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Table 5 Most frequent drug-drug exposures with a strong inhibitor in all patients (n = 1221). Classification of the potential drug-drug exposure was determined by the content of the prescribing information associated with the brand-name drug

From: Frequency and clinical relevance of potential cytochrome P450 drug interactions in a psychiatric patient population – an analysis based on German insurance claims data

Potential drug-drug exposure (bold = strong inhibitor)

Frequency

Events per 100 person-years (95%CI)

Number of patients with at least one DDE (%)

Clinical relevance of a potential interaction (as per prescribing information)

amitriptyline & paroxetine

29

0.56 (0.37–0.80)

9 (0.74)

Patients taking SSRIs should only be treated with amitriptyline with particular caution [35] [reason not given]

paroxetine & risperidone

21

0.40 (0.25–0.62)

6 (0.49)

Paroxetine increases the plasma-concentration of risperidone [36]

codeine & fluoxetine

8

0.15 (0.07–0.30)

5 (0.41)

not mentioned [37, 38]

amitriptyline & fluoxetine

16

0.31 (0.18–0.50)

5 (0.41)

Taking fluoxetine and amitriptyline in parallel might result in an increased plasma-concentration of amitriptyline Dose-reduction might be necessary [33]

fluoxetine & tramadol

42

0.81 (0.58–1.09)

5 (0.41)

Taking tramadol and fluoxetine in parallel can induce serotonin syndrome [32]

amlodipine & clarithromycin

5

0.10 (0.03–0.22)

4 (0.33)

Taking clarithromycin and amlodipine parallel might result in an increased plasma concentration of amlodipine [39]

clomipramine & paroxetine

76

1.46 (1.15–1.82)

4 (0.33)

Paroxetine can increase the plasma concentration of clomipramine [40]

paroxetine & tramadol

6

0.12 (0.04–0.25)

4 (0.33)

Taking tramadol and SSRIs [i.e., paroxetine] in parallel can induce serotonin syndrome [32]. Patients taking tramadol and paroxetine must be monitored closely [35]

    

Sum

380

7.29 (6.57–8.06)

90