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  2. 6-Monoacetylmorphine - Wikipedia

    en.wikipedia.org/wiki/6-monoacetylmorphine

    The production of black tar heroin results in significant amounts of 6-MAM in the final product. [citation needed] 6-MAM is approximately 30 percent more active than diacetylmorphine itself, [citation needed] This is why despite lower heroin content, black tar heroin may be more potent than some other forms of heroin. 6-MAM can be synthesized from morphine using glacial acetic acid with an ...

  3. Ropinirole - Wikipedia

    en.wikipedia.org/wiki/Ropinirole

    Ropinirole can cause nausea, dizziness, hallucinations, orthostatic hypotension, and sudden sleep attacks during the daytime.Unusual side effects specific to D 3 agonists such as ropinirole and pramipexole can include hypersexuality, punding and compulsive gambling, even in patients without a history of these behaviours.

  4. Lists of drugs - Wikipedia

    en.wikipedia.org/wiki/Lists_of_drugs

    Many drugs have more than one name and, therefore, the same drug may be listed more than once. Brand names and generic names are differentiated by capitalizing brand names. See also the list of the top 100 bestselling branded drugs , ranked by sales.

  5. Methenamine - Wikipedia

    en.wikipedia.org/wiki/Methenamine

    The drug is distributed widely throughout the body, including in saliva, bile, cerebrospinal fluid, synovial fluids, and pleural effusions. [2] In accordance with its presence in cerebrospinal fluid, methenamine is known to cross the blood–brain barrier and enter the central nervous system .

  6. Bictegravir - Wikipedia

    en.wikipedia.org/wiki/Bictegravir

    Bictegravir (INN; BIC, formerly known as GS-9883) [1] [2] is a second-generation integrase inhibitor (INSTI) class that was structurally derived from an earlier compound dolutegravir by scientists at Gilead Sciences. In vitro and clinical results were presented by Gilead in the summer of 2016.

  7. Lamivudine - Wikipedia

    en.wikipedia.org/wiki/Lamivudine

    As a result, lamivudine was identified as a less toxic agent to mitochondria DNA than other retroviral drugs. [18] [19] Lamivudine was approved by the US Food and Drug Administration (FDA) in November 1995, for use with zidovudine (AZT) and again in 2002. It is on the World Health Organization's List of Essential Medicines. [10]

  8. Two Indian companies indicted in US for importing ingredients ...

    www.aol.com/news/two-indian-companies-indicted...

    Two Indian chemical companies have been indicted for allegedly importing ingredients for the highly addictive opioid fentanyl into the United States and Mexico, the U.S. Department of Justice said ...

  9. Lamivudine/zidovudine - Wikipedia

    en.wikipedia.org/wiki/Lamivudine/zidovudine

    Lamividine/zidovudine interacts with stavudine and zalcitabine by competing intracellularly for activation and results in inhibiting phosphorylation. [ 3 ] [ 12 ] There is also a known interaction with nephrotoxic or bone marrow suppressive agents (e.g. doxorubicin ) which increases the risk of hematologic toxicity of zidovudine. [ 13 ]

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