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  2. Ondansetron - Wikipedia

    en.wikipedia.org/wiki/Ondansetron

    A vial of Zofran 4 mg containing ondansetron for intravenous injection Ondansetron (marketed under the brand name Zofran) was developed in the mid-1980s by GlaxoSmithKline in London. It was granted U.S. patent protection in September 1987, [ 37 ] received a use patent June 1988, [ 38 ] and was approved by the U.S. Food and Drug Administration ...

  3. 5-HT3 antagonist - Wikipedia

    en.wikipedia.org/wiki/5-HT3_antagonist

    0.25 mg dose Ramosetron: Benzimidazole derivative 5-HT 3 receptor antagonist 5.8 hours 300 μg/kg Tropisetron [30] Indole: 5-HT 3 receptor antagonist 5.6 hours CYP 3A3/4/5, CYP2D6: 200 μg/kg Vortioxetine: Phenylpiperazine: 5-HT 3 receptor antagonist Antidepressant 66h CYP 2D6/ 2A6/CYP2B6/CYP2C8/9, CYP2C19: 5 mg, 10 mg, 20 mg doses

  4. Chemotherapy-induced nausea and vomiting - Wikipedia

    en.wikipedia.org/wiki/Chemotherapy-induced...

    Aprepitant has also been shown to increase the activity of the 5-HT 3 receptor antagonists ondansetron and the corticosteroid dexamethasone, which are also used to prevent nausea and vomiting caused by chemotherapy. [11] Netupitant has recently been approved by USFDA. It has also been marketed in combination with palonosetron.

  5. Postoperative nausea and vomiting - Wikipedia

    en.wikipedia.org/wiki/Postoperative_nausea_and...

    Serotonin (5-HT3) receptor antagonists can be administered as a single dose at the end of surgery. Adverse effects include prolongation of the QT interval on electrocardiogram (EKG). Medications include ondansetron, granisetron, and dolasetron. Anticholinergics can be used as a long-acting patch placed behind the patient's ear. Adverse effects ...

  6. Zofran - Wikipedia

    en.wikipedia.org/?title=Zofran&redirect=no

    From or to a drug trade name: This is a redirect from (or to) the trade name of a drug to (or from) the international nonproprietary name (INN).

  7. Loading dose - Wikipedia

    en.wikipedia.org/wiki/Loading_dose

    That immediately gets the drug's concentration in the body up to the therapeutically-useful level. First day: 1000 mg; the body clears 100 mg, leaving 900 mg. On the second day, the patient takes 100 mg, bringing the level back to 1000 mg; the body clears 100 mg overnight, still leaving 900 mg, and so forth.

  8. Route of administration - Wikipedia

    en.wikipedia.org/wiki/Route_of_administration

    The term injection encompasses intravenous (IV), intramuscular (IM), subcutaneous (SC) and intradermal (ID) administration. [ 35 ] Parenteral administration generally acts more rapidly than topical or enteral administration, with onset of action often occurring in 15–30 seconds for IV, 10–20 minutes for IM and 15–30 minutes for SC. [ 36 ]

  9. Post-anesthesia care unit - Wikipedia

    en.wikipedia.org/wiki/Post-anesthesia_care_unit

    Patients do receive antiemetic medications, such as Ondansetron and Dexamethasone, during the surgical procedure if the patient is at risk for it. [ 1 ] [ 6 ] Along with PONV, there are numerous complications that can happen with many different organ systems, the most threatening of which involves the respiratory system , and cardiovascular ...

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