MESO-Rx

Anabolic Steroids

MESO-Rx Sponsor Pharmacom Labs officials and our Basicstero.com store

Basicstero's 2023 WINTER PROMO is Active!

Pay with cryptocurrency and get FREE bonuses as follows:
$100 of FREE bonus items for orders over $200.
$300 of FREE bonus items for orders over $500.
$600 of FREE bonus items for orders over $800.
$800 of FREE bonus items for orders over $1000.

Bonuses are picked during the ordering process and shipped together with the main order. No promo code is needed.
This promo is valid for orders from the International Warehouse only!
Please plan accordingly for international transit times.

In case of seizures/lost-packs only items that were paid for are reshipped, not free bonuses (please understand this means promo free bonus items are not included in a reship).
If you need discreet shipping please select the "Discreet Shipping" option during the check-out process on the "Address" page when you enter your order.
Pharmatropin GH is not participating in this promotion.
Nothing new with these terms and conditions - just the typical rules for many Basicstero promos.

Make Winter a Powerful Season with Basicstero!
 
Check out these informative posts to learn more about some of Pharmacom Labs innovative products!


• The NEW Fat-Loss Product TESOS (Tesofensine):
RThoads said:
TESOS – An Exciting NEW Fat-Loss Product from Pharmacom Labs! – is Now Available in the Basicstero Store.
Code: 
https://basicstero.ws/fat-loss/tesos
This innovative Oral-Line Fat-Loss product is currently offered as a 50 count blister strip of 0.5 mg tablets (1 BLISTER, 50 PILLS).

Tesofensine Information:
Tesofensine is a unique new generation Triple Serotonin Norepinephrine Dopamine Reuptake Inhibitor (SNDRI).
SNDRI belong to the class of psychoactive antidepressants. They affect neurotransmitters in the brain, exactly serotonin, norepinephrine and dopamine. Tesofensin affects the brain qualitatively, helping a person to feel maximum saturation during eating, and reduce appetite significantly.
Tesofensin was originally developed and patented by NeuroSearch A/S (Denmark) to cure Parkinson's and Alzheimer's diseases.
• acts centrally, suppress appetite, regulate the availability of dopamine receptors and stimulate α1-adrenergic receptors.
• appetite decreases within 14 days, there is a higher level of satiety and less desire to eat.
• increases significantly fat oxidation and reduces adipose tissue.
• improves the level of insulin sensitivity, which leads to higher glucose metabolism.
• alters the expression of dopaminergic receptors in the striatum of the brain, as well as their binding.
• the energy consumption increases greatly within 14 days.
• The drug has a long half-life, which is 8-9 days, and metabolized mainly in the liver by CYP3A4 to the disalkyl metabolite M1 (NS-2360), which is the only metabolite found in human blood plasma.

Chemical name: (1R,2R,3S,5S)-3-(3,4-dichlorophenyl)-2-(ethoxymethyl)-8-methyl-8-azabicyclo[3.2.1]octane
Formula: C17H23Cl2NO
Anabolic activity index: not a steroid
Androgenic activity index: not a steroid
ACTIVE HALF-LIFE: 9 days
CLASSIFICATION: psychoactive antidepressants.
DOSAGE: 0.25 mg -1 mg
ACNE: no
WATER RETENTION: no
HBR: Perhaps
HEPATOXITY: Low
AROMATIZATION: no

The Basicstero Team hopes this NEW Pharmacom Labs Fat-Loss product will help you reach your goals!
Click to expand...


• Toremifene vs. Tamoxifen: Why Toremifene is a healthier SERM and less toxic than Tamoxifen:
RThoads said:
Addendum: structural considerations and an explanation of toremifene’s decreased carcinogenicity.

Why is Tamoxifen Carcinogenic? What Makes Toremifene Less Toxic?
zVWoHo2.jpg


Most of these compounds may lead to long-term toxic effects. For instance, tamoxifen induces liver cancer in rats after prolonged administration, which has been attributed to the generation of DNA-alkylating species from the metabolism of the stilbene framework. It has been proposed that cytochrome P450 hydroxylates tamoxifen at the allylic position of the ethyl side chain, leading to an alcohol, which can generate a highly delocalized allylic cation 3.6 and therefore alkylate DNA to give product 3.7 through an SN1 mechanism (Fig. 3.6 below).
(Reference: Triphenylethylene - an overview | ScienceDirect Topics)

k1BUSJ8.jpg



This proposal also explains the lack of carcinogenicity of toremifene, which can be attributed to destabilization of the positive charge in 3.8 by the inductive effect of the chlorine substituent at the position adjacent to the allylic carbon (Fig. 3.7 below).
(Reference: Triphenylethylene - an overview | ScienceDirect Topics)

Nl4CHEb.jpg
Click to expand...


• FARESTOS (Toremifene) a More Modern SERM:
RThoads said:
Toremifene (Fareston) – A More Modern SERM – is Available in the Basicstero Store

Toremifene Citrate is a selective estrogen receptor modulator (SERM) derived from triphenylethylene. It was patented and approved in Europe in the mid 1990's to treat metastatic ER+ breast cancer in postmenopausal women. Toremifene (Fareston) is an analogue of Tamoxifen and Clomid which can be used to replace these older compounds.
JpCWPh6.jpg
In bodybuilding toremifene citrate is used by men as a drug for post-cycle therapy (PCT) to counteract and/or block some of the effects of excessive estradiol in the body as a result of aromatization of various androgens used. In particular, toremifene is used to restore levels of endogenous testosterone in blood as well as to prevent the estrogen-related side effect of gynecomastia.
In its chemical structure toremifene is very similar to tamoxifen and clomiphene. However, toremifene is a new generation drug and has less toxic side effects than tamoxifen.

For a more effective boost in testosterone production toremifene dosage should be in the range of up to 120 mg per day. This dose can be maintained for a first week of PCT; then, 100mg/day for the second week of PCT; and, finally 60mg/day for the remaining 3 – 4 weeks of PCT. Of course, exact dosages should be determined individually based on blood work results.

This innovative SERM is currently available as a 50 count blister strip of 20 mg tablets at the link in the "code" box below:
Code: 
https://basicstero.ws/pct/farestos-pills-20mg

Toremifene Information:
lGWzNBU.jpg


Toremifene Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is an anti-estrogenic drug, specifically classified as a Selective Estrogen-Receptor Modulator (SERM) with mixed agonist and antagonist properties. It is a non-steroidal triphenylethylene derivative, similar in structure and action to both Nolvadex (tamoxifen citrate) and Clomid (clomiphene citrate). Toremifene citrate is used for the treatment of breast cancer in postmenopausal women with estrogen-receptor positive or estrogen-receptor unknown (unsure if the cancer is estrogen responsive) tumors. It works by attaching to the estrogen receptor in various tissues in a competitive manner, blocking endogenous estrogen from exerting biological activity. As an anti-estrogen in many tissues, male bodybuilders and athletes may use toremifene citrate to counter some of the side effects associated with the use of aromatizable or estrogenic anabolic/androgenic steroids. This may include gynecomastia, body fat gain, and increased water retention.

The triphenylethylene compounds (toremifene citrate, tamoxifen citrate, clomiphene citrate) tend to be somewhat intrinsically estrogenic in the liver. This means that while they can block estrogenic activity in some areas of the body, they can actually act as estrogens in this other key area. Estrogenic action in the liver is important in the regulation of serum cholesterol (it tends to support HDL synthesis and LDL reductions). Since steroid-using bodybuilders are already dealing with the negative cardiovascular effects of these drugs, compounding the issue with aromatase inhibitors (which will lower total serum estrogen levels) may not always be the best option. Using a drug that blocks gynecomastia, for example, while at the same time supporting improved cholesterol values, might be much more ideal. In terms of which triphenylethylene agent is most effective in this regard, evidence suggests that the positive lipid altering benefits of toremifene are significantly stronger than those of tamoxifen, a drug normally favored for this purpose. Toremifene citrate may, therefore, be the preferred antiestrogen among those concerned about their lipid profiles.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate was approved by the FDA as a prescription drug in 1997. It is sold in the U.S. under the Fareston brand name, which is made by GTx, Inc. Fareston is also available in over two dozen other countries including Australia, Austria, Belgium, Czech Republic, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Mexico, Netherlands, New Zealand, Portugal, Russia, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, and the United Kingdom.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is classified as a selective estrogen receptor modulator, with both agonist and antagonist properties. It has the chemical designation 2-{p-[(Z)-4-chloro-1,2-diphenyl-1-butenyl]phenoxy}-N,N-dimethylethylamine citrate (1:1).

Side Effects (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate appears to be well tolerated, with a low incidence of serious side effects. In clinical trials, common side effects associated with its use included hot flashes (35%), sweating (20%), elevated liver enzymes (19%), nausea (14%), vaginal discharge (13%), dizziness (95%), edema (5%), vomiting (4%), and vaginal bleeding (2%). Other observed rare adverse events that may or may not be linked to toremifene citrate administration include low white blood cell and platelet counts, skin discoloration or dermatitis, constipation, difficulty breathing, partial motor paralysis, tremor, vertigo, itching, anorexia, visual disturbances, loss of strength, hair loss, depression, jaundice, and rigors (stiffening of the muscles). Antiestrogens may harm the developing fetus and should never be used during pregnancy.

Administration (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is FDA approved for the treatment of metastatic breast cancer in postmenopausal women with estrogen-receptor positive or unknown tumors. The recommended dose is one 60 mg tablet administered once per day. When used (off-label) to mitigate the estrogenic side effects of anabolic/androgenic steroid use, male athletes and bodybuilders may use 30 mg to 60 mg per day during steroid treatment.

Availability (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Toremifene citrate is widely available under the Fareston brand name. It is not commonly sold on the black market, nor is it a high-profile item for counterfeiters.
Click to expand...


• DROLOS (Superdrol):
RThoads said:
DROLOS – The New SUPERDROL Product from Pharmacom Labs! – is Now Available in the Basicstero Store.

Methyldrostanolone is scientifically known as Superdrol and it is arguably the most effective and potent oral anabolic steroid to be utilized over the last decade. Superdol is very similar to Masteron, with the only difference being that Masteron though is lacking an ester chain. The name Superdrol is a combination of the words “super” and “anadrol." Superdrol is an awesome steroid for bulking, though some bodybuilders also use it as part of their cut as it yields very dry and hard gains with no bloating or water retention. It was created back in the 1950s by doctors who were looking to create a drug to destroy tumors. Sadly, this wasn’t achievable, but they did find that the oral steroid promoted huge increases in lean muscle mass and strength. However, Superdol wasn’t released until 2005.

The active steroidal hormone in Superdrol is Methyldrostanolone. It is a structurally altered form of Drostanolone, with an added methyl group at the 17th carbon position. There is also an added methyl group at the carbon 2 position. These changes ramp-up the anabolic potential of this drug, giving it an anabolic rating of 400.

Effects:
• Increases muscle mass.
• Improves recovery.
• Improves athletic performance.

This Powerful Oral-Line product is currently offered as 10 mg tablets available at the link in the "code" box below:
Code: 
https://basicstero.ws/oral-steroids/drolos

Superdrol Information:

Superdrol Description (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone, also known as methasteron, is a potent oral anabolic steroid that was never sold as a prescription drug. In structure, this steroid is a close derivative of drostanolone (Masteron). The only difference in this case is the addition of a c-17 alpha methyl group, a modification that gives this steroid high oral bioavailability. The two agents remain very comparable, however. Both methyldrostanolone and drostanolone are nonaromatizable, so there is no difference in the estrogenicity of these two steroids, and both steroids retain favorable anabolic to androgenic ratios. Lab assays do put Superdrol ahead here, however, showing it to possess 4 times the anabolic potency of oral methyltestosterone while displaying only 20% of the androgenicity (a 20:1 ratio, compared to 3:1 ). The exact real-world relevance of these figures remains to be seen, however. Methyldrostanolone is favored by athletes for its moderate anabolic properties, which are usually accompanied by fat loss and minimal androgenic side effects.

History (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone was first described in 1959.1 This steroid was developed by the international pharmaceuticals giant Syntex, alongside such other wellknown anabolic agents as drostanolone propionate and oxymetholone. Unlike rostanolone and oxymetholone, however, this steroid (at least in its basic form) was never released as a medicinal product. It was only sold for a brief period of time as a modified hormone called dimethazine. Dimethazine is made from two molecules of methyldrostanolone that are bonded together, which are later metabolically separated to yield free methyldrostanolone. So while technically methyldrostanolone itself was never sold as a prescription agent, we can say that the drug was one utilized medicinally (for more information see the Roxilon drug profile). Otherwise, the methyldrostanolone molecule remained an obscure research steroid only, and was never itself approved for use in humans. Methyldrostanolone was released in early 2005 as an over the counter "grey market" anabolic steroid in the United States. The drug was being sold without restrictions as a nutritional supplement product, barring some minimum age disclaimers by the manufacturer. No State or Federal laws identify this drug as an anabolic steroid, which remove the legalities associated with being a Class Ill controlled substance like other steroids. This is simply due to the fact that methyldrostanolone was not in commerce at the time such laws were written, and was unknown to lawmakers. It was never legal to sell as a dietary supplement, however, and in late 2005 the FDA angrily acknowledged methyldrostanolone was being sold on the sports supplement market. In early 2006, the FDA sent letters to the manufacturer and a distributor demanding it be pulled from commerce. Superdrol has since been discontinued.

Structural Characteristics (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone is a modified form of dihydrotestosterone. 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-2 (alpha), which considerably increases the anabolic strength of the steroid by heightening its resistance to metabolism by the 3-hydroxysteroid dehydrogenase enzyme in skeletal muscle tissue.

Side Effects (Estrogenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals. Since estrogen is the usual culprit with water retention, methyldrostanolone instead produces a lean, quality look to the physique with no fear of excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are major concerns.

Side Effects (Androgenic) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Although classified as an anabolic steroid,androgenic side effects are still possible with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are 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. Methyldrostanolone is a steroid with relatively low androgenic activity relative to its tissuebuilding actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone, methandrostenolone, or fluoxymesterone. Note that methyldrostanolone is unaffected by the 5-alpha reductase enzyme, so its relative androgenicity is not affected by the concurrent use of finasteride or dutasteride.

Side Effects (Hepatotoxicity) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone is a cl 7-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral administration. Cl 7-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. Note that although no human data can be found to make reference of, doses of 1 0 mg and 20 mg per day have been sufficient to produce high elevations of liver enzymes in consumers, as reported by private lab test results. Also, a small number of serious adverse events relating to liver toxicity have been reported with the use of this substance. 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.

Side Effects (Cardiovascular) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL cholesterol values and increase LDL 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. Methyldrostanolone has a strong effect on the hepatic management of cholesterol due to its non-aromatizable nature, 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. To help reduce card iovascular 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.

Side Effects (Testosterone Suppression) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
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.

Administration (Men) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methydrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. An effective dosage of methyldrostanolone for physique- or performance-enhancing purposes seems to begin in the range of 10-20 mg per day, taken for no longer than 6 or 8 weeks. At this level it seems to impart a measurable muscle-building effect, which is usually accompanied by fat loss and increased definition. Don't expect to gain 30 pounds on this agent (its name, which is short for "Super Anadrol," is more marketing than reality), but many do walk away with more than 10 pounds of solid muscle gain when using this agent alone. In determining an optimal daily dosage, some do find the drug to be measurably more effective when venturing up to the 30 mg range. Potential hepatotoxicity should definitely be taken into account with such use, however. To avoid further escalating liver strain, 20 mg daily of methyldrostanolone is sometimes stacked with a nontoxic injectable steroid, such as testosterone for massbuilding phases of training, or nandrolone or boldenone for more lean tissue gain and definition, instead of simply increasing the dosage. The drug also works well in cutting cycles, where its lack of estrogenicity is highly favored. Often it is combined here with a non-aromatizable injectable steroid like Primobolan or Parabolan.

Administration (Women) (credit: Llewellyn, William. “ANABOLICS” 11th ed. 2017.):
Methyldrostanolone was never approved for use in humans. Prescribing guidelines are unavailable. In the athletic arena, an effective oral daily dosage would fall around 2.5 mg per day, taken in cycles lasting no more than 4-6 weeks to minimize the chance for virilization. The main point of contention with females is probably going to be the 10 mg product, which is far too high to use. Application would require splitting contents up into 4 separate doses. As with all steroids, virilization is still possible.
Code: 
https://basicstero.ws
Click to expand...
 
luex said:
I received my order, but a few items were missing. I took an unboxing video. Now support is telling me to upload the video to YouTube???? @Pharmacom Support @RThoads
Click to expand...
Is the file size too large to send as an attachment in an email?

Sorry to hear that some items were missing. The source will replace it for you; we just need to get the video to them. It sucks that a video is required but unfortunately scammers ruined things for us all by making false claims and exploiting the source's good will.

If you do choose to use YouTube to have a link to easily share the video with the source, please make sure to set the video visibility (privacy) to "unlisted" so the public cannot find the video.

See the screenshot below. Setting the visibility to "unlisted" will make it so that only someone with the link can see the video; it will not be searchable to the public. Also, so not name the title or any description with any info that can identify you or the contents (I recommend title just says "unpacking" and no added description).
Then, after the source views the video and issue is resolved, delete the upload.
JIkiiBz.jpg
 
DROLOS (MethylDrostanolone aka Superdrol) is an anabolic steroid that is an oral version of the well-known Drostanolone (Masteron).

The product does not aromatize and does not have progestagenic activity.
This product does not cause gynecomastia and does not cause water retention.
The effect is comparable to a greatly enhanced and significantly more powerful version of injectable masteron with side effects closer to other very strong orals such as halotestin.

MethylDrostanolone is effective for quality weight gain and/or fat percentage reduction, and confidently lowers SHBG!

Anabolic activity = 400.
Androgenic activity = 20.
Working dosage is 20 - 40mg per day, for up to 4 weeks.

With the powerful addition of Drolos, Pharmaсom Labs has another promising product in its product line which is useful for both beginners and more advanced athletes.
Code: 
https://basicstero.ws/superdrol/drolos
 
TESOS (Tesofensine) is a product developed for the treatment of obesity.
Code: 
https://basicstero.ws/fat-loss/tesos
It acts as an appetite suppressant.
Increases energy expenditure at rest.
It has a slight antidepressant effect.
Increases fat oxidation.
Improves insulin sensitivity.
Increases glucose metabolism.

In total, this allows for more comfortable weight loss while successfully maintaining a caloric deficit.

It is not an anabolic steroid; as such PCT is not needed after use and there is no classic HPTA setback.
The product does not cause water retention, nor cause acne, nor affect the prostate.
The effect on the liver is insignificant and does not require monitoring.

Tesofensine is a more modern analog of sibutramine and is already available in the Basicstero store!
 
Ester-Free Testosterone (pure testosterone in its own right without the addition of any slow-release ester) differs from version with esters in its unique properties.
  1. First of all, the preparation is very quickly put to work.
    A noticeable effect is already felt 30-minutes after the injection; and, it reaches its maximum level after an hour.
    Due to this, base testosterone is often used as a pre-workout!
  2. The second difference is that 100mg of the product contains exactly 100mg of testosterone - the active ingredient.
    For example, 100mg of testosterone propionate contains 83.7mg of testosterone, the remaining 16.3mg is the mass of ester (propionate); likewise, testosterone enanthate contains 72mg of testosterone per 100mg, the rest is ester mass. But the mass of ester-free base is all active testosterone.
  3. Due to the absence of an ester, this product is quickly absorbed, gives a powerful surge of testosterone levels (3-4 times stronger than Test-propionate) and is also quickly excreted - after 16-20 hours its effect decreases significantly.
  4. The powerful and short testosterone surge gives an emotional boost and accelerated recovery, while the product does not have time to convert significantly into estradiol and dihydrotestosterone. As a result, estrogenic and androgenic side effects are less frequently encountered than with the same amount of test-propionate, and aromatase inhibitors are usually not required.
  5. The product can be used: as a pre-workout, as a preparation for competitions, as a basis for a bulking cycle, as a supplement for a mass-building cycle, as a preparation for increasing explosive endurance and aggression.

Pharmacom Labs currently offers two types of ester-free testosterone: the well-known suspension in water (PharmaTest 100) and unique ester-free testosterone base in oil (PharmaTest OIL 100); the latter of which can be mixed with any other oil-based AAS.
Both are available in vials or ampules!

• PharmaTest 100 (water suspension) available in vials at:
Code: 
https://basicstero.ws/testosterones/pharmatest-100
and in ampules at:
Code: 
https://basicstero.ws/testosterones/pharmatest-100-ampules

• PharmaTest OIL 100 (oil base) available in vials at:
Code: 
https://basicstero.ws/testosterones/pharmatest-100-oil-base
and in ampules at:
Code: 
https://basicstero.ws/testosterones/pharmatest-100-oil-base-ampules

But Pharmacom has gone further and also released an esterless trenbolone suspension in water (PharmaTren 50), which has all the properties of trenbolone + it's esterless, with all the benefits described above!

• PharmaTren 50 (water suspension) is available now at:
Code: 
https://basicstero.ws/trenbolone/pharmatren-50-waterbase

If you didn't know what ester-free is and therefore haven't tried ester-free testosterone or trenbolone, now you do.
All that's left now is to try it!
 
I hope everyone had a good weekend and a nice start to the new week.

Reminder: Basicstero's Winter Promo is active; please see the post quoted below for more details.
PHL Official said:
Basicstero's 2023 WINTER PROMO is Active!

Pay with cryptocurrency and get FREE bonuses as follows:
$100 of FREE bonus items for orders over $200.
$300 of FREE bonus items for orders over $500.
$600 of FREE bonus items for orders over $800.
$800 of FREE bonus items for orders over $1000.

Bonuses are picked during the ordering process and shipped together with the main order. No promo code is needed.
This promo is valid for orders from the International Warehouse only!
Please plan accordingly for international transit times.

In case of seizures/lost-packs only items that were paid for are reshipped, not free bonuses (please understand this means promo free bonus items are not included in a reship).
If you need discreet shipping please select the "Discreet Shipping" option during the check-out process on the "Address" page when you enter your order.
Pharmatropin GH is not participating in this promotion.
Nothing new with these terms and conditions - just the typical rules for many Basicstero promos.

Make Winter a Powerful Season with Basicstero!
Click to expand...
 
I just ordered a few vials of the no ester Test-base in oil to try for the first time.
I've never used anything no ester but just wanting to try something for a little short-term boost on specific days.
 
RThoads said:
I just ordered a few vials of the no ester Test-base in oil to try for the first time.
I've never used anything no ester but just wanting to try something for a little short-term boost on specific days.
Click to expand...
Pretty decent as a pre workout at 100mg. Main thing I noticed is I get very hot and sweat way more. Strength stayed the same but focus was better.
 
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