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ACD Solution Modified

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Overview

What is ACD Solution Modified?

Each 100 mL vial contains 80 mg citric acid, 224 mg sodium citrate anhydrous, and 120 mg dextrose anhydrous in a sterile, non-pyrogenic solution of 10 mL. The pH of the solution has been adjusted to be between 4.5 to 5.5



What does ACD Solution Modified look like?



What are the available doses of ACD Solution Modified?

Sorry No records found.

What should I talk to my health care provider before I take ACD Solution Modified?

Sorry No records found

How should I use ACD Solution Modified?

ACD solution modified is to be used in the labeling of red blood cells for intravenous administration with Cr-51 Sodium Chromate.

Red Blood Cell Labeling Procedure


What interacts with ACD Solution Modified?

Sorry No Records found


What are the warnings of ACD Solution Modified?

Sorry No Records found


What are the precautions of ACD Solution Modified?

Sorry No Records found


What are the side effects of ACD Solution Modified?

Sorry No records found


What should I look out for while using ACD Solution Modified?

There are no known contraindications.


What might happen if I take too much ACD Solution Modified?

Sorry No Records found


How should I store and handle ACD Solution Modified?

Sorry No Records found


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Clinical Information

Chemical Structure

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Clinical Pharmacology

In vitro, citrate ions combine with ionic calcium in the blood and the resulting

lack of ionic calcium prevents coagulation. Blood that has been treated with citrate anticoagulants is nontoxic to the body when injected in small amounts intravenously. After injection, citrate ions are rapidly removed from the blood by the liver, polymerized into glucose, and then metabolized in the usual manner

Non-Clinical Toxicology
There are no known contraindications.

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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.

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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. 315.72
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Tips

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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).