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  2. Rivastigmine - Wikipedia

    en.wikipedia.org/wiki/Rivastigmine

    [4] [6] [7] Rivastigmine can be administered orally or via a transdermal patch; the latter form reduces the prevalence of side effects, [8] which typically include nausea and vomiting. [9] Rivastigmine is eliminated through the urine, and appears to have relatively few drug-drug interactions. [9] It was patented in 1985 and came into medical ...

  3. Transdermal patch - Wikipedia

    en.wikipedia.org/wiki/Transdermal_patch

    The patch is labelled with the time and date of administration as well as the administrator's initials. Microneedle patch size comparison [1] A transdermal patch is a medicated adhesive patch that is placed on the skin to deliver a specific dose of medication through the skin and into the bloodstream. An advantage of a transdermal drug delivery ...

  4. Deprescribing - Wikipedia

    en.wikipedia.org/wiki/Deprescribing

    Deprescribing can improve adherence, cost, and health outcomes but may have adverse drug withdrawal effects. More specifically, deprescribing is the planned and supervised process of intentionally stopping a medication or reducing its dose to improve the person's health or reduce the risk of adverse side effects. Deprescribing is usually done ...

  5. Dosage (pharmacology) - Wikipedia

    en.wikipedia.org/wiki/Dosage_(pharmacology)

    In pharmacology and medicine, dosage refers to the prescribed regimen for administering a medication or substance, encompassing the amount, frequency, and duration of use. [1] It is distinct from dose, which denotes a single, specific quantity of a drug or substance given at one time. [2] Dosage typically includes information on the number of ...

  6. Medication discontinuation - Wikipedia

    en.wikipedia.org/wiki/Medication_discontinuation

    Medication discontinuation is the ceasing of a medication treatment for a patient by either the clinician or the patient themself. [ 1 ] [ 2 ] When initiated by the clinician, it is known as deprescribing . [ 3 ]

  7. Equianalgesic - Wikipedia

    en.wikipedia.org/wiki/Equianalgesic

    Acute use (1–3 days) yields a potency about 1.5× stronger than that of morphine and chronic use (7 days+) yields a potency about 2.5 to 5× that of morphine. Similarly, the effect of tramadol increases after consecutive dosing due to the accumulation of its active metabolite and an increase of the oral bioavailability in chronic use.

  8. Cholinesterase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Cholinesterase_inhibitor

    Paraoxon and rivastigmine are both acetylcholinesterase inhibitors and butyrylcholinesterase inhibitors. [14] [11] [7]In 2015, the United States Food and Drug Administration's Adverse Event Reporting System database compared rivastigmine to the other ChEI drugs donepezil and galantamine found that rivastigmine was associated with a higher frequency of reports of death as an adverse event.

  9. Ibuprofen - Wikipedia

    en.wikipedia.org/wiki/Ibuprofen

    Allowing sufficient time between doses of ibuprofen and immediate-release (IR) aspirin can avoid this problem. The recommended elapsed time between a dose of ibuprofen and a dose of aspirin depends on which is taken first. It would be 30 minutes or more for ibuprofen taken after IR aspirin, and 8 hours or more for ibuprofen taken before IR aspirin.