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DHA (docosahexaenoic acid), Vit.A (beta-carotine), Vit.C (ascorbic acid), Vit.D-3 (cholecalciferol), Vit.E (d-alpha-tocopheryl acetate), Vit.B-1 (thiamine HCl), Vit.B-2 (riboflavin), Vit.B-3 (niacinamide), Vit.B-6 (pyridoxine HCl), Folate (1.85 mg (6S)-5-methyltetrahydrofolate-Quatrefolic), Vit.B-12 (cyanocobalamin), Iron (carbonyl iron -Ferronyl and ferrous bis-glycinate chelate -Ferrochel), Magnesium (magnesium oxide), Zinc (zinc bis-glycinate chelate -TRAACS), Selenium (sodium selenate), Docusate Sodium

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Overview

What is Folet DHA?

Folet DHA combination pack is a prescription prenatal vitamin and mineral supplementation with DHA taken through pregnancy and during the portnatal period for both lactating and non-lactating mothers. Folet DHA combination pack is also useful in improving nutritional status prior to conception.

It is recommended that for all women folate levels should be high for at least one month prior to possible conception and continued at that level for the first three months of pregnancy.



What does Folet DHA look like?



What are the available doses of Folet DHA?

Sorry No records found.

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

Sorry No records found

How should I use Folet DHA?

One tablet and one softgel daily or as direct by a physician.


What interacts with Folet DHA?

Sorry No Records found


What are the warnings of Folet DHA?

Sorry No Records found


What are the precautions of Folet DHA?

Sorry No Records found


What are the side effects of Folet DHA?

Sorry No records found


What should I look out for while using Folet DHA?

Folet DHA is contraindicated in patients with a known hypersensitivity to any of the components of this product. Hemochromatosis and hemosiderosis are contraindications to iron therapy.


What might happen if I take too much Folet DHA?

Sorry No Records found


How should I store and handle Folet DHA?

Sorry No Records found


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Non-Clinical Toxicology
Folet DHA is contraindicated in patients with a known hypersensitivity to any of the components of this product. Hemochromatosis and hemosiderosis are contraindications to iron therapy.

WARNINGS:

PRECAUTIONS:

Ingestion of more than 3 grams per day of omega-3 fatty acids, such as DHA (docosahexaenoic acid) has been shown to have potential anti-thrombotic effects, including increased bleedng times. Administration of Folet DHA Omega-3 Fatty Acids should be avoided in patients taking anticoagulants.

Allergic sensitization has been reported following both oral and parenteral administration of folic acid.

To report a serious adverse event or to obtain product information, contact (866) 703-3508.

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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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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).