What is the chemical formula for tramadol Ultram?

What is the chemical formula for tramadol Ultram?

Full Prescribing Information DESCRIPTION ULTRAM (tramadol hydrochloride) tablets is a centrally acting analgesic. The chemical name for tramadol hydrochloride is (±) cis -2-[(dimethylamino)methyl]-1-(3­ methoxyphenyl) cyclohexanol hydrochloride. Its structural formula is: The molecular weight of tramadol hydrochloride is 299.8.

What are the side effects of long term use of tramadol?

Long-term use of opioid medication may affect fertility (ability to have children) in men or women. It is not known whether opioid effects on fertility are permanent. Common tramadol side effects may include: constipation, nausea, vomiting, stomach pain; dizziness, drowsiness, tiredness; headache; or. itching.

What is the generic name for tramadol pain medicine?

Generic name: tramadol (TRAM a dol) Brand name: ConZip, Qdolo, Ultram, Ultram ER Drug class: Narcotic analgesics. Medically reviewed by Kaci Durbin, MD. Last updated on July 12, 2021. Uses; Warnings; Dosage; What to avoid; Side effects; Interactions; FAQ; What is tramadol? Tramadol is a pain medicine similar to an opioid.

When did tramadol become a Schedule IV drug?

Tramadol was initially approved by the FDA in 1995 and classified as a non-scheduled drug — meaning the drug was not regulated by the DEA and carried fewer restrictions than other opioids. Tramadol was finally listed as a Schedule IV substance in 2014 after numerous reports revealed the drug was associated with high rates of abuse and dependence.

Are there any side effects to taking tramadol extended release?

The extended-release form of tramadol is not for use on an as-needed basis for pain. Seizures have been reported in patients taking tramadol. Your risk of seizures is higher if you are taking higher doses of tramadol over what is recommended.

How is tramadol related to morphine and codeine?

Clinical pharmacology of tramadol Tramadol, a centrally acting analgesic structurally related to codeine and morphine, consists of two enantiomers, both of which contribute to analgesic activity via different mechanisms. (+)-Tramadol and the metabolite (+)-O-desmethyl-tramadol (M1) are agonists of the mu opioid receptor.

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