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ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, folic acid, pyridoxine hydrochloride, cyanocobalamin, biotin, calcium carbonate, ferrous fumarate, magnesium oxide, lactic acid and doconexent

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Overview

What is PRENATE Restore?

DESCRIPTION:

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What does PRENATE Restore look like?



What are the available doses of PRENATE Restore?

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

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How should I use PRENATE Restore?

INDICATIONS:

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DOSAGE AND ADMINISTRATION:


What interacts with PRENATE Restore?

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What are the warnings of PRENATE Restore?

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What are the precautions of PRENATE Restore?

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What are the side effects of PRENATE Restore?

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What should I look out for while using PRENATE Restore?

CONTRAINDICATIONS:

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KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.


What might happen if I take too much PRENATE Restore?

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How should I store and handle PRENATE Restore?

HOW SUPPLIED:


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
CONTRAINDICATIONS:

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KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

(See  .) Verapamil hydrochloride injection has been used concomitantly with other cardioactive drugs (especially digitalis) without evidence of serious negative drug interactions. In rare instances, including when patients with severe cardiomyopathy, congestive heart failure, or recent myocardial infarction were given beta-adrenergic blocking agents or disopyramide concomitantly with verapamil, serious adverse effects have occurred. Concomitant use of verapamil hydrochloride with β-adrenergic blockers may result in an exaggerated hypotensive response. Such an effect was observed in one study, following the concomitant administration of verapamil and prazosin. It may be necessary to decrease the dose of verapamil and/or dose of the neuromuscular blocking agent when the drugs are used concomitantly. As verapamil is highly bound to plasma proteins, it should be administered with caution to patients receiving other highly protein-bound drugs.









































PRECAUTIONS:

ADVERSE REACTIONS:

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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).