Multi Vitamin Concentrate
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Multi Vitamin Concentrate Side Effects Center
Medical Editor: John P. Cunha, DO, FACOEP
M.V.I. Adult (multi-vitamin infusion) is used as daily multivitamin maintenance dosage for adults and children aged 11 years and above receiving parenteral nutrition. It is a vitamin supplement. Side effects are uncommon, but may include rash, itching, hives, headache, dizziness, agitation, or double vision.
For intravenous feeding, administer one daily dose of M.V.I. Adult (5 mL of Vial 1 plus 5 mL of Vial 2) added directly to 500 mL to 1,000 mL of intravenous dextrose, saline or similar infusion solutions. M.V.I. Adult may interact with acetazolamide, chlorothiazide sodium, aminophylline, ampicillin, tetracycline, vitamin K, antibiotics, phenytoin, or levodopa. Tell your doctor all medications and supplements you use. Pregnant women and nursing mothers should follow the U.S. Recommended Daily Allowances for their condition. Consult your doctor before becoming pregnant or breastfeeding.
Our M.V.I. Adult (multi-vitamin infusion) Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
What is Prescribing information?
The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.
Multi Vitamin Concentrate FDA Prescribing Information: Side Effects
There have been rare reports of anaphylactoid reactions following large intravenous doses of thiamine. The risk, however, is negligible if thiamine is co-administered with other vitamins in the B group. There have been no reports of fatal anaphylactoid reactions associated with M.V.I. Adult.
There have been rare reports of the following types of reactions:
Ophthalmic - diplopia
Read the entire FDA prescribing information for Multi Vitamin Concentrate (Multi Vitamin Concentrate (intravenous infusion)) »
Additional MVI Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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