Trastuzumab 440mg Injection

Trastuzumab 440mg is a HER2-directed monoclonal antibody used in HER2-positive breast cancer and selected advanced gastric or gastro-oesophageal cancers. HER2 testing identifies cancers that may benefit.
The reconstituted medicine is diluted for intravenous infusion. The first infusion is generally given over about 90 minutes, with later infusions shortened if tolerated. Weekly and three-weekly regimens use different doses.
Trastuzumab binds HER2 on tumour cells, reduces growth signalling and helps immune cells recognise and attack the cancer.
Fever, chills, headache, nausea and infusion reactions can occur. Reduced heart pumping function and serious lung reactions are important risks.
Heart function is assessed before and during treatment, especially with prior anthracycline exposure. Effective contraception is needed during treatment and for 7 months after the last dose.
Can reduce recurrence or progression when incorporated into a suitable HER2-directed cancer regimen.
The target protein must be present at the required level or genetic pattern for the proposed treatment setting.
No. Those are antibody-drug conjugates with different doses, indications and toxicities.
A decline in pumping function can appear before breathlessness or swelling and may change the treatment plan.
No. These powder-vial presentations are for intravenous infusion; dedicated subcutaneous products use different formulations.
HER2: a growth receptor present at high levels in some tumours. Monoclonal antibody: a targeted immune-system protein. LVEF: a measure of the heart’s pumping function.; AR: Trastuzumab 440mg حقن; FR: Trastuzumab 440mg injection; PT: Trastuzumab 440mg injeção; ES: Trastuzumab 440mg inyección; RU: Trastuzumab 440mg инъекция; ID: Trastuzumab 440mg suntikan; VI: Trastuzumab 440mg thuốc tiêm; MS: Trastuzumab 440mg suntikan; TL: Trastuzumab 440mg iniksyon; ZH-SG: Trastuzumab 440mg 注射剂
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Trastuzumab 440mg Injection