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Multi-Vitamin With Fluoride

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Overview

What is Multi-Vitamin With Fluoride?

Active ingredient for caries prophylaxis:

Inactive ingredients:



What does Multi-Vitamin With Fluoride look like?



What are the available doses of Multi-Vitamin With Fluoride?

Sorry No records found.

What should I talk to my health care provider before I take Multi-Vitamin With Fluoride?

Sorry No records found

How should I use Multi-Vitamin With Fluoride?

Supplementation of the diet with ten essential vitamins.

Supplementation of the diet with fluoride for caries prophylaxis.

Multi-Vitamin with Fluoride Chewable Tablets

Multi-Vitamin with Fluoride Chewable Tablets

Multi-Vitamin with Fluoride Chewable Tablets

Multi-Vitamin with Fluoride Chewable Tablets

The American Academy of Pediatrics recommends that children up to age 16, in areas where drinking water contains less than optimal levels of fluoride, receive daily fluoride supplementation.

Children using should regularly receive semi-annual dental examinations. Teeth brushing and good oral hygiene practices are essential as well.

One tablet daily or as prescribed.


What interacts with Multi-Vitamin With Fluoride?

Sorry No Records found


What are the warnings of Multi-Vitamin With Fluoride?

Sorry No Records found


What are the precautions of Multi-Vitamin With Fluoride?

Sorry No Records found


What are the side effects of Multi-Vitamin With Fluoride?

Sorry No records found


What should I look out for while using Multi-Vitamin With Fluoride?

AS IN THE CASE OF ALL MEDICATIONS, KEEP OUT OF THE REACH OF CHILDREN.

This tablet should be chewed. This product, as with all chewable tablets, are not recommended for children under age 4 due to risk of choking.


What might happen if I take too much Multi-Vitamin With Fluoride?

Sorry No Records found


How should I store and handle Multi-Vitamin With Fluoride?

Store original packages at room temperature; avoid excessive heat. Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets Multi-Vitamin with Fluoride Chewable Tablets


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Significant decrease in the incidence of dental caries can be linked to the fluoridation of the water supply (1ppm fluoride) during the period of tooth development.

Multi-Vitamin with Fluoride Chewable Tablets

Hydroxyapatite is the principal crystal for all calcified tissue in the human body. The fluoride ion reacts with the hydroxyapatite in the tooth as it is formed to produce the more caries-resistant crystal, fluorapatite.

The reaction may be expressed by the equation:

Ca(PO)(OH) + 2F-  —————> Ca(PO)F + 2OH-

(Hydroxyapatite)                                   (Fluorapatite)

Three stages of fluoride deposition in tooth enamel can be distinguished:

1. Small amounts (reflecting the low levels of fluoride in tissue fluids) are incorporated into the enamel crystals while they are being formed.

2. After enamel has been laid down, fluoride deposition continues in the surface enamel. Diffusion of fluoride from the surface inward is apparently restricted.

3. After eruption, the surface enamel acquires fluoride from the water, food, supplementary fluoride and smaller amounts from saliva.

Non-Clinical Toxicology
AS IN THE CASE OF ALL MEDICATIONS, KEEP OUT OF THE REACH OF CHILDREN.

This tablet should be chewed. This product, as with all chewable tablets, are not recommended for children under age 4 due to risk of choking.

When probenecid is used to elevate plasma concentrations of penicillin, or other beta-lactams, or when such drugs are given to patients taking probenecid therapeutically, high plasma concentrations of the other drug may increase the incidence of adverse reactions associated with that drug. In the case of penicillin, or other beta-lactams, psychic disturbances have been reported.

The use of salicylates antagonizes the uricosuric action of probenecid (see ). The uricosuric action of probenecid is also antagonized by pyrazinamide.

Probenecid produces an insignificant increase in free sulfonamide plasma concentrations but a significant increase in total sulfonamide plasma levels. Since probenecid decreases the renal excretion of conjugated sulfonamides, plasma concentrations of the latter should be determined from time to time when a sulfonamide and probenecid and colchicine are coadministered for prolonged periods. Probenecid may prolong or enhance the action of oral sulfonylureas and thereby increase the risk of hypoglycemia.

It has been reported that patients receiving probenecid require significantly less thiopental for induction of anesthesia. In addition, ketamine and thiopental anesthesia were significantly prolonged in rats receiving probenecid.

The concomitant administration of probenecid increases the mean plasma elimination half-life of a number of drugs which can lead to increased plasma concentrations. These include agents such as indomethacin, acetaminophen, naproxen, ketoprofen, meclofenamate, lorazepam, and rifampin. Although the clinical significance of this observation has not been established, a lower dosage of the drug may be required to produce a therapeutic effect, and increases in dosage of the drug in question should be made cautiously and in small increments when probenecid is being co-administrated. Although specific instances of toxicity due to this potential interaction have not been observed to date, physicians should be alert to this possibility.

Probenecid given concomitantly with sulindac had only a slight effect on plasma sulfide levels, while plasma levels of sulindac and sulfone were increased. Sulindac was shown to produce a modest reduction in the uricosuric action of probenecid, which probably is not significant under most circumstances.

In animals and in humans, probenecid has been reported to increase plasma concentrations of methotrexate (see ).

Falsely high readings for theophylline have been reported in an study, using the Schack and Waxler technique, when therapeutic concentrations of theophylline and probenecid were added to human plasma.

The suggested dose of should not be exceeded, since dental fluorosis may result from continued ingestion of large amounts of fluoride.

Before prescribing

Allergic rash and other idiosyncrasies have been rarely reported.

Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-1800-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

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).