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Metoclopramide nausea/vomiting

Common adverse events sedation, respiratory depression, pruritus, nausea/vomiting, constipation, and urinary retention, which are treated with a naloxone 40-80 pg IV bolus followed by an infusion of 50-100 pg/h. However, these adverse events are relatively less commonly observed with epidural hydromorphone than with neuraxial morphine regimens. Pruritus is treated with a naloxone infusion of 50-100 pg/h, diphenhydramine 12.5-50 mg or propofol infusion of 10 mg/h. Nausea and vomiting is best treated with either ondansetron (4-8 mg IV), low-dose droperidol (0.625-1.25 mg IV), metoclopramide (10 mg IV every 4-6 h), or transdermal scopolamine patch during the first 10 hours following administration. [Pg.190]

Wallenborn J, Gelbrich G, Bulst D et al (2006) Prevention of postoperative nausea and vomiting by metoclopramide combined with dexamethasone randomised double blind multicentre trial. Br Med J 333 324-327... [Pg.462]

Metoclopramide is used for its antiemetic properties in patients with diabetic gastroparesis and with dexamethasone for prophylaxis of delayed nausea and vomiting associated with chemotherapy administration. [Pg.313]

Chlorpromazine, prochlorperazine, promethazine, methylprednisolone, lorazepam, metoclopramide, dexamethasone, or dronabinol may be used for adult patients. Around the clock dosing should be considered. The choice of specific agent should based on patient specific factors, including potential for adverse drug reactions, and cost. SSRIs are effective for breakthrough nausea and vomiting but they are not superior to the less expensive antiemetics above. [Pg.316]

The severe nausea and vomiting induced by cytotoxic drugs and radiation in man can be reduced by metoclopramide given either atone or in combination with other drugs, such as dexamethasone. However, the extrapyramidal side-effects induced by metoclopramide, due to antagonism of dopamine re-... [Pg.247]

Metoclopramide may have some potential value (10 mg orally or IV 30 minutes before each meal and at bedtime) in nausea and vomiting of a variety of etiologies (uncontrolled studies report 80% to 90% efficacy), including emesis during pregnancy and labor (5 to 10 mg orally or 5 to 20 mg IV or IM, 3 times a day). [Pg.976]

Even after an effective regimen for prophylaxis, nausea or vomiting can begin again or persist 24 h or more after chemotherapy, particularly with cisplatin. Concurrent use of oral dexamethasone (8 mg twice daily for 2 d, then 4 mg twice daily for 2 d) and oral metoclopramide (0.5 mg/kg four times daily for 4 d) has been effective for this condition. Ondansetron alone has not been effective for treatment of delayed emesis following high doses of cisplatin. [Pg.233]

The absorption of paracetamol is decreased by anion exchange resins (colestyramine), whereas some drugs used to control nausea and vomiting, such as metoclopramide and domperidone, hasten the absorption of paracetamol. [Pg.762]

Uses. Metoclopramide is used for nausea and vomiting associated with gastrointestinal disorders, and with cytotoxic drugs and radiotherapy. It is also an effective antiemetic in migraine and is used as a prokinetic agent (see above). [Pg.635]


See other pages where Metoclopramide nausea/vomiting is mentioned: [Pg.72]    [Pg.1179]    [Pg.1112]    [Pg.233]    [Pg.1080]    [Pg.743]    [Pg.431]    [Pg.543]    [Pg.205]    [Pg.461]    [Pg.472]    [Pg.303]    [Pg.303]    [Pg.506]    [Pg.727]    [Pg.615]    [Pg.284]    [Pg.248]    [Pg.330]    [Pg.382]    [Pg.699]    [Pg.44]    [Pg.521]    [Pg.360]    [Pg.205]    [Pg.567]    [Pg.117]    [Pg.582]    [Pg.404]    [Pg.1498]    [Pg.426]    [Pg.342]    [Pg.461]    [Pg.215]    [Pg.602]    [Pg.332]    [Pg.611]    [Pg.635]   
See also in sourсe #XX -- [ Pg.635 , Pg.648 ]




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