L-Isoleucine
USP 0.352 g
L-Leucine
USP 0.490 g
L-Lysine
Hydrochloride USP 0.430 g
L-Methionine
USP 0.225 g
L-Phenylalanine
USP 0.533 g
L-
Threonine USP 0.250 g
L-Tryptophan
USP 0.090 g
L-Valine
USP 0.360 g
L-Histidine
USP 0.250 g
L-Tyrosine
USP 0.025 g
Non-Essential
Amino Acids
L-Arginine
USP 0.500 g
L-Aspartic
Acid USP 0.250 g
L-Glutamic
Acid BP 0.075 g
L-Alanine
USP 0.200 g
L-Cysteine
BP 0.010 g
Glycine
USP 0.760 g
L-Proline
USP 0.100 g
L-Serine
USP 0.100 g
Carbohydrate
D-Sorbitol
BP 5.000 g
Electrolytes
(mmol/L)
Sodium
(Na+) 35.5
Potassium
(K+) 25.0
Magnesium
(Mg++) 2.5
Chloride
(CI-) 53.4
Acetate (CH3COO-) 25.0
Description
Amino
Acid, D-Sorbitol and Electrolytes is a
sterile aqueous solution of crystalline Amino Acids and D-Sorbitol with
electrolytes, which is
necessary
as the nitrogen sources for parenteral nutrition. Nitrogen is provided in the
form of essential and non-essential amino acids. The solution is clear,
colorless, having a pH lying in the range of 5.7 to 7.0.
Clinical
Pharmacology
Amino
Acid, D-Sorbitol and Electrolytes contains all 18 essential and non-essential
amino acid needed for protein synthesis. The amino acid composition is such that
positive nitrogen balance can be achieved in the postoperative period and during
extended periods of intravenous nutrition.
Indication
Amino
Acid, D-Sorbitol and Electrolytes is indicated as a source of amino acids for
protein synthesis in patients needing intravenous nutrition. Aminosin is
particularly suitable for patients with basal amino acid requirements. Aminosin
is also indicated in faster recovery in surgery, burns, renal insufficiency,
hepatic insufficiency and effective management of cancer.
Dosage
Adult: The
nitrogen requirement for maintenance of body protein mass depends on the
patient's condition (nutritional state and degree of metabolic stress). The
requirements are 0.10-0.15g nitrogen/kg/day (no or minor metabolic stress and
normal nutritional state), 0.15-0.20g nitrogen/kg/day (moderate metabolic
stress with or without malnutrition) and up to 0.20-0.25g nitrogen/kg/day
(severe catabolism as in burns, sepsis and trauma). The dosage range 0.10-0.25g
nitrogen/kg/day corresponds to 15-35 ml Aminosin/kg/day. In obese patients, the
dose should be based on the estimated ideal weight. Depending upon patients
requirements, 1000-2000 ml Aminosin may be infused intravenously per 24 hours.
Aminosin should be infused slowly, at rates 1.4-2.8 ml (30-60 drops) per
minute.
Infant
and children:
In
children and infants, the rate of infusion is 28-35 ml/kg body weight per day
is recommended, with a step wise increase in the rate of administration during
the first week.
Adverse
Effect
Amino
Acid, D-Sorbitol and Electrolytes is usually well tolerated. Nausea Occurs
rarely. Vomiting, flushing and sweating have been observed during infusion of
Aminosin at rates exceeding the recommended maximal rate. Transient
increases
liver test during intravenous nutrition have been reported. The reasons are at
present unclear.The underlying disease and the components and their amount in
the intravenous feeding regimens have been suggested. Hypersensitivity
reactions have been reported. As with all hypertonic infusion solution, thrombophlebitis
may occur when peripheral veins are used. The Incidence may be reduced by the simultaneous
infusion of 10% fat emulsion. If given to severely ill, premature infants, hyperphenylalaninemia
may occur.
Contraindication
Amino
Acid, D-Sorbitol and Electrolytes is contraindicated in patients with inborn
errors of amino acids metabolism, irreversible liver damage and severe uremia
when dialysis facilities are not available.
Use
in Pregnancy
Successful
and safe administration of amino acid solutions during pregnancy in the human
has been reported. Animal reproduction studies have not been carried out with Amino
Acid, D-Sorbitol and Electrolytes.
Drug
Interaction
At
the recommended dosage the amino acid in Aminosin solutions have no
pharmacological effects and is not expected to interact with other medicaments.
Compatibility
Amino
Acid, D-Sorbitol and Electrolytes containing amino acids should not be mixed
with other preparations because of the increased risk of microbial
contamination and incompatibility.
Precaution
Hyperphenylalaninemia has been noted in severely ill,
premature infants. In these patients, monitoring of the phenylalanine levels is
recommended and the infusion rate is adjusted as needed. Do not use if the solution
is turbid or contains particles. Discard any unused portion
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