Term
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Definition
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Term
channel-forming ionophore |
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Definition
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Term
2 kinds of weakly basic drugs |
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Definition
antihistamines, antidepressants |
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Term
2 kinds of weakly acidic drugs |
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Definition
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Term
drug that increases the small bowel transit time |
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Definition
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Term
2 drugs that have increased absorption with a slower transit time |
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Definition
riboflavin, digoxin (as slow dissolving tablet) |
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Term
drug that reduces small bowel transit time |
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Definition
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Term
2 acid-labile drugs that will degrade in stomach if rate of gastric emptying slows |
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Definition
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Term
3 drugs that reduce rate of gastric empyting |
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Definition
anticholinergics narcotic analgesics ethanol |
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Term
drug that increases rate of gastric emptying |
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Definition
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Term
4 drugs which will irritate GI mucosa if rate of gastric emptying is reduced |
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Definition
erythromycin, iron salts, aspirin, NSAIDs |
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Term
drug that forms complex with bile salts |
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Definition
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Term
drug that forms complex with Ca++ from milk |
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Definition
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Term
drug that forms complex from excipients in medicine |
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Definition
carboxymethylcellulose and amphetamines |
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Term
2 water soluble drugs that form a lipid soluble complex |
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Definition
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Term
drug that forms a complex with PEG to increase absorption of poorly water-soluble drugs |
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Definition
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Term
enteric coated tablet to protect lining of stomach |
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Definition
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Term
2 drugs administered in form of buccal/sublingual |
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Definition
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Term
drugs administered rectally |
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Definition
aspirin acetaminophen theophylline prochlorperazine barbiturates |
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Term
the amorphous form of this drug is 10 x more absorbed than the crystallized form |
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Definition
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Term
the anhydrous form of these 2 drugs dissolve more rapidly than the hydrates |
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Definition
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Term
drug that is better absorbed in the presence of food |
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Definition
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Term
drug that is better absorbed on a full stomach (presence of fat) |
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Definition
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Term
2 drugs absorbed in colon |
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Definition
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Term
2 drugs that have low therapeutic index |
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Definition
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