Ultima Pharmaceuticals is a leading manufacturer of high-quality performance-enhancing drugs (PEDs). The company's products are used by athletes, bodybuilders, and fitness enthusiasts around the world to improve their performance and achieve their fitness goals.
Ultima Pharmaceuticals is committed to providing its customers with the highest quality PEDs available. The company's products are manufactured in state-of-the-art facilities and undergo rigorous testing to ensure their safety and efficacy. Ultima Pharmaceuticals also offers a wide range of support services to help its customers get the most out of their PEDs.
If you are looking for the best PEDs on the market, look no further than Ultima Pharmaceuticals. The company's products are safe, effective, and affordable. With Ultima Pharmaceuticals, you can achieve your fitness goals faster and easier than ever before.
Clomiphene, also known by its trade names Clomid and Serophene, is a medication widely used in the field of reproductive medicine. It falls into the class of drugs known as selective estrogen receptor modulators (SERMs) and is primarily prescribed to women who experience fertility issues due to anovulation, a condition where ovulation does not occur regularly or at all.
At its core, clomiphene works by stimulating the release of certain hormones in the brain that are responsible for initiating the process of ovulation. It achieves this by blocking the negative feedback mechanism of estrogen on the hypothalamus, a region of the brain that plays a crucial role in regulating the menstrual cycle. By interfering with this feedback loop, clomiphene increases the production of follicle-stimulating hormone (FSH) and luteinizing hormone (LH), both of which are essential for the development and release of mature eggs from the ovaries.
When prescribed clomiphene, women typically start taking the medication on the third, fourth, or fifth day of their menstrual cycle. The recommended dosage may vary depending on the individual's specific circumstances, and it is essential to follow the doctor's instructions carefully. Treatment usually lasts for five consecutive days, with ovulation typically occurring between the sixth and tenth day after the last pill is taken.
One of the advantages of clomiphene is its relative affordability and ease of administration compared to other fertility treatments. It is available in pill form, making it convenient for women to take at home without the need for invasive procedures. However, it is crucial to note that clomiphene is a prescription medication and should only be used under the guidance of a qualified healthcare professional.
Clomiphene is most effective for women who have irregular menstrual cycles or those who do not ovulate regularly. It is commonly prescribed for women diagnosed with polycystic ovary syndrome (PCOS), a condition characterized by hormonal imbalances that can lead to irregular or absent ovulation. By stimulating the release of eggs, clomiphene helps increase the chances of successful conception for women with ovulatory disorders.
During treatment, women taking clomiphene are often monitored closely through regular ultrasound scans and hormone level measurements. These monitoring procedures aim to assess the response to the medication and determine the optimal timing for sexual intercourse or other fertility interventions, such as intrauterine insemination (IUI).
While clomiphene is generally well-tolerated, it is not without potential side effects. Common side effects include hot flashes, breast tenderness, mood swings, and abdominal discomfort. In rare cases, clomiphene may cause ovarian hyperstimulation syndrome (OHSS), a condition characterized by enlarged ovaries and fluid accumulation in the abdomen. OHSS is typically mild, but severe cases can be potentially dangerous and require medical intervention.
For couples undergoing fertility treatments, the success rate of clomiphene varies depending on factors such as the woman's age, overall health, and the underlying cause of infertility. Studies have shown that approximately 70% of women treated with clomiphene will ovulate, and about 30-40% will achieve pregnancy within six cycles of treatment. If clomiphene alone does not result in pregnancy, other assisted reproductive technologies, such as in vitro fertilization (IVF), may be considered.
It is worth mentioning that clomiphene is not recommended for women who have blocked fallopian tubes, severe male factor infertility, or ovarian failure. In these cases, alternative treatments or interventions may be necessary to achieve pregnancy.
In conclusion, clomiphene is a medication widely used in reproductive medicine to treat anovulation and promote ovulation in women. By stimulating the release of hormones essential for egg development and release, clomiphene increases the chances of successful conception for women struggling with fertility issues. While it is generally well-tolerated, it is important to use clomiphene under the guidance of a healthcare professional and be aware of potential side effects. With proper monitoring and appropriate use, clomiphene can be a valuable tool in helping couples achieve their dream of starting or expanding their family.
GHK-Cu (glycyl-histidyl-lysine-copper) is a peptide that consists of three amino acids: glycine, histidine, and lysine, along with a copper ion. This peptide is derived from a larger protein called copper-binding protein, which is naturally present in our bodies.
GHK-Cu has gained significant attention in the field of skincare and anti-aging due to its potential benefits. It has been found to have several biological activities that make it appealing for its potential use in skincare products.
1. Skin rejuvenation: GHK-Cu has been shown to promote collagen production, which helps to improve skin elasticity and firmness. Collagen is a crucial protein responsible for maintaining the structure and strength of the skin. By stimulating collagen synthesis, GHK-Cu may help to reduce the appearance of fine lines and wrinkles, making the skin look more youthful.
2. Wound healing: GHK-Cu has been extensively studied for its wound healing properties. It has been shown to accelerate the healing process by promoting the migration of cells involved in tissue repair, such as fibroblasts and keratinocytes. Additionally, it has anti-inflammatory effects that can help to reduce inflammation and redness associated with wounds.
3. Antioxidant activity: GHK-Cu has antioxidant properties, meaning it can help protect the skin from damage caused by free radicals. Free radicals are unstable molecules that can damage cells and contribute to the aging process. By neutralizing free radicals, GHK-Cu may help to prevent oxidative stress and maintain a healthier skin appearance.
4. Anti-inflammatory effects: GHK-Cu has been found to have anti-inflammatory properties, which can help to soothe and calm the skin. It can reduce the production of pro-inflammatory molecules and inhibit the activation of inflammatory pathways. This makes it beneficial for individuals with skin conditions such as acne, rosacea, or dermatitis.
GHK-Cu is available in various forms, including creams, serums, and gels, for topical application. It is essential to note that GHK-Cu is a potent peptide and should be used as directed by professionals or according to product instructions. It is advisable to consult a dermatologist or healthcare provider before incorporating GHK-Cu into your skincare routine, especially if you have any underlying skin conditions or are taking medication.
Overall, GHK-Cu peptide shows promise in promoting skin rejuvenation, wound healing, antioxidant protection, and anti-inflammatory effects. It is important to stay updated with scientific research and consult professionals for the most accurate and up-to-date information on its benefits and usage.
Ultima-Test/EQ 200 Mix is a steroid mix of: Boldenone Undecylenate (100 mg) and Testosterone Enanthate (100 mg).
Testosterone Enanthate is the strongest steroid with anabolic and androgenic activity. Dissolved ester in oil, enters gradually in the blood. Due to the fact that there is Enanthate, it has a positive effect on the body more than one month.
Boldenone Undecylenate – is a derived synthetic anabolic steroid, which includes a derivative of the male hormone testosterone. Equipoise is considered one of the few drugs with no flavorings.
Boldenone is a very popular steroid among bodybuilders, weightlifters, and those who prefer the power load. The key to this success is the main feature of Boldenone: stimulation of the formation of the hormone erythropoietin which is responsible for the creation of red blood cells. Incidentally, a drug characterized in that, it enables to work on the dry weight of an athlete.
Testosterone Enanthate helps to increase strength, burn fat, and Boldenone allows you to gain quality mass with a minimum of side effects. After Ultima-Test/EQ 200 Mix cycle, you should take Anastrozole (Arimidex) to reduce side effects of Testosterone Enanthate (possible water retention, appearance of gynecomastia).
Now, EQ/Test E recommended dosage is 250-600 mg once a week. These dosages are for beginners who have just started to take the Anabolic Steroids.
ACTIVE HALF-LIFE 8-12 hours
CLASSIFICATION Anabolic Steroid
DOSAGE 10-20 mg/day
ACNE Rarely
WATER RETENTION No
HBR Yes
HEPATOTOXICITY High
AROMATIZATION No
MANUFACTURER Rx Pharmaceuticals
SUBSTANCE Methyldrostanolone,
Superdrol – trademark of anabolic steroid Methyldrostanolone.
Also called Metasteron, this steroid is a powerful oral anabolic agent, which was never produced as a commercial medical product.
Its chemical structure is very similar to Masteron (Drostanolone).
The only difference – the addition being 17 alpha-methyl group, a modification that gives this steroid a highly availability by oral administration.
In many cases, with 17 alpha-alkylation, it changes the nature of the steroid, in this case this does not happen.
Like its parent Drostanolone – aromatizing, so there is no estrogenic difference in these two steroids. Neither should not produce the side effects of estrogen. In addition, both steroids remain with very favorable ratio of anabolic effect of androgen.
Laboratory tests have shown that its anabolic activity is 4 times higher than that of oral Methyltestosterone and its relationship to androgenic anabolic effect of 20:1.
Masteron tests, as shown, that it is as powerful as an anabolic agent as Testosterone, but only 25-40% of androgens. It is – still a very good anabolic steroid, but by all accounts its rate is 3:1 instead of 20:1.
The effective Ultima-Superdrol dosage seems to start in the range of 10-20 mg per day for men. At this dosage level, it provides good anabolic effect which is usually accompanied by loss of fat and muscle expression appearance. But do not expect to obtain 10-15 kg with this steroid, growth is mostly 5-7 kg of quality weight if used solo.
In determining the optimum daily dosage, some do find that the drug is more effective in the range of up to 30mg. At higher dosage begins to develop the potential hepatotoxicity of the drug. In many cases, the best choice would be to use Ultima-Superdrol at 20 mg per day + any non-toxic injectable steroid (Nandrolone or Boldenone).
You can consider the possibility of using injectable Primobolan or Trenbolone for such cycles, instead of adding 17-alpha alkylated anabolic steroids.
Since this steroid has a very high ratio of the anabolic effect of androgen, it may be interesting for representatives of women’s bodybuilders. Ultima-Superdrol is less androgenic than the majority of popular Winstrol and Primobolan. The closest to it is Anavar (Oxandrolone), which according to some ratio of anabolic and androgenic effect is 30:1.
However, this steroid deserves interest. The main point of the problems with the use of women may be the dosage that is too high (10mg per tablet) Women are better to experiment with 1-2mg per day.
Admittedly not a comfortable experience, but nevertheless it will be effective. As with all steroids, there is a danger of virilization.
When using 17 alpha alkylation oral steroids is necessary to bear in mind the possibility of liver damage. For the most, Ultima-Superdrol best cycle is 4-6 weeks in length, that does not prevent some bodybuilders to use it for 8 consecutive weeks. This is due to the fact that among bodybuilders is widely believed that Ultima-Superdrol is less toxic to the liver than Oxymetholone, Dianabol and Winstrol.
We can tell you with little confidence that this is – a lie!
Ultima-Superdrol – really powerful oral anabolic steroid, it is an effective drug with a very favorable ratio of anabolic to androgenic effect, but also there is a significant possibility of liver damage in the event of misuse.
Warnings: Keep out of reach of children. For adults only.
OZEMPIC 1mg (blue) - NOVO NORDISK
In the box: 3 Kits for the Price of 2!
1 pen x 3 ml x 1.34 mg/ml
Set dosage: 1mg
Indications and Limitations of Use
Ozempic® (semaglutide) injection 0.5 mg, 1 mg, or 2 mg is indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus and to reduce the risk of major adverse cardiovascular (CV) events (CV death, nonfatal myocardial infarction, or nonfatal stroke) in adults with type 2 diabetes mellitus and established CV disease.
Ozempic® has not been studied in patients with a history of pancreatitis. Consider other antidiabetic therapies in patients with a history of pancreatitis.
Ozempic® is not indicated for use in patients with type 1 diabetes mellitus.
Important Safety Information cont.
Contraindications
Ozempic® is contraindicated in patients with a personal or family history of MTC or in patients with MEN 2, and in patients with a hypersensitivity reaction to semaglutide or to any of the excipients in Ozempic®. Serious hypersensitivity reactions including anaphylaxis and angioedema have been reported with Ozempic®.
Warnings and Precautions
Risk of Thyroid C-Cell Tumors: Patients should be referred to an endocrinologist for further evaluation if serum calcitonin is measured and found to be elevated or thyroid nodules are noted on physical examination or neck imaging.
Pancreatitis: Acute and chronic pancreatitis have been reported in clinical studies. Observe patients carefully for signs and symptoms of pancreatitis (persistent severe abdominal pain, sometimes radiating to the back with or without vomiting). If pancreatitis is suspected, discontinue Ozempic® promptly, and if pancreatitis is confirmed, do not restart.
Diabetic Retinopathy Complications: In a 2-year trial involving patients with type 2 diabetes and high cardiovascular risk, more events of diabetic retinopathy complications occurred in patients treated with Ozempic® (3.0%) compared with placebo (1.8%). The absolute risk increase for diabetic retinopathy complications was larger among patients with a history of diabetic retinopathy at baseline than among patients without a known history of diabetic retinopathy.
Rapid improvement in glucose control has been associated with a temporary worsening of diabetic retinopathy. The effect of long-term glycemic control with semaglutide on diabetic retinopathy complications has not been studied. Patients with a history of diabetic retinopathy should be monitored for progression of diabetic retinopathy.
Never Share an Ozempic® Pen Between Patients: Ozempic® pens must never be shared between patients, even if the needle is changed. Pen-sharing poses a risk for transmission of blood-borne pathogens.
Hypoglycemia: Patients receiving Ozempic® in combination with an insulin secretagogue (eg, sulfonylurea) or insulin may have an increased risk of hypoglycemia, including severe hypoglycemia. Inform patients using these concomitant medications of the risk of hypoglycemia and educate them on the signs and symptoms of hypoglycemia.
Acute Kidney Injury: There have been postmarketing reports of acute kidney injury and worsening of chronic renal failure, which may sometimes require hemodialysis, in patients treated with GLP-1 receptor agonists. Some of these events have been reported in patients without known underlying renal disease. A majority of the reported events occurred in patients who had experienced nausea, vomiting, diarrhea, or dehydration. Monitor renal function when initiating or escalating doses of Ozempic® in patients reporting severe adverse gastrointestinal reactions.
Hypersensitivity: Serious hypersensitivity reactions (eg, anaphylaxis, angioedema) have been reported in patients treated with Ozempic®. If hypersensitivity reactions occur, discontinue use of Ozempic®; treat promptly per standard of care, and monitor until signs and symptoms resolve. Use caution in a patient with a history of angioedema or anaphylaxis with another GLP-1 receptor agonist.
Acute Gallbladder Disease: Acute events of gallbladder disease such as cholelithiasis or cholecystitis have been reported in GLP-1 receptor agonist trials and postmarketing. In placebo-controlled trials, cholelithiasis was reported in 1.5% and 0.4% of patients treated with Ozempic® 0.5 mg and 1 mg, respectively, and not reported in placebo-treated patients. If cholelithiasis is suspected, gallbladder studies and appropriate clinical follow-up are indicated.
Adverse Reactions
The most common adverse reactions, reported in ≥5% of patients treated with Ozempic® are nausea, vomiting, diarrhea, abdominal pain, and constipation.
Drug Interactions
When initiating Ozempic®, consider reducing the dose of concomitantly administered insulin secretagogue (such as sulfonylureas) or insulin to reduce the risk of hypoglycemia.
Ozempic® causes a delay of gastric emptying and has the potential to impact the absorption of concomitantly administered oral medications, so caution should be exercised.
Use in Specific Populations
There are limited data with semaglutide use in pregnant women to inform a drug-associated risk for adverse developmental outcomes. Discontinue Ozempic® in women at least 2 months before a planned pregnancy due to the long washout period for semaglutide.
Tri Testosterone Lite 350mg/ml is a popular anabolic steroid that is used by bodybuilders and athletes to enhance their performance and improve muscle mass. It is a combination of three different forms of testosterone, including Testosterone Propionate, Testosterone Enanthate, and Testosterone Decanoate.
Each milliliter of Tri Testosterone Lite contains a total of 350mg of testosterone, making it a potent and effective compound. The combination of these three forms of testosterone provides a quick and sustained release of the hormone, leading to increased muscle growth, strength gains, and improved athletic performance.
Testosterone Propionate is a fast-acting ester that helps to kickstart the effects of the steroid. It quickly enters the bloodstream and increases protein synthesis, leading to enhanced muscle growth and recovery. Testosterone Enanthate is a longer-acting ester that ensures a sustained release of testosterone into the body over a longer period of time. This allows for consistent levels of testosterone, promoting continuous muscle growth and strength gains.
Testosterone Decanoate is another long-acting ester that further extends the release of testosterone. It helps maintain a stable hormone level in the body and contributes to the overall effectiveness of Tri Testosterone Lite.
Tri Testosterone Lite 350mg/ml is typically administered through intramuscular injections, usually once or twice a week. The dosage and frequency may vary depending on individual goals, experience, and tolerance. It is important to consult with a healthcare professional or an experienced coach to determine the appropriate dosage and cycle duration.
Like other anabolic steroids, Tri Testosterone Lite carries potential side effects. These can include estrogenic effects such as water retention, gynecomastia (development of breast tissue in males), and increased blood pressure. Androgenic side effects may also occur, such as acne, oily skin, and accelerated hair loss in individuals predisposed to male pattern baldness. Additionally, the use of Tri Testosterone Lite can suppress natural testosterone production, leading to a decrease in endogenous testosterone levels.
To mitigate the potential risks and side effects, users often incorporate post-cycle therapy (PCT) after discontinuing the use of Tri Testosterone Lite. PCT helps restore natural testosterone production and minimize the negative effects associated with steroid use.
It is crucial to note that the use of Tri Testosterone Lite or any other anabolic steroid should always be done under the guidance of a healthcare professional. Misuse or abuse of these substances can have serious health consequences.
ULTIMA-CYP 250 is a type of anabolic steroid that is widely used in the bodybuilding and fitness community. It belongs to the class of drugs known as androgenic-anabolic steroids, which are synthetic derivatives of the male sex hormone testosterone. ULTIMA-CYP 250 is specifically formulated with the active ingredient Testosterone Cypionate, which is a long-acting ester of testosterone.
Testosterone is naturally produced in the human body and plays a crucial role in the development of male sexual characteristics, muscle growth, bone density, and overall well-being. However, ULTIMA-CYP 250 is typically used by individuals who aim to enhance their athletic performance, increase muscle mass, improve strength, and accelerate recovery after intense workouts.
ULTIMA-CYP 250 is administered through intramuscular injection, typically into the gluteal muscles. The esterification of testosterone in ULTIMA-CYP 250 allows for a slower release into the bloodstream, resulting in a sustained elevation of testosterone levels over a longer period compared to other shorter-acting forms of testosterone. This makes ULTIMA-CYP 250 more convenient for users, as it requires less frequent dosing.
As with any anabolic steroid, ULTIMA-CYP 250 carries both benefits and risks. The primary benefits include increased muscle mass, enhanced strength and endurance, improved recovery, and a boost in overall performance. It can also have positive effects on libido and mood.
However, it is important to note that ULTIMA-CYP 250, like other anabolic steroids, is associated with potential side effects. These can include acne, oily skin, increased body hair growth, male pattern baldness, testicular atrophy (shrinkage of the testicles), and mood swings. In females, it may cause masculinizing effects such as a deepening of the voice and enlargement of the clitoris.
Moreover, ULTIMA-CYP 250 can negatively affect cholesterol levels, potentially leading to an increase in LDL (bad) cholesterol and a decrease in HDL (good) cholesterol. It can also negatively impact the natural production of testosterone in the body, leading to suppression of the hypothalamic-pituitary-gonadal axis. This can result in testicular atrophy and temporary infertility.
Like all anabolic steroids, ULTIMA-CYP 250 is a controlled substance and its use without a prescription is illegal in many countries. It should only be used under the guidance of a medical professional who can monitor its effects and mitigate potential risks.
In conclusion, ULTIMA-CYP 250 is a widely used anabolic steroid that contains Testosterone Cypionate. It is used to enhance athletic performance, increase muscle mass, and improve strength. However, its use comes with potential risks and side effects, and it should only be used under medical supervision.
CHARACTERISTICS
ACTIVE HALF-LIFE
36 HOURS
CLASSIFICATION
PDE5 INHIBITOR
DOSAGE
100 MG/DAY
ACNE
NO
WATER RETENTION
NO
HBR
PERHAPS
HEPATOTOXICITY
NO
AROMATIZATION
NO
ACTIVE SUBSTANCE
SILDENAFIL
FORM
50 TABS X 100 MG/TAB
MANUFACTURER
RX Pharmaceuticals
DESCRIPTION
Chemical name: 1-((3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo(4,3-d)pyrimidin-5-yl)-4-ethoxyphenyl)sulfonyl)-4-methylpiperazine citrate
Formula: C28H38N6O11S
Anabolic activity index: not a steroid
Androgenic activity index: not a steroid
VIAGRA
50 pills x 100 mg/tab
Viagra is used for treating erectile dysfunction (e.g., male impotence). In combination with sexual stimulation, this medicine works by helping the blood flow into the penis to achieve and maintain an erection. This medicine is not intended for use in women or children. This medicine will not protect against sexually transmitted diseases including HIV infection. Use ‘safe sex’ practices such as latex condoms.
VIagra is to be taken 30 minutes to 1 hour before sexual activity. Viagra’s effect lasts for about 4 hours. Ultima-VIagra is not supposed to be taken more than 4 pills (100mg) per day.
VIagra is a phosphodiesterase type 5 inhibitor and it works by helping the blood flow into the penis to achieve and maintain an erection during sexual stimulation.
Warnings/Precautions
Do not take VIagra if you are also using a nitrate drug for chest pain or heart problems, including nitroglycerin (Nitrostat, Nitrolingual, Nitro-Dur, Nitro-Bid, Minitran, Deponit, Transderm-Nitro), isosorbide dinitrate (Dilatrate-SR, Isordil, Sorbitrate), and isosorbide mononitrate (Imdur, ISMO, Monoket), or recreational drugs such as amyl nitrate or nitrite (“poppers”).
Before taking VIagra, tell your doctor about all other medications you use for erectile dysfunction, or if you are using any of the following medications:
bosentan (Tracleer);
a blood thinner such as warfarin (Coumadin);
cimetidine (Tagamet, Tagamet HB);
an antibiotic such as erythromycin (E-Mycin, Eryc, Ery-Tab) or clarithromycin (Biaxin);
ACTIVE HALF-LIFE
CLASSIFICATION
DOSAGE
ACNE
WATER RETENTION
HBR
HEPATOTOXICITY
AROMATIZATION
ACTIVE SUBSTANCE
FORM
MANUFACTURER
