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  2. Morphine - Wikipedia

    en.wikipedia.org/wiki/Morphine

    Morphine pharmaceuticals are subject to annual manufacturing quotas; in 2017 these quotas were 35.0 tonnes of production for sale, and 27.3 tonnes of production as an intermediate, or chemical precursor, for conversion into other drugs. [154] Morphine produced for use in extremely dilute formulations is excluded from the manufacturing quota.

  3. Intrathecal administration - Wikipedia

    en.wikipedia.org/wiki/Intrathecal_administration

    Intrathecal administration is often used for a single 24-hour dose of analgesia (opioid with local anesthetic). Caution should be exercised with intrathecal opioids due to the risk of late onset hypoventilation. The use of intrathecal morphine may be limited by severe pruritus and urinary retention. [citation needed]

  4. Paroxysmal sympathetic hyperactivity - Wikipedia

    en.wikipedia.org/wiki/Paroxysmal_sympathetic...

    Morphine has been found to be effective in aborting episodes; sometimes it is the only medication that can combat the sympathetic response. Morphine helps lower respiration rates and hypertension. It is given in doses of two milligrams to eight milligrams but can be administered up to twenty milligrams. Nausea and vomiting are common side effects.

  5. Opioid - Wikipedia

    en.wikipedia.org/wiki/Opioid

    Opioids work on opioid receptors in the brain and other organs to produce a variety of morphine-like effects, including pain relief. [2] [3] The terms 'opioid' and 'opiate' are sometimes used interchangeably, but the term 'opioid' is used to designate all substances, both natural and synthetic, that bind to opioid receptors in the brain. [4]

  6. μ-opioid receptor - Wikipedia

    en.wikipedia.org/wiki/Μ-opioid_receptor

    Miosis and reduced bowel motility tend to persist; little tolerance develops to these effects. [citation needed] The canonical MOR1 isoform is responsible for morphine-induced analgesia, whereas the alternatively spliced MOR1D isoform (through heterodimerization with the gastrin-releasing peptide receptor) is required for morphine-induced itching.

  7. Morphine - Wikipedia

    en.wikipedia.org/wiki/(+)-Morphine

    To the contrary, in rats, (+)-morphine acts as an antianalgesic and is approximately 71,000 times more potent as an antianalgesic than (−)-morphine is as an analgesic. [ 1 ] (+)-Morphine derives its antianalgesic effects by being a selective-agonist of the Toll-like receptor 4 (TLR4), which due to not binding to opioid receptors allows it to ...

  8. Analgesic - Wikipedia

    en.wikipedia.org/wiki/Analgesic

    An analgesic drug, also called simply an analgesic, antalgic, pain reliever, or painkiller, is any member of the group of drugs used for pain management.Analgesics are conceptually distinct from anesthetics, which temporarily reduce, and in some instances eliminate, sensation, although analgesia and anesthesia are neurophysiologically overlapping and thus various drugs have both analgesic and ...

  9. Apomorphine - Wikipedia

    en.wikipedia.org/wiki/Apomorphine

    As the drug is known to be reasonably safe for use in humans, it is a viable target for repurposing. Apomorphine has been researched as a possible treatment for erectile dysfunction and female hypoactive sexual desire disorder, though its efficacy has been limited.