1993-94 Regular Season
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | 1 | 1993-11-05 | 21-228 | PHI | WSB | W (+12) | 1 | 29:00 | .233 | .167 | 0.0 | 17.6 | 9.1 | 5.2 | 1.8 | 18.1 | 13.4 | 22.5 | 52 | 79 | 3.6 | -6.6 | |
2 | 2 | 1993-11-06 | 21-229 | PHI | @ | ORL | L (-25) | 1 | 24:00 | .274 | .182 | 8.3 | 11.8 | 9.8 | 14.3 | 4.1 | 5.7 | 23.9 | 28.4 | 58 | 108 | 1.7 | -8.4 |
3 | 3 | 1993-11-09 | 21-232 | PHI | @ | NYK | L (-9) | 1 | 33:00 | .250 | .250 | 3.8 | 11.6 | 8.3 | 10.5 | 3.0 | 8.7 | 25.0 | 21.4 | 48 | 94 | 2.4 | -5.4 |
4 | 4 | 1993-11-10 | 21-233 | PHI | BOS | L (-2) | 1 | 36:00 | .463 | .455 | 7.0 | 19.0 | 13.3 | 14.6 | 4.5 | 4.8 | 20.2 | 18.8 | 88 | 94 | 10.7 | 0.2 | |
5 | 5 | 1993-11-12 | 21-235 | PHI | @ | WSB | L (-12) | 1 | 34:00 | .601 | .444 | 0.0 | 13.4 | 6.5 | 9.3 | 1.4 | 11.4 | 20.5 | 18.1 | 101 | 97 | 12.8 | 2.9 |
6 | 6 | 1993-11-13 | 21-236 | PHI | @ | NJN | W (+1) | 1 | 30:00 | .617 | .563 | 16.3 | 9.8 | 13.1 | 8.6 | 1.7 | 5.8 | 5.1 | 27.8 | 132 | 104 | 20.2 | 8.1 |
7 | 7 | 1993-11-15 | 21-238 | PHI | HOU | L (-4) | 1 | 28:00 | .190 | .143 | 0.0 | 15.6 | 8.4 | 12.6 | 3.9 | 0.0 | 20.2 | 17.2 | 43 | 95 | -0.9 | -9.2 | |
8 | 8 | 1993-11-17 | 21-240 | PHI | ATL | L (-2) | 1 | 13:00 | .347 | .000 | 7.9 | 22.6 | 15.4 | 10.3 | 4.0 | 5.4 | 46.5 | 34.6 | 49 | 88 | -0.6 | -17.4 | |
9 | 9 | 1993-11-19 | 21-242 | PHI | UTA | W (+9) | 0 | 8:00 | .000 | .000 | 0.0 | 27.9 | 16.0 | 0.0 | 0.0 | 0.0 | 0.0 | 11.4 | 0 | 121 | -1.6 | -21.6 | |
10 | 10 | 1993-11-21 | 21-244 | PHI | @ | DET | L (-14) | 0 | 30:00 | .360 | .308 | 0.0 | 29.5 | 13.8 | 23.2 | 0.0 | 2.4 | 12.6 | 23.8 | 78 | 112 | 5.3 | -5.2 |
11 | 11 | 1993-11-24 | 21-247 | PHI | @ | IND | W (+11) | 0 | 28:00 | .258 | .222 | 10.1 | 23.8 | 17.1 | 8.2 | 0.0 | 9.7 | 14.7 | 22.8 | 65 | 101 | 3.2 | -10.7 |
12 | 12 | 1993-11-26 | 21-249 | PHI | GSW | L (-12) | 0 | 29:00 | .536 | .500 | 7.0 | 19.2 | 12.9 | 22.5 | 3.7 | 8.6 | 30.0 | 20.1 | 88 | 102 | 10.5 | 3.1 | |
13 | 13 | 1993-11-27 | 21-250 | PHI | @ | ATL | L (-32) | 1 | 28:00 | .479 | .333 | 19.8 | 18.7 | 19.2 | 22.5 | 1.7 | 11.2 | 32.4 | 25.4 | 82 | 100 | 12.2 | 4.9 |
14 | 14 | 1993-11-30 | 21-253 | PHI | SEA | L (-12) | 1 | 16:00 | .500 | .500 | 0.0 | 15.8 | 8.2 | 31.0 | 3.3 | 4.3 | 66.7 | 17.9 | 49 | 98 | 0.2 | -5.0 | |
15 | 15 | 1993-12-04 | 21-257 | PHI | SAS | L (-8) | 1 | 27:00 | .125 | .125 | 9.9 | 10.5 | 10.1 | 11.8 | 0.0 | 0.0 | 11.1 | 15.6 | 51 | 107 | -0.9 | -11.4 | |
16 | 16 | 1993-12-08 | 21-261 | PHI | CHI | W (+7) | 1 | 45:00 | .430 | .444 | 5.6 | 20.0 | 13.2 | 12.4 | 0.0 | 8.5 | 16.8 | 24.2 | 80 | 86 | 11.7 | -1.7 | |
17 | 17 | 1993-12-10 | 21-263 | PHI | SAC | L (-6) | 1 | 36:00 | .467 | .438 | 3.0 | 13.0 | 7.8 | 13.0 | 2.8 | 9.9 | 9.9 | 24.0 | 96 | 109 | 15.2 | 0.2 | |
18 | 18 | 1993-12-11 | 21-264 | PHI | @ | MIL | W (+13) | 1 | 20:00 | .500 | .500 | 14.5 | 20.0 | 17.8 | 0.0 | 0.0 | 3.5 | 27.3 | 25.7 | 80 | 97 | 2.7 | -11.7 |
19 | 19 | 1993-12-13 | 21-266 | PHI | @ | BOS | L (-5) | 1 | 19:00 | .286 | .286 | 5.9 | 5.9 | 5.9 | 7.9 | 0.0 | 11.6 | 22.2 | 19.5 | 62 | 114 | 2.0 | -9.7 |
20 | 20 | 1993-12-15 | 21-268 | PHI | DEN | W (+8) | 1 | 20:00 | .417 | .417 | 23.5 | 9.6 | 16.6 | 0.0 | 2.5 | 16.2 | 14.3 | 28.7 | 92 | 88 | 8.5 | -1.0 | |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
21 | 21 | 1993-12-17 | 21-270 | PHI | LAL | W (+11) | 1 | 36:00 | .340 | .300 | 9.8 | 22.7 | 16.7 | 10.8 | 0.0 | 3.7 | 14.5 | 17.0 | 84 | 100 | 5.4 | -7.4 | |
22 | 22 | 1993-12-18 | 21-271 | PHI | @ | MIA | L (-23) | 1 | 22:00 | .410 | .333 | 10.1 | 21.3 | 15.6 | 14.2 | 4.8 | 5.7 | 21.5 | 19.6 | 83 | 109 | 6.0 | 0.1 |
23 | 23 | 1993-12-20 | 21-273 | PHI | DET | W (+29) | 1 | 27:00 | .588 | .636 | 17.8 | 39.1 | 31.1 | 0.0 | 7.3 | 11.0 | 13.6 | 24.7 | 106 | 68 | 19.4 | 6.8 | |
24 | 24 | 1993-12-22 | 21-275 | PHI | MIA | L (-8) | 1 | 16:00 | .333 | .333 | 31.6 | 0.0 | 16.2 | 15.0 | 0.0 | 0.0 | 25.0 | 44.7 | 65 | 119 | -1.3 | -25.6 | |
25 | 25 | 1993-12-27 | 21-280 | PHI | @ | LAC | L (-10) | 1 | 34:00 | .592 | .500 | 4.9 | 12.0 | 8.4 | 0.0 | 1.4 | 7.4 | 27.0 | 21.8 | 90 | 91 | 11.4 | -0.5 |
26 | 26 | 1993-12-28 | 21-281 | PHI | @ | GSW | W (+17) | 1 | 18:00 | .205 | .250 | 0.0 | 16.0 | 8.6 | 6.3 | 0.0 | 3.3 | 29.1 | 15.3 | 39 | 90 | -2.1 | -12.0 |
27 | 27 | 1993-12-30 | 21-283 | PHI | @ | PHO | L (-12) | 1 | 35:00 | .571 | .571 | 14.1 | 9.4 | 11.6 | 28.2 | 0.0 | 9.0 | 6.3 | 20.7 | 126 | 122 | 19.1 | 7.2 |
28 | 28 | 1994-01-02 | 21-286 | PHI | @ | DEN | W (+16) | 1 | 35:00 | .597 | .600 | 4.0 | 11.9 | 8.6 | 10.2 | 4.4 | 5.6 | 31.5 | 20.5 | 87 | 78 | 10.2 | 2.7 |
29 | 29 | 1994-01-04 | 21-288 | PHI | @ | SAS | L (-23) | 1 | 35:00 | .401 | .429 | 10.4 | 7.4 | 9.1 | 10.2 | 0.0 | 0.0 | 11.0 | 22.7 | 84 | 121 | 5.6 | -6.8 |
30 | 30 | 1994-01-07 | 21-291 | PHI | @ | DAL | W (+10) | 1 | 23:00 | .434 | .500 | 0.0 | 17.8 | 9.7 | 12.7 | 4.5 | 22.1 | 25.8 | 15.5 | 74 | 77 | 8.7 | 8.2 |
31 | 31 | 1994-01-08 | 21-292 | PHI | @ | HOU | L (-7) | 1 | 31:00 | .470 | .429 | 6.7 | 14.1 | 10.3 | 6.0 | 6.4 | 6.9 | 6.3 | 23.5 | 95 | 91 | 13.4 | 3.7 |
32 | 32 | 1994-01-10 | 21-294 | PHI | BOS | W (+5) | 1 | 31:00 | .313 | .273 | 8.4 | 17.9 | 13.0 | 19.8 | 0.0 | 7.0 | 19.0 | 21.7 | 74 | 96 | 5.6 | -6.4 | |
33 | 33 | 1994-01-12 | 21-296 | PHI | LAC | W (+19) | 1 | 29:00 | .833 | .875 | 5.2 | 29.7 | 18.6 | 4.7 | 1.7 | 7.2 | 22.7 | 19.6 | 122 | 92 | 15.8 | 5.1 | |
34 | 34 | 1994-01-14 | 21-298 | PHI | IND | W (+2) | 1 | 37:00 | .697 | .667 | 7.3 | 18.3 | 13.3 | 8.8 | 0.0 | 10.9 | 21.8 | 18.2 | 114 | 97 | 14.5 | 5.3 | |
35 | 35 | 1994-01-15 | 21-299 | PHI | @ | CLE | L (-43) | 1 | 43:00 | .246 | .167 | 5.3 | 14.7 | 9.8 | 0.0 | 1.2 | 4.5 | 29.7 | 20.9 | 40 | 115 | -3.0 | -13.6 |
36 | 36 | 1994-01-17 | 21-301 | PHI | @ | CHI | L (-30) | 1 | 27:00 | .654 | .583 | 4.9 | 18.2 | 11.9 | 22.6 | 0.0 | 0.0 | 26.7 | 32.2 | 102 | 131 | 11.0 | -2.9 |
37 | 37 | 1994-01-19 | 21-303 | PHI | @ | CHH | L (-12) | 1 | 27:00 | .354 | .333 | 7.7 | 21.7 | 14.3 | 4.7 | 0.0 | 6.5 | 33.6 | 22.2 | 57 | 105 | 0.6 | -11.6 |
38 | 38 | 1994-01-22 | 21-306 | PHI | ORL | L (-9) | 1 | 33:00 | .585 | .588 | 7.3 | 11.2 | 9.2 | 13.0 | 3.0 | 1.9 | 4.6 | 28.4 | 122 | 119 | 18.6 | 3.5 | |
39 | 39 | 1994-01-23 | 21-307 | PHI | @ | NYK | W (+7) | 1 | 34:00 | .159 | .143 | 16.8 | 16.0 | 16.4 | 21.9 | 0.0 | 5.9 | 27.6 | 28.7 | 51 | 98 | -2.6 | -13.4 |
40 | 40 | 1994-01-26 | 21-310 | PHI | DAL | W (+14) | 1 | 33:00 | .912 | .857 | 6.6 | 12.1 | 9.5 | 9.9 | 3.0 | 4.0 | 15.4 | 17.9 | 158 | 91 | 20.5 | 9.1 | |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
41 | 41 | 1994-01-28 | 21-312 | PHI | PHO | L (-5) | 1 | 32:00 | .671 | .625 | 18.8 | 19.2 | 19.0 | 5.4 | 0.0 | 1.9 | 17.7 | 30.8 | 120 | 115 | 18.1 | 1.3 | |
42 | 42 | 1994-01-29 | 21-313 | PHI | MIL | W (+5) | 1 | 25:00 | .200 | .200 | 7.7 | 24.6 | 15.1 | 6.6 | 2.1 | 11.3 | 28.6 | 23.9 | 42 | 87 | -1.2 | -15.9 | |
43 | 43 | 1994-02-04 | 21-319 | PHI | WSB | L (-7) | 1 | 30:00 | .258 | .222 | 7.0 | 7.1 | 7.0 | 9.2 | 1.8 | 0.0 | 14.7 | 21.1 | 62 | 116 | -0.3 | -15.1 | |
44 | 44 | 1994-02-05 | 21-320 | PHI | @ | MIA | W (+2) | 1 | 36:00 | .359 | .375 | 3.5 | 14.8 | 9.6 | 13.3 | 1.4 | 1.7 | 29.1 | 16.8 | 64 | 96 | 2.2 | -6.0 |
45 | 45 | 1994-02-07 | 21-322 | PHI | CHH | W (+8) | 1 | 31:00 | .545 | .545 | 9.7 | 12.4 | 11.1 | 8.0 | 0.0 | 5.2 | 31.3 | 19.9 | 84 | 110 | 6.9 | -7.0 | |
46 | 46 | 1994-02-09 | 21-324 | PHI | NYK | L (-35) | 1 | 31:00 | .428 | .429 | 9.9 | 25.8 | 17.9 | 14.3 | 0.0 | 9.4 | 18.6 | 29.5 | 79 | 110 | 10.2 | 0.4 | |
47 | 47 | 1994-02-15 | 21-330 | PHI | @ | SEA | L (-28) | 1 | 30:00 | .663 | .615 | 0.0 | 8.6 | 5.3 | 19.8 | 0.0 | 6.1 | 17.3 | 24.4 | 113 | 131 | 15.1 | 3.5 |
48 | 48 | 1994-02-16 | 21-331 | PHI | @ | SAC | L (-2) | 1 | 30:00 | .311 | .143 | 3.6 | 13.3 | 8.7 | 15.9 | 0.0 | 2.1 | 29.3 | 21.3 | 59 | 98 | -0.2 | -11.6 |
49 | 49 | 1994-02-18 | 21-333 | PHI | @ | POR | L (-16) | 1 | 1:00 | .000 | .000 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 40.8 | 0 | 117 | -0.7 | -40.0 |
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