PACLITAXEL injection, solution

Kraj: Stany Zjednoczone

Język: angielski

Źródło: NLM (National Library of Medicine)

Składnik aktywny:

PACLITAXEL (UNII: P88XT4IS4D) (PACLITAXEL - UNII:P88XT4IS4D)

Dostępny od:

Actavis Pharma, Inc.

INN (International Nazwa):

PACLITAXEL

Skład:

PACLITAXEL 6 mg in 1 mL

Droga podania:

INTRAVENOUS

Typ recepty:

PRESCRIPTION DRUG

Wskazania:

Paclitaxel Injection, USP is indicated as subsequent therapy for the treatment of advanced carcinoma of the ovary. As first-line therapy, Paclitaxel Injection, USP is indicated in combination with cisplatin. Paclitaxel Injection, USP is indicated for the adjuvant treatment of node-positive breast cancer administered sequentially to standard doxorubicin-containing combination chemotherapy. In the clinical trial, there was an overall favorable effect on disease-free and overall survival in the total population of patients with receptor-positive and receptor-negative tumors, but the benefit has been specifically demonstrated by available data (median follow-up 30 months) only in the patients with estrogen and progesterone receptor-negative tumors (see CLINICAL STUDIES, Breast Carcinoma). Paclitaxel Injection, USP is indicated for the treatment of breast cancer after failure of combination chemotherapy for metastatic disease or relapse within 6 months of adjuvant chemotherapy. Prior therapy should have included a

Podsumowanie produktu:

Paclitaxel Injection, USP (6 mg/mL) is available as follows: NDC 45963-613-56         30 mg/5 mL multidose vial individually packaged in a carton. NDC 45963-613-53         100 mg/16.7 mL multidose vial individually packaged in a carton. NDC 45963-613-59         300 mg/50 mL multidose vial individually packaged in a carton. Storage Store the vials in original cartons between 20°–25°C (68°–77°F). [See USP Controlled Room Temperature.] Retain in the original package until time of use to protect from light. See DOSAGE AND ADMINISTRATION, Preparation and Administration Precautions. Sterile, Nonpyrogenic, Preservative-free. The container closure is not made with natural rubber latex.

Status autoryzacji:

Abbreviated New Drug Application

Charakterystyka produktu

PACLITAXEL- PACLITAXEL INJECTION, SOLUTION
ACTAVIS PHARMA, INC.
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PACLITAXEL INJECTION, USP
(FOR INTRAVENOUS USE ONLY)
RX ONLY
WARNING
Paclitaxel Injection, USP should be administered under the supervision
of a physician
experienced in the use of cancer chemotherapeutic agents. Appropriate
management of
complications is possible only when adequate diagnostic and treatment
facilities are readily
available.
Anaphylaxis and severe hypersensitivity reactions characterized by
dyspnea and hypotension
requiring treatment, angioedema, and generalized urticaria have
occurred in 2 to 4% of patients
receiving paclitaxel in clinical trials. Fatal reactions have occurred
in patients despite
premedication. All patients should be pretreated with corticosteroids,
diphenhydramine, and H
antagonists (see DOSAGE AND ADMINISTRATION). Patients who experience
severe
hypersensitivity reactions to paclitaxel should not be rechallenged
with the drug.
Paclitaxel Injection, USP therapy should not be given to patients with
solid tumors who have
baseline neutrophil counts of less than 1,500 cells/mm and should not
be given to patients with
AIDS-related Kaposi’s sarcoma if the baseline neutrophil count is
less than 11,000 cells/mm . In
order to monitor the occurrence of bone marrow suppression, primarily
neutropenia, which may
be severe and result in infection, it is recommended that frequent
peripheral blood cell counts be
performed on all patients receiving Paclitaxel Injection, USP.
DESCRIPTION
Paclitaxel Injection, USP is a clear, colorless to slightly yellow
viscous solution. It is supplied as a
nonaqueous solution intended for dilution with a suitable parenteral
fluid prior to intravenous infusion.
Paclitaxel Injection, USP is available in 30 mg (5 mL), 100 mg (16.7
mL), and 300 mg (50 mL) multidose
vials. Each mL of sterile nonpyrogenic solution contains 6 mg
paclitaxel USP, 527 mg of purified
Cremophor
EL (polyoxyethylated castor oil), 2 mg citric acid anhydrous, USP and
48.7% (v/v)
dehydrated alcohol, USP.
Paclitaxel, USP