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. 2014 Apr 3;2014(4):CD006531. doi: 10.1002/14651858.CD006531.pub2

Summary of findings 10. Paroxetine compared with fluvoxamine for depression.

Paroxetine compared with fluvoxamine for depression
Patient or population: patients with depression
 Settings: in‐ and out‐patients
 Intervention: paroxetine
 Comparison: fluvoxamine
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of Participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Fluvoxamine Paroxetine
Failure to respond at endpoint (6‐12 weeks) 466 per 1000 510 per 1000 
 (386 to 629) OR 1.19 
 (0.72 to 1.94) 261
 (3 studies) ⊕⊕⊕⊝
 moderate1  
Failure to respond at 1‐4 weeks Study population OR 0.71 
 (0.41 to 1.24) 281
 (3 studies) ⊕⊕⊕⊝
 moderate1  
769 per 1000 703 per 1000 
 (577 to 805)
Moderate
   
Failure to respond at 16‐24 weeks See comment See comment Not estimable 0
 (0)   No trial reported this outcome.
Failure to remit at endpoint 752 per 1000 703 per 1000 
 (571 to 807) OR 0.78 
 (0.44 to 1.38) 261
 (3 studies) ⊕⊕⊕⊝
 moderate1  
SMD at endpoint   The mean SMD at endpoint in the intervention groups was
 0.09 standard deviations higher 
 (0.43 lower to 0.6 higher)   58
 (1 study) ⊕⊕⊕⊝
 moderate1 This effect approaches zero.
Failure to complete ‐ any cause ‐ 293 per 1000 285 per 1000 
 (183 to 416) OR 0.96 
 (0.54 to 1.72) 261
 (3 studies) ⊕⊕⊕⊝
 moderate1  
Participants with at least some Side Effects 609 per 1000 636 per 1000 
 (395 to 822) OR 1.12 
 (0.42 to 2.97) 261
 (3 studies) ⊕⊕⊕⊝
 moderate1  
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: Confidence interval; SMD: standardized mean difference; OR: Odds ratio;
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low quality: We are very uncertain about the estimate.

1 Blinding stated but not tested. No information on randomisation procedures and allocation concealment.