Product Images Perjeta

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 4 images provide visual information about the product associated with Perjeta NDC 50242-145 by Genentech, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Figure 1 - perjeta 01

Figure 1 - perjeta 01

This is a statistical report for a clinical trial study comparing the effectiveness of different treatments for a medical condition. The hazard ratio (HR) for one treatment compared to the other is 0.62, with a 95% confidence interval of 0.51 to 0.75, which suggests that the treatment with the lower HR is more effective. The p-value obtained is less than 0.0001, indicating statistically significant results. The figure shows the proportion of patients that remain event-free over time, for each treatment group. The treatments being compared are Bertugumab and Trastuzymab + Docotaxel, placebo + Trasilzumad + Bocetaxel, and Pz +T+D with Pa+T+D.*

Figure 2 - perjeta 02

Figure 2 - perjeta 02

Figure 3 - perjeta 03

Figure 3 - perjeta 03

This appears to be a figure/table containing survival or event-free survival data for two groups of patients receiving different treatments. The first row shows the proportion of patients who remained event-free over time for each treatment group. The p-value and hazard ratio with confidence interval are also provided, suggesting that there may be a statistically significant difference between the two groups. The number of patients at risk is also given for each treatment group over time. However, there is not enough information to determine what type of event was being measured or what the specific treatments were.*

PRINCIPAL DISPLAY PANEL - 14 mL Vial Carton - perjeta 04

PRINCIPAL DISPLAY PANEL - 14 mL Vial Carton - perjeta 04

This is a description of Perjeta, a medication that comes in a single-dose vial with a strength of 420 mg/14 mL (30 mg/mL) and the active ingredient Pertuzumab. It should be diluted prior to use and administered via intravenous infusion only. There is no preservative, and unused portions should be discarded. The National Drug Code (NDC) for this medication is 50242-145-01.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.