carboplatin injection Other

()

Logo

Rx only

PREPARATION OF INTRAVENOUS SOLUTIONS

Carboplatin Injection 10 mg/mL is supplied as a Ready To Use (RTU) sterile solution in 5 mL, 15 mL, 45 mL or 60 mL vials. Total content of carboplatin per vial is described in following table:

Vial StrengthDiluent Volume
50 mg5 mL
150 mg15 mL
450 mg45 mL
600 mg60 mL

Carboplatin Injection aqueous solution can be further diluted to concentrations as low as 0.5 mg/mL with 5% Dextrose in Water (D5W) or 0.9% Sodium Chloride Injection, USP.

When prepared as directed, Carboplatin Injection aqueous solutions are stable for 8 hours at room temperature (25°C). Since no antibacterial preservative is contained in the formulation, it is recommended that Carboplatin Injection aqueous solutions be discarded 8 hours after dilution.

HANDLING AND DISPOSAL

Caution should be exercised in handling and preparing Carboplatin Injection. Several guidelines on this subject have been published.1–4

To minimize the risk of dermal exposure, always wear impervious gloves when handling vials containing Carboplatin Injection. If Carboplatin Injection contacts the skin, immediately wash the skin thoroughly with soap and water. If Carboplatin Injection contacts mucous membranes, the membranes should be flushed immediately and thoroughly with water. More information is available in the references listed below.

Logo

Distributed by Hospira, Inc. Lake Forest, IL 60045

LAB-1014-4.0

Revised: 8/2021

Find carboplatin injection medical information:

Find carboplatin injection medical information:

Our scientific content is evidence-based, scientifically balanced and non-promotional. It undergoes rigorous internal medical review and is updated regularly to reflect new information.

carboplatin injection Quick Finder

Prescribing Information
Download Prescribing Information

Health Professional Information

Other

Logo

Rx only

PREPARATION OF INTRAVENOUS SOLUTIONS

Carboplatin Injection 10 mg/mL is supplied as a Ready To Use (RTU) sterile solution in 5 mL, 15 mL, 45 mL or 60 mL vials. Total content of carboplatin per vial is described in following table:

Vial StrengthDiluent Volume
50 mg5 mL
150 mg15 mL
450 mg45 mL
600 mg60 mL

Carboplatin Injection aqueous solution can be further diluted to concentrations as low as 0.5 mg/mL with 5% Dextrose in Water (D5W) or 0.9% Sodium Chloride Injection, USP.

When prepared as directed, Carboplatin Injection aqueous solutions are stable for 8 hours at room temperature (25°C). Since no antibacterial preservative is contained in the formulation, it is recommended that Carboplatin Injection aqueous solutions be discarded 8 hours after dilution.

HANDLING AND DISPOSAL

Caution should be exercised in handling and preparing Carboplatin Injection. Several guidelines on this subject have been published.1–4

To minimize the risk of dermal exposure, always wear impervious gloves when handling vials containing Carboplatin Injection. If Carboplatin Injection contacts the skin, immediately wash the skin thoroughly with soap and water. If Carboplatin Injection contacts mucous membranes, the membranes should be flushed immediately and thoroughly with water. More information is available in the references listed below.

Logo

Distributed by Hospira, Inc. Lake Forest, IL 60045

LAB-1014-4.0

Revised: 8/2021

Medication Guide

Health Professional Information

{{section_name_patient}}

{{section_body_html_patient}}

Resources

Didn’t find what you were looking for? Contact us.

MI Digital Assistant

Chat online with Pfizer Medical Information regarding your inquiry on a Pfizer medicine.

Call 800-438-1985*

*Speak with a Pfizer Medical Information Professional regarding your medical inquiry. Available 9AM-5Pm ET Monday to Friday; excluding holidays.

Medical Inquiry

Submit a medical question for Pfizer prescription products.

Report Adverse Event

Pfizer Safety

To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for this product, adverse events should be reported to your coordinating study site.

If you cannot use the above website, or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at (800) 438-1985.

FDA Medwatch

You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or call (800) 822-7967.