Tomexa 200 μg/2mL; 400 μg/4mL; 1000 μg/10 mL Concentrate for solution for infusion

    Tomexa 200 μg/2mL; 400 μg/4mL; 1000 μg/10 mL Concentrate for solution for infusion

    S5
    PDF Leaflet Revision Date: 24 February 2025

    API: Dexmedetomidine | Company: Pharmacorp

    Clinical Summary

    Quick overview from the medicine insert

    Indication

    Sedation in ICU and monitored anaesthesia care.

    Dosage (summary)

    Loading: 1.0 mcg/kg over 10 mins; Maintenance: 0.2-0.7 mcg/kg/hr.

    Special Populations

    • Elderly
    • Hepatic impairment
    • Renal impairment

    Pregnancy & Breastfeeding

    Not recommended in pregnancy; excreted in breast milk.

    Key Drug Interactions

    • Enhanced effects with sedatives and opioids
    • Caution with beta blockers

    Contraindications

    • Hypersensitivity to dexmedetomidine
    • Sepsis
    • Unstable trauma
    • Hypovolaemia
    • Heart block
    • Uncontrolled cardiac failure

    Common side effects

    • Hypotension
    • Bradycardia
    • Hypertension
    • Nausea
    • Dry mouth

    Counselling Points

    • Avoid driving for 24 hours post-sedation
    • Monitor for signs of agitation after stopping
    • Fluid supplementation is necessary

    Serious warnings

    • Serious bradycardia and sinus arrest
    • Careful titration in elderly
    • Continuous monitoring required
    Important Disclaimer

    The Tomexa 200 μg/2mL; 400 μg/4mL; 1000 μg/10 mL Concentrate for solution for infusion professional information leaflet below is the property of Pharmacorp and is provided on Medinsert exactly as issued, with no.. alterations or editorial changes. We make every effort to keep content current by updating documents as soon as new versions become available. Medinsert serves as a trusted access point for healthcare professionals, but does not replace official sources or clinical judgement. For more details, please read our full disclaimer. read more>>

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