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Lytensopril

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Overview

What is Lytensopril?

PRODUCT DESCRIPTION Primary Ingredients Hypertensa consists of a proprietary formulation of L-Arginine, Choline Bitartrate, Whey Protein Hydrolysate, Cocoa, Cinnamon, Ginseng, L-Leucine, L-Glutamine, LHistidine, Caffeine, L-Cysteine, and Grape Seed Extract in specific proportions. These ingredients fall into the classification of Generally Recognized as Safe (GRAS) as defined by the Food and Drug Administration (FDA) (Sections 201(s) and 409 of the Federal Food, Drug, and Cosmetic Act). A GRAS substance is distinguished from a food additive on the basis of the common knowledge about the safety of the substance for its intended use. The standard for an ingredient to achieve GRAS status requires not only technical demonstration of non-toxicity and safety, but also general recognition of safety through widespread usage and agreement of that safety by experts in the field. Many ingredients have been determined by the FDA to be GRAS, and are listed as such by regulation, in Volume 21 Code of Federal Regulations (CFR) Sections 182, 184, and 186. Amino AcidsAmino Acids are the building blocks of protein and are GRAS listed as they have been safely ingested by humans for thousands of years. The formulations of the amino acids in Hypertensa are equivalent to those found in the usual human diet. Patients with hypertension may require an increased amount of certain amino acids that cannot be obtained from normal diet alone. Arginine, for example, is a conditional amino acid. The body can make arginine in the liver, but the liver produced arginine can only be used in the liver itself. Arginine is needed to produce nitric oxide (NO). NO is required to dilate the constricted blood vessels that are the cause of high blood pressure. Patients with hypertension have an increase in the enzyme, arginase that degrades arginine before it can be used to produce NO. Some patients with hypertension have a resistance to the use of arginine that is similar to the mechanism found in insulin resistance that is genetically determined. Patients with hypertension cannot obtain sufficient arginine from the diet without ingesting a prohibitively large amount of calories, particularly calories from protein. FlavonoidsFlavonoids are a group of phytochemical compounds found in all vascular plants including fruits and vegetables. They are a part of a larger class of compounds known as polyphenols. Many of the therapeutic or health benefits of colored fruits and vegetables, cocoa, red wine, and green tea are directly related to their flavonoid content. The specially formulated flavonoids found in Hypertensa cannot be obtained from conventional foods in the necessary proportions to elicit a therapeutic response. Other IngredientsHypertensa contains the following “inactive” or other ingredients, as fillers, excipients, and colorings: Tricalcium Phosphate, Gelatin, Silicone Dioxide, Vegetable Magnesium Stearate, Microcrystalline Cellulose, Chlorophyllin Copper Complex, Titanium Dioxide. Physical DescriptionHypertensa is a yellow to light brown powder. Hypertensa consists of a proprietary formulation of L-Arginine, Choline Bitartrate, Whey Protein Hydrolysate, Cocoa, Cinnamon, Ginseng, L-Leucine, L-Glutamine, L-Histidine, Caffeine, L-Cysteine, and Grape Seed Extract.



What does Lytensopril look like?



What are the available doses of Lytensopril?

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

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How should I use Lytensopril?

INDICATIONS FOR USEHypertensa is intended for the clinical dietary management of the metabolic processes of hypertension.

DOSAGE AND ADMINISTRATIONRecommended AdministrationFor the dietary management of the metabolic processes associated with hypertension. Take two (2) capsules twice daily or as directed by physician.As with most amino acid formulations Hypertensa should be taken without food to increase the absorption of key ingredients.


What interacts with Lytensopril?

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What are the warnings of Lytensopril?

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What are the precautions of Lytensopril?

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What are the side effects of Lytensopril?

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What should I look out for while using Lytensopril?

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What might happen if I take too much Lytensopril?

OVERDOSEThere is a negligible risk of overdose with Hypertensa as the total amount of amino acids in a two week supply (60 capsules) is less than 12 grams.Overdose symptoms may include diarrhea, weakness, and nausea.


How should I store and handle Lytensopril?

Store bottles at controlled room temperature, 59° to 86°F (15° to 30°C) and dispense in tight, light-resistant containers (USP).How SuppliedHypertensa is supplied in green and white, size 0 capsules in bottles of 60 and 90 capsules.Physician SupervisionHypertensa is a Medical Food product available by prescription only and may be used per FDA law, and product labeling while the patient is under ongoing physician supervision. U.S. patent pendingManufactured by Arizona Nutritional Supplements, Inc. Chandler AZ 85225Distributed exclusively by Physician Therapeutics LLC, a wholly owned subsidiary of Targeted Medical Pharma Inc. Los Angeles, CA.www.ptlcentral.comNDC: 68405-007-02NDC: 68405-007-03


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Clinical Information

Chemical Structure

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Clinical Pharmacology

CLINICAL PHARMACOLOGYMechanism of ActionHypertensa acts by restoring and maintaining the balance of Nitric Oxide (NO) in patients with hypertension.MetabolismThe amino acids in Hypertensa are primarily absorbed by the stomach and small intestines. All cells metabolize the amino acids in Hypertensa. Circulating tryptophan, arginine and choline blood levels determine the production of serotonin, nitric oxide, and acetylcholine.ExcretionHypertensa is not an inhibitor of cytochrome P450 1A2, 2C9, 2C19, 2D6, or 3A4. These isoenzymes are principally responsible for 95% of all detoxification of drugs, with CYP3A4 being responsible for detoxification of roughly 50% of drugs. Amino acids do not appear to have an effect on drug metabolizing enzymes.

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

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