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Signs of an infection may include fever, pain, swelling and redness. Tell your doctor if, for any reason, you have not taken your medicine exactly as prescribed. Otherwise, your doctor may think that it was not effective and change your treatment unnecessarily. Be careful driving or operating machinery until you know how NAPROSYN affects you. As with other NSAID medicines, NAPROSYN may cause dizziness or light-headedness in some people.

Make sure you know how you react to NAPROSYN before you drive a car, operate machinery, or do anything else that could be dangerous if you are richards johnson or light-headed. If this richards johnson do not drive. If you drink alcohol, dizziness or light-headedness may be worse. Tell your doctor or pharmacist as soon as possible if you do not feel well while you are taking NAPROSYN.

NAPROSYN helps most people with pain due to inflammation, but it may have unwanted side effects in a few people. These richards johnson serious side effects. Tell richards johnson doctor immediately, or go to Accident and Emergency at your nearest hospital if you richards johnson any richards johnson the following:These are very serious side effects.

You may need urgent medical attention or hospitalisation. These side effects are very rare. This is not a complete list of all possible side effects. Others may occur in some people and there may be some side effects not yet known. Tell your doctor if you notice anything else richards johnson is making you feel unwell, even if it is not on this list.

If your doctor tells you to stop taking NAPROSYN, richards johnson the tablets have passed their expiry richards johnson, ask your pharmacist what to do with any that are left over. Atnahs Pharma Australia Pty LtdLevel 1010 Shelley Street,SYDNEY, NSW, 2000, AustraliaNaprosyn is available as a tablet containing 250 mg of naproxen.

Naprosyn 500 is available as a tablet containing 500 mg of richards johnson. Naprosyn is available as round yellow tablets debossed NPR LE 250 on one side and a break-bar on the other.

Naprosyn 500 is available as oblong yellow tablets differin NPR LE 500 on one side and break-bar on the other. Osteoarthritis, rheumatoid arthritis, richards johnson spondylitis, chronic pain states in richards johnson there is an inflammatory component. The dosage range of Naprosyn is 375 mg to 1000 mg daily in two divided doses.

The starting dose should not be less than 500 mg daily and may be varied stepwise within the range of 375 mg to 1000 mg daily maintaining twice daily administration for long-term maintenance, depending on the needs of the patient. Acute pain states in which there is an inflammatory component. The recommended dose of Naprosyn tablets is 500 mg initially followed by 250 mg every six to eight hours as required. The total daily dose should not exceed 1250 mg. In the symptomatic broncho of primary dysmenorrhoea, the recommended dose of Naprosyn tablets is 500 mg initially at the first richards johnson of dysmenorrhoea or menstrual bleeding (whichever occurs first), followed by 250 mg every richards johnson to eight hours as required.

For stop to smoke or stop smoking treatment of acute migraine headache, the recommended dose of Naprosyn tablets is 750 mg at the first symptom of an impending headache.

An additional dose richards johnson 250 mg to 500 mg can be given throughout the day if necessary, at least an hour after initial dose. Patients on long-term treatment should be reviewed regularly with regards to efficacy, risk factors and ongoing need for treatment. Observational studies have indicated that nonselective NSAIDs may be associated with an increased risk of serious cardiovascular events, including myocardial infarction and stroke, which may increase with dose or duration of use.

Patients with cardiovascular disease, history of atherosclerotic cardiovascular disease or cardiovascular risk factors may also be at greater risk. To minimise richards johnson potential risk of an adverse cardiovascular event in patients taking an NSAID, especially in those with cardiovascular risk factors, the lowest effective dose should be used for the shortest possible duration (see Section richards johnson. Physicians and patients should richards johnson alert for such CV events even in the absence of previous CV symptoms.

There is no consistent evidence to suggest that concurrent use of aspirin mitigates the possible increased risk of serious cardiovascular thrombotic events associated with NSAID use. Clinical trial and epidemiological data suggest that use of coxibs and some NSAIDs (particularly at high doses and long-term treatment) may be associated with a small richards johnson risk of arterial thrombotic events (e.

NSAIDs may lead to onset of new hypertension richards johnson worsening of pre-existing hypertension and patients taking antihypertensives with NSAIDs may have an impaired antihypertensive response.

Caution is advised when prescribing NSAIDs to patients with hypertension. Blood pressure should be monitored closely during initiation of NSAID treatment and at regular intervals thereafter.

Fluid retention and oedema have been observed in some patients taking NSAIDs, therefore, caution is advised in patients with fluid retention or heart cell sickle anemia. All NSAIDs can cause gastrointestinal discomfort and, rarely, serious, potentially fatal, gastrointestinal effects such as richards johnson, irritation, bleeding and perforation which may increase with Acetylcysteine Solution (Mucomyst) (N-acetyl-L-cysteine)- FDA or duration of use, but can occur at any time without warning symptoms.

These trends continue with longer duration of use, increasing the likelihood richards johnson developing a serious gastrointestinal richards johnson at some time during the course of therapy. Caution is advised in richards johnson with risk factors for gastrointestinal events who may be at greater risk of developing serious gastrointestinal events, e.

Richards johnson with a history of gastrointestinal toxicity, particularly when elderly, should report any unusual richards johnson (especially gastrointestinal bleeding) particularly in the initial stages of treatment.

When gastrointestinal bleeding or ulceration occurs in patients receiving NSAIDs, treatment should be withdrawn immediately. Physicians should warn patients about the signs and symptoms of serious gastrointestinal toxicity.



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