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Sodium Sulfacetamide, Sulfur

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Overview

What is Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

DESCRIPTION: 



What does Sodium Sulfacetamide 9.8%, Sulfur 4.8% look like?



What are the available doses of Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

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What should I talk to my health care provider before I take Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

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How should I use Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

INDICATIONS:

DOSAGE AND ADMINISTRATION:


What interacts with Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

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What are the warnings of Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

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What are the precautions of Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

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What are the side effects of Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

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What should I look out for while using Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

CONTRAINDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN.


What might happen if I take too much Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

Sorry No Records found


How should I store and handle Sodium Sulfacetamide 9.8%, Sulfur 4.8%?

Store at 20°C to 25°C (68°F to 77°F) [See USP controlled room temperature]. Protect from moisture.HOW SUPPLIED:


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

CLINICAL PHARMACOLOGY:

Propionibacterium acnes

Non-Clinical Toxicology
CONTRAINDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN.

Oral metronidazole has been reported to potentiate the anticoagulant effect of coumarin and warfarin resulting in a prolongation of prothrombin time. The effect of topical metronidazole on prothrombin time is not known.

PRECAUTIONS: FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

ADVERSE REACTIONS:

Call your doctor for medical advice about side effects. To report SUSPECTED ADVERSE REACTIONS, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

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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).