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Romazicon (Flumazenil). IndicationBenzodiazepine antagonistReverses sedative effects of benzodiazepines used in conscious sedation and general anesthesiaTreatment of benzodiazepine overdose. Mechanism of Action. Competitively inhibits the activity at the benzodiazepine receptor site on the GABA
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1. Romazicon ® and Narcan ® Nicole Clark PharmD, BCPS
Hallmark Health System
2. Romazicon® (Flumazenil) Indication
Benzodiazepine antagonist
Reverses sedative effects of benzodiazepines used in conscious sedation and general anesthesia
Treatment of benzodiazepine overdose
3. Mechanism of Action Competitively inhibits the activity at the benzodiazepine receptor site on the GABA/benzodiazepine receptor complex
Does not antagonize the CNS effects of other GABA antagonists (ethanol, barbituates or general anesthetics)
Does not reverse narcotics/opiods
4. Adult Dosing – Reversal of conscious sedation & general anesthesia Initial dose
0.2mg IV over 15 seconds
Repeat dose (max 4 doses)
0.2mg may be repeated at 1 minute intervals
Maximum total cumulative dose
1mg (usual dose: 0.6-1mg)
5. Adult Dosing – Suspected benzodiazepine overdose Initial dose
0.2 mg IV over 30 seconds
if the desired level of consciousness is not obtained, 0.3 mg can be given over 30 seconds
Repeat Dose
0.5 mg over 30 seconds repeated at 1-minute intervals
6. Adult Dosing – Suspected benzodiazepine overdose Maximum total cumulative dose
3 mg (usual dose: 1-3 mg)
Patients with a partial response at 3 mg may require additional titration up to total dose of 5 mg
If a patient has not responded 5 minutes after cumulative dose of 5 mg the major cause of sedation is unlikely to be due to benzodiazepines
7. Resedation Repeated doses may be given at 20 - minute intervals as needed
Maximum of 1mg/dose
(rate of 0.5mg/minute)
Maximum of 3mg/hr
8. Special Populations Elderly
No dose adjustments required
Since generally will have received smaller doses of agonist, flumazenil should be adm slowly, in incremental doses of 0.1 mg, titrated to effect
Renal impairment
No dose adjustments required
Hepatic impairment
Due to the clearance being decreased, use caution with initial and/or repeated doses in patients with liver disease
9. Pregnancy/Lactation Pregnancy Risk Factor C
Teratogenic effects not seen in animal studies – no adequate human studies
Embryocidal effects seen at large doses
Use only if clearly needed
Lactation
Excretion in breast milk unknown/use caution
10. Initial Response 1 –2 minutes
Mean time from flumazenil administration to eye opening was 3.1 minutes and the mean time to self-identification was 4.4 minutes
Peak Response
6-10 minutes
11. Duration of Action Single dose 1 – 4 hours
After intoxication with high doses of benzodiazepines the duration of a single dose of flumazenil is not expected to exceed 1 hour
Most patients with a benzodiazepine overdose with respond to a cumulative dose of 1-3 mg and doses > 3 mg do not reliably produce additional effects
12. Black Box Warning May result in seizures in some patients
Pts on benzodiazepines for long-term sedation
Tricyclic antidepressant overdose pts
Concurrent major sedative-hypnotic drug withdrawal
Recent therapy with repeated doses of parenteral benzodiazepines
Myoclonic jerking or seizure activity prior to flumazenil administrations
Use caution of patients relying on a benzodiazepine for seizure control
13. Cautions/Concerns Does not consistently reverse amnesia
Should not rely upon to reverse respiratory depression/hypoventilation
Use with caution in pts with head injury
May provoke panic attacks in patients with history of panic disorder
Caution in pts with mixed drug overdoses; toxic effects of other drugs may emerge once benzodiazepine effects are reversed
14. Adverse Effects Most Frequent
Ataxia, blurred vision, dizziness, feeling agitated, headache, hyperhidrosis, injection site sequelae, nausea, tonic clonic seizure, vertigo, visual changes, vomiting
Less Frequent
Hypertension, mood changes, paresthesia, sedation, skin rash
15. Adverse Effects Rare
Conduction disorder of the heart, dysphasia, fatigue, flushing, general weakness, hallucinations, hearing disorder, hyperacusis, impaired cognition, malaise, panic disorder, pruritus of skin, seizure disorder, thrombophlebitis, urticaria
16. Physical Assesment/Monitoring Asses level of consciousness frequently
Monitor vital signs and airways closely
ECG monitoring & oxygentation via pulse oximetry is highly recommended
Observe continually for resedation, respiratory depression, and preseizure activity
May require pain medication soon after reversal
Asses for nausea and vomiting
17. Narcan Indication
Opiod Antagonist
Complete or partial reversal of opioid drug effects, including respiratory depression
Management of known or suspected overdose
Diagnosis of suspected opioid dependence or acute opioid overdose
Mechanism of action
Pure opioid antagonist that competes and displaces narcotics at opioid receptor sites
18. Adult Dosing- Opioid intoxication: Respiratory Depression 0.4-2 mg IV (over 30 seconds)
May need to repeat doses every 2-3 minutes
After reversal may need to readminister at a later interval depending on type/duration of opioid (long acting opioids)
If no response observed after 10 mg consider other causes of respiratory depression
Opioid-dependent patients may require lower doses (0.1mg) titrated incrementally to avoid precipitating acute withdrawal
19. Continuous Infusion Calculate dosage/hour based on effective intermittent dose/duration of adequate response seen
Typically 0.25 – 6.25mg/hr
˝ of the initial bolus dose should be readministered after infusion started to prevent drop in levels
To prepare infusion
2 mg naloxone in 500 mL of 0.9% sodium chloride or D5W (final concentration: 40 mcg/mL)
20. Adult Dosing: Postoperative reversal 0.1-0.2mg IV every 2-3 minutes until desired response
Repeat doses may be needed within 1-2 hour intervals depending on type, dose and timing of last dose of opioid administered
21. Pregnacy/Lactation Pregnancy Risk Factor C
Consider benefit to the mother and risk to the fetus before administering to a pregnant women who is opioid dependent
May precipitate withdrawal in both the mother and fetus
Lactation
Excretion in breast milk unknown/not recommended
22. Cautions/Concerns Use caution in patients with cardiovascular disease or in patients receiving medications with potential adverse cardiovascular effects
Use caution in patients with history of seizures
23. Adverse Reactions Adverse events occur secondarily to reversal of narcotic analgesia and sedation
Less frequent
Conduction disorder of the heart, excitement, hyperhidrosis, hypertension, hypotension, irritability, nausea, nervousness, tachyarrhythmia, tremors, vomiting
24. References Lexi Comp
Micromedex
Medscape/drug info