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Oxycodone is a semisynthetic derivative of codeine that acts as a narcotic analgesic more potent and addicting than codeine. An extended-release (ER) form of oxycodone (Xtampza ER) was approved for the management of daily, around-the-clock pain management in April 2016.

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Buy oxycodone without prescription online

Oxycodone is a semisynthetic opioid synthesized from thebaine, an opioid alkaloid, and one of the many alkaloids found in the opium poppy. It is a moderately potent opioid pain medication, generally indicated for relief of moderate to severe pain as one of several semi-synthetic opioids in an attempt to improve on the existing opioids.

Uses: 

Oxycodone is used to help relieve moderate to severe pain.
Oxycodone belongs to a class of drugs known as opioid (narcotic) analgesics.
It works in the brain to change how your body feels and responds to pain.

Side Effects:

Nausea and vomiting.
Fatigue.
Depression.
Coughing.
Diarrhea.
Runny nose.
Teary eyes.
Sweating.

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Oxycodone is a semisynthetic derivative of codeine that acts as a narcotic analgesic more potent and addicting than codeine. An extended-release (ER) form of oxycodone (Xtampza ER) was approved for the management of daily, around-the-clock pain management in April 2016.

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Associated Conditions :
Severe Pain
Severe, Chronic Pain
Acute, moderate Pain
Acute, severe Pain
Chronic, moderate Pain

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Oxycodone, a semisynthetic opiate agonist derived from the opioid alkaloid, thebaine, is similar to other phenanthrene derivatives such as hydrocodone and morphine. Oxycodone is available in combination with aspirin or acetaminophen to control pain and restless leg and Tourette syndromes.

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Mechanism of Action of Oxycodone :

Oxycodone acts as a weak agonist at mu, kappa, and delta-opioid receptors within the central nervous system (CNS). Oxycodone primarily affects mu-type opioid receptors, which are coupled with G-protein receptors and function as modulators, both positive and negative, of synaptic transmission via G-proteins that activate effector proteins.

Binding of the opiate stimulates the exchange of GTP for GDP on the G-protein complex. As the effector system is adenylate cyclase and CAMP located at the inner surface of the plasma membrane, opioids decrease intracellular cAMP by inhibiting adenylate cyclase.

Subsequently, the release of nociceptive neurotransmitters such as substance P, GABA, dopamine, acetylcholine, and noradrenaline is inhibited. Opioids such as oxycodone also inhibit the release of vasopressin, somatostatin, insulin, and glucagon.

Opioids close N-type voltage-operated calcium channels (kappa-receptor agonist) and open calcium-dependent inwardly rectifying potassium channels (mu and delta receptor agonist). This results in hyperpolarization and reduced neuronal excitability. 

Toxicity :

Symptoms of overdose include respiratory depression, somnolence progressing to stupor or coma, skeletal muscle flaccidity, cold and clammy skin, constricted pupils, bradycardia, hypotension, and death.

HOW SHOULD I TAKE OXYCODONE :

If you are taking the Oxycodone extended-release tablets, swallow them whole; do not chew, break, divide, crush, or dissolve them. Do not presoak, lick or otherwise wet the tablet prior to placing in the mouth. Swallow each tablet right after you put it in your mouth.

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