contraindications Male breast or prostate cancer, liver disease, known or suspected pregnancy, or known hypersensitivity to this drug prohibits its use.
In males, used as replacement therapy in conditions associated with symptoms of deficiency or absence of endogenous testosterone. In females, for palliation of androgenresponsive recurrent mammary cancer in women who are more than one year but less than five years postmenopausal.
Halotestin 5mg (Fluoxymesterone) Upjohn
Kind Protein Organism Human Pharmacological action unknown Actions antagonist General Function: Zinc ion binding Specific Function: Receptor for glucocorticoids (GC). Has a dual mode of action: as a transcription factor that binds to glucocorticoid response elements (GRE), both for nuclear and mitochondrial DNA, and as a modulator of other transcription factors. Affects inflammatory responses, cellular proliferation and differentiation in target tissues. Could act as a coactivator for STAT5-dependent transcription upon grow. Gene Name: NR3C1 Uniprot ID: P04150 Molecular Weight: 85658.57 Da
A common dosage of Stenox is in the range of 20-30 mg which is between 8 and 12 tablets for a 4-6 week cycle. At this level an athlete can expect massive strength gains with a very low tendency of water and salt retention. Stenox is considered to be the most toxic oral steroid and has a high rate of side effect occurrences. This fact has kept most people, especially women, away from this compound.
NOT COVERED – Drugs that are not covered by the plan.