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Methenamine, Sodium Phosphate Monobasic, Methylene Blue, Hyoscyamine Sulfate

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Overview

What is UTA?

UTA CAPSULES for oral administration.Each capsule contains:Methenamine....................................................120 mgSodium Phosphate Monobasic..........................40.8 mgMethylene Blue...................................................10 mgHyoscyamine Sulfate........................................0.12 mg

METHENAMINE (hexamethylenetetramine) exists as colorless, lustrous crystals or white crystalline powder. Its solutions are alkaline to litmus. Freely soluble in water, soluble in alcohol and in chloroform.

SODIUM PHOSPHATE MONOBASIC exists as a white powder. It is freely soluble in water and practically insoluble in alcohol.

METHYLENE BLUE (methylthionine chloride) exists as dark green crystals. It is soluble in water and in chloroform; sparingly soluble in alcohol.

HYOSCYAMINE SULFATE is an alkaloid of belladonna. Exists as a white crystalline powder. Its solutions are alkaline to litmus. Affected by light. It is slightly soluble in water; freely soluble in alcohol; sparingly soluble in ether.

UTA CAPSULES contains inactive ingredients: Microcrystalline Cellulose, Magnesium Stearate, Mannitol and Croscarmellose.



What does UTA look like?



What are the available doses of UTA?

Sorry No records found.

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

Sorry No records found

How should I use UTA?

UTA CAPSULES are indicated for the treatment of symptoms of irritative voiding, the relief of local symptoms, such as inflammation, hypermotility, and pain, which accompany lower urinary tract infections, and the relief of urinary tract symptoms caused by diagnostic procedures.

Adults

Older children


What interacts with UTA?

Sorry No Records found


What are the warnings of UTA?

Sorry No Records found


What are the precautions of UTA?

Sorry No Records found


What are the side effects of UTA?

Please report Adverse Reactions to SJ Pharmaceuticals; Attention: Adverse Reactions; 1212 Collier Rd. NWAtlanta, GA 30318. (877) 604-7575

Cardiovascular

Central Nervous system

Respiratory

Genitourinary

Gastrointestinal


What should I look out for while using UTA?

Hypersensitivity to any of the ingredients is possible. Risk-benefit should be carefully considered when the following medical problems exist: cardiac desease (especially cardiac arrhythmias, congestive heart failure, coronary heart disease, mitral stenosis); gastrointestinal tract obstructive disease; glaucoma; myasthenia gravis; acute urinary retention may be precipitated in obstructive uropathy (such as bladder neck obstruction due to prostatic hypertrophy).

Do not exceed recommended dosage. If rapid pulse, dizziness, or blurring of vision occurs discontinue use immediately.


What might happen if I take too much UTA?

Emesis or gastric lavage. Slow intravenous administration of physostigmine in doses of 1 to 4 mg (0.5 to 1 mg in children) repeated as needed in one to two hours to reverse severe antimuscarinic symptoms. Administration of small doses of diazepam to control excitement and seizures. Artificial respiration with oxygen if needed for respiratory depression. Adequate hydration. Symptomatic treatment as necessary.


How should I store and handle UTA?

ArrayUTA Capsules are blue/blue capsules imprinted "SJ 646" NDC 24839-699-01, bottles of 100 capsules and a unit dose pack of 1 capsule (24839-699-99).


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Clinical Information

Chemical Structure

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Clinical Pharmacology

METHENAMINE degrades in an acidic urine environment releasing formaldehyde which provides bactericidal or bacteriostatic action. It is well absorbed from the gastrointestinal tract. 70%-90% reaches the urine unchanged at which point it is hydrolyzed if the urine is acidic. Within 24 hours it is almost completely (90%) excreted; of this at pH5, approximately 20% is formaldehyde. Protein binding - some formaldehyde is bound to substances in the urine and surrounding tissues. Methenamine is freely distributed to body tissue and fluids but is not clinically significant as it does not hydrolyze at pH greater than 6.8.

SODIUM PHOSPHATE MONOBASIC an acidifier, helps to maintain an acid pH in the urine necessary for the degradation of methenamine.

METHYLENE BLUE possesses weak antiseptic properties. it is well absorbed by the gastrointestinal tract and is srapidly reduced to leukomethylene blue which is stabilized in some combination form in the urine. 75% is excreted unchanged.

HYOSCYAMINE is a parasympatholytic, which relaxes smooth muscles and thus produces an antispasmodic effect. It is well absorbed from the gastrointestinal tract and is rapidly distributed throughout body tissues. Most is excreted in the urine within 12 hours, 13% to 50% being unchanged. Its biotransformation is hepatic. Its protein binding is moderate.

Non-Clinical Toxicology
Hypersensitivity to any of the ingredients is possible. Risk-benefit should be carefully considered when the following medical problems exist: cardiac desease (especially cardiac arrhythmias, congestive heart failure, coronary heart disease, mitral stenosis); gastrointestinal tract obstructive disease; glaucoma; myasthenia gravis; acute urinary retention may be precipitated in obstructive uropathy (such as bladder neck obstruction due to prostatic hypertrophy).

Do not exceed recommended dosage. If rapid pulse, dizziness, or blurring of vision occurs discontinue use immediately.

Temporary resistance to prothrombin-depressing anticoagulants may result, especially when larger doses of phytonadione are used. If relatively large doses have been employed, it may be necessary when reinstituting anticoagulant therapy to use somewhat larger doses of the prothrombin-depressing anticoagulant or to use one which acts on a different principle, such as heparin sodium.

Cross sensitivity and/or related problems

Pregnancy/Reproduction (FDA Pregnancy category C)

Breast feeding

Prolonged use

Pediatric

Geriatric

Drug Interactions

Please report Adverse Reactions to SJ Pharmaceuticals; Attention: Adverse Reactions; 1212 Collier Rd. NWAtlanta, GA 30318. (877) 604-7575

Cardiovascular

Central Nervous system

Respiratory

Genitourinary

Gastrointestinal

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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

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