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Phenoxybenzamine Hydrochloride Tablets

Function and Efficacy

Pharmacological action Phenoxybenzamine hydrochloride tablets are long-acting α-receptor blockers (α1, α2). They act on postganglionic α-adrenaline receptors, prevent or reverse the effects of endogenous or exogenous catecholamines, dilate peripheral blood vessels, and increase blood flow. Blood pressure drops slightly when lying down, and drops significantly when standing upright. A drop in blood pressure can reflexively cause an increase in heart rate.

Ingredients

The main ingredients and chemical names of this product are: N-(1-methyl-2-phenoxyethyl)-N-(2-chloroethyl)benzylamine hydrochloride

Name Description Content CAS NO. Manufacturer
Phenoxybenzamine hydrochlorideIngredients

Phenoxybenzamine hydrochloride tablets are long-acting α-receptor blockers (α1, α2). They act on postganglionic α-adrenaline receptors to prevent or reverse the effects of endogenous or exogenous catecholamines, causing peripheral vasodilation and increased blood flow. Blood pressure drops slightly when lying down and can drop significantly when standing upright. A drop in blood pressure can reflexively cause an increase in heart rate.

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Appearance

This product is white tablets

Indication

1. Treatment and preoperative preparation for pheochromocytoma. 2. Peripheral vasospasm. 3. Urinary retention caused by prostatic hyperplasia.

Usage and Dosage

Dosing should be individualized, and the dosage should be adjusted according to clinical response and the content of catecholamines and their metabolites in urine. Initially, 10 mg once a day, twice a day, and increase by 10 mg every other day until the expected clinical efficacy is achieved or mild adverse reactions of α receptor blockade occur. Maintain at 20-40 mg twice a day.

Adverse Reactions

Common symptoms include postural hypotension, nasal congestion, dry mouth, pupil constriction, reflex heart rate tachycardia and gastrointestinal irritation. Rare symptoms include confusion, fatigue, headache, impotence, drowsiness, and occasionally angina pectoris and myocardial infarction.

Precautions

1. Hypotension. 2. Angina pectoris, myocardial infarction. 3. Allergic to this product.

Special Population Medication

Precautions for children: Oral administration, start with 0.2 mg per kg of body weight, twice a day; or 6-10 mg per square meter of body surface area, once a day. Increase the dose every 4 days until the effect is achieved. The maintenance dose is 0.4-1.4 mg per kg of body weight or 12-36 mg per square meter of body surface area, taken orally in 3-4 times. Precautions for pregnancy and lactation: The effect of this product on pregnancy has not been fully studied. This product can only be used by pregnant women when it is absolutely necessary. It is not known whether this product is secreted through breast milk, but for the sake of caution, lactating women should choose to stop taking the drug or stop breastfeeding. Precautions for the elderly: The elderly are sensitive to its antihypertensive effect, are prone to hypothermia, and have poor renal function. They should be cautious when using this product.

Drug Interactions

1. When used in combination with sympathomimetic amines, the pressor effect is weakened or eliminated; 2. When used in combination with guanethidine, orthostatic hypotension is likely to occur; 3. When used in combination with diazoxide, it antagonizes the latter's inhibitory effect on insulin release; 4. This product can block the hyperthermia caused by L-norepinephrine, and can also block the hypothermia caused by reserpine.

Storage

Keep in a sealed container

Packaging Specification

10mg

Validity Period

24 months

Manufacturer

Dingfukang Pharmaceutical Co., Ltd.

  • Founded in:

    2003-06-23
  • Address:

    No. 1 Lianbo Avenue, Queshan County, Henan Province
  • Tax NO.:

    91411700745750818R
  • Registered Funds:

    60 million yuan
  • Email:

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