Article Contents ::
- 1 The Brand Name CARDIFORCE Has Generic Salt :: Dobutamine
- 2 CARDIFORCE Is From Company TORRENT Priced :: Rs. 350
- 3 CARDIFORCE have Dobutamine is comes under Sub class #N/A of Main Class #N/A
- 4 Main Medicine Class:: #N/A Sub Medicine Class :: #N/A
- 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.
The Brand Name CARDIFORCE Has Generic Salt :: Dobutamine
CARDIFORCE Is From Company TORRENT Priced :: Rs. 350
CARDIFORCE have Dobutamine is comes under Sub class #N/A of Main Class #N/A
Main Medicine Class:: #N/A Sub Medicine Class :: #N/A
|Salt Name : OR Generic Name||Form||Price : MRP /Probable||Packing|
|Dobutamine||INJ||Rs. 350||20ML V.|
Indications for Drugs ::
Heart failure, Cardiac stress test
Drug Dose ::
Adult: IV Acute heart failure 2.5-10 mcg/kg, up to 0.5-40 mcg/kg according to response. Cardiac stress test As 1 mg/mL soln: 5 mcg/kg/min for 8 mins, increase dose at 5 mcg/kg/min until 20 mcg/kg/min, w/ each dose being infused for 8 mins before the next increase. Because of its short half-life, Dobutamine Hydrochloride must be administered as a continuous intravenous infusion. Following the initiation of a constant rate infusion, or upon changing the rate, a steady-state dobutamine plasma concentration is achieved within approximately 10 minutes. Thus, loading doses or bolus injections are not necessary and are not recommended. Recommended Dosage The rate of infusion needed to increase cardiac output has ranged from 2.5 to 10 mcg/kg/min in the majority of patients. Frequently, doses up to 20 mcg/kg/min are required for adequate haemodynamic improvement. The rate of administration and the duration of therapy should be adjusted according to the patient’s response, The indicators are: haemodynamic parameters such as heart rate and rhythm, arterial pressure, and, whenever possible, cardiac output and measurements of ventricular filling pressures and signs of pulmonary congestion. Concentrations up to 5,000 mg/L have been administered to humans. The final volume administered should be determined by the fluid requirements of the patient. Rather than abruptly discontinuing therapy with Dobutamine Hydrochloride, it is often advisable to decrease the dosage gradually. Rates of Infusion Based on Concentration of Dobutamine Hydrochloride The rates of fluid infusion that are required to deliver specific dosages are a function of the concentration of Dobutamine Hydrochloride in the infusate.
Hypersensitivity; idiopathic hypertrophic subaortic stenosis (IHSS).
Drug Precautions ::
Correct hypovolaemia prior to treatment. Increased risk of rapid ventricular response in patients with atrial fibrillation. Insufficient data to determine the safety and efficacy of dobutamine use after acute MI. Elderly. Neonates. Pregnancy.
Drug Side Effects ::
Increased heart rate and BP, ectopic beats, palpitation. Nausea, headache, chest pain, palpitation, dyspnoea, paraesthesia, leg cramps. Tissue necrosis at site of extravasation. Potentially Fatal: Cardiac arrhythmias, allergy (rare), MI and hypotension.
Pregnancy category ::
Drug Mode of Action ::
Dobutamine increases contractility and heart rate by stimulating ?-adrenergic receptors in the cardiac tissues.
Drug Interactions ::
Increased cardiac output when used with nitroprusside. Increased vasopressor effect of dobutamine when used with bretylium, guanethidine, oxytocic drugs or TCAs.