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UNI-DUR 400 MG SR 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:

400 MG

 

GENERIC NAME:

THEOPHYLLINE

 

MANUFACTURER:

SCHERING CORP

 

UNIT:

 

ADMINISTRATION ROUTE:

 

FDA PREGNANCY GROUP:

C

 

INDICATIONS:

Asthma

Bronchitis, chronic

Emphysema

 

SIDE EFFECTS:

abdominal pain

agitation

anorexia

anxiety

atrial fibrillation

atrial flutter

atrial tachycardia

cardiac arrest

diuresis

dizziness

headache

hematemesis

hypokalemia

hypotension

insomnia

metabolic acidosis

nausea/vomiting

palpitations

premature ventricular contractions (PVCs)

restlessness

seizures

sinus tachycardia

supraventricular tachycardia (SVT)

urticaria

ventricular tachycardia

 

ABSOLUTE CONTRAINDICATIONS :

 

RELATIVE CONTRAINDICATIONS :

acidemia

breast-feeding

cardiac arrhythmias

cardiac disease

cholestasis

cor pulmonale

corn hypersensitivity

coronary artery disease

cystic fibrosis

elderly

fever

gastritis

gastroesophageal reflux disease (GERD)

heart failure

hepatic disease

hepatitis

hiatal hernia

hyperthyroidism

hypothyroidism

hypoxemia

infants

myocardial infarction

neonates

peptic ulcer disease

pregnancy

prostatic hypertrophy

pulmonary edema

respiratory infection

seizure disorder

sepsis

shock

 

ADULT DOSE:

Bronchodilator-Oral, the equivalent of anhydrous theophylline, initially, 300 mg per day. If tolerated, the dosage may be increased after three days, to 400 mg per day. After three more days, the dosage may be increased, if tolerated, to 600 mg per day without measurement of serum concentration. One-half the daily theophylline dose may be given at twelve hour intervals. However, certain patients metabolize theophylline more rapidly, especially the young and those that smoke, and may require dosing at eight hour intervals. Note: If the 600-mg-per-day dose is to be maintained or exceeded, monitoring of serum theophylline concentration and patient response is recommended to achieve the optimal therapeutic theophylline dosage and minimize the risk of toxicity.

 

MAXIMUM ADULT DOSE:

 

PEDIATRIC DOSE:

Bronchodilator-Children 1 year of age and older, weighing less than 45 kg: Oral, the equivalent of anhydrous theophylline, 12 to 14 mg per kg of body weight, up to a maximum of 300 mg, per day in divided doses. The dosage may be increased, if tolerated, after three days to 16 mg per kg of body weight, up to a maximum of 400 mg, per day. After three more days, if tolerated, the dosage may be increased to 20 mg per kg of body weight up to a maximum of 600 mg, per day. One-half of the daily theophylline dose may be given at twelve-hour intervals. However, younger patients may require dosing at eight-hour intervals. Children weighing more than 45 kg: See Usual adult dose. Children 6 to 16 years of age: See Usual adult dose . 

 

MAXIMUM PEDIATRIC DOSE:

 

ELDERLY DOSE:

 

 

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