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TENORMIN 25 MG TABLETS

 

 
 

 

GENERIC NAMES

MANUFACTURERS 

MEDICAL GROUP

MEDICAL ARTICLES

 

DRUGS IN :

 

 

FDA DRUGS

UNITED STATES

CANADA

UNITED KINGDOM

AUSTRALIA

GERMANY

FRANCE

MIDDLE EAST

KUWAIT

LEBANON

EGYPT

SYRIA

BAHRAIN

IRAN

JORDAN

SAUDI ARABIA

UNITED ARAB EMIRATES

 

 

 
 

SIZE:

25 MG

 

GENERIC NAME:

ATENOLOL

 

MANUFACTURER:

ASTRA ZENECA

 

UNIT:

 

ADMINISTRATION ROUTE:

 

FDA PREGNANCY GROUP:

C

 

INDICATIONS:

Angina pectoris

Hypertension, essential

Myocardial infarction

 

SIDE EFFECTS:

alopecia

AV block

bronchospasm

depression

diabetes mellitus

diarrhea

dizziness

drowsiness

dyspnea

elevated hepatic enzymes

fatigue

hallucinations

headache

heart failure

hyperbilirubinemia

hyperglycemia

hypertriglyceridemia

hypoglycemia

hypotension

impotence

lupus-like symptoms

nausea/vomiting

nightmares

orthostatic hypotension

psoriaform rash

psoriasis

psychosis

purpura

rash (unspecified)

sinus bradycardia

skin hypopigmentation

syncope

teratogenesis

thrombocytopenia

vertigo

visual impairment

wheezing

xerophthalmia

xerostomia

 

ABSOLUTE CONTRAINDICATIONS :

 

RELATIVE CONTRAINDICATIONS :

asthma

breast-feeding

bronchitis

chronic obstructive pulmonary disease (COPD)

depression

diabetes mellitus

dialysis

driving or operating machinery

elderly

emphysema

heart failure

hyperthyroidism

hypotension

myasthenia gravis

peripheral vascular disease

pheochromocytoma

pregnancy

psoriasis

pulmonary disease

Raynaud's disease

renal disease

renal failure

renal impairment

surgery

thyroid disease

thyrotoxicosis

vasospastic angina

 

ADULT DOSE:

Antianginal-Oral, initially 50 mg once a day, the dosage being increased gradually to 100 mg a day after one week if necessary and tolerated . Some patients may require up to 200 mg a day. Antihypertensive-Oral, initially 25 to 50 mg once a day, the dosage being increased to 50 to 100 mg a day after two weeks if necessary and tolerated. Myocardial infarction-In patients who tolerate the full intravenous dose: Oral, initially 50 mg ten minutes after the last intravenous dose, followed by another 50 mg twelve hours later . A dose of 100 mg once a day or 50 mg two times a day may then be given for six to nine days or until discharge from the hospital . Note: Geriatric patients may have increased or decreased sensitivity to the effects of the usual adult dose. For patients with severe renal function impairment, the following maximum doses are recommended: Creatinine clearance Maximum (mL/min/1.73m) dose 15-35 50 mg per day <15 50 mg every second day

 

MAXIMUM ADULT DOSE:

 

PEDIATRIC DOSE:

Dosage has not been established.  

 

MAXIMUM PEDIATRIC DOSE:

 

ELDERLY DOSE:

 

 

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