Axomadol

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Axomadol Structure.svg

Axomadol is a synthetic opioid analgesic that is used for the treatment of moderate to severe pain. It is structurally related to tramadol and functions as a centrally acting analgesic. Axomadol is known for its dual mechanism of action, which includes both opioid receptor agonism and inhibition of serotonin and norepinephrine reuptake.

Pharmacology[edit | edit source]

Axomadol exerts its analgesic effects primarily through its action on the mu-opioid receptor (MOR). By binding to these receptors, it mimics the effects of endogenous endorphins, leading to pain relief. Additionally, axomadol inhibits the reuptake of serotonin and norepinephrine, which enhances its analgesic properties and contributes to its effectiveness in treating neuropathic pain.

Mechanism of Action[edit | edit source]

The dual mechanism of action of axomadol involves:

  • Agonism at the mu-opioid receptor, which provides potent analgesia.
  • Inhibition of the reuptake of serotonin and norepinephrine, which modulates pain perception and provides additional analgesic effects.

Clinical Use[edit | edit source]

Axomadol is prescribed for the management of moderate to severe pain, including both acute and chronic pain conditions. It is particularly useful in cases where other analgesics, such as nonsteroidal anti-inflammatory drugs (NSAIDs), are ineffective or contraindicated.

Side Effects[edit | edit source]

Common side effects of axomadol include:

Serious side effects may include:

Contraindications[edit | edit source]

Axomadol should not be used in patients with:

Interactions[edit | edit source]

Axomadol may interact with other medications, including:

Regulation[edit | edit source]

As an opioid analgesic, axomadol is subject to regulation under various national and international drug control laws. It is classified as a controlled substance in many countries due to its potential for abuse and dependence.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD