Bridion

Bridion

sugammadex

Manufacturer:

MSD

Distributor:

Zuellig Pharma
Concise Prescribing Info
Contents
Sugammadex
Indications/Uses
Reversal of rocuronium- or vecuronium-induced neuromuscular blockade in patients ≥2 yr.
Dosage/Direction for Use
IV Single bolus inj given rapidly, w/in 10 sec into existing IV line. Adult Routine reversal 4 mg/kg if recovery reached at least 1-2 post-tetanic counts (PTC) or 2 mg/kg if spontaneous recovery occurred up to reappearance of T2 following rocuronium- or vecuronium-induced blockade. Immediate reversal of rocuronium-induced blockade 16 mg/kg administered 3 min after bolus dose of rocuronium Br 1.2 mg/kg. Recurrence of neuromuscular blockade post-op Repeat dose of 4 mg/kg after initial dose of 2 mg/kg or 4 mg/kg. Childn & adolescent ≥2 yr Routine reversal of rocuronium- or vecuronium-induced blockade 4 mg/kg if recovery reached at least 1-2 PTC or 2 mg/kg at re-appearance of T2.
Contraindications
Special Precautions
Hypersensitivity including anaphylactic reactions. Not to be used to reverse block induced by nonsteroidal neuromuscular blockers (eg, succinylcholine or benzylisoquinolinium compd) or steroidal neuromuscular blockers other than rocuronium or vecuronium; reversal of pancuronium-induced blockade. Prolonged aPTT & PT (INR); marked bradycardia. Increased risk of recurrence of neuromuscular blockade w/ low doses. Signs of light anesth when neuromuscular blockade was reversed intentionally in the middle of anesth. Waiting times for re-administration w/ neuromuscular blocking agents. Patients receiving rocuronium or vecuronium in ICU setting; on controlled Na diet. Delayed recovery time in CV disease, elderly or edematous state. Provide adequate ventilation. Monitor coagulation parameters in patients w/ known coagulopathies & those using anticoagulants; hemodynamic changes during & after reversal. Monitor for signs of recurrence of neuromuscular blockade approx up to 15 min after parenteral administration of another medicinal product occurring w/in 7.5 hr. Concomitant use w/ medicinal products which potentiate neuromuscular blockade in post-op period; hormonal contraceptives; toremifene & fusidic acid. Not recommended in severe renal impairment including those requiring dialysis (CrCl <30 mL/min). Severe hepatic impairment or hepatic impairment accompanied by coagulopathy. Pregnancy & lactation. Immediate reversal in childn & adolescents. Not recommended in term newborn infants (<30 days) & infants (30 days to 2 yr).
Adverse Reactions
Airway complication of anesth, anesth complication, procedural hypotension & complication; cough.
Drug Interactions
Displacement of vecuronium or rocuronium w/ toremifene. Delayed recovery time w/ IV fusidic acid. Reduced effectiveness of hormonal contraceptives eg, progestogen. Interference w/ serum progesterone assay.
MIMS Class
Antidotes & Detoxifying Agents
ATC Classification
V03AB35 - sugammadex ; Belongs to the class of antidotes. Used to reverse neuromuscular blockade caused by rocuronium or vecuronium.
Presentation/Packing
Form
Bridion soln for inj 100 mg/mL
Packing/Price
2 mL x 10 × 1's
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