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Superior Peptide TB-500

TB-500 (Thymosin Beta-4) 10 mg x 1 vial – Superior Peptide

4,100.00
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HGH-FRAG (Fragment 176-191) 6 mg x 1 vial – Superior Peptide

2,500.00
Superior Peptide HGH-FRAG

Description

DESCRIPTION

Superior Peptide HGH is a sterile, non-pyrogenic, white lyophilized powder intended for subcutaneous or intramuscular injection, after reconstitution with bacteriostatic water for injection.

U.S.P. PHARMACOLOGY:

In vitro, preclinical, and clinical tests have demonstrated that somatropins are therapeutically equivalent to human growth hormone of pituitary origin and achieve similar pharmacokinetic profiles in normal adults. In pediatric patients who have growth hormone deficiency (GHD), treatment with somatropin stimulates linear growth and normalizes concentrations of Insulin-like Growth Factor -I (IGF-I).In adults with GHD, treatment with somatropin results in reduced fat mass, increased lean body mass, metabolic alterations that include beneficial changes in lipid metabolism, and normalization of IGF-I concentrations.

PHARMACOKINETICS

Absorption: Following a subcutaneous injection of a single dose of 4 mg Somatotropin in healthy male and female adults, the extent of absorption (AUC) was 291 hr.μg/L and the peak concentration (Cmax) was 37 μg/L. There are no pharmacokinetic data from patients with GHD.

Distribution: The mean volume of distribution of Somatotropin following administration to healthy adults was estimated to be 1.4 L/kg.

Metabolism: The metabolic fate of Somatotropin was not studied. However, it is presumed that the metabolic fate of Somatotropin involves classical protein catabolism in both the liver and kidneys.

Excretion: The mean clearance subcutaneously administered Somatotropin in healthy adults was 0.23 (± 0.04) L/hrkg. The mean terminal half-life of Somatotropin after a single subcutaneous injection in healthy adults is 2.4 hours

INDICATIONS AND USAGE:

HGH is indicated for:

  • Long-term treatment of pediatric patients who have growth failure due to an inadequate secretion of endogenous growth hormone.
  • Long-term replacement therapy in adults with growth hormone deficiency (GHD) of either childhood- or adult-onset etiology. GHD should be confirmed by an appropriate growth hormone stimulation test.

INDICATIONS AND USAGE:

The dosage of HGH must be adjusted for the individual patient. The weekly dose should be divided into daily subcutaneous injections (administered preferably in the evening). HGH may be given in the thigh, buttocks, or abdomen; the site of SC injections should be rotated daily to help prevent lipoatrophy. Pediatric GHD Patients: Generally, a dose of 0.16 to 0.24 mg/kg body weight/week is recommended. Adult GHD Patients: The recommended dosage at the start of therapy is not more than 0.04 mg/kg/week. The dose may be increased at 4- to 8-week intervals according to individual patient requirements to a maximum of 0.08 mg/kg/week, depending upon patient tolerance of treatment. Clinical response, side effects, and determination of age-adjusted serum IGF-I may be used as guidance in dose titration. This approach will tend to result in weight-adjusted doses that are larger for women compared with men and smaller for older and obese patients.

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