Article Contents ::
- 1 Details About Generic Salt :: Rapacuro
- 2 Main Medicine Class:: Muscle relaxant,nondepolarizing neuromuscular blocker
- 3 (rah-pah-cure-OH-nee-uhm BROE-mide) Raplon Class: Muscle relaxant/nondepolarizing neuromuscular blocker
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Rapacuro
Main Medicine Class:: Muscle relaxant,nondepolarizing neuromuscular blocker
(rah-pah-cure-OH-nee-uhm BROE-mide)
Raplon
Class: Muscle relaxant/nondepolarizing neuromuscular blocker
Drugs Class ::
Action Binds competitively to cholinergic receptors on motor end-plate to antagonize action of acetylcholine, resulting in block of neuromuscular transmission.
Indications for Drugs ::
Indications Adjunct to general anesthesia to facilitate tracheal intubation; provide skeletal muscle relaxation during surgery.
Drug Dose ::
Route/Dosage
ADULTS: IV Initial dose: 1.5 mg/kg; maintenance dose: Up to three doses of 0.5 mg/kg. CESAREAN SECTION: 2.5 mg/kg with thiopental induction. CHILDREN 1 MO TO 12 YR: IV 2 mg/kg. CHILDREN 13 TO 17 YR: IV Determine dose by physical maturity, height, and weight using above dosing recommendations.
Contraindication ::
Contraindications Standard considerations.
Drug Precautions ::
Precautions
Pregnancy: Category C. Lactation: Undetermined. Children < 1 mo: Safety and efficacy not established; has not been studied in patients 13 to 17 yr. Hepatic insufficiency: Use with caution, resistance to neuromuscular blockade and prolonged duration of blockade may occur. Obesity: Base initial dose in obese patients (body mass index ³ 30) on actual body weight; consider dosing morbidly obese patients (body mass index ³40) on ideal body weight. Renal failure: Onset time may be slowed and duration of blockade may be prolonged.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CV Hypotension; tachycardia; bradycardia; extrasystoles; arrhythmias; cardiac failure; MI. RESP: Bronchospasm. GI: Vomiting; nausea. DERM: Erythematous rash.
Drug Mode of Action ::
Action Binds competitively to cholinergic receptors on motor end-plate to antagonize action of acetylcholine, resulting in block of neuromuscular transmission.
Drug Interactions ::
Interactions
Antibiotics (eg, aminoglycosides, bacitracin, colistin, polymyxin, tetracyclines, vancomycin), inhalational anesthetics, lithium, local anesthetics, magnesium salts, procainamide, quinidine: Prolonged neuromuscular blockade may occur. Anticonvulsants (eg, carbamazepine, phenytoin): Shortened duration of action and decreased effectiveness. Incompatibilities: Cefuroxime, danaparoid, diazepam, nitroglycerin, thiopental.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history including drug history and any known allergies.
- Monitor the patient, including drug history and any known allergies.
- Monitor vital signs and keep airway clear of secretions.
- Use nerve stimulator to assess neuromuscular blockade.
- Continually monitor patient’s hemodynamic status including bradycardia, tachycardia, hypotension, and hypertension.
- Monitor for ECG abnormalities and tachyphylaxis following repeated and large single doses.
- Ensure that a peripheral nerve simulator is available and used to monitor patient’s responses to drug and recovery from neuromuscular block.
- Monitor for possible occurrence (rare) of malignant hyperthermia.
- Maintain patent airway, adequate oxygenation, and controlled ventilation in the case the neuromuscular block and subsequent respiratory depression extends beyond the time needed for surgery and anesthesia.
- Closely monitor patients with hepatic, respiratory, cardiac, muscular, and renal disease.
- Monitor patients with myasthenia gravis or Eaton-Lambert syndrome for potential profound and prolonged effects.
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Drug Storage/Management ::
Administration/Storage
- Store at 2° to 25°C (36° to 77°F).
- When reconstituted with sterile water, keep vial at room temperature or refrigerate at 2° to 25°C (36° to 77°F) and use within 24 hrs. For single use only, discard unused portion. Do not use if particulate matter is present.
- When reconstituted with bacteriostatic water, store at room temperature or refrigerate at 2° to 25°C (36° to 77°F) and use within 24 hrs.
- Do not administer to newborn infants if reconstituted with bacteriostatic water as it contains benzyl alcohol.
- Administer IV only in carefully adjusted doses individualized to patient needs by or under the supervision of experienced clinicians who are familiar with the drug actions and possible complications.
- Do not administer unless personnel and facilities for resuscitation and life support (tracheal intubation, artificial ventilation, oxygen therapy) and an antagonist (anticholinesterase [eg, neostigmine]) of the drug are available, and a peripheral nerve simulator to measure neuromuscular function are immediately available.
- Administration must be accompanied by adequate anesthesia or sedating agents.
Drug Notes ::
Patient/Family Education
- Explain that drug will be administered while patient is unconscious.
- Inform family of the usual length and nature of the unit’s routine as they are often in the waiting room.
- Inform family of patient’s condition during the procedure and in the recovery room.
- Inform patient and family that hoarseness and sore throat may be experienced.
- Report any residual muscle weakness to primary caregiver.