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Halotestin , WTF

DrS

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Oct 9, 2010
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48
I was chatting with a few old school BB'ers , and we had a 20 min conversation on the extinction of Halo. It isn't very popular any more and mainly it seems because the most of the Halo around is bunk or anadrol. My buddy was talking about work outs on it where he would have such pumps he wouldn't leave the mirror. I was recently in the hunt for Halo and told them how out of 5 company's I tried only 2 were real and one was actually mg'd correctly. Unreal... Wanted to see what was the best Halotestin you ever had ?????
 
gauls was quite potent also theres a new prohormone out called bolasterone or something along those lines thats supposed to be very similar to halo i pre ordered it cant wait to try it
 
gauls was quite potent also theres a new prohormone out called bolasterone or something along those lines thats supposed to be very similar to halo i pre ordered it cant wait to try it

hahaha im beta testing Boladrol along with my cycle.... holy shit... im up 7lbs in 9days, and not watery gains at all. stuff feels amazing thus far.
 
Well

If it is close to halo, that sounds about right. Halo is one of the most potent oral out there , it is unreal and little to no water retention. It is very toxic for the liver but it is worth it,
 
i've heard of guys going to the ER

Showing up yellow Jaundice, But I haven't found one person that knows of somebody that it happend too!
 
Have only tried halo one time, and it was compounded from a real pharmacy at 11mg/cap. Tried it at 11mg/ED for 10 days and didn't notice much of anything. I suppose the dose was simply too low.

For those that love it, they use it for strength purposes, and NOT to gain weight... for example PL or MMA where there are weight classes.
 
7lbs in 9 days and it's not water :eek: lol

ok, when i say that im meaning its not subcutaneous water retention but rather pushing wayer into muscle tissue, it doesnt have that watery look, its a very dry gain.

its also burning fat in the other testers.
 
hahaha im beta testing Boladrol along with my cycle.... holy shit... im up 7lbs in 9days, and not watery gains at all. stuff feels amazing thus far.

Just ordered some today. Any sides? Tiredness, hunger problems, etc.
 
ok, when i say that im meaning its not subcutaneous water retention but rather pushing wayer into muscle tissue, it doesnt have that watery look, its a very dry gain.

its also burning fat in the other testers.

Sound like what I'm looking for... Thanks for the info. bro!! I just ordered some from G
 
I wonder if anyone here has had their liver values tested while on Halo? Maybe that's something I'll do when I try it out. Not to HJ the thread, But, I was on 100mg of var for most of the summer and got tested. AST was 99 ALT was 170. That was on 3-23-10. Cleaned out for a while and got tested again on 10-7-10 AST was 44 ALT was 39... Curious to see if Halo is much worse than that.
 
dont want to hijack the thread but found this on another site....

Here is the entire bolasterone write from Anabolics 9th edition. (quoted from jbryand101b's post over on AM)
Androgenic 300
Anabolic 575
Standard Methyltestosterone (oral)
Chemical Names 17beta-Hydroxy-7,17alpha-dimethylandrost-4-en-3-one 7,17-dimethyltestosterone
Estrogenic Activity high
-------------
Bolasterone is a modified form of testosterone. It differs by: 1) the addition of a methyl group at carbon 17-alpha, which helps protect the hormone during oral administration, and 2) the introduction of a methyl group at carbon 7 (alpha), which inhibits 5-alpha reduction and shifts the anabolic to androgenic ratio in favor of the former. 7,17-dimethylated steroids also tend to be very resistant to metabolism and serum-binding proteins, greatly enhancing their relative biological activity.
-----------------

Bolasterone is an oral anabolic steroid structurally related to methyltestosterone. It differs only by the addition of a methyl group at c-7, which accounts for its given chemical name, 7,17-dimethyltestosterone. The added c-7 methyl group makes the activity of this steroid far removed from methyltestosterone, however, such that any direct comparison is difficult to justify. For starters, bolasterone is a fairly potent steroid, measured in human subjects to have approximately twice the anabolic effect of methandrostenolone.636 This is in contrast to methyltestosterone, which is considerably less potent than methandrostenolone. Despite being a testosterone derivative, bolasterone is also much more anabolic than androgenic in nature. At a given -therapeutic level, it is much less likely to cause androgenic/virilizing side effects. It does have one strong similarity to methyltestosterone, however, which lies in the fact that bolasterone too is quite estrogenic. Both agents are, therefore, most appropriately used during bulking phases or training.
--------------
Bolasterone was first described in 1959.637 It was closely evaluated for anabolic and androgenic effect approximately 3 years later.638 The drug was developed by Upjohn, and sold in the U.S. during the 1960's under the Myagen brand name. It was mainly indicated for the treatment of advanced breast cancer in women, although the agent was also investigated for its stimulatory effect on blood cells and its general anabolic (lean-tissue sparing) activity. Bolasterone was ultimately a short-lived drug, disappearing from the U.S. market shortly after its release. By the 1980's, bolasterone had been out of commerce for so long that it was all but forgotten among athletes. Although bolasterone is no longer produced, the drug remains listed in the U.S. Pharmacopeias, suggesting it would not be impossible to see this agent for sale (legally) in the U.S. again, perhaps under order by a private compounding pharmacy. The reemergence of an actual commercial bolasterone compound, however, remains very unlikely. Huh, little did he know...
---------------
Bolasterone is aromatized by the body, and is considered a highly estrogenic steroid due to its conversion to 7,17dimethylestradiol (an estrogen with high biological activity). Gynecomastia may be a concern during treatment, especially when higher than normal therapeutic doses are used. At the same time water retention can' become a problem, causing a notable loss of muscle definition as both subcutaneous water retention and fat! levels build. To avoid strong estrogenic side effects, it may' be necessary to use an anti-estrogen such as Nolvadex®. One may alternately use an aromatase inhibitor like
Arimidex® (anastrozole), which is a more effective remedyl for estrogen control. Aromatase inhibitors, however, can bel' quite expensive in comparison to standard estrogen maintenance therapies,and may also have negative effects on blood lipids.
--------------------
Although bolasterone is classified as an anabolic steroid, androgenic side effects are still possible with this substance.These may include bouts of oily skin, acne, and body/facial hair growth. Higher doses are more likely to cause such side effects. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are additionally warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Bolasterone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride. Note that studies administering 1mg and 2mg of bolasterone per day have shown no outward androgenic side effects in children and hypogonadotrophic males, as would be characterized by public hair growth, genital changes, voice changes, and acne. Higher doses remain likely to induce androgenic effects. Bolasterone is considered to have a comparable ratio of anabolic to androgenic effect as oxymetholone and methandrostenolone (superdrol).
-------------
Side Effects (Hepatotoxicity):
Bolasterone is a c17-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage ofthe drug entry into the bloodstream following oral administration. ell-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life-threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6-8 weeks, in an effort to avoid escalating liver strain. Studies adm.inistering 1mg and 2mg of bolasterone daily for 6 weeks to 27 patients have demonstrated a trend toward increases in serum alkaline phosphatase (a marker of liver stress), although no significant untoward effects on the liver were documented.
The use of a liver detoxification supplement such as Liver Stabil, Liv-52, or Essentiale Forte is advised while taking any hepatotoxic anabolic/androgenic steroids.
------------------
Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Bolasterone has a strong effect on the hepatic management of cholesterol due to its structural resistance to liver breakdown and route of administration. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction. Studies administering 1mg and 2mg of bolasterone daily for 6 weeks to 27 patients have demonstrated a trend toward increased serum cholesterol. Although no HDL and LDL breakdown was provided, it can be assumed based on the structure and route of administration that bolasterone significantly shifted the ratio of these two fractions of cholesterol further apart, measurably increasing atherogenic risk.
To help reduce cardiovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.
-----------------
All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.
The above side effects are not inclusive. For more detailed discussion ofpotential side effects, see the Steroid Side Effects section ofthis book.
------------
Studies have shown that taking an oral anabolic steroid with food may decrease its bioavailability.639 This is caused by the fat-soluble nature of steroid hormones, which can allow some of the drug to dissolve with undigested dietary fat, reducing its absorption from the gastrointestinal tract. For maximum utilization,this steroid should be taken on an empty stomach.
----------------
Administration (Men):
Clinical studies have demonstrated that significant nitrogen retention and weight gain can be induced with a daily dosage of 1-2mg per day. In the athletic arena, doses of 2-5 mg daily seem to be most reasonable, taken in cycles lasting no more than 6-8 weeks in length to minimize hepatotoxicity. This level is sufficient fer strong increases in muscle size and strength, although such gains will likely be accompanied by significant water retention.
----------------
Administration (Women):
Bolasterone was not widely used with women in clinical medicine. When applied, it was most often used as a secondary medication during inoperable breast cancer, when other therapies have failed to produce a desirable effect. The dosage used for this application would be as high as 10 mg per day, a level that has caused significant virilization among patients. Bolasterone is generally not recommended for women for physique-.or performanceenhancing purposes due to its very strong nature and tendency to produce virilizing side effects.
------------------
Bolasterone is no longer produced as a prescription drug, although a handful of underground laboratories have taken to selling this material.
__________________

sounds harsh on the system
 
i love halo:love:! i used to take one single stenox tab [2.5mgs] a day and it would feel amazing, i cant believe i would get such a boost in strength with such a low dose!.
 
MG/Body weight

I do 5mg per 50lbs per day. So when I was 200lbs I did 20mg a day. I did 10mg tabs twice a day. When I had 5mg tabs I broke it down to every few hrs a tab. 20mg worked great


11mg is a little low IMO!!


If I would do Halo again I'm 230 right now I would do 30mg a day for 4weeks.
 
I was chatting with a few old school BB'ers , and we had a 20 min conversation on the extinction of Halo. It isn't very popular any more and mainly it seems because the most of the Halo around is bunk or anadrol. My buddy was talking about work outs on it where he would have such pumps he wouldn't leave the mirror. I was recently in the hunt for Halo and told them how out of 5 company's I tried only 2 were real and one was actually mg'd correctly. Unreal... Wanted to see what was the best Halotestin you ever had ?????

"Wanted to see what was the best Halotestin you ever had ?????" Stenox
 
It's funny, a lot of guys on this thread that THINK they used Halo did not, as those are not Halo's effects.

I used Upjohn Halotestin over almost 2 decades. Still have some, but it's long expired as Upjohn discountinued it a long time ago.
 
It's funny, a lot of guys on this thread that THINK they used Halo did not, as those are not Halo's effects.

I used Upjohn Halotestin over almost 2 decades. Still have some, but it's long expired as Upjohn discountinued it a long time ago.

Ok, Now I'm wondering if I shoud even bother :eek:

Are you saying most Halo is fake these days?
 
It's funny, a lot of guys on this thread that THINK they used Halo did not, as those are not Halo's effects.

I used Upjohn Halotestin over almost 2 decades. Still have some, but it's long expired as Upjohn discountinued it a long time ago.

Do you think it loose his potency? totally? Because some years ago a guy used a 4 years expired Dynabolon and all gone well. i think it's more easy to preserve tablets.
 
Ok, Now I'm wondering if I shoud even bother :eek:

Are you saying most Halo is fake these days?

I have no idea what's fake or not, but the effects most of the guys in this thread are describing, are not what Halo does.
 

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