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Ethiodol

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Overview

What is Ethiodol?

Ethiodol, brand of ethiodized oil, is a sterile injectable radio-opaque diagnostic agent for use in hysterosalpingography and lymphography. It contains 37% iodine (475 mg/mL) organically combined with ethyl esters of the fatty acids (primarily as ethyl monoiodostearate and ethyl diiodostearate) of poppyseed oil. Stabilized with poppyseed oil, 1%. The precise structure of Ethiodol is unknown at this time. Ethiodol is a straw to amber colored, oily fluid, which because of simplified molecular structure, possesses a greatly reduced viscosity (1.280 specific gravity at 15° C yields viscosity of 0.5 - 1.0 poise). This high fluidity provides a new flexibility for radiographic exploration.



What does Ethiodol look like?



What are the available doses of Ethiodol?

Sorry No records found.

What should I talk to my health care provider before I take Ethiodol?

Sorry No records found

How should I use Ethiodol?

Ethiodol is indicated for use as a radio-opaque medium for hysterosalpingography and lymphography.


What interacts with Ethiodol?

Sorry No Records found


What are the warnings of Ethiodol?

Sorry No Records found


What are the precautions of Ethiodol?

Sorry No Records found


What are the side effects of Ethiodol?

Sorry No records found


What should I look out for while using Ethiodol?

Sorry No records found


What might happen if I take too much Ethiodol?

Sorry No Records found


How should I store and handle Ethiodol?

Store the kit at 2°-8°C (36°-46°F) and protect from light.ArrayStore the kit at 2°-8°C (36°-46°F) and protect from light.ArrayEthiodol (ethiodized oil for injection) is supplied in a box of two 10 ml ampules, NDC 0281-7062-37.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from light. Remove from carton only upon use.Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Ethiodol brand of ethiodized oil for injection is straw to amber color under normal conditions. (See ).A development of Guerbet Laboratories.Ethiodol (ethiodized oil for injection) is supplied in a box of two 10 ml ampules, NDC 0281-7062-37.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from light. Remove from carton only upon use.Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Ethiodol brand of ethiodized oil for injection is straw to amber color under normal conditions. (See ).A development of Guerbet Laboratories.Ethiodol (ethiodized oil for injection) is supplied in a box of two 10 ml ampules, NDC 0281-7062-37.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from light. Remove from carton only upon use.Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Ethiodol brand of ethiodized oil for injection is straw to amber color under normal conditions. (See ).A development of Guerbet Laboratories.Ethiodol (ethiodized oil for injection) is supplied in a box of two 10 ml ampules, NDC 0281-7062-37.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from light. Remove from carton only upon use.Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. Ethiodol brand of ethiodized oil for injection is straw to amber color under normal conditions. (See ).A development of Guerbet Laboratories.


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Clinical Information

Chemical Structure

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Clinical Pharmacology

There has been little detailed investigation of the metabolic fate of Ethiodol in either man or animals. However, the fate of Ethiodol following Lymphangiography in dogs has been reported. Koehler et al. employed I–tagged Ethiodol for lymphangiography in dogs and analyses of individual organs at various time intervals were done. The investigators reported an average of only 25% of the injected medium was retained in the lymphatics at the end of three days. An average of 50% was recovered from the lungs. They found the remainder of injected activity was fairly uniformly distributed throughout the body. Urinary excretion in the form of inorganic iodine was revealed as the chief mode of iodine loss from the system.

Non-Clinical Toxicology
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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

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).