Ethoheptazine
Ethoheptazine[edit | edit source]
Ethoheptazine is a synthetic opioid analgesic drug that belongs to the class of phenazocine derivatives. It was first synthesized in the 1960s and was primarily used as a pain reliever. Ethoheptazine is known for its potent analgesic properties and has been used in various medical settings.
History[edit | edit source]
Ethoheptazine was developed by pharmaceutical company Merck in the 1960s. It was initially introduced as a safer alternative to other opioid analgesics available at the time. The drug gained popularity due to its effectiveness in managing moderate to severe pain.
Pharmacology[edit | edit source]
Ethoheptazine acts as a selective agonist of the μ-opioid receptor, which is responsible for mediating the analgesic effects of opioids. It also exhibits some affinity for the κ-opioid receptor. By binding to these receptors, ethoheptazine inhibits the transmission of pain signals in the central nervous system, resulting in pain relief.
Medical Uses[edit | edit source]
Ethoheptazine was primarily used for the management of moderate to severe pain. It was commonly prescribed for postoperative pain, cancer-related pain, and other chronic pain conditions. However, due to the potential for abuse and addiction, its use has been limited in recent years.
Side Effects[edit | edit source]
Like other opioids, ethoheptazine can cause various side effects. Common side effects include drowsiness, dizziness, constipation, nausea, and respiratory depression. Long-term use of ethoheptazine can lead to tolerance, dependence, and addiction.
Legal Status[edit | edit source]
The legal status of ethoheptazine varies from country to country. In some countries, it is classified as a controlled substance due to its potential for abuse and addiction. In other countries, it may be available only by prescription or completely banned.
References[edit | edit source]
See Also[edit | edit source]
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