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When used for opioid addiction it is recommended that a health care provider observe the person while they take the medication. For longer term treatment of addiction a combination formulation of buprenorphine/naloxone is usually recommended. Maximum pain relief is generally within an hour with effects up to 24 hours.

Side effects may include respiratory depression (decreased breathing), sleepiness, adrenal insufficiency, QT prolongation, low blood pressure, allergic reactions, and opioid addiction. Among those with a history of seizures, there is a risk of further seizures. Opioid withdrawal following stopping is generally mild. It is unclear if use during pregnancy is safe and use while breastfeeding is not recommended. Buprenorphine affects different types of opioid receptors in different ways. Depending on the type of receptor it may be an agonist, partial agonist, or antagonist.

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Boldenone Cypionate is an injectable steroid Boldenone was developed to be used in veterinary practice for horses and cattle. This drug is administered via intramuscular route, i.e. it is injected directly into the muscle tissue. The process makes absorption faster. Boldenone Cypionate affects the body in the same way testosterone producing androgens does. The latter induces virilization crucial for muscle bulking and cutting.

Boldenone Cypionate is designed to be membrane permeable allowing it to pass through the membrane into the cell nucleus where it targets androgen receptors located in the cytoplasm. This process affects genes, as well as signals activating cells. Various steroids may cause different effects.

The side effects of Boldenone Cypionate are increased cholesterol, hypertension, gynecomastia and testicular size reduction. As for additional side effects, a user may experience acne, oily skin, unnatural hair growth or vice versa unusual hair loss and an increased appetite. Despite all these downsides, Boldenone Cypionate still has great benefits needed for bulking.

Boldenone Cypionate increases protein content and reduces recovery time in workouts. Inhibiting the effects of stress hormone cortisol, the protein shortens the time a body needs to rest after a hard workout. Innovagen Ultrabolan may lead to increased appetite as it boosts basal metabolic rate. This process conduces to differentiation of muscle cells, but not fat ones.

By increasing circulation, this steroid increases endurance, bone marrow production, oxygen uptake and triggers hemoglobin increase. All these leads to enhanced sustaining power.

For women daily dosage is 35-50mg weekly, while for men it ranges between 300-600mg per week.

This steroid may help a bodybuilder to skip estrogen-related issues. It’s worth mentioning that this steroid stays in the body for 16-18 months after a cycle completion. Therefore, it is not recommended to use it if you are going to undergo routine or random drug screenings.

Taking into account the modest effect of the drug, it cannot provide fast results. The progress stimulated by the steroid is similar to that of Primobolan, since the effects emerge slowly and uniformly, but the result is quite stable. The drug does not result in excess water retention and aromatization.

Therefore, at first, it may seem the drug does not cause growth in comparison with testosterone, which during the first weeks leads to increased body weight due to fluid retention. However, be aware that the level of fluid returns to normal after the end of the cycle, and if using boldenone you can build up 1 lb of muscle mass per week, the other drugs are hardly to provide better results.

Boldenone can be combined with other steroids such as Primombolan (methenolone) or Masteron (drostanolone). Since boldenone produces small amounts of estrogen, it helps to build lean mass muscle, which is easier to be maintained.

The following are the examples of boldenone cycles (sometimes it’s recommended to use 500iu of HCG per week from the very beginning to the end of the cycle, as it minimizes the hormonal fluctuations and contributes to recovery processes).

Example of low aromatase bulking cycle:

Boldenone Cypionate – 800 mg per week, from the 1st to the 12th week.

Primobolan (methenolone enanthate) – 600 mg per week, from the 1st to the 13th week.

(At user’s option – Anavar (oxandrolone) 40 mg daily from the 1st to the 16th week).

Clomid recovery treatment – 3 weeks after last Primombolan injection.

 

Specifications:

TEST ITEMS SPECIFICATION RESULTS
Description White or almost white crystalline powder Conforms
Melting Point 95°C min 99.0~105.0°C
Loss On Drying 0.5%max 0.30%
Heavy Metals 10PPm max Conforms

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Methadone (Adolan, Dolophine, Methadose) is a synthetic, acyclic analog of morphine and heroin that acts on µ-opioid receptors (Ki = 0.72 nM) to produce a long-acting analgesic effect. It is used as maintenance therapy in the treatment of opioid dependence.

This medication is used to treat addiction to opioids (such as heroin) as part of an approved treatment program. Methadone belongs to a class of drugs known as opioid analgesics. It helps prevent withdrawal symptoms caused by stopping other opioids.

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Buy Lysergic Acid Diethylamide, first synthesized in 1938, is an extremely potent hallucinogen. It is synthetically made from lysergic acid, which is found in ergot, a fungus that grows on rye and other grains. It is so potent its doses tend to be in the microgram (mcg) range. Its effects, often called a “trip”, can be stimulating, pleasurable, and mind-altering or it can lead to an unpleasant, sometimes terrifying experience called a “bad trip.

Appearance;

LSD is produced in crystalline form and then mixed with other inactive ingredients, or diluted as a liquid for production in ingestible forms. It is odorless, colorless, and has a slightly bitter taste. LSD is under more than 80 street names including Acid, Blotter, acid, Doses, Dots, Trips, Mellow Yellow, Window Pane, as well as names that reflect the designs on sheets of blotter paper.

Qualities;

LSD does not appear to be addictive, although tolerance may occur with the use of increasing doses. Adverse psychiatric reactions are possible, such as anxiety, paranoia, and delusions. Distressing flashbacks might occur in spite of no further use, a condition called hallucinogen persisting perception disorder.

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LSD was first made by Albert Hofmann in 1938 from lysergic acid, a chemical from the fungus ergot. Hofmann discovered its hallucinogenic properties in 1943. In the 1950s, the Central Intelligence Agency (CIA) believes that the drug might be useful for mind control, so they test it on people, some without their knowledge, in a program called MKUltra. LSD was sold as a medication for research purposes under the trade-name Delysid in the 1950s and 1960s.

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Lysergic Acid Diethylamide is a mind-altering drug. It is LSD causes its characteristic hallucinogenic effects via interaction with the serotonin receptors in the brain.

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Phenobarbital, also known as phenobarbitone or phenobarb, is a medication recommended for the treatment of certain types of epilepsy in developing countries In the developed world it is commonly used to treat seizures in young children, while other medications are generally used in older children and adults. It may be used intravenously, injected into a muscle, or taken by mouth. The injectable form may be used to treat status epilepticus. It is occasionally used to treat trouble sleeping, anxiety, and drug withdrawal and to help with surgery.

Medical uses
It is used in the treatment of all types of seizures except absence seizures. It is no less effective at seizure control than phenytoin, however phenobarbital is not as well tolerated. It may provide a clinical advantage over carbamazepine for treating partial onset seizures. Carbamazepine may provide a clinical advantage over phenobarbital for generalized onset tonic-clonic seizures.

It  is the first-line choice for the treatment of neonatal seizures.

It is sometimes used for alcohol detoxification and benzodiazepine detoxification for its sedative and anticonvulsant properties. The benzodiazepines chlordiazepoxide (Librium) and oxazepam (Serax) have largely replaced phenobarbital for detoxification.

It’s properties can effectively reduce tremors and seizures associated with abrupt withdrawal from benzodiazepines.

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