Esocard
Esocard Uses, Dosage, Side Effects, Food Interaction and all others data.
Esocard Hydrochloride is a beta-1 selective (cardioselective) adrenergic receptor blocking agent with rapid onset, a very short duration of action, and no significant intrinsic sympathomimetic or membrane stabilizing activity at therapeutic dosages. Its elimination half-life after intravenous infusion is approximately 9 minutes. Esocard Hydrochloride inhibits the beta 1 receptors located chiefly in cardiac muscle, but this preferential effect is not absolute and at higher doses it begins to inhibit beta 2 receptors located chiefly in the bronchial and vascular musculature.
Trade Name | Esocard |
Availability | Prescription only |
Generic | Esmolol |
Esmolol Other Names | Esmolol |
Related Drugs | amlodipine, lisinopril, metoprolol, losartan, furosemide, hydrochlorothiazide, propranolol, Xarelto, atenolol, diltiazem |
Type | Injection |
Formula | C16H25NO4 |
Weight | Average: 295.374 Monoisotopic: 295.178358293 |
Protein binding | 55% bound to human plasma protein, while the acid metabolite is 10% bound. |
Groups | Approved |
Therapeutic Class | Anti adrenergic agent (Beta blockers) |
Manufacturer | Samarth Life Sciences Pvt Ltd |
Available Country | India |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
Esocard Hydrochloride is a beta adrenergic blocker used for the short-term
treatment of:
- Control of ventricular rate in supraventricular tachycardia including atrial fibrillation and atrial flutter and control of heart rate in noncompensatory sinus tachycardia.
- Control of perioperative tachycardia and hypertension.
Pediatric Use: The safety and effectiveness of Esocard Hydrochloride in pediatric patients have not been established.
Geriatric Use: Clinical studies of Esocard Hydrochloride did not include sufficient numbers of subjects aged 65 and over to determine whether they responded differently from younger subjects.
Hepatic Impairment: No special precautions are necessary in patients with hepatic impairment because Esocard Hydrochloride is metabolized by red-blood cell esterases.
Renal Impairment: No dosage adjustment is required for esmolol in patients with renal impairment receiving a maintenance infusion of esmolol 150 mcg/kg for 4 hours.
Esocard is also used to associated treatment for these conditions: Atrial Fibrillation, Tachycardia, Supraventricular, Intraoperative Hypertension, Intraoperative Tachycardia, Noncompensatory Sinus tachycardia, Postoperative Hypertension, Postoperative Tachycardia
How Esocard works
Similar to other beta-blockers, esmolol blocks the agonistic effect of the sympathetic neurotransmitters by competing for receptor binding sites. Because it predominantly blocks the beta-1 receptors in cardiac tissue, it is said to be cardioselective. In general, so-called cardioselective beta-blockers are relatively cardioselective; at lower doses they block beta-1 receptors only but begin to block beta-2 receptors as the dose increases. At therapeutic dosages, esmolol does not have intrinsic sympathomimetic activity (ISA) or membrane-stabilizing (quinidine-like) activity. Antiarrhythmic activity is due to blockade of adrenergic stimulation of cardiac pacemaker potentials. In the Vaughan Williams classification of antiarrhythmics, beta-blockers are considered to be class II agents.
Dosage
Esocard dosage
Administer intravenously. Titrate using ventricular rate or blood pressure at ≥4 minute intervals. Supraventricular tachycardia (SVT) or noncompensatory sinus tachycardia-
- Optional loading dose: 500 mcg per kg infused over one minute
- Then 50 mcg per kg per minute for the next 4 minutes
- Adjust dose as needed to a maximum of 200 mcg per kg per minute
- Additional loading doses may be administered
- Loading dose: 500 mcg per kg over 1 minute for gradual control (1 mg per kg over 30 seconds for immediate control).
- Than 50 mcg per kg per minute for gradual control (150 mcg per kg per minute for immediate control) adjusted to a maximum of 200 (tachycardia) or 300 (hypertension) mcg per kg per minute.
Side Effects
Most common adverse reactions (incidence> 10%) are symptomatic hypotension (hyperhidrosis, dizziness) and asymptomatic hypotension.
Toxicity
Symptoms of overdose include cardiac arrest, bradycardia, hypotension, electromechanical dissociation and loss of consciousness.
Precaution
- Risk of hypotension, bradycardia, and cardiac failure: Reduce or discontinue use
- Risk of exacerbating reactive airway disease
- Diabetes mellitus: Increases the effect of hypoglycemic agents and masks hypoglycemic tachycardia
- Risk of unopposed alpha-agonism and severe hypertension in untreated pheochromocytoma
- Risk of myocardial ischemia when abruptly discontinued in patients with coronary artery disease
Interaction
- Digitalis glycosides: Risk of bradycardia
- Anticholinesterases: Prolongs neuromuscular blockade
- Antihypertensive agents: Risk of rebound hypertension
- Sympathomimetic drugs: Dose adjustment needed
- Vasoconstrictive and positive inotropic effect substances: Avoid concomitant use
Food Interaction
No interactions found.Esocard Alcohol interaction
[Moderate]
Many psychotherapeutic and CNS-active agents (e.g., anxiolytics, sedatives, hypnotics, antidepressants, antipsychotics, opioids, alcohol, muscle relaxants) exhibit hypotensive effects, especially during initiation of therapy and dose escalation.
Coadministration with antihypertensives and other hypotensive agents, in particular vasodilators and alpha-blockers, may result in additive effects on blood pressure and orthostasis.
Caution and close monitoring for development of hypotension is advised during coadministration of these agents.
Some authorities recommend avoiding alcohol in patients receiving vasodilating antihypertensive drugs.
Patients should be advised to avoid rising abruptly from a sitting or recumbent position and to notify their physician if they experience dizziness, lightheadedness, syncope, orthostasis, or tachycardia.
Esocard Drug Interaction
Moderate: epinephrine, epinephrine, meperidine, meperidine, midazolam, midazolamMinor: aspirin, aspirinUnknown: sulfamethoxazole / trimethoprim, sulfamethoxazole / trimethoprim, acetaminophen, acetaminophen, tramadol, tramadol, valproic acid, valproic acid, ascorbic acid, ascorbic acid, phytonadione, phytonadione
Esocard Disease Interaction
Major: bradyarrhythmia/AV block, cardiogenic shock/hypotension, CHF, diabetes, hypersensitivity, ischemic heart disease, PVDModerate: cerebrovascular insufficiency, glaucoma, hyperthyroidism, myasthenia gravis, pheochromocytoma, psoriasis, tachycardia, asthma/COPD, renal dysfunction
Elimination Route
Rapidly absorbed, steady-state blood levels for dosages from 50-300 µg/kg/min (0.05-0.3 mg/kg/mm) are obtained within five minutes.
Half Life
Rapid distribution half-life of about 2 minutes and an elimination half-life of about 9 minutes. The acid metabolite has an elimination half-life of about 3.7 hours.
Clearance
- 20 L/kg/hr [Men]
Elimination Route
Consistent with the high rate of blood-based metabolism of esmolol hydrochloride, less than 2% of the drug is excreted unchanged in the urine. The acid metabolite has an elimination half-life of about 3.7 hours and is excreted in the urine with a clearance approximately equivalent to the glomerular filtration rate. Excretion of the acid metabolite is significantly decreased in patients with renal disease, with the elimination half-life increased to about ten-fold that of normals, and plasma levels considerably elevated.
Pregnancy & Breastfeeding use
Pregnancy Category C. Esocard hydrochloride has been shown to produce increased fetal resorptions with minimal maternal toxicity in rabbits when given in doses approximately 8 times the maximum human maintenance dose (300 mcg/kg/min). There are no adequate and well-controlled studies in pregnant women. Esocard Hydrochloride should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from Esocard Hydrochloride, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
Contraindication
- Severe sinus bradycardia
- Heart block greater than first degree
- Sick sinus syndrome
- Decompensated heart failure
- Cardiogenic shock
- Coadministration of IV cardiodepressant calcium-channel antagonists (e.g. verapamil) in close proximity to Esocard hydrochloride
- Pulmonary hypertension
- Known hypersensitivity to esmolol
Storage Condition
Keep below 25°C temperature, away from light & moisture. Keep out of the reach of children.
Innovators Monograph
You find simplified version here Esocard
Esocard contains Esmolol see full prescribing information from innovator Esocard Monograph, Esocard MSDS, Esocard FDA label