Parenteral Manual

Metoclopramide HCl

Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Alternate Name(s): 
MAXERAN®, REGLAN®
Classification: 
Upper GIT motility modifier, antiemetic
Original Date: 
August 2005
Revised Date: 
December 2019
Indications: 
  • Management of delayed gastric emptying/reflux if oral therapy not feasible
  • Adjunct to facilitate small bowel intubations; in diagnostic radiology to facilitate gastroduodenal evacuation of barium meal
  • Prevention of nausea and vomiting during chemotherapy or postoperatively  
  • Migraine 
Reconstitution and Stability: 
  • Available as a 5 mg/mL colourless injection. Store at room temperature 
  • Diluted solutions stable 48 hours at room temperature when protected from light 
Compatibility: 
  • Solutions Compatible: D5W, 0.9% NaCl, D5W/0.45%NaCl, ringer's solution, ringer's lactate
  • Additive/Above Cassette Compatible: aminophylline, atropine, benztropine, dexamethasone, dimenhydrinate, diphenhydramine, fentanyl, heparin, hydromorphone, hydroxyzine, meperidine, methylprednisolone sodium succinate, morphine, midazolam, KCL (up to 30 mmol/L), ranitidine
  • Y-site Compatible: ciprofloxacin, cisatracurium, fluconazole, meropenem, TPN (amino acids/dextrose)

Incompatible: ampicillin, chloramphenicol, furosemide, penicilin G, propofol, sodium bicarbonate

Administration: 

(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)

SC NO
IM YES
Usual dilution: 5 mg/mL
IV Direct

NO

IV Intermittent Infusion

YES

Usual dilution Hem/Onc only: 1 mg/mL

Usual dilution other wards/ER: 0.5 mg/mL

Infusion time: 15-30 minutes
Infusion rate: do not exceed 5 mg/minute

IV Continuous Infusion YES
Usual dilution: 1 mg/mL
Dosage: 

(For neonatal dosages, refer to Neonatal IV Drug Manual.)

Pediatric:

- Gastroesophageal reflux: 0.4 -0.8 mg/kg/day IM/IV QID, 30 minutes before meals and at bedtime (maximum 15 mg QID)

- Chemotherapy-Induced Nausea/Vomiting: 0.5-1 mg/kg/dose IV given 30 minutes before chemotherapy Q 2-4 hours PRN (maximum 25 mg/dose)

** Administer diphenhydramine 1 mg/kg/dose (max 50 mg) concurrently to prevent dystonic reactions

- Postoperative Nausea/Vomiting: 0.1-0.2 mg/kg/dose IV Q6-8 hours PRN (maximum 10 mg/dose)

- Migraine: Pediatric dose guidelines for migraines do not exist in the literature.If required, a reasonable approach would be to use dosing similar to that used for postop nausea and vomiting: 0.1-0.2 mg/kg/dose IV (maximum dose: 10 mg/dose) x 1

- Small Bowel Intubation:

           < 6 yrs: 0.1 mg/kg IV x 1 dose 5 minutes prior to intubation

           6-14 yrs: 2.5-5 mg IV x 1 dose 5 minutes prior to intubation

           > 14 yrs: 10 mg IV x 1 dose 5 minutes prior to intubation

Adult:

- Gastroesophageal reflux: 10-15 mg IM/IV QID, 30 minutes before meals and at bedtime

- Chemotherapy-Induced Nausea/Vomiting: 1-2 mg/kg/dose IV given 30 minutes before chemotherapy Q 2-4 hours PRN (maximum 10 mg/kg/day)

** Administer diphenhydramine 1 mg/kg/dose (max 50 mg) concurrently to prevent dystonic reactions

- Postoperative Nausea/Vomiting: 10 mg IV Q 6-8 hours PRN

DOSE ADJUSTMENT IN RENAL FAILURE:

CrCl: 40-50 mL/minute: Administer 75% of recommended dose

CrCl: 10-40 mL/minute: Administer 50% of recommended dose

CrCl: < 10 mL/minute: Administer 25-50% of recommended dose

Migraine - 10 mg IV x 1 dose

Potential hazards of parenteral administration: 
  • IV Direct may cause transient feelings of anxiety and restlessness, followed by drowsiness
  • Extrapyramidal reactions within 24-48 hours: Treatment: diphenhydramine 1 mg/kg IV stat
  • Diarrhea, Fluid retention, urinary frequency
  • Insomnia, headache, visual disturbances- less common
  • Transient flushing after large dose
  • May increase seizure frequency in epileptics
Notes: 
  • Monitor renal function, BP, HR
  • Contraindicated in pheochromocytoma, GI obstruction, history of seizure disorder or patients receiving drugs likely to cause extrapyramidal symptoms
  • May alter the absorption of oral medications (e.g: decrease digoxin absorption, increases cyclosporine and tacrolimus absorption)
  • Concomitant use with MAO inhibitors increases hypertensive episodes

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