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Naprosyn (naproxen, naproxen) 250 mg, compared to 50% on placebo.

Naprosyn the dose may be increased to a maximum recommended dose of 100 mg or decreased to 25 mg. For people with potency problems.

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Naproxen
Clinical data
Pronunciation/ n ə ˈ p r ɒ k s ən /
Trade namesAleve, Naprosyn, Anaprox, Naprelan, Flanax, Aflaxen, others [1]
AHFS/Drugs.comMonograph
MedlinePlusa681029
License dataUS  DailyMed:  43871
Pregnancy categoryAU: C US: C (Risk not ruled out)
Routes of administrationOral
ATC codeG02CC02 ( WHO ) M01AE02 ( WHO ), M02AA12 ( WHO )
Legal status
Legal statusAU: S2 (Pharmacy only) when in preparations that contain no more than 15 days' supply. Otherwise it is Schedule 4 (Prescription only). [2] CA : OTC UK: POM (Prescription only) Pharmacy medicine (P) only for treatment of primary dysmenorrhoea in women aged 15-50 years subject to a maximum single dose of 500mg, maximum daily dose of 750mg for a maximum of 3 days, and max pack size of 9x250mg tablets [3] US: OTC
Pharmacokinetic data
Bioavailability95% (oral)
Protein binding99%
MetabolismHepatic (to 6-desmethylnaproxen)
Elimination half-life12–17 hours (adults) [4]
ExcretionRenal

What is Naproxen

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Naprosyn info
Tablets name naprosyn
Naprosyn synonym naprolag, naproxenum natricum, naproxène, naproxenum natricum
Active substance naproxen, naproxen
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Use of naproxen may blunt the CV effects of several therapeutic agents used to treat these medical conditions e. Clinical studies, as well as post-marketing observations, showed that NSAIDs reduced the natriuretic effect of loop diuretics e.

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Renal toxicity has also been seen in patients in whom renal prostaglandins have a compensatory role in the maintenance of renal perfusion. Cholestyramine Concomitant administration of cholestyramine can delay the absorption of naproxen. A clinical study found gastrointestinal reactions to be more frequent and more severe in rheumatoid arthritis patients taking daily doses of mg naproxen compared to those taking mg naproxen.

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