Irinotecan hydrochloride Injection 100 mg in 5 mL (10)

Country: Awstralja

Lingwa: Ingliż

Sors: Department of Health (Therapeutic Goods Administration)

Ingredjent attiv:

irinotecan hydrochloride trihydrate, Quantity: 20 mg/mL

Disponibbli minn:

Pfizer (Perth) Pty Ltd

Għamla farmaċewtika:

Injection, concentrated

Kompożizzjoni:

Excipient Ingredients: sorbitol; water for injections; lactic acid

Rotta amministrattiva:

Intravenous

Unitajiet fil-pakkett:

1 X 5 mL

Tip ta 'preskrizzjoni:

(S1) This Schedule is intentionally blank

Indikazzjonijiet terapewtiċi:

Irinotecan is indicated for single-agent or combination treatment of patients with: ? Metastatic carcinoma of the colon or rectum that has recurred or progressed following 5-fluorouracil (5-FU)-based therapy ? Irinotecan in combination with cetuximab is indicated for the treatment of patients with epidermal growth receptor (EGFR)-expressing metastatic colorectal cancer after failure of irinotecan-including cytotoxic therapy. ? Previously untreated metastatic carcinoma of the colon or rectum ? Advanced cervical squamous cell carcinoma ? Irinotecan in combination with 5-FU, folinic acid (FA) and bevacizumab is indicated for first-line treatment of patients with metastatic carcinoma of the colon or rectum.

Sommarju tal-prodott:

Visual Identification: Clear, light yellow solution, free from visible particles.; Container Type: Vial; Container Life Time: 36 Months; Container Temperature: Store below 25 degrees Celsius; Container Closure: Neither child resistant closure nor restricted flow insert

L-istatus ta 'awtorizzazzjoni:

Listed (Export Only)

Data ta 'l-awtorizzazzjoni:

2019-09-03