Innovagen Stromba tablets (Stanozolol) – is an anabolic steroid, which is a modified form of DHT. It has few differences: 1) addition of a methyl group at 17-alpha position in order to protect the drug from metabolism during oral administration and 2) change of a usual 3-keto group on the pyrazole group.
The drug becomes heterocyclic steroid (17b-hydroxy-17-methyl-5a-androstane-[3,2-c]-pyrazole). This change affects the increasing of anabolic strength of steroid greatly, thus reducing its androgenity.
Stanozolol is much less similar to the androgen receptors than to testosterone and dihydrotestosterone. Moreover, it has long half-life and lower ability to bind blood proteins. It has one of the biggest differences between the anabolic and androgenic activities among all steroids available on the market, it is not aromatized.
Due to the recent research, it became known that the main mechanism of drug’s action involves interaction with the cell androgen receptors. It cannot be fully explained, but stanozolol has some unique ability to antagonism of progesterone receptors, it inhibits the binding of glucocorticoids with their receptors.
But in order to see such a result you need more than therapeutic dose. In addition, it inhibits the binding proteins of the blood. During one study, 25 men showed a 48.4% reduction of SHBG level at a dose of 0.2mg per pound, i.e. 18mg per person weighing 200 lbs.
Binding proteins, such as SHBG, can limit activity of steroids in the body and reduce the percentage of the active substance in the blood. Combined oral administration of stanozolol with another binding steroid may promote an increase of free steroid amount in the blood.
Penetrating into the cell’s nucleus, stanozolol activates the cells genetic apparatus, which leads to an increase of DNA, RNA and structure proteins synthesis, enzyme level activation and increase of tissue respiration, oxidative phosphorylation, ATP synthesis and accumulation of macroergs in the cell.
It exerts a stimulating effect on the production of calcium and inhibits catabolic processes which are caused by glucocorticoids. The drug improves tissue trophism, promotes the deposition of calcium in the bones, and retains nitrogen, phosphorus and sulfur in the body. Hematopoietic effect is associated with an increase of the erythropoietin’s synthesis. Antiallergic effect is caused by increasing concentration of C1 fraction complement. Androgenic activity can lead to the development of male secondary sex characteristics.
Stanozolol steroid profile
1. Activity of substance: 8 hours
2. Classification: steroid of anabolic / androgenic origin
3. Method of use: injection / tablets
4. Dosage: for males it constitutes 50-100 mg per day, for females - 5-10 mg / day.
5. Acne: not often
6. Water Retention: No
7. High blood pressure: Yes
8. Hepatotoxicity: Yes (both injectable form and tablets are alkylated on 17-alpha; injectable form can be taken orally, but injections increase the effectiveness in half a time, injection form of stanozolol promotes slower process of passing to the liver due to intramuscular administration. Stanozolol in tablet form passes through the liver immediately after the intake, but as injectable form works only 8 hours)
9. Aromatase: No
10. Progestogenic activity: low
11. DHT (dihydrotestosterone) conversion: No
12. Decrease of HPTA function (testosterone production): None
13. Other information: Anabolic activity 320% / androgenic activity 30%
14. Detection time - 3 weeks
Effects of Stanozolol
• Affects the increase of cutting and muscle stiffness
• increasing rates of power (explosive strength) and endurance
• Improves appetite
• Has a fat burning effect
• Withdraws fluid from the body
Use of Stanozolol
Due to recent studies it was found that oral administration of AAS simultaneously with food reduces the bioavailability of the drug. This happens because AAS have liposoluble nature that makes part of the drug dissolve in the food fat and it reduces the absorption of AAS in the gastrointestinal tract. In order to achieve the maximum effect, this drug should be taken on an empty stomach.
Administration (for men):
Stanozolol was used for medical purposes at doses of 6 mg per day (3 times a day at 2mg). To improve the physical characteristics it was administered by at 30-50mg a day for 6-8 weeks. In sport it is used at a dose of 50mg per day. Stanozolol is often combined with other drugs for the effect enhancement. For example, during the courses of weight gain it may be taken with testosterone (200-400mg per week) to reduce fat and increase water retention. During cutting cycles stanozolol may be easily combined with primobolan (400-600 mg) or trenbolone (150mg). In order to gain the lean mass it is combined with nandrolone decanoate (400-600 mg per week), or with boldenone.
Administration (for women):
In medicine, stanozolol is used by females in a dose of 4 mg per day (at 2mg twice per day). If it was used for sporting purposes, dose grew up to 5-10 mg per day, in the course of 4-6 weeks, while the risk of verilization was great and, as a rule, women took more safe drugs. Injectable stanozolol is not used by females due to the fact that it is difficult to control its level in the blood.
Stanozolol side effects
Stanozolol does not aromatize, it does not have estrogenic activity. Antiestrogens are not needed, even sensitive to the drug people do not feel the symptoms of gynecomastia. Normally, estrogen causes water retention, but when you take this steroid you see that it increases quality mass without excess fluid.
In this regard, it is good to administer it during cutting courses, when the primary concern is the water retention and fat. Stanozolol is widely used by athletes involved in speed-power sports, such as athletics. In these disciplines the extra weight is not needed, and it tends to generate, if you take aromatizing agents.
Stanozolol is referred to anabolic but the risk of androgenic side effects is still present (for example, increased oiliness of the skin, acne, hair growth on the body and face). They can be caused by high doses. Anabolic steroids may cause hair loss of male type. Women should remember about potential virilizing effects of AAS. They are deepening of voice, irregular periods, change in skin texture, facial hair growth, and clitoral enlargement. Stanozolol does not react with 5a-reductase, its androgenity cannot be changed by simultaneous use of finasteride or dutasteride. Stanozolol – is steroid with relatively low androgenic activity, however threshold of androgenic side effects is not as high as when taking testosterone, methandrostenolone or fluoxymesterone.
Stanozolol – is 17-alpha alkylated drug. This modification protects the drug from deactivation by the liver, allowing most of medication entering the bloodstream after oral administration. Alkylated AAS can be hepatotoxic. The use of alkylated AAS usually does not exceed 6-8 weeks, in order to avoid increasing stress of liver.
Stanozolol is less harmful for liver than the same dose of methandrostenolone. Studies, during which stanozolol was taken in a dosage of 12 mg per day for 27 weeks, have showed no significant changes in markers of liver stress, including ALT, AST, GGT, bilirubin, and alkaline phosphatase. While increasing the dosage or combining it with other medications the situation may change. Injectable agent has hepatotoxicity, it is not used as a non-toxic alternatives.
Indications to drug administration
Break of the proteins’ synthesis, cachexia of various origins, injuries, burns, pre- and postoperative periods, recovery period after infectious diseases; toxic goiter, muscular dystrophy, osteoporosis, negative nitrogen balance in corticosteroid therapy, hypo-and aplastic anemia.
Contraindications to drug administration
Hypersensitivity to the drug’s components; prostate cancer, breast cancer in men, breast carcinoma in women with hypercalcemia; coronary heart disease, atherosclerosis; hepatic and renal failure; acute and chronic prostatitis; period of pregnancy and breastfeeding; childhood.
- perfect Review by bigTrev
- worked just like its suppose to. Hardened up quite a bit just off 30-40 mg a day. (Posted on 12/22/2019)