Multi Vitamin Infusion Pediatric Prescribing Information

Multi Vitamin Infusion Pediatric Description

M.V.I. Pediatric® is a lyophilized, sterile powder intended for reconstitution and dilution in intravenous infusions. Each 5 mL of reconstituted product provides:

Ascorbic acid (vitamin C)………………………………………………………………………80 mg

Vitamin A* (retinol)………………………………………………………………………..0.7 mg (a)

Ergocalciferol*

(vitamin D)………………………………………………………………………………10 mcg (b)

Thiamine (vitamin B1)

(as the hydrochloride)………………………………………………………………………..1.2 mg

Riboflavin (vitamin B2) (as riboflavin-

5-phosphate sodium)…………………………………………………………………………...1.4 mg

Pyridoxine (vitamin B6)

(as the hydrochloride)………………………………………………………………………….1 mg

Niacinamide…………………………………………………………………………………….17 mg

Dexpanthenol

(d-pantothenyl alcohol)………………………………………………………………………...5 mg

Vitamin E* (dl-alpha

tocopheryl acetate)…………………………………………………………………………7 mg (c)

Biotin…………………………………………………………………………………………..20 mcg

Folic acid……………………………………………………………………………………..140 mcg

Cyanocobalamin

(vitamin B12)………………………………………………………………………………….1 mcg

Phytonadione*

(vitamin K1)………………………………………………………………………………...200 mcg

with 375 mg mannitol; sodium hydroxide for pH adjustment; 50 mg polysorbate 80; 0.8 mg polysorbate 20; 58 mcg butylated hydroxytoluene; 14 mcg butylated hydroxyanisole.

*Oil-soluble vitamins A, D, E and K1 water-solubilized with polysorbate 80.

(a) 0.7 mg vitamin A equals 2,300 USP units.

(b) 10 mcg ergocalciferol equals 400 USP units.

(c) 7 mg vitamin E equals 7 USP units.

Multivitamin Formula for Intravenous Infusion: M.V.I. Pediatric® (Multi- Vitamin for Infusion) provides a combination of important oil-soluble and water-soluble vitamins, formulated especially for incorporation into intravenous infusions after reconstitution. Through special processing techniques, the liposoluble vitamins A, D, E and K1 have been water solubilized with polysorbate 80, permitting intravenous administration of these vitamins.

Related/similar drugs

acetylcysteine, ascorbic acid, biotin, multivitamin, Dextrose, l-methylfolate, Deplin

Indications and Usage for Multi Vitamin Infusion Pediatric

This formulation is indicated as daily multivitamin maintenance dosage for infants and children up to 11 years of age receiving parenteral nutrition.

It is also indicated in other situations where administration by the intravenous route is required. Such situations include surgery, extensive burns, fractures and other trauma, severe infectious diseases, and comatose states, which may provoke a "stress" situation with profound alterations in the body’s metabolic demands and consequent tissue depletion of nutrients.

The physician should not await the development of clinical signs of vitamin deficiency before initiating vitamin therapy.

M.V.I. Pediatric® (reconstituted and administered in intravenous fluids under proper dilution) contributes intake of these necessary vitamins toward maintaining the body’s normal resistance and repair processes.

Patients with multiple vitamin deficiencies or with markedly increased requirements may be given multiples of the daily dosage for two or more days as indicated by the clinical status. Blood vitamin concentrations should be monitored to ensure maintenance of adequate levels, particularly in patients receiving parenteral multivitamins as their sole source of vitamins for long periods of time.

Contraindications

Known hypersensitivity to any of the vitamins or excipients in this product or a pre-existing hypervitaminosis.

Allergic reaction has been known to occur following intravenous administration of thiamine and vitamin K. The formulation is contraindicated prior to blood sampling for detection of megaloblastic anemia, as the folic acid and cyanocobalamin in the vitamin solution can mask serum deficits.

Warnings

WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.

Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.

Precautions

Adverse Reactions/Side Effects

There have been rare reports of anaphylactic reactions following parenteral multivitamin administration. Rare reports of anaphylactoid reactions have also been reported after large intravenous doses of thiamine. The risk, however, is negligible if thiamine is coadministered with other vitamins in the B group. There have been no reports of fatal anaphylactoid reactions associated with M.V.I. Pediatric®.

There have been rare reports of the following types of reactions:

Dermatologic - rash, erythema, pruritus

CNS - headache, dizziness, agitation, anxiety

Ophthalmic -diplopia

Allergic - urticaria, shortness of breath, wheezing, and angioedema

Overdosage

The possibility of hypervitaminosis A or D should be borne in mind. Clinical manifestations of hypervitaminosis A have been reported in patients with renal failure receiving 1.5 mg/day retinol. Therefore, vitamin A supplementation of renal failure patients should be undertaken with caution.

Multi Vitamin Infusion Pediatric Dosage and Administration

The single dose vial of M.V.I. Pediatric® is reconstituted by adding 5 mL of Sterile Water for Injection USP, Dextrose Injection USP 5%, or Sodium Chloride Injection to the 10 mL vial.

The vial may be swirled gently after the addition of the water to hasten reconstitution. Use of this product is restricted to a suitable work area, such as a laminar flow hood. The reconstituted solution is ready within three minutes for immediate use. The withdrawal of container contents should be accomplished without delay. However, should this not be possible, a maximum time of 4 hours from initial closure entry is permitted to complete fluid transfer operations. The amount to be administered should be added to appropriate intravenous infusion fluids (see below).

The reconstituted M.V.I. Pediatric® should not be given as a direct, undiluted intravenous injection as it may give rise to dizziness, faintness and possible tissue irritation.

For a single dose, 5 mL of reconstituted M.V.I. Pediatric® should be added directly to not less than 100 mL of intravenous dextrose, saline or similar infusion solutions.

Infants weighing less than 1 kg: The daily dose is 30% (1.5 mL) of a single full dose (5 mL). Do not exceed this daily dose.

Infants weighing 1 to 3 kg: The daily dose is 65% (3.25 mL) of a single full dose (5 mL). Multiples of this recommended dose should not be given to infants weighing less than 3 kg. A supplemental vitamin A may be required for low birth weight infants.

Infants and children weighing 3 kg or more up to 11 years of age: The daily dose is 5 mL unless there is clinical or laboratory evidence for increasing or decreasing the dosage.

DISCARD ANY UNUSED PORTION.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

After M.V.I. Pediatric® is reconstituted it should be immediately diluted into the intravenous solution. The resulting solution should be administered immediately. Some of the vitamins in this product, particularly vitamins A and D and riboflavin, are light-sensitive and exposure to light should be minimized.

How is Multi Vitamin Infusion Pediatric supplied

M.V.I. Pediatric® is available as:

NDC 61703-421-53, Single Dose Vial, Boxes of 10.

Store under refrigeration, 2 to 8°C (36 to 46°F).

Revised: August, 2007

005036

Manufactured for:

Hospira, Inc.

Lake Forest, IL 60045 USA EN-1593

RL-2156