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Omnitrope 10mg 30IU pen (Somatropin 150iu kit – 5 x 10mg(30iu) 1.5ml HGH cartridges Injection) Drug Information: Description, User Reviews, Drug Side Effects, Interactions – Prescribing Information
Omnitrope Drug Description
OMNITROPE (somatropin [rDNA origin]) Injection
Omnitrope 10mg 30IU (somatropin-[rDNA] origin) is a polypeptide hormone of recombinant DNA origin. It has 191 amino acid residues and a molecular weight of 22,125 daltons. The amino acid sequence of the product is identical to that of human growth hormone of pituitary origin (somatropin). Omnitrope® is synthesized in a strain of. Escherichia coli that has been modified by the addition of the gene for human growth hormone. Omnitrope 10mg 30IU Cartridge is a clear, colorless, sterile solution for subcutaneous injection. Omnitrope 10mg 30IU for Injection is a lyophilized powder that is reconstituted for subcutaneous injection.
What are the possible side effects of somatropin?
If you have Prader-Willi syndrome, call your doctor promptly if you develop signs of lung or breathing problems such as shortness of breath, coughing, or new or increased snoring. Rare cases of serious breathing problems have occurred in patients with Prader-Willi syndrome who use somatropin.
Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any of these serious Side Effects Omnitrope 10mg 30IU (Somatropin 150iu kit – 5 x 10mg(30iu) 1.5ml HGH cartridges Injection) Drug Information: Description, User Reviews, Drug Side Effects, Interactions – Prescribing Information:
severe pain in your upper stomach spreading to your…
DOSAGE AND ADMINISTRATION
The weekly dose should be divided over 6 or 7 days of subcutaneous injections. Therapy with Omnitrope 10mg 30IU should be supervised by a physician who is experienced in the diagnosis and management of pediatric patients with short stature associated with GHD, Prader-Willi Syndrome (PWS), those who were born small for gestational age (SGA), Idiopathic Short Stature (ISS) and adult patients with either childhood onset or adult onset GHD.