What is Infuvite Pediatric IV and how is it used?
Infuvite Pediatric IV is a prescription medicine used as a vitamin supplement for infusion for pediatric patients receiving parenteral nutrition. Infuvite Pediatric IV may be used alone or with other medications.
Infuvite Pediatric IV belongs to a class of drugs called Vitamins and Mineral Combinations.
It is not known if Infuvite Pediatric IV is safe and effective in children up to 11 years of age.
What are the possible side effects of Infuvite Pediatric IV?
Infuvite Pediatric IV may cause serious side effects including:
- difficulty breathing,
- swelling of your face, lips, tongue, or throat,
- severe dizziness,
- dizziness, and
- blurred vision
Get medical help right away, if you have any of the symptoms listed above.
The most common side effects of Infuvite Pediatric IV include:
- skin redness,
- double vision,
- shortness of breath,
- wheezing, and
- skin swelling
Tell the doctor if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of Infuvite Pediatric IV. For more information, ask your doctor or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
INFUVITE PEDIATRIC (multiple vitamins injection) is a sterile product consisting of 2 vials provided as a pharmacy bulk package for intravenous use:
- Vial 1 (40 mL Fill in 50 mL Vial); and
- Vial 2 (10 mL).
A pharmacy bulk package is a container of a sterile preparation for parenteral use that contains many single doses. The contents are intended for use in a pharmacy admixture program and are restricted to the preparation of admixtures for intravenous infusion [see DOSAGE AND ADMINISTRATION].
Each 4 mL of Vial 1 contains 10 vitamins (see Table 2).
Table 2: Active Ingredients in 4 mL of Vial 1
|Ascorbic acid (Vitamin C)||80 mg|
|Vitamin A* (as palmitate)||2,300 IU
(equals 0.7 mg)
|Vitamin D3* (cholecalciferol)||400 IU
(equals 10 mcg)
|Thiamine (Vitamin B1) (as the hydrochloride)||1.2 mg|
|Riboflavin (Vitamin B2) (as riboflavin 5-phosphate sodium)||1.4 mg|
|Pyridoxine HCl (Vitamin B6)||1 mg|
|Dexpanthenol (as d-pantothenyl alcohol)||5mg|
|Vitamin E* (dl-α-tocopheryl acetate)||7 IU (equals 7 mg)|
|Vitamin K1*||0.2 mg|
|*Polysorbate 80 is used to water solubilize the oil-soluble vitamins A, D, E, and K.|
Inactive ingredients in Vial 1: 50 mg polysorbate 80, sodium hydroxide and/or hydrochloric acid for pH adjustment, and water for injection. Each 1 mL of Vial 2 contains 3 vitamins (see Table 3).
Table 3: Active Ingredients in 1 mL of Vial 2
|Folic acid||140 mcg|
|Vitamin B12 (cyanocobalamin)||1 mcg|
Inactive ingredients in Vial 2: 75 mg mannitol, citric acid and/or sodium citrate for pH adjustment and water for injection.
INFUVITE PEDIATRIC (multiple vitamins injection) makes available a combination of oil-soluble and water-soluble vitamins in an aqueous solution, formulated for incorporation into intravenous solutions. The liposoluble vitamins A, D, E, and K have been solubilized in an aqueous medium with polysorbate 80, permitting intravenous administration of these vitamins.
INFUVITE PEDIATRIC contains no more than 30 mcg/L of aluminum (combined Vials 1 and 2).
INFUVITE PEDIATRIC is a combination of vitamins indicated for the prevention of vitamin deficiency in pediatric patients up to 11 years of age receiving parenteral nutrition.
The physician should not await the development of clinical signs of vitamin deficiency before initiating vitamin therapy.
DOSAGE AND ADMINISTRATION
Important Dosage And Administration Instructions
INFUVITE PEDIATRIC is a combination product that contains the following vitamins: ascorbic acid, vitamin A, vitamin D, thiamine, riboflavin, pyridoxine, niacinamide, dexpanthenol, vitamin E, vitamin K1, folic acid, biotin, and vitamin B12 [see Dosage Information].
INFUVITE PEDIATRIC is supplied as a pharmacy bulk package, and consists of two pharmacy bulk vials which must be combined and diluted prior to intravenous administration [see Preparation And Administration Instructions]. As a pharmacy bulk vial, INFUVITE PEDIATRIC is intended for dispensing of single doses to many patients in a pharmacy admixture program and is restricted to the preparation of admixtures for infusion. Each closure shall be penetrated only one time with a suitable sterile transfer device or dispensing set that allows measured dispensing of the contents. INFUVITE PEDIATRIC is to be used only in a suitable work area such as a laminar flow hood (or an equivalent clean air compounding area).
Dispensing from a pharmacy bulk vial should be completed within 4 hours after the vial is penetrated. After combining contents of the two vials, a specified volume of INFUVITE PEDIATRIC is added to intravenous fluids prior to intravenous administration [see Preparation And Administration Instructions]. Do not administer INFUVITE PEDIATRIC as a direct, undiluted intravenous injection as it may cause dizziness, faintness, and possible tissue irritation.
The recommended daily dosage volume of 1.5 mL, 3.25 mL, or 5 mL of the combined contents of Vials 1 and 2 is based on the patient's actual weight of less than 1 kg, 1 kg to less than 3 kg, and more than or equal to 3 kg, respectively (see Table 1). One daily dose of combined content of vials 1 and 2 (1.5 mL, 3.25 mL or 5 mL) is then added directly to the intravenous fluid [see Preparation And Administration Instructions]. Patients with multiple vitamin deficiencies or with increased vitamin requirements may need multiple daily dosages as indicated or additional doses of individual vitamins. However, additional daily dosages in infants are not recommended [see WARNINGS AND PRECAUTIONS]. Supplemental vitamin A may be required for low-birth weight infants.
Table 1: Recommended Weight-Based Dosage of INFUVITE
|Less than 1 kg||≥ 1 kg and < 3 kg||More than or equal to 3 kg|
|Daily Dosage Volume||1.5 mL||3.25 mL||5 mL|
|Ascorbic acid (Vitamin C)||24 mg||52 mg||80 mg|
|Vitamin A (as palmitate)||690 IU (equals 0.2 mg)||1495 IU (equals 0.5 mg)||2,300 IU (equals 0.7 mg)|
|Vitamin D3 (cholecalciferol)||120 IU (equals 3 mcg)||260 IU (equals 7 mcg)||400 IU (equals 10 mcg)|
|Thiamine (Vitamin B1) (as the hydrochloride)||0.4 mg||0.8 mg||12 mg|
|Riboflavin (Vitamin B2) (as riboflavin 5-phosphate sodium)||0.4 mg||0.9 mg||1.4 mg|
|Pyridoxine HCl (Vitamin B6)||0.3 mg||0.7 mg||1 mg|
|Niacinamide||5.1 mg||11.1 mg||17 mg|
|Dexpanthenol (as J-pantothenyl alcohol)||15 mg||3.3 mg||5 mg|
|Vitamin E (dl-a-tocopheryl acetate)||2.1 IU (equals 2 mg)||4.6 IU (equals 5 mg)||7 IU (equals 7 mg)|
|Vitamin K1||0.1 mg||0.1 mg||0.2 mg|
|Folic acid||42 mcg||91 mcg||140 mcg|
|Biotin||6 mcg||13 mcg||20 mcg|
|Vitamin B12 (cyanocobalamin)||0.3 mcg||0.7 mcg||1 mcg|
Preparation And Administration Instructions
INFUVITE PEDIATRIC is supplied as a pharmacy bulk package. It consists of two pharmacy bulk vials that must be combined and diluted prior to intravenous administration.
- Transfer the contents of Vial 2 (10 mL of solution) into the contents of Vial 1 (40 mL of solution). The mixed solution (50 mL) will provide thirty-three 1.5 mL single doses, fifteen 3.25 mL single doses or ten 5 mL single doses.
- Add one dose directly to at least 100 mL of intravenous dextrose or saline solution for each patient. INFUVITE PEDIATRIC must be diluted in an intravenous infusion; it is not intended for direct infusion.
- Visually inspect for particulate matter and discoloration prior to administration.
- After puncture, complete dispensing from the pharmacy bulk vial should be completed within 4 hours.
- After INFUVITE PEDIATRIC is diluted in an intravenous infusion, refrigerate the resulting solution unless it is to be used immediately, and use the solution within 24 hours after dilution.
- Minimize exposure to light because some of the vitamins in INFUVITE PEDIATRIC, particularly A, D and riboflavin, are light sensitive.
- Discard unused portion.
Monitoring Vitamin Blood Levels
Blood vitamin concentrations should be monitored to ensure maintenance of adequate levels, particularly in patients receiving parenteral multivitamins as the only credit of vitamins for long periods of time.
- INFUVITE PEDIATRIC is not physically compatible with moderately alkaline solutions such as a sodium bicarbonate solution and other alkaline drugs such as acetazolamide sodium, aminophylline, ampicillin sodium, tetracycline HCl and chlorothiazide sodium.
- Folic acid is unstable in the presence of calcium salts such as calcium gluconate.
- Vitamin A and thiamine in INFUVITE PEDIATRIC may react with bisulfite solutions such as sodium bisulfite or vitamin K bisulfate.
- Do not add INFUVITE PEDIATRIC directly to intravenous fat emulsions.
- Consult appropriate references for listings of physical and chemical compatibility of solutions and drugs with the vitamin infusion. In such circumstances, admixture or Y-site administration with vitamin solutions should be avoided.
Dosage Forms And Strengths
INFUVITE PEDIATRIC is an injection consisting of two vials labeled Vial 1 (40 mL Fill in 50 mL Vial) and Vial 2 (10 mL). The mixed solution (50 mL) will provide thirty-three 1.5 mL single doses, fifteen 3.25 mL single doses or ten 5 mL single doses. For the vitamin strengths, see Dosage Information and DESCRIPTION.
Storage And Handling
INFUVITE PEDIATRIC (multiple vitamins injection) is supplied as a pharmacy bulk package available in boxes containing 2 vials â€“ Vial 1 (40 mL Fill in 50 mL Vial) and Vial 2 (10 mL). Mix contents of Vial 2 with Vial 1 to provide thirty-three 1.5 mL single doses, fifteen 3.25 mL single doses or 10 single 5 mL doses [see Dosage Information and Preparation And Administration Instructions].
NDC 54643-5647-0 Store at 2-8°C (36-46°F).
Manufactured by: Sandoz Canada Inc., 145 Jules-LÃ©ger Street Boucherville, Qc, Canada, J4B 7K8. Distributed by: Baxter Healthcare Corporation, Clintec Nutrition Division Deerfield, IL 60015 USA, Revised: Jul 2014
The following adverse reactions are discussed in greater detail in other sections of the labeling.
- Allergic reactions to thiamine [see WARNINGS AND PRECAUTIONS].
- Hypervitaminosis A [see WARNINGS AND PRECAUTIONS]
The following adverse reactions have been identified during postapproval use of the vitamins in INFUVITE PEDIATRIC. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Dermatologic: rash, erythema, pruritis
CNS: headache, dizziness, agitation, anxiety
Drug Interactions Affecting Co-administered Drugs
A number of interactions between vitamins and drugs have been reported. The following are examples of these types of interactions:
Warfarin: Vitamin K, a component of INFUVITE PEDIATRIC, antagonizes the anticoagulant action of warfarin. In patients who are co-administered warfarin and INFUVITE PEDIATRIC, blood levels of prothrombin/INR should be periodically monitored to determine if dose of warfarin needs to be adjusted.
Bleomycin: Ascorbic acid and riboflavin inactivate bleomycin in vitro, thus the activity of bleomycin may be reduced.
Levodopa: Pyridoxine may increase the metabolism of levodopa (decrease blood levels of levodopa) and decrease its efficacy.
Methotrexate: Folic acid may decrease a patient's response to methotrexate therapy.
Drug Interactions Affecting Vitamin Levels
Concomitant administration of hydralazine or isoniazid may increase pyridoxine requirements.
Phenytoin may decrease serum folic acid concentrations.
Included as part of the PRECAUTIONS section.
INFUVITE PEDIATRIC contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration in pediatric patients with renal impairment. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solution, which contain aluminum.
Patients with renal impairment, 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. Consider periodic monitoring of aluminum levels with prolonged parenteral administration of INFUVITE PEDIATRIC.
Allergic Reactions To Thiamine
Allergic reactions such as urticaria, shortness of breath, wheezing and angioedema have been reported following intravenous administration of thiamine, which is found in INFUVITE PEDIATRIC. There have been rare reports of anaphylaxis following intravenous doses of thiamine. No fatal anaphylaxis associated with INFUVITE PEDIATRIC has been reported.
Hypervitaminosis A, manifested by nausea, vomiting, headache, dizziness, blurred vision has been reported in patients with renal failure receiving 1.5 mg/day retinol and in patients with liver disease. Therefore, supplementation of renal failure patients and patients with liver disease with vitamin A, an ingredient found in INFUVITE PEDIATRIC, should be undertaken with caution [See Use in Specific Populations]. Blood levels of Vitamin A should be monitored periodically.
Vitamin K Antagonizes The Anticoagulant Action Of Warfarin
Vitamin K, which is found in INFUVITE PEDIATRIC, antagonizes the anticoagulant action of warfarin. In patients who are on warfarin anticoagulant therapy receiving parenteral multivitamins such as with INFUVITE PEDIATRIC blood levels of prothrombin/INR should be periodically monitored to determine if dose of warfarin needs to be adjusted.
Interferes With Diagnosis Of Megaloblastic Anemia
Avoid the use of INFUVITE PEDIATRIC in patients with suspected or diagnosed megaloblastic anemia prior to blood sampling for the detection of the folic acid and cyanocobalamin deficiencies. The folic acid and the cyanocobalamin in INFUVITE PEDIATRIC can mask serum deficits of folic acid and cyanocobalamin in these patients.
Potential To Develop Vitamin Deficiencies Or Excesses
In patients receiving parenteral multivitamins such as with INFUVITE PEDIATRIC, blood concentration should be periodically monitored to determine if vitamin deficiencies or excesses are developing. INFUVITE PEDIATRIC may not correct long-standing specific vitamin deficiencies. The administration of additional doses of specific vitamins may be required [see DOSAGE AND ADMINISTRATION].
Interference With Urine Glucose Testing
Vitamin E Overdose In Infants Receiving Additional Vitamin E
Avoid additional oral or parental doses of vitamin E in infants. Daily dose of INFUVITE PEDIATRIC contains adequate concentrations of vitamin E required to achieve normal blood levels of vitamin E. Therefore, additional vitamin E supplementations of patients receiving INFUVITE PEDIATRIC may result in elevated blood concentrations of vitamin E and potential vitamin E toxicity in infants.
Risk Of Low Vitamin A Levels
Vitamin A may adhere to plastic, resulting in lower vitamin A concentrations after administration of INFUVITE PEDIATRIC. Therefore, blood vitamin concentrations should be periodically monitored and the administration of additional therapeutic doses of vitamin A may be required, especially in low-birth weight infants.
Risk Of E-Ferol Syndrome In Low-Birth Weight Infants
E-Ferol syndrome manifested by thrombocytopenia, renal dysfunction, hepatomegaly, cholestasis, ascites, hypotension and metabolic acidosis has been reported in low-birth weight infants following administration of polysorbates which are found in INFUVITE PEDIATRIC. No E-Ferol syndrome associated with INFUVITE PEDIATRIC has been reported.
Carcinogenesis, Mutagenesis, Impairment Of Fertility
Carcinogenicity, mutagenicity, and fertility studies have not been performed with INFUVITE PEDIATRIC.
Use In Specific Populations
Pregnancy Category C.
INFUVITE PEDIATRIC has not been studied in pregnant women. Pregnant women should follow the U.S. recommended daily allowances for pregnancy because their vitamin requirements may exceed those of non-pregnant women. Animal reproduction studies have not been conducted with INFUVITE PEDIATRIC (multiple vitamins injection).
INFUVITE PEDIATRIC has not been studied in nursing mothers. Lactating women may have vitamin requirements that exceed those of non-lactating women. Caution should be exercised when INFUVITE PEDIATRIC is administered to nursing mothers.
INFUVITE PEDIATRIC is approved for the prevention of vitamin deficiency in pediatric patients up to 11 years old receiving parenteral nutrition. INFUVITE PEDIATRIC has not been studied in pediatric patients older than 11 years.
INFUVITE PEDIATRIC contains aluminum that may be toxic for premature neonates. Aluminum levels should be monitored periodically during administration of INFUVITE PEDIATRIC to premature neonates [see WARNINGS AND PRECAUTIONS].
Additional vitamin E supplementations of infants receiving INFUVITE PEDIATRIC may result in elevated blood concentrations of vitamin E and potential vitamin E toxicity [see WARNINGS AND PRECAUTIONS].
E-Ferol syndrome has been reported in low-birth weight infants following administration of polysorbates which are found in INFUVITE PEDIATRIC. No E-Ferol syndrome associated with INFUVITE PEDIATRIC has been reported [see WARNINGS AND PRECAUTIONS].
INFUVITE PEDIATRIC has not been studied in patients with renal impairment. Monitor renal function, calcium, phosphorus and vitamin A levels in patients with renal impairment [see WARNINGS AND PRECAUTIONS].
INFUVITE PEDIATRIC has not been studied in patients with liver impairments. Monitor vitamin A levels in patients with liver disease [see WARNINGS AND PRECAUTIONS].
Signs and symptoms of acute or chronic overdosage may be those of individual INFUVITE PEDIATRIC component toxicity. There is no clinical experience with INFUVITE PEDIATRIC overdosage.
INFUVITE PEDIATRIC is contraindicated in patients who have:
- An existing hypervitaminosis, or
- A history of hypersensitivity due to any vitamins or excipients contained in this formulation.
Instruct caregiver(s) and patients (if age appropriate) that:
- Caregivers should watch patients for signs of allergic reactions such as urticaria, shortness of breath, wheezing and angioedema, which have been reported following intravenous administration of thiamine.
- If patients have renal impairment caregivers should watch for and immediately report signs of hypervitaminosis A, manifested by nausea, vomiting, headache, dizziness, blurred vision.
- Instruct caregivers to report other adverse reactions that patients may experience such as rash, erythema, pruritus, headache, dizziness, agitation, anxiety, and diplopia.
- If patients who are on warfarin anticoagulant therapy, instruct caregivers that patients will be monitored periodically with blood prothrombin/ INR levels to determine if the dose of warfarin needs to be adjusted.
- Explain to caregivers the significance of periodic monitoring of blood vitamin concentrations to determine if vitamin deficiencies or excesses are developing and the need to monitor renal function, calcium, phosphorus, aluminum and vitamin A levels in patients with renal impairment.
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