Proviten JR IV(Vitamin A, Vitamin-B complex, Vitamin-C , Vitamin-D and Vitamin E)

Therapeutic Group: Vitamins and Minerals

Presentation

Proviten JR IV for infusion: Proviten JR IV is a lyophilized, sterile powder/cake for infusion which contains both water soluble and fat soluble vitamins.

Each vial of Proviten Jr IV contains:

Vitamin A 2300 IU

Vitamin D3 400 IU

Vitamin E 7 mg

Vitamin C 80 mg

Vitamin B1 1.2 mg

Vitamin B2 1.4 mg

Vitamin B6 1 mg

Vitamin B12 0.001 mg

Folic acid 0.14 mg

Dexpanthenol 5 mg

Biotin 0.02 mg

Nicotinamide 17 mg

Vitamin K1 0.2 mg

Description

Proviten JR IV is a sterile, lyophilized powder/cake for infusion which contains nine water-soluble and four fat soluble vitamins. Mixed micelles is used as a solubilizing agent. It is presented as a lyophilized, orange-yellow, sterile powder cake that is to be reconstituted with 5 ml of Water for injections or other parenteral fluids, (e.g. as 0.9% Sodium chloride or 5% Dextrose solution), prior to administration by parenteral route.

Indications

Proviten JR IV is indicated as a daily multivitamin maintenance dosage for infants and children aged up to 11 years 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.

Dosage & Administration

Dosage
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). 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.
Administration
The single dose vial of Proviten JR IV is reconstituted by adding 5 ml of sterile Water for injection or other intravenous fluids like 0.9% Sodium Chloride injection or 5% dextrose injection. 5 ml of diluent should be added by means of sterile syringe into the vial and gently mixed to dissolve the lyophilized powder/cake. The product will form a clear and yellow color solution after reconstitution. The reconstituted solution is ready within three minutes for immediate use. After Proviten JR IV 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, D and riboflavin are light-sensitive and exposure to light should be minimized. The reconstituted Proviten
JR IV 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 Proviten JR IV should be added directly to not less than 100 ml of intravenous dextrose, saline or similar infusion solutions.
DISCARD ANY UNUSED PORTION.

Side Effects

There have been rare reports of anaphylactic reactions following parenteral multivitamin administration. Rare reports of anaphylactic reactions have also been reported after large intravenous doses of thiamine. The risk is negligible if thiamine is co-administered with
other vitamins in the B group. There have been rare reports of the following types of reactions:- rash, erythema, pruritus, headache, dizziness, agitation, anxiety, diplopia, urticaria, shortness of breath, wheezing, and angioedema.

Precautions

Caution should be exercised when administering this multivitamin formulation to patients on warfarin sodium-type anticoagulant therapy as it contains Vitamin K. Larger doses or supplementation with oral or parenteral vitamin E are not recommended because elevated blood levels of vitamin E may result. Additional vitamin A supplementation may be
required, especially in low birth weight infants. Polysorbates have been associated with the E-Ferol syndrome (thrombocytopenia, renal dysfunction, hepatomegaly, cholestasis, ascites, hypotension, and metabolic acidosis) in low birth weight infants. This product contains aluminum. 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.

Use in Pregnancy & Lactation

Not recommended