๐Ÿฉบ CARDIAC THERAPY ๐Ÿท๏ธ Sympathomimetics Inotropic Beta 1-agonist
๐Ÿ‘จโ€โš•๏ธ Clinically Reviewed by: PakistaniBano Medical Editorial Board (Pharm.D Panel)
๐Ÿ“… Reviewed: November 2026 โ€ข ๐Ÿ” Authority: DRAP / WHO ATC
๐Ÿ“ฆ Formulations, Pack Sizes & Retail Prices Currency: Rs.
Dosage Form Reg. No Pack Size Trade Price (TP) Maximum Retail Price (MRP)
Inj250 mg 019474 1 Vialx5 ml Rs.260.67 Rs.306.68

๐Ÿ“‹ Indications & Clinical Dosage

*Inotropic support in infarction, cardiac surgery, cardiomyopathies, septic shock, cardiogenic shock, and during positive end expiratory pressure ventilation:* BY IV INF: Adult: 2.5-10 mcg/kg/min, adjusted according to response, alternatively0.5-40 mcg/kg/min Children: Neonate, initially 5 mcg/kg/minute continuous IV INF adjusted according to response to 2-15 mcg/ kg/minute; max. 20 mcg/kg/minute; 1 mth-18 yr, initially 5 mcg/kg/minute adjusted according to response to 2-20 mcg/kg/minute. *Cardiac stress testing:* BY IV INF: Adult: Consult product literature.

๐Ÿ’Š Mode of Administration

Always administer via infusion device; administer into large vein.Dilute concentrate with at least 50 ml compatible IV soln. A common dilution is 500 mg (40 ml from 250 ml bag) in 210 ml D5W or NS to yield 2000 mcg/ml or dilute 1000 mg (80 ml from 250 ml bag) in 170 ml D5W or NS to yield 4000 mcg/ml. Adjust max conc. according to patients fluid requirements as prescribed. Do not exceed 5000 mcg/ml.

โ›” Contraindications

Pheochromocytoma.

โš ๏ธ Precautions & Warnings

Do not add to alkaline solutions, acute myocardial infarction; correct hypovolaemia, correct atrial fibrillation with rapid ventricular response with digitalis; peripheral vascular resistance may increase if beta-blocker received recently, marked mechanical obstruction. Monitor ECG, blood pressure, pulmonary wedge pressure, cardiac output. Safety in children and pregnancy MI established. Avoid cyclopropane or halogenated hydrocarbon anaesthetics.

๐Ÿ”„ Drug Interactions

General anaesthetics, bretylium, beta-blockers (non-selective ones), guanethidine, MAO inhibitors, methyldopa, reserpine, and tricyclic antidepressants, beta-adrenergic blockers.

โš ๏ธ Adverse Reactions / Side Effects

Nausea; hypotension, hypertension, arrhythmias, palpitations, chest pain; dyspnoea, bronchospasm; headache; fever; increased urinary urgency; eosino-philia; rash, phlebitis; very rarely myocardial infarction, hypokalaemia: coronary artery spasm and thrombocytopenia also reported.

๐Ÿคฐ Pregnancy & Lactation Safety

Pregnancy Risk:
Caution advised
Lactation / Breastfeeding:
Caution advised

๐Ÿงช Compatibility & Storage Stability

Compatibility: Stable in D5LR, D5 'ANS, D5NS, D5W, 010W, LR, VAS, NS, mannitol 20%. .

Stability & Storage: Remix solution every 24 hrs. Store reconstituted solutionin refrigerator for 48 hrs or 6 hrs at room temp. Stability of parenteral admixture at room temp (25C) is 48 hrs; at refrigeration (4C) stability is 7 days.

๐Ÿ“š Official Regulatory & Clinical References

  • Drug Regulatory Authority of Pakistan (DRAP): Drug Registration, S.R.O. Price Gazettes & National Essential Medicines List (NEML).
  • World Health Organization (WHO): Collaborating Centre for Drug Statistics Methodology (ATC/DDD Index).
  • Formulary Standards: British National Formulary (BNF) & Pakistan National Formulary (PNF) guidelines.

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