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PRODUCT INFORMATION

Tecentriq Hybreza 125mg/2000units/ml injection 1vial x 15ml (atezolizumab and hyaluronidase-tqjs)

atezolizumab and hyaluronidase-tqjs

Tecentriq Hybreza 125mg/2000units/ml injection 1vial x 15ml (atezolizumab and hyaluronidase-tqjs)
Reference priceCNY ¥630.00Original source price: INR 52,500.00. Converted estimates are available by currency selection.
BrandTecentriq Hybreza
ManufacturerGENENTECH USA
Prescription requiredYes

Description

Tecentriq Hybreza 125mg/2000units/ml injection 1vial x 15ml(/) (atezolizumab and hyaluronidase-tqjs) is a medicine catalog record in the MediPriceHub database. Active ingredient: atezolizumab and hyaluronidase-tqjs. Clinical use summary: See the Benefits field on this page for the product-specific indication or intended use. That field is kept separate from catalog metadata so users can distinguish clinical information from packaging information. Manufacturer or supplier: GENENTECH USA. Therapeutic category: Medicine Library > Oncology Medicines > Soft Tissue Sarcoma Drugs. Pack information: 1875 30000 / 15 (125 2000 / ). Origin country or market: United States. This page is for medicine catalog reference only and should be read together with the approved prescribing information in the patient or buyer's country.

Benefits

TECENTRIQ HYBREZA is a combination of atezolizumab, a programmed death-ligand 1 (PD-L1) blocking antibody, and hyaluronidase, an endoglycosidase indicated: Non-Small Cell Lung Cancer (NSCLC) Small Cell Lung Cancer (SCLC) Hepatocellular Carcinoma (HCC) Melanoma Alveolar Soft Part Sarcoma (ASPS) Muscle Invasive Bladder Cancer (MIBC) as adjuvant treatment following resection and platinum-based chemotherapy for adult patients with Stage II to IIIA NSCLC whose tumors have PD-L1 expression on ≥ 1% of tumor cells, as determined by an FDA-authorized test. for the first-line treatment of adult patients with metastatic NSCLC whose tumors have high PD-L1 expression (PD-L1 stained ≥ 50% of tumor cells [TC ≥ 50%] or PD-L1 stained tumor-infiltrating immune cells [IC] covering ≥ 10% of the tumor area [IC ≥ 10%]), as determined by an FDA-authorized test, with no EGFR or ALK genomic tumor aberrations. in combination with bevacizumab, paclitaxel, and carboplatin, for the first-line treatment of adult patients with metastatic non-squamous NSCLC with no EGFR or ALK genomic tumor aberrations. in combination with paclitaxel protein-bound and carboplatin for the first-line treatment of adult patients with metastatic non-squamous NSCLC with no EGFR or ALK genomic tumor aberrations. for the treatment of adult patients with metastatic NSCLC who have disease progression during or following platinum-containing chemotherapy. Patients with EGFR or ALK genomic tumor aberrations should have disease progression on FDA-approved therapy for NSCLC harboring these aberrations prior to receiving TECENTRIQ HYBREZA. in combination with carboplatin and etoposide, for the first-line treatment of adult patients with extensive-stage small cell lung cancer (ES-SCLC). in combination with lurbinectedin, for the main

How to Use

Use atezolizumab and hyaluronidase-tqjs under the supervision of a qualified healthcare professional. It should be prepared and administered only by trained healthcare professionals in a setting appropriate for injectable or infusion medicines. Do not start, stop, change the dose, split or crush a dosage form, mix with other medicines, or repeat a course unless the approved product information or a clinician confirms that it is appropriate. Check the local prescribing information for age limits, dose adjustments, missed-dose instructions, storage after opening or reconstitution, and monitoring requirements.

Specification

Active ingredient: atezolizumab and hyaluronidase-tqjs. Pack size: 1875 30000 / 15 (125 2000 / ). Pack unit: bottle. Manufacturer: GENENTECH USA. Origin country: United States. Source category: Medicine Library > Oncology Medicines > Soft Tissue Sarcoma Drugs. Availability, prescription status, storage, and exact approved use may vary by country. Check the local product information before clinical or procurement decisions.

Side Effects

Cancer medicines may cause fatigue, nausea, vomiting, diarrhea or constipation, appetite changes, mouth sores, rash, changes in blood counts, infection risk, liver or kidney test changes, bleeding risk, neuropathy, infusion reactions, or organ-specific toxicity depending on the medicine. Injectable and infusion products may also cause administration-site pain, swelling, infection, infusion reactions, or hypersensitivity. Seek urgent medical care for severe allergic symptoms, breathing difficulty, fainting, severe skin reactions, chest pain, confusion, serious bleeding, signs of infection, or rapidly worsening symptoms. The approved local prescribing information is the controlling source for the complete adverse-reaction profile.

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