doctor can adjust the dose up or down based on the efficacy evaluation and adverse reactions, but the number of tablets and specification itself will not change.

It should be noted that cabozantinib sold in different regions may have differences in packaging labeling, language instructions, etc., but the number of tablets and configuration basically follows the unified international standards. For patients who learn about the drug through overseas or Hong Kong channels, clarifying "how many tablets a box contains" can help to reasonably estimate the treatment cycle and medication cost.

In addition, because cabozantinib has not yet been launched in China, there are no official circulation specifications in the mainland market, and most of the specification information that patients are exposed to comes from overseas markets. Therefore, before actual use, it is still necessary to carefully confirm the specific dosage and packaging information based on doctor's advice and legal channels.

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Reference materials:https://medlineplus.gov/druginfo/meds/a616037.html