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. 2008 May 16;66(2):266–275. doi: 10.1111/j.1365-2125.2008.03200.x

Table 3.

Main results in gabapentin trials

Efficacy % with
Subgroup Number of patients Relative benefit (95% CI) NNT (95% CI) Placebo Gabapentin
Lack of efficacy withdrawal
All 1425 0.41 (0.19, 0.87) −56 (−510, −30) 3 1
PEE 639 0.41 (0.14, 1.2) −55 (140, −23) 3 2
NEE 786 0.40 (0.14, 1.1) −55 (430, −26) 3 1
1800 mg 287 0.98 (0.21, 4.5) 250 (25, −31) 2 3
2400 mg 644 0.30 (0.09, 1.0) −44 (3000, −22) 3 1
3600 mg 494 0.33 (0.09, 1.2) −41 (360, −19) 4 1
Harm
% with
Subgroup Number of patients Relative risk (95% CI) NNH (95% CI) Placebo Gabapentin
Adverse event withdrawal
All 1546 1.4 (1.1, 1.9) 26 (14, 140) 9 13
PEE 639 1.4 (0.88, 2.1) 31 (12, −47) 12 15
NEE 907 1.5 (1.0, 2.3) 27 (13, −2700) 8 11
1800 mg 408 1.8 (0.82, 3.8) 21 (10, −810) 5 10
2400 mg 644 1.4 (0.91, 2.0) 25 (11, −72) 12 16
3600 mg 494 1.4 (0.85, 2.4) 27 (11, −57) 9 12
Somnolence
All 1526 3.4 (2.5, 4.7) 6.4 (5.3, 8.1) 6 22
PEE 639 2.9 (1.7, 5.0) 8.8 (6.2, 15) 6 17
NEE 887 3.3 (2.6, 5.4) 5.2 (4.2, 6.8)a 7 26
1800 mg 396 2.9 (1.6, 5.4) 7.2 (4.9, 14) 7 21
2400 mg 682 3.0 (1.9, 4.8) 7.1 (5.3, 11) 7 21
3600 mg 448 4.7 (2.6, 8.5) 5.1 (3.8, 7.6) 5 25
Dizziness
All 1576 3.5 (2.7, 4.9) 5.3 (4.5, 6.5) 7 26
PEE 639 3.2 (2.1, 4.9) 4.9 (3.9, 6.9) 9 29
NEE 937 3.8 (2.6, 5.6) 5.7 (4.6, 7.6) 6 24
1800 mg 396 4.5 (2.3, 8.7) 5.0 (3.8, 7.5) 6 26
2400 mg 682 2.8 (1.9, 4.0) 5.5 (4.2, 7.9) 10 28
3600 mg 498 4.3 (2.6, 8.2) 5.3 (4.0, 7.8) 5 24

1800 mg, 2400 mg and 3600 mg refer to the maximum available daily doses of gabapentin. For the analysis of dizziness, the 3600 mg subgroup also contains one trial [45] using 4200 mg gabapentin as the maximum available daily dose. a) P = 0.019 for the comparison PEE vs. NEE.