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Rx Item-Clolar 20Mg 20Ml Vial By Aventis Pharma

NDC 00024-5860-01 UPC/GTIN No.3-00245-86001-9 Mfg.Part No.586001BRAND: CLOLAR  NDC: 00024-5860-01,24586001 UPC: 3-00245-86001-9,300245860019 Aventis Pharmaceuticals/DsOnly Lic.-Physician,Pharmacy,Dentist,Drug Mfg,Dist.,Gov,Hospital,Lic.Lab,Naturalist,Naturopath,NP,Optometrist,Pharmacist,PA,Physical Therapist,Podiatrist,Research Co.,Uni.,VA,Vet & Wholesalers in scopWant to do Research on this Med or need a large quantity? Email Details with quantity required to:sales@AmericanPharmaWholesale.comVisit AmericanPharmaWholesale.com for over 100,000 items of Health & Beauty at Retail@Wholesale prices.Clolar 20mg 20ml Vial by Aventis Pharma

Rx Item-Clolar 20Mg 20Ml Vial By Aventis Pharma

$3901.18$3715.41

Item No.:RX367538, Item No. RX862817, 862817, NDC No.: 00024-5860-01, 00024-860-01, 0002486001, 00024586001, 5860-01, 586001 UPC No. 3-00245-86001-9, 300245-860019, 300245860019, Rx Item-Clolar 20Mg 20Ml Vial By Aventis Pharma Only Physician, Pharmacy Or Licensed Facility Can purchase this RX Item Brand/Generic: , Drug Category: Antineoplastics-Antimetabolites Antineoplastic AgentDrug Class: 10000000 Antineoplastic Agents

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CLOLAR- clofarabine injection
sanofi-aventis U.S. LLC

1 INDICATIONS AND USAGE

Clolar� (clofarabine) Injection is indicated for the treatment of pediatric patients 1 to 21 years old with relapsed or refractory acute lymphoblastic leukemia after at least two prior regimens. This indication is based upon response rate. There are no trials verifying an improvement in disease-related symptoms or increased survival with Clolar.

2 DOSAGE AND ADMINISTRATION

2.1 Recommended Dosage
Administer the recommended pediatric dose of 52 mg/m2 as an intravenous infusion over 2 hours daily for 5 consecutive days.

Treatment cycles are repeated following recovery or return to baseline organ function, approximately every 2 to 6 weeks. The dosage is based on the patient's body surface area (BSA), calculated using the actual height and weight before the start of each cycle. To prevent drug incompatibilities, no other medications should be administered through the same intravenous line.
Provide supportive care, such as intravenous fluids, antihyperuricemic treatment, and alkalinize urine throughout the 5 days of Clolar administration to reduce the effects of tumor lysis and other adverse events.
Discontinue Clolar if hypotension develops during the 5 days of administration.
Monitor renal and hepatic function during the 5 days of Clolar administration [see Warnings and Precautions (5.7, 5.8)].
Monitor patients taking medications known to affect blood pressure. Monitor cardiac function during administration of Clolar.
Reduce the dose by 50% in patients with creatinine clearance (CrCL) between 30 and 60 mL/min. There is insufficient information to make a dosage recommendation in patients with CrCL less than 30 mL/min [see Use in Specific Populations (8.7) ].
2.2 Supportive Medications and Medications to Avoid
Consider prophylactic anti-emetic medications as Clolar is moderately emetogenic.
Consider the use of prophylactic steroids to mitigate Systemic Inflammatory Response Syndrome (SIRS) or capillary leak syndrome (e.g., hypotension, tachycardia, tachypnea, and pulmonary edema).
Minimize exposure to drugs with known renal toxicity during the 5 days of Clolar administration since the risk of renal toxicity may be increased.
Consider avoiding concomitant use of medications known to induce hepatic toxicity.
2.3 Dose Modifications and Reinitiation of Therapy
Hematologic Toxicity
Administer subsequent cycles no sooner than 14 days from the starting day of the previous cycle and provided the patient's ANC is ?0.75 � 109 /L.
If a patient experiences a Grade 4 neutropenia (ANC <0.5 � 109 /L) lasting ?4 weeks, reduce dose by 25% for the next cycle.
Non-hematologic Toxicity
Withhold Clolar if a patient develops a clinically significant infection, until the infection is controlled, then restart at the full dose.
Withhold Clolar for a Grade 3 non-infectious non-hematologic toxicity (excluding transient elevations in serum transaminases and/or serum bilirubin and/or nausea/vomiting controlled by antiemetic therapy). Re-institute Clolar administration at a 25% dose reduction when resolution or return to baseline.
Discontinue Clolar administration for a Grade 4 non-infectious non-hematologic toxicity.
Discontinue Clolar administration if a patient shows early signs or symptoms of SIRS or capillary leak (e.g., hypotension, tachycardia, tachypnea, and pulmonary edema) occur and provide appropriate supportive measures.
Discontinue Clolar administration if Grade 3 or higher increases in creatinine or bilirubin are noted. Re-institute Clolar with a 25% dose reduction, when the patient is stable and organ function has returned to baseline. If hyperuricemia is anticipated (tumor lysis), initiate measures to control uric acid.

NDC 00024-5860-01 UPC/GTIN No.3-00245-86001-9 Mfg.Part No.586001
RX ITEM-Clolar 20Mg 20Ml Vial By Aventis
NDC 00024-5860-01 UPC/GTIN No.3-00245-86001-9 Mfg.Part No.586001

BRAND: CLOLAR  NDC: 00024-5860-01,24586001 UPC: 3-00245-86001-9,300245860019 Aventis Pharmaceuticals/Ds
Clolar 20mg 20ml Vial by Avent
BRAND: CLOLAR NDC: 00024-5860-01,24586001 UPC: 3-00245-86001-9,300245860019 Aventis Pharmaceuticals/Ds

Only Lic.-Physician,Pharmacy,Dentist,Drug Mfg,Dist.,Gov,Hospital,Lic.Lab,Naturalist,Naturopath,NP,Optometrist,Pharmacist,PA,Physical Therapist,Podiatrist,Research Co.,Uni.,VA,Vet & Wholesalers in scop
CLOFARABINE INTRAVEN VIAL
Only Lic.-Physician,Pharmacy,Dentist,Drug Mfg,Dist.,Gov,Hospital,Lic.Lab,Naturalist,Naturopath,NP,Optometrist,Pharmacist,PA,Physical Therapist,Podiatrist,Research Co.,Uni.,VA,Vet & Wholesalers in scop

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Visit AmericanPharmaWholesale.com for over 100,000 items of Health & Beauty at Retail@Wholesale prices.
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Clolar 20mg 20ml Vial by Aventis Pharma
Clolar 20mg 20ml Vial by Avent
Clolar 20mg 20ml Vial by Aventis Pharma