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CPDA-1 Blood Bag Collection System
Overview
What is Leukotrap WB System?
CPDA-1 Blood Collection Set, Double Bag with WBF2 Filter and Sampling System
Instruction for Use for Systems Containing a Y Sampling Site (YSS) or Sample Diversion Pouch (with or without a pre-attached Samp Vacuum Tube Holder). Refer to unit foil package label for specific product description being used.
Sterile, nonpyrogenic fluid path. Sterilized by steam.
Rx only.
This product is free of natural rubber latex.
What does Leukotrap WB System look like?
What are the available doses of Leukotrap WB System?
Sorry No records found.
What should I talk to my health care provider before I take Leukotrap WB System?
Sorry No records found
How should I use Leukotrap WB System?
Indicated for collection of blood and preparation of red blood cells and plasma with pre-storage leukocyte reduction. Platelet concentrates are not intended to be made with this product.
What interacts with Leukotrap WB System?
Sorry No Records found
What are the warnings of Leukotrap WB System?
Photosensitivity manifested by an exaggerated sunburn reaction has been observed in some individuals taking tetracyclines. Patients apt to be exposed to direct sunlight or ultraviolet light should be advised that this reaction can occur with tetracycline drugs, and treatment should be discontinued at the first evidence of skin erythema.
What are the precautions of Leukotrap WB System?
Sorry No Records found
What are the side effects of Leukotrap WB System?
There are no known potential adverse reactions associated specifically with the Leukotrap WB System with CPDA-1.
What should I look out for while using Leukotrap WB System?
Failure to achieve and maintain a closed system during processing would result in a product that must be transfused within 24 hours.
What might happen if I take too much Leukotrap WB System?
Sorry No Records found
How should I store and handle Leukotrap WB System?
Dispense in a well-closed container as defined in the USP, with a child-resistant closure.Store at 20°-25°C (68°-77°F). [See USP controlled room temperature].Dispense in a well-closed container as defined in the USP, with a child-resistant closure.Store at 20°-25°C (68°-77°F). [See USP controlled room temperature].Each shipping case contains 6 foil envelopes. Within each foil envelope resides 3 units of the collection system. Each unit consists of a collection bag with 70 ml of CPDA-1 solution and two empty bags.
Clinical Information
Chemical Structure
No Image foundClinical Pharmacology
Non-Clinical Toxicology
Failure to achieve and maintain a closed system during processing would result in a product that must be transfused within 24 hours.Because tetracyclines have been shown to depress plasma prothrombin activity, patients who are on anticoagulant therapy may require downward adjustment of their anticoagulant dosage.
Since bacteriostatic drugs may interfere with the bactericidal action of penicillin, it is advisable to avoid giving tetracyclines in conjunction with penicillin.
Absorption of tetracyclines is impaired by antacids containing aluminum, calcium, or magnesium, and iron-containing preparations.
Absorption of tetracyclines is impaired by bismuth subsalicylate.
Barbiturates, carbamazepine, and phenytoin decrease the half-life of doxycycline.
The concurrent use of tetracycline and Penthrane (methoxyflurane) has been reported to result in fatal renal toxicity.
Concurrent use of tetracycline may render oral contraceptives less effective.
Use Aseptic Technique.
Use only if solution is clear.
Store CPDA-1 preserved red blood cells at 1—6 °C for up to 35 days and use as indicated.
* During processing, always observe the following precautions:
1. Sealing should be done in a manner that avoids fluid splatter.
2. Always dispose of blood-contaminated products in a manner consistent with established BIOHAZARD safety procedures.
There are no known potential adverse reactions associated specifically with the Leukotrap WB System with CPDA-1.
Reference
This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"
While we update our database periodically, we cannot guarantee it is always updated to the latest version.
Review
Professional
Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72Tips
Tips
Interactions
Interactions
A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).