1994-95 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 | 1994-11-09 | 26-167 | PHI | WSB | W (+1) | 0 | 19:00 | .365 | .273 | 6.0 | 6.6 | 6.3 | 0.0 | 0.0 | 0.0 | 7.5 | 29.9 | 78 | 112 | 1.7 | -12.2 | |
2 | 2 | 1994-11-11 | 26-169 | PHI | DAL | L (-7) | 0 | 14:00 | .600 | .600 | 7.8 | 9.3 | 8.5 | 0.0 | 0.0 | 0.0 | 16.7 | 17.8 | 108 | 118 | 2.9 | -6.0 | |
3 | 3 | 1994-11-12 | 26-170 | PHI | ORL | L (-13) | 0 | 24:00 | .545 | .500 | 11.8 | 14.0 | 12.8 | 0.0 | 0.0 | 0.0 | 12.7 | 25.9 | 107 | 122 | 8.4 | -1.8 | |
4 | 4 | 1994-11-15 | 26-173 | PHI | @ | DET | L (-1) | 0 | 33:00 | .760 | .750 | 10.4 | 7.9 | 9.2 | 12.2 | 3.2 | 6.3 | 10.1 | 27.1 | 141 | 105 | 24.0 | 20.4 |
5 | 5 | 1994-11-16 | 26-174 | PHI | MIA | W (+13) | 1 | 34:00 | .558 | .389 | 4.4 | 18.8 | 12.8 | 14.2 | 0.0 | 0.0 | 7.9 | 18.2 | 130 | 114 | 10.2 | -3.7 | |
6 | 6 | 1994-11-18 | 26-176 | PHI | LAC | W (+14) | 1 | 29:00 | .472 | .417 | 6.4 | 10.1 | 8.2 | 0.0 | 0.0 | 0.0 | 0.0 | 20.5 | 112 | 96 | 6.1 | -4.4 | |
7 | 7 | 1994-11-22 | 26-180 | PHI | @ | ATL | L (-3) | 1 | 38:00 | .528 | .438 | 6.8 | 9.7 | 8.3 | 4.4 | 1.5 | 0.0 | 0.0 | 27.7 | 119 | 121 | 14.0 | -2.1 |
8 | 8 | 1994-11-25 | 26-183 | PHI | @ | MIN | W (+38) | 1 | 29:00 | .376 | .250 | 0.0 | 10.6 | 6.2 | 7.9 | 0.0 | 2.3 | 34.9 | 22.6 | 63 | 85 | -1.0 | -15.6 |
9 | 9 | 1994-11-26 | 26-184 | PHI | BOS | L (-9) | 1 | 38:00 | .412 | .357 | 8.6 | 13.7 | 10.9 | 11.6 | 2.6 | 2.1 | 0.0 | 18.2 | 104 | 110 | 10.9 | -0.9 | |
10 | 10 | 1994-12-02 | 26-190 | PHI | SAC | W (+3) | 0 | 30:00 | .668 | .654 | 8.0 | 18.8 | 13.0 | 0.0 | 0.0 | 2.4 | 0.0 | 27.0 | 148 | 107 | 18.4 | 12.2 | |
11 | 11 | 1994-12-03 | 26-191 | PHI | @ | CLE | W (+5) | 0 | 22:00 | .438 | .438 | 0.0 | 9.3 | 4.8 | 0.0 | 0.0 | 0.0 | 11.1 | 21.4 | 73 | 100 | 1.4 | -6.6 |
12 | 12 | 1994-12-05 | 26-193 | PHI | NYK | L (-5) | 0 | 31:00 | .446 | .313 | 0.0 | 20.8 | 10.2 | 15.2 | 0.0 | 0.0 | 4.5 | 34.1 | 95 | 103 | 8.5 | -1.9 | |
13 | 13 | 1994-12-07 | 26-195 | PHI | @ | MIA | W (+9) | 0 | 24:00 | .985 | .929 | 7.1 | 10.0 | 8.8 | 44.4 | 0.0 | 3.1 | 23.7 | 24.2 | 160 | 111 | 17.3 | 15.2 |
14 | 14 | 1994-12-09 | 26-197 | PHI | IND | L (-6) | 0 | 26:00 | .660 | .636 | 4.9 | 18.9 | 12.0 | 8.4 | 0.0 | 2.7 | 26.8 | 33.5 | 102 | 108 | 9.8 | 3.1 | |
15 | 15 | 1994-12-10 | 26-198 | PHI | @ | NYK | L (-4) | 1 | 38:00 | .558 | .472 | 7.9 | 9.7 | 8.7 | 5.5 | 0.0 | 0.0 | 12.2 | 29.6 | 110 | 125 | 12.9 | -0.6 |
16 | 16 | 1994-12-13 | 26-201 | PHI | MIA | W (+15) | 1 | 43:00 | .846 | .763 | 11.4 | 9.9 | 10.6 | 21.5 | 1.2 | 3.7 | 3.1 | 32.1 | 182 | 99 | 49.6 | 30.7 | |
17 | 17 | 1994-12-14 | 26-202 | PHI | @ | MIL | L (-3) | 1 | 43:00 | .645 | .594 | 9.7 | 8.6 | 9.2 | 4.1 | 1.2 | 0.0 | 18.7 | 26.8 | 116 | 114 | 16.4 | 0.6 |
18 | 18 | 1994-12-16 | 26-204 | PHI | CLE | L (-4) | 1 | 46:00 | .336 | .321 | 0.0 | 7.0 | 4.1 | 21.9 | 3.7 | 0.0 | 16.8 | 20.2 | 67 | 101 | 3.8 | -5.5 | |
19 | 19 | 1994-12-17 | 26-205 | PHI | DET | L (-5) | 1 | 38:00 | .571 | .571 | 3.6 | 14.0 | 8.9 | 17.2 | 1.5 | 2.3 | 12.5 | 20.2 | 122 | 116 | 11.8 | 3.2 | |
20 | 20 | 1994-12-22 | 26-210 | PHI | @ | CHH | L (-12) | 1 | 27:00 | .286 | .286 | 4.2 | 8.7 | 6.4 | 5.7 | 2.0 | 0.0 | 22.2 | 15.2 | 58 | 116 | 0.1 | -11.4 |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
21 | 21 | 1994-12-26 | 26-214 | PHI | @ | POR | W (+7) | 0 | 27:00 | .656 | .550 | 0.0 | 14.2 | 8.5 | 18.5 | 0.0 | 0.0 | 7.6 | 24.1 | 129 | 106 | 11.7 | 5.9 |
22 | 22 | 1994-12-28 | 26-216 | PHI | @ | SEA | L (-19) | 0 | 35:00 | .475 | .441 | 7.4 | 0.0 | 4.0 | 21.8 | 0.0 | 0.0 | 5.3 | 23.8 | 106 | 130 | 8.7 | -2.4 |
23 | 23 | 1994-12-30 | 26-218 | PHI | @ | SAC | L (-3) | 1 | 41:00 | .582 | .542 | 0.0 | 2.9 | 1.4 | 10.2 | 3.8 | 1.9 | 28.0 | 19.0 | 88 | 95 | 7.8 | -0.9 |
24 | 24 | 1995-01-04 | 26-223 | PHI | @ | PHO | L (-5) | 1 | 42:00 | .794 | .767 | 0.0 | 3.4 | 1.8 | 3.3 | 0.0 | 2.0 | 14.5 | 22.9 | 132 | 141 | 17.4 | 0.0 |
25 | 25 | 1995-01-05 | 26-224 | PHI | @ | LAC | L (-2) | 1 | 31:00 | .380 | .214 | 0.0 | 15.5 | 7.6 | 14.3 | 3.6 | 0.0 | 30.3 | 19.6 | 72 | 107 | 3.0 | -7.0 |
26 | 26 | 1995-01-07 | 26-226 | PHI | @ | UTA | L (-21) | 0 | 9:00 | .092 | .000 | 0.0 | 14.4 | 6.8 | 15.7 | 0.0 | 0.0 | 0.0 | 27.6 | 35 | 125 | -1.5 | -20.2 |
27 | 27 | 1995-01-11 | 26-230 | PHI | CHI | L (-38) | 0 | 29:00 | .775 | .778 | 0.0 | 4.7 | 2.2 | 8.0 | 0.0 | 0.0 | 32.6 | 24.9 | 97 | 134 | 6.5 | -2.0 | |
28 | 28 | 1995-01-25 | 26-244 | PHI | MIL | L (-1) | 0 | 32:00 | 1.047 | 1.143 | 0.0 | 6.4 | 3.7 | 22.5 | 0.0 | 0.0 | 24.1 | 30.2 | 122 | 116 | 23.7 | 14.8 | |
29 | 29 | 1995-01-27 | 26-246 | PHI | PHO | L (-1) | 1 | 36:00 | .690 | .667 | 0.0 | 15.9 | 7.6 | 30.1 | 2.9 | 0.0 | 22.5 | 20.9 | 124 | 114 | 15.4 | 7.3 | |
30 | 30 | 1995-01-28 | 26-247 | PHI | @ | IND | L (-3) | 1 | 42:00 | .720 | .692 | 0.0 | 3.6 | 1.7 | 4.2 | 2.7 | 2.3 | 17.8 | 19.5 | 125 | 115 | 13.2 | 5.6 |
31 | 31 | 1995-01-30 | 26-249 | PHI | SEA | L (-5) | 1 | 42:00 | .813 | .700 | 0.0 | 0.0 | 0.0 | 11.3 | 0.0 | 0.0 | 19.4 | 24.0 | 142 | 138 | 17.3 | 2.1 | |
32 | 32 | 1995-02-01 | 26-251 | PHI | WSB | W (+9) | 1 | 34:00 | .660 | .545 | 0.0 | 8.5 | 4.7 | 0.0 | 0.0 | 0.0 | 12.8 | 20.9 | 117 | 100 | 10.4 | -1.9 | |
33 | 33 | 1995-02-03 | 26-253 | PHI | NYK | L (-20) | 1 | 30:00 | .344 | .150 | 8.9 | 5.0 | 7.1 | 5.8 | 1.9 | 0.0 | 31.4 | 30.9 | 60 | 130 | -1.4 | -17.0 | |
34 | 34 | 1995-02-04 | 26-254 | PHI | @ | MIL | W (+6) | 1 | 18:00 | .750 | .750 | 0.0 | 8.6 | 3.6 | 9.5 | 3.0 | 0.0 | 14.3 | 17.6 | 138 | 110 | 4.6 | 1.8 |
35 | 35 | 1995-02-06 | 26-256 | PHI | ATL | L (-15) | 1 | 44:00 | .656 | .571 | 3.2 | 3.1 | 3.2 | 7.7 | 1.3 | 0.0 | 14.6 | 22.4 | 123 | 127 | 14.8 | 1.5 | |
36 | 36 | 1995-02-07 | 26-257 | PHI | @ | CLE | L (-6) | 1 | 27:00 | .375 | .375 | 0.0 | 0.0 | 0.0 | 5.8 | 0.0 | 3.2 | 11.1 | 16.5 | 73 | 115 | 0.4 | -9.4 |
37 | 37 | 1995-02-15 | 26-265 | PHI | MIN | L (-4) | 1 | 28:00 | .717 | .625 | 6.9 | 12.9 | 9.5 | 25.7 | 1.9 | 0.0 | 6.4 | 24.0 | 152 | 114 | 17.7 | 12.1 | |
38 | 38 | 1995-02-17 | 26-267 | PHI | @ | ORL | L (-46) | 1 | 23:00 | .295 | .227 | 8.0 | 5.5 | 7.0 | 14.0 | 2.2 | 0.0 | 14.4 | 24.2 | 76 | 139 | 1.4 | -10.4 |
39 | 39 | 1995-02-18 | 26-268 | PHI | DEN | W (+6) | 1 | 37:00 | .505 | .318 | 3.8 | 2.8 | 3.2 | 8.1 | 1.5 | 0.0 | 27.5 | 28.5 | 83 | 106 | 4.9 | -9.9 | |
40 | 40 | 1995-02-20 | 26-270 | PHI | @ | GSW | L (-13) | 1 | 35:00 | .354 | .167 | 0.0 | 3.2 | 1.4 | 9.1 | 1.4 | 0.0 | 16.2 | 21.5 | 75 | 105 | 0.7 | -11.6 |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
41 | 41 | 1995-02-22 | 26-272 | PHI | @ | LAL | L (-12) | 1 | 38:00 | .422 | .396 | 0.0 | 0.0 | 0.0 | 15.4 | 2.7 | 0.0 | 3.9 | 28.5 | 98 | 123 | 10.8 | -2.0 |
42 | 42 | 1995-02-23 | 26-273 | PHI | @ | DEN | L (-30) | 1 | 29:00 | .534 | .346 | 0.0 | 11.8 | 5.1 | 15.5 | 0.0 | 0.0 | 9.7 | 29.7 | 118 | 121 | 10.4 | 3.2 |
43 | 43 | 1995-02-26 | 26-276 | PHI | @ | NYK | L (-5) | 0 | 20:00 | .254 | .125 | 0.0 | 14.4 | 7.3 | 6.9 | 0.0 | 0.0 | 12.7 | 33.7 | 56 | 112 | -3.0 | -20.2 |
44 | 44 | 1995-02-28 | 26-278 | PHI | @ | WSB | W (+4) | 0 | 18:00 | .379 | .273 | 5.6 | 14.8 | 9.5 | 7.8 | 0.0 | 0.0 | 7.0 | 31.0 | 95 | 111 | 2.9 | -11.1 |
45 | 45 | 1995-03-03 | 26-281 | PHI | @ | NJN | W (+4) | 0 | 6:00 | .340 | .200 | 0.0 | 18.6 | 9.6 | 0.0 | 0.0 | 0.0 | 25.4 | 55.6 | 60 | 110 | -1.2 | -32.5 |
46 | 46 | 1995-03-04 | 26-282 | PHI | CHI | L (-12) | 0 | 28:00 | .406 | .406 | 0.0 | 14.3 | 6.3 | 6.7 | 1.8 | 0.0 | 20.0 | 31.1 | 74 | 112 | 0.8 | -9.9 | |
47 | 47 | 1995-03-08 | 26-286 | PHI | NJN | L (-7) | 0 | 32:00 | .446 | .423 | 3.1 | 3.0 | 3.0 | 13.3 | 0.0 | 0.0 | 27.1 | 23.2 | 80 | 122 | 1.0 | -10.0 | |
48 | 48 | 1995-03-10 | 26-288 | PHI | SAS | L (-6) | 0 | 20:00 | .508 | .429 | 0.0 | 5.1 | 2.6 | 0.0 | 0.0 | 0.0 | 27.6 | 24.5 | 77 | 121 | 1.2 | -9.2 | |
49 | 49 | 1995-03-12 | 26-290 | PHI | CLE | L (-20) | 0 | 18:00 | .405 | .167 | 6.3 | 8.9 | 7.4 | 0.0 | 0.0 | 0.0 | 10.4 | 27.4 | 86 | 115 | 2.0 | -9.6 | |
50 | 50 | 1995-03-14 | 26-292 | PHI | HOU | L (-29) | 0 | 17:00 | .557 | .500 | 0.0 | 7.6 | 3.9 | 25.1 | 0.0 | 5.0 | 9.2 | 27.7 | 111 | 139 | 7.6 | -1.0 | |
51 | 51 | 1995-03-16 | 26-294 | PHI | @ | SAS | L (-26) | 1 | 30:00 | .597 | .600 | 3.0 | 4.0 | 3.4 | 0.0 | 1.6 | 2.5 | 0.0 | 15.4 | 122 | 119 | 9.5 | 0.2 |
52 | 52 | 1995-03-17 | 26-295 | PHI | @ | DAL | L (-2) | 1 | 35:00 | .618 | .583 | 7.4 | 10.4 | 9.1 | 0.0 | 0.0 | 3.4 | 12.7 | 21.7 | 113 | 118 | 12.2 | -3.3 |
53 | 53 | 1995-03-19 | 26-297 | PHI | @ | HOU | L (-11) | 1 | 5:00 | .333 | .333 | 0.0 | 0.0 | 0.0 | 31.6 | 0.0 | 0.0 | 0.0 | 26.7 | 94 | 134 | 0.6 | -10.1 |
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