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Table 2 Most occurring potential drug-drug interaction for each level of severity

From: Prevalence and nature of potential drug-drug interactions among hospitalized HIV patients presenting with suspected meningitis in Uganda

Severitya

Drug 1

Drug 2

% pDDI overallb

Level of evidencec

Proposed effect summary

Contraindicated

 

Fluconazole

Ondansetron

3.6

Fair

Risk of QT interval prolongation

 

Fluconazole

Haloperidol

2.8

Fair

Increased haloperidol exposure, risk of QT interval prolongation

 

Fluconazole

Ritonavir

1.1

Fair

Increased ritonavir exposure, risk of QT interval prolongation

 

Artane

Potassium (oral)

0.8

Fair

Gastrointestinal lesions

 

Fluconazole

Atazanavir

0.8

Fair

Increased atazanavir exposure, risk of QT interval prolongation

 

Fluconazole

Artemether- lumefantrine

0.7

Fair

Risk of QT interval prolongation

 

Dihydroartemisinin-piperaquine

Efavirenz

0.2

Fair

Risk of QT interval prolongation

 

Fluconazole

Dihydroartemisinin-piperaquine

0.2

Fair

Risk of QT interval prolongation

 

Haloperidol

Metoclopramide

0.2

Fair

Increased extrapyramidal reactions and neuroleptic malignant syndrome

 

Fluconazole

Quinine

0.1

Fair

Increased quinine levels, risk of QT interval prolongation

Major

 

Co-trimoxazole

Fluconazole

18

Fair

Cardiotoxicity (QT prolongation, torsades)

 

Efavirenz

Fluconazole

8.6

Fair

Risk of QT interval prolongation

 

Codeine

Fluconazole

4.8

Fair

Increased codeine concentration

 

Isoniazid

Rifampin

4.5

Good

Hepatotoxicity

 

Co-trimoxazole

Haloperidol

2.4

Fair

Cardiotoxicity (QT prolongation, torsades)

 

Pyrazinamide

Rifampin

2.4

Good

Hepatotoxicity

 

Fluconazole

Metronidazole

2.3

Fair

Risk of QT interval prolongation and arrhythmias

 

Efavirenz

Ondansetron

1.3

Fair

QT interval prolongation

 

Codeine

Efavirenz

1.1

Fair

Decreased codeine efficacy

 

Codeine

Metoclopramide

1.1

Fair

Increased CNS depression

 

Azithromycin

Fluconazole

1.1

Fair

Risk of QT interval prolongation

 

Ciprofloxacin

Fluconazole

1.1

Fair

Risk of QT interval prolongation

 

Fluconazole

Tramadol

0.9

Fair

Increased tramadol exposure and increased risk of respiratory depression

 

Acetaminophen

Isoniazid

0.9

Excellent

Hepatotoxicity

 

Efavirenz

Rifampin

0.9

Fair

Decreased serum efavirenz concentration

Moderate

 

Fluconazole

Zidovudine

4.2

Good

Increased zidovudine serum concentration

 

Fluconazole

Rifampin

2.2

Excellent

Decreased fluconazole serum concentration

 

Artane

Haloperidol

1.2

Good

Excessive anticholinergic effects

 

Acetaminophen

Zidovudine

0.9

Good

Hepatotoxicity (acetaminophen driven)

Minor

 

Co-trimoxazole

Zidovudine

3.6

Good

Increased zidovudine serum concentration

  1. a Severity classification for clinical purposes per IBM Micromedex DRUGDEX® database definitions
  2. b Percent of overall pDDI for study, % reported as (n/ 4582 total pDDI events) * 100
  3. c Strength of scientific data for the interaction per IBM Micromedex DRUGDEX® database; (i) excellent – clearly documented well controlled studies support the interaction; (ii) good – studies strongly suggest that interaction exists however there are not well controlled studies; (iii) fair – available evidence is poor but clinicians suspect the interaction exists based on pharmacology or the available evidence is good for a pharmacologically similar drug; and (iv) unknown – interaction documentation is unknown