PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
14566199-4	2003	The role of paroxetine in clinically significant drug-drug interactions, especially involving metabolic inhibitory effects on the substrates of cytochrome p450 2D6, has long been suspected, but only isolated cases provide any evidence.	Paroxetine	12-22	cytochrome P450 2D6	Homo sapiens	144-163	
16542048-11	2006	Caution should also be exercised when prescribing strong cytochrome P450 2D6 inhibitors, such as paroxetine or fluoxetine, to women who are taking tamoxifen.	Paroxetine	97-107	cytochrome P450 2D6	Homo sapiens	57-76	
12404553-1	2001	Paroxetine inhibits cytochrome P(450) 2D6, which is involved in the metabolism of mirtazapine.	Paroxetine	0-10	cytochrome P450 2D6	Homo sapiens	20-41	
8861776-4	1996	For example, fluoxetine and paroxetine produce clinically significant inhibition of cytochrome P450 2D6 at their usually effective antidepressant dose, whereas citalopram, fluvoxamine or sertraline do not.	Paroxetine	28-38	cytochrome P450 2D6	Homo sapiens	84-103