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Silver Nitrate

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Overview

What is GRAFCO?



What does GRAFCO look like?



What are the available doses of GRAFCO?

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

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How should I use GRAFCO?

INDICATIONS:  For cauterization of skin or mucous membrane and for removing warts and granulated tissue.

DIRECTIONS:  The healthcare professional moistens the applicator tip with distilled water and applies the silver nitrate to the affected area by holding, rubbing, or rotating the tip along the affected tissue.  The strength of the action is controlled by the dilution with distilled water.  One Grafco silver nitrate applicator is generally sufficient for each application. 


What interacts with GRAFCO?

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What are the warnings of GRAFCO?

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What are the precautions of GRAFCO?

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What are the side effects of GRAFCO?

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What should I look out for while using GRAFCO?

CONTRAINDICATIONS:  Silver salts stain tissue black due to depositon of reduced silver.  The stain gradually disappears within a period of two weeks.


What might happen if I take too much GRAFCO?

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How should I store and handle GRAFCO?

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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
CONTRAINDICATIONS:  Silver salts stain tissue black due to depositon of reduced silver.  The stain gradually disappears within a period of two weeks.

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WARNINGS:  KEEP OUT OF REACH OF CHILDREN.  The active ingredients are poisonous and may be fatal when ingested in sufficient doses.  The symptoms include toxic gastroenteritis, which may lead to coma, convulsion, paralysis and profound alteration of respiration.  If poisoning occurs, consult a physician.  In case of eye contact, hold eyes open and immediately flush thoroughly with water for a least 15 minutes and consult a physician.

PRECAUTION:  Silver nitrate is a caustic substance.  Wear appropriate personal protective equipment as needed.  Take care to confine the silver nitrate to the area being treated by using an appropriate physical or chemical barrier to prevent staining or burning of untreated tissue. 

Prolonged ingestion or absorption of silver compounds (organic or inorganic); whether originating industrially or therapeutically, leads to deposition of silver in connective tissues producing a slate-blue discoloration of the skin known as argyria.  This discoloration may also appear on mucous membranes such as the margins of gums.  The sclera of the eye is also stained.  The nature of the pigment is not definitely known, it may be metallic silver or oxide.  This discoloration exists throughout life but does not cause any systematic symptoms.  While small patches may be removed, this method is so tedous and painful as to be impractical for large areas. 

CAUTION:  FEDERAL LAW PROHIBITS DISPENSING WITHOUT PRESCRIPTION. 

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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

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