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Drugs enteric-coated

Oral administration of bicarbonate may decrease the absorption of ketoconazole. Increased blood levels of quinidine, flecainide, or sympatiiomimetics may occur when these agents are administered with bicarbonate There is an increased risk of crystalluria when bicarbonate is administered with the fluoroquinolones. Fbssible decreased effects of lithium, methotrexate, chlorpropamide, salicylates, and tetracyclines may occur when these drag s are administered with sodium bicarbonate. Sodium bicarbonate is not administered within 2 hours of enteric-coated drugs the protective enteric coating may disintegrate before the drug reaches the intestine. [Pg.640]

Most pancreatic enzyme supplements are enteric coated to release enzymes in the alkaline environment of the intestine this minimizes enzyme destruction in the stomach. Enteric-coated pancreatic enzyme supplements require fewer daily dosage units, but delivery of the drug to the site of action and effectiveness may be delayed by gastric emptying time.41... [Pg.343]

A drug should always be ingested with a cup of water ( 8 oz) to insure easy transit down the esophagus and to provide fluid for disintegration and dissolution. Whether or not the drug should be taken on an empty stomach (e.g., enteric-coated tablets) or with food will depend upon the specific drug as noted above. [Pg.56]

Which of the following is unlikely to be associated with oral drug administration of an enteric-coated dosage form ... [Pg.34]

Over the years, dissolution testing has expanded beyond ordinary tablets and capsules—first to extended-release and delayed-release (enteric-coated) articles, then to transder-mals, multivitamin and minerals products, and to Class Monographs for non-prescription drug combinations. (Note at the time, sustained-release products were being tested, unofficially, in the NF Rotating Bottle apparatus). [Pg.11]

The solubility should be measured at all of these pH values with a suitable, validated method such as shake-flask or pSol (2) at 37°C to determine whether the (envisaged) dose of the drug can be completely dissolved at all points of interest in the GI tract (see Chapter 11 for more discussion of solubility determination). Typically, this would be the upper GI pH (stomach and proximal small intestine) for immediate release (IR) products, the pH in the small intestine for enteric-coated products and, additionally for MR dosage forms intended to release over a period of six hours or more, the pH in the proximal colon. [Pg.196]

The protection of a drug substance from the destructive influence of gastric acid after oral administration (such as enteric-coated tablets)... [Pg.380]

Attempts have been made to achieve colon-speeifie delivery of drugs. These include prodrugs and enteric coated polymers that are sensitive to degradation by bacterial enzymes, and matrices and hydrogels suseeptible to degradation by baeterial enzymes. [Pg.45]

Voltarol is a brand-name preparation for diclofenac (NSAID) and modified-release tablets are available in 75 mg and 100 mg strength. Nu-seals is a proprietary preparation of enteric-coated aspirin 75 mg. Fentanyl, co-codamol and Suboxone (buprenorphine and naloxone) consist of opioid drugs. [Pg.112]

Behrend M, Braun F. (2005) Enteric-coated mycophenolate sodium Tolerability profile compared with mycophenolate mofetil. Drugs 65 1037-1050. [Pg.159]

Enteric coating materials not only protect a dosage form from the acidic environment in the stomach and allow drug delivery to the small intestine, they may also pass through the... [Pg.161]

Duloxetine hydrochloride, a novel anti-depressive, is known to be acid labile and, consequently, it has been formulated as an enteric-coated tablet. Interestingly, Jansen et al. [97] subsequently found that the drug was destabilised by degradation products within these enteric polymers. The authors found that succinyl and phthalyl residues from the hydroxypropyl methylcellulose acetate succinate (HPMCAS) and hydroxypropyl methylcellulose phthalate (HPMCP) formed... [Pg.39]

Taste masking Control of drug release phthalate (for enteric coatings)... [Pg.98]

Rheumatoid arthritis (RA enteric-coated tablets) Treatment of patients with RA who have responded inadequately to salicylates or other nonsteroidal anti-inflammatory drugs (NSAIDs). [Pg.943]


See other pages where Drugs enteric-coated is mentioned: [Pg.96]    [Pg.476]    [Pg.482]    [Pg.54]    [Pg.1525]    [Pg.20]    [Pg.235]    [Pg.27]    [Pg.54]    [Pg.58]    [Pg.327]    [Pg.504]    [Pg.577]    [Pg.675]    [Pg.753]    [Pg.564]    [Pg.231]    [Pg.49]    [Pg.674]    [Pg.35]    [Pg.472]    [Pg.7]    [Pg.199]    [Pg.219]    [Pg.463]    [Pg.167]    [Pg.349]    [Pg.48]    [Pg.49]    [Pg.157]    [Pg.161]    [Pg.162]    [Pg.10]    [Pg.98]    [Pg.99]    [Pg.48]   
See also in sourсe #XX -- [ Pg.25 , Pg.40 ]

See also in sourсe #XX -- [ Pg.25 , Pg.40 ]

See also in sourсe #XX -- [ Pg.25 , Pg.40 ]




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Drug-coating

Enteral

Enteric

Enteric coat

Enteric coated

Enteric coatings

Entering

Oral drug administration enteric coatings

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