| NAPRO
Naproxen

Description:
Napro is
a preparation of naproxen, which is a non-steroidal anti-inflammatory
agent. The drug exhibits anti-inflammatory, analgesic and antipyretic
activity. Naproxen is an inhibitor of prostaglandin synthesis.
Composition:
Napro Tablet:
Each tablet contains 250 mg Naproxen.
Napro-500
Tablet: Each Tablet contains 500 mg Naproxen.
Indications:
Napro is
indicated in the active stages of inflammatory rheumatic diseases,
rheumatoid arthritis, ankylosing spondylitis, in soft tissue
rheumatism & musculoskeletal disorders, acute gout, dysmenorrhoea.
Dosage &
Administration:
In rheumatic disorders,
the usual initial dose of naproxen is 250 mg twice daily adjusted
to 500 mg to 1000 mg daily in 2 divided doses. A dose of 10
mg/kg body weight daily in 2 divided doses is used for children
over 5 years of age with juvenile arthritis. In acute gout an
initial dose of 750 mg followed by 250 mg every 8 hours has
been suggested. In dysmenorrhoea, 500 mg may be given initially
followed by 250 mg in every 6-8 hours.
Contra-indications:
History of asthma
attacks or urticaria triggered by acetylsalicylic acid or other
prostaglandin synthesis inhibitors.
Precautions:
Use of Naproxen
should be avoided in patients with gastrointestinal disorders
and gastro-duodenal ulcer. In case of severe hepatic or renal
damage or disturbance of cardiac function a close medical surveillance
is indicated. Blood counts including platelet counts, as well
as monitoring of hepatic and renal functions are recommended,
particularly in patients under long-term therapy.
Unwanted effects:
Naproxen is generally
well tolerated, but occasionally patient may complain gastric
discomfort, nausea & dizziness. In exceptional cases,
very sensitive patients may suffer from gastro-intestinal bleeding,
skin rashes, thrombocytopenia.
Drug Interactions:
Antacid: The absorption
of naproxen can be altered by antacids.
Aspirin: Plasma
concentration of Naproxen can be reduced when aspirin is given
concomitantly, this appeared to be due to increased excretion
of naproxen.
Diuretics: Naproxen
diminish the effect of furosemide.
Probenecid: It
increase the plasma concentration of naproxen.
Overdosage:
Significant overdosage
of the drug may be characterized by drowsiness, heart-burn,
indigestion, nausea or vomiting. It is not known what dose of
the drug would be life threatening.
Pharmaceutical
precautions:
Protect from light
& store in a cool, dry place. Keep out of the reach of children.
Packing:
Box containing
5 x 10's tablets of 250 mg in blister pack.
Box containing
3 x 10's/5 x 10's tablets of 500 mg in blister pack. |