Noflash 0.1mg

Generic: Clonidine Hydrochloride

Manufacturer

Veritas Pharmaceuticals Ltd.

৳ 8

Overdose Effects

Overdose may causes Hypotension, Bradicardia, Respiratory Depression, Hypothermia, Sedation, Abnormal Reflexes, Weakness & Miosis.

Therapeutic Class

Centrally acting antihypertensive drugs (central sympatholytic)

Storage Conditions

Keep below 30°C temperature, away from light & moisture. Keep out of the reach of children.

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Description

Indications

Noflash is indicated in the treatment of hypertension. It may be employed alone or concomitantly with other anti-hypertensive agent. Noflash is also indicated for the treatment of menopausal flushing, opioid withdrawal & alcohol withdrawal syndrome. Noflash extended release tablet is indicated for the treatment of attention deficit hyperactivity disorder (ADHD) as monotherapy.

Pharmacology

Clonidine Hydrochloride stimulates alpha adrenoceptors in the brain stem. With immediate-release clonidine, blood pressure declines within 30 to 60 minutes after an oral dose, the maximum decrease occurring within 2 to 4 hours. Renal blood flow and glomerular filtration rate remain essentially unchanged. Normal postural reflexes are intact; therefore, orthostatic symptoms are mild and infrequent.

Dosage & Administration

Adult: The dose of Clonidine must be adjusted according to the patient’s individual blood pressure response.

Initial dose: 0.1 mg twice a day (morning & bed time). Elderly patients may be benefited from a lower initial dose.

Maintenance dose: Further increments of 0.1 mg per day may be made at weekly intervals if necessary, until the desired result is achieved. The therapeutic dose most commonly employed have ranged from 0.2 mg to 0.6 mg per day given in divided doses. In renal impairment, dose of Clonidine Hydrochloride must be adjusted according to the degree of impairment & patient should be monitored carefully.

Attention deficit hyperactivity disorder: Clonidine IR 5 mcg/kg/day or Clonidine ER 0.1 mg/day for 8 weeks

Menopausal flushing: 0.1 mg to 0.4 mg daily

Alcohol withdrawal: 0.3 to 0.6 mg every 6 hourly or as directed by the physician.

Use in Children & Adolescents: Safety and effectiveness in pediatric patients have not been established in adequate and well-controlled trials.

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