Glycopyrrolate: Difference between revisions

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==Administration==
==Administration==
*Type: [[Anticholinergics]]
*Class: [[Anticholinergics]]
*Dosage Forms: Oral tab 1mg; INJ
*Routes of Administration: Oral, IV, IM
*Routes of Administration: Oral, IM, IV
*Dosage Forms: 1-2 mg tablets, 1 mg/5mL oral solution, 0.2 mg/mL injectable solution
*Common Trade Names: Robinul
*Common Trade Names: Robinul, Cuvposa


==Adult Dosing==
==Adult Dosing==
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***Start: 1 mg PO tid
***Start: 1 mg PO tid
***Max: 8 mg/day
***Max: 8 mg/day
**IM/IV Dose: 0.1-0.2 mg IM/IV tid-qid
**IM/IV Dose: 0.1-0.2 mg IM/IV tid-QID
***Max: 0.8 mg/day
***Max: 0.8 mg/day
***Space dose 4h apart
***Space dose 4h apart
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==Special Populations==
==Special Populations==
*[[Drug pregnancy categories|Pregnancy Rating]]: B; No known risk of teratogenicity w/ INJ form at 5x MRHD and w/ PO form at 320x MRHD
*[[Drug pregnancy categories|Pregnancy Rating]]: B; No known risk of teratogenicity with INJ form at 5x MRHD and with PO form at 320x MRHD
*Lactation risk: L3; Safety unknown
*Lactation risk: L3; Safety unknown


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*Intestinal atony in elderly, debilitated pts
*Intestinal atony in elderly, debilitated pts
*[[Myasthenia gravis]]
*[[Myasthenia gravis]]
*Acute hemorrhage w/ unstable cardiovascular status
*Acute hemorrhage with unstable cardiovascular status
*Caution if CAD
*Caution if CAD
*Caution if [[HTN]]
*Caution if [[HTN]]
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*Caution if [[febrile]]
*Caution if [[febrile]]
*Caution if [[ulcerative colitis]]
*Caution if [[ulcerative colitis]]
*Caution if hiatal hernia w/ reflux [[esophagitis]]
*Caution if hiatal hernia with reflux [[esophagitis]]


==Adverse Reactions==
==Adverse Reactions==

Latest revision as of 17:14, 6 May 2022

Administration

  • Class: Anticholinergics
  • Routes of Administration: Oral, IV, IM
  • Dosage Forms: 1-2 mg tablets, 1 mg/5mL oral solution, 0.2 mg/mL injectable solution
  • Common Trade Names: Robinul, Cuvposa

Adult Dosing

  • PUD, adjunct tx
    • PO Dose: 1-2 mg PO bid-tid;
      • Start: 1 mg PO tid
      • Max: 8 mg/day
    • IM/IV Dose: 0.1-0.2 mg IM/IV tid-QID
      • Max: 0.8 mg/day
      • Space dose 4h apart
  • Antisialagogue
    • PO Dose: 1-2 mg PO bid-tid;
      • Max: 8 mg/day
    • Parenteral Dose: 0.1-0.2 mg SC/IM/IV q4-8h PRN
      • Max: 0.8 mg/day

Pediatric Dosing

  • Antisialagogue
    • PO Dose, 2+ yo: 0.04-0.1 mg/kg PO q4-8h PRN
      • Max: 1-2 mg/dose, 8mg/day
    • Parenteral Dose, 2+ yo: 0.0004-0.01 mg/kg SC/IM/IV q4-8h PRN
      • Max: 0.1-0.2 mg/dose, 0.8 mg/day

Special Populations

  • Pregnancy Rating: B; No known risk of teratogenicity with INJ form at 5x MRHD and with PO form at 320x MRHD
  • Lactation risk: L3; Safety unknown

Renal Dosing

  • Adult: Not defined; consider decreased dose.
  • Pediatric: No defined; consider decreased dose.

Hepatic Dosing

  • Adult: Not defined.
  • Pediatric: Not defined.

Contraindications

  • Allergy to class/drug
  • Neonates (benzyl alcohol-containing INJ forms)
  • Glaucoma, angle-closure
  • Obstructive uropathy
  • GI Obstruction
  • Paralytic ileus
  • Toxic megacolon
  • Ulcerative colitis, severe
  • Intestinal atony in elderly, debilitated pts
  • Myasthenia gravis
  • Acute hemorrhage with unstable cardiovascular status
  • Caution if CAD
  • Caution if HTN
  • Caution if CHF
  • Caution if arrhythmia
  • Caution in elderly/debilitated pts
  • Caution if renal impairment
  • Caution if pulmonary disease
  • Caution if hyperthyroidism
  • Caution if autonomic neuropathy
  • Caution if BPH
  • Caution if high environmental temperature
  • Caution if febrile
  • Caution if ulcerative colitis
  • Caution if hiatal hernia with reflux esophagitis

Adverse Reactions

Serious

Common

Pharmacology

  • Half-life: 0.83h
  • Metabolism: Unknown
  • Excretion: Urine 85%, bile

Mechanism of Action

  • Antagonizes acetylcholine receptors.

Comments

See Also

References