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Magnesium Naproxen

Figure 10 Controlling the outcome of mechanochemical synthesis by variation of water activity in the grinding liquid used for LAG (a) the synthesis of zinc fumarate anhydrous and hydrated coordination polymers from ZnO and (b) screening for magnesium naproxen pharmaceutical derivatives of different levels of hydration and polymerization... Figure 10 Controlling the outcome of mechanochemical synthesis by variation of water activity in the grinding liquid used for LAG (a) the synthesis of zinc fumarate anhydrous and hydrated coordination polymers from ZnO and (b) screening for magnesium naproxen pharmaceutical derivatives of different levels of hydration and polymerization...
Cj]HyBrMgO 38046-82-1) see Naproxen (5)-2-(5-bromo-6-methoxy-2-naphthyl)propanoic acid (Ci4Hi BrO 84236-26-0) see Naproxen bromo(3-methoxyphenyl)magnesium (C7H7BrMgO 36282-40-3) see Tramadol (/f)-2-bromo-A -[2-(4-methoxyphenyl)-l-methylethyl]-acetamide... [Pg.2314]

Naprosyn (naproxen) suspension for oral administration contains 125 mg/5 mL of naproxen in a vehicle containing sucrose, magnesium aluminum silicate, sorbitol solution, and sodium chloride (30 mg/5 mL, 1.5 mEq),... [Pg.163]

Fig. 2 Solubility-pH profiles, 5x of naproxen and four salts A, potassium salt o, sodium salt , magnesium salt and V, calcium salt. (From Ref. l)... Fig. 2 Solubility-pH profiles, 5x of naproxen and four salts A, potassium salt o, sodium salt , magnesium salt and V, calcium salt. (From Ref. l)...
Figure 10.3 Mean plasma concentrations ( [ g cm of naproxen in 14 male volunteers with and without intake of sodium bicarbonate, magnesium oxide or aluminium hydroxide. Figure 10.3 Mean plasma concentrations ( [ g cm of naproxen in 14 male volunteers with and without intake of sodium bicarbonate, magnesium oxide or aluminium hydroxide.
Clinically important, potentially hazardous interactions with acitretin, aldesleukin, aminoglycosides, amiodarone, amoxicillin, ampicillin, aspirin, bacampicillin, bismuth, carbenicillin, chloroquine, cisplatin, cloxacillin, co-trimoxazole, dapsone, demeclocycline, dexamethasone, diclofenac, dicloxacillin, etodolac, etoricoxib, etretinate, fenoprofen, flurbiprofen, folic acid antagonists, haloperidol, hydrocortisone, ibuprofen, indomethacin, influenza vaccines, ketoprofen, ketorolac, lithium, magnesium trisalicylate, meclofenamate, mefenamic acid, methicillin, mezlocillin, minocycline, nabumetone, nafcillin, naproxen, NSAIDs, omeprazole, oxacillin, oxaprozin, oxytetracycline, paromomycin, penicillin G, penicillin V, penicillins, phenylbutazone, piperacillin, piroxicam, polypeptide antibiotics, prednisolone, prednisone, probenecid, procarbazine, rofecoxib, salicylates, salsalate, sapropterin, sulfadiazine, sulfamethoxazole, sulfapyridine, sulfasalazine, sulfisoxazole, sulindac, tazobactum, tenoxicam, tetracycline, ticarcillin, tolmetin, trimethoprim, vaccines... [Pg.369]

Naproxen was introduced to the market by Syntex in 1976 as a nonsteroidal antiinflammatory drug in an optically pure form. The original manufacturing process (Scheme 1) before product launch started from P-naphthol (1) which was brominated in methylene chloride to produce 1,6-dibromonaphthol (2). The labile bromine at the 1-position was removed with bisulfite to give 2-bromo-6-hydroxy-naphthalene that was then methylated with methyl chloride in water-isopropanol to obtain 2-bromo-6-methoxynaphthalene (3) in 85-90% yield from p-naphthol. The bromo compound was treated with magnesium followed by zinc chloride. The resultant naphthylzinc was coupled with ethyl bromopropionate to give naproxen ethyl ester that was hydrolyzed to afford the racemic acid 4. The final optically active naproxen (5) was obtained by a classic resolution process. The racemic acid 4 was treated with cinchonidine to fonn diastereomeric salts. The S -naproxen-cinchonidine salt was crystallized and then released with acid to give S -naproxen (5) in 95% of the theoretical yield (48% chemical yield) [8,9]. [Pg.118]

Fenoprofen Magnesium salicylate Meclofenamate Mefenamic acid Naproxen Naproxen sodium Sodium salicylate... [Pg.71]

Naproxen is absorbed fully when administered orally. Food delays the rate but not the extent of absorption. Peak concentrations in plasma occur within 2 to 4 hours and are somewhat more rapid after the administration of naproxen sodium. Absorption is accelerated by the concurrent administration of sodium bicarbonate but delayed by magnesium oxide or aluminum hydroxide. Naproxen also is absorbed rectally, but more slowly than after oral administration. The half-life of naproxen in plasma is variable. It is about 14 hours in the young, but it may increase about twofold in the elderly because of age-related decline in renal function. [Pg.483]

Magnesium Hydroxide Magnesium Silicate Hydroxide Menthol Methane Methyl Alcohol Methyl Mercaptan Methyl-t-butyl Ether Monosodium Glutamate N,N-Diethyl-3-Methyl-benzamide Naphthalene Naproxen Niacin Nicotine Nitric Acid Nitroglycerin Nylon 6 and Nylon 66 Oxalic Acid Pectin Penicillin Petrolatum Petroleum Phenol... [Pg.899]

With respect to concomitant antacid administration past studies have shown that sodium bicarbonate enhances the rate of naproxen absorption, magnesium carbonate caused a slight reduction, and a mixture of magnesium oxide and aluminium hydroxide gave a clear reduction in the rate of naproxen absorption (17). [Pg.364]

A small reduction in ketoprofen absorption occurred with aluminium-magnesium hydroxide, but dexketoprofen, ibuprofen and flurbiprofen were not affected, and naproxen showed a slight increase in rate and extent of absorption. Aluminium phosphate had no effect on ketoprofen absorption. [Pg.140]

Sodium bicarbonate increased the rate of naproxen absorption, and aluminium hydroxide and magnesium oxide decreased it. Dimeticone did not affect ketoprofen bioavailability. [Pg.140]

Sodium bicarbonate 700 mg or 1.4 g increased the rate of absorption of a single 300-mg dose of naproxen in 14 healthy fasted subjects, whereas magnesium oxide or aluminium hydroxide 700 mg had the opposite effect, and reduced the rate of absorption. Magnesium carbonate had little effect. On the other hand when 15 or 60 mL of aluminium/magnesium hydroxide (Maalox) was given, the rate and extent of absorption of naproxen were slightly increased. ... [Pg.141]

Aspirin 1.3 to 3.6 g daily more than halved the serum levels of ibuprofen 800 mg to 2.4 g daily, without affecting salicylate levels. There was little additional clinical benefit from the combination. Similarly, aspirin reduced the AUC of flurbiprofen by about two-thirds, but without any clear changes in clinical effectiveness. The pharmacokinetics of the aspirin were unchanged by flurbiprofen. Aspirin 3.9 g daily also virtually halved the AUC of fenoprofen 2.4 g daily,and reduced the AUC of ke-toprofen 200 mg daily by about one-third. The AUC of naproxen was only minimally reduced (by 10 to 15%). Choline magnesium trisalicylate increased the clearance of naproxen by 56% and decreased its serum levels by 26% in one study. ... [Pg.143]

Sucralfate appears not to have a clinically important effect on the pharmacokinetics of aspirin, choline-magnesium trisalicylate, diclofenac, ibuprofen, indometacin, ketoprofen, naproxen or pirox-icam. [Pg.157]


See other pages where Magnesium Naproxen is mentioned: [Pg.181]    [Pg.182]    [Pg.181]    [Pg.182]    [Pg.152]    [Pg.424]    [Pg.78]    [Pg.3179]    [Pg.17]    [Pg.398]    [Pg.178]    [Pg.95]    [Pg.305]    [Pg.217]    [Pg.157]    [Pg.649]    [Pg.351]    [Pg.247]    [Pg.180]    [Pg.495]    [Pg.415]   


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Magnesium oxide Naproxen

Naproxen

Naproxen Magnesium hydroxide

Naproxen magnesium salt

Naproxene

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