1992-93 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 | 1992-11-21 | 30-036 | PHI | @ | NJN | W (+9) | 0 | 7:00 | .000 | .000 | 12.7 | 12.5 | 12.6 | 0.0 | 0.0 | 0.0 | 0.0 | 5.8 | 59 | 101 | -0.1 | -10.4 |
2 | 2 | 1992-11-28 | 30-043 | PHI | BOS | L (-8) | 0 | 3:00 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0 | 127 | -0.4 | -11.0 | ||||
3 | 3 | 1992-12-09 | 30-054 | PHI | SEA | W (+11) | 0 | 7:00 | .521 | .500 | 19.0 | 0.0 | 8.6 | 0.0 | 0.0 | 8.5 | 41.0 | 29.9 | 69 | 110 | 1.0 | -14.2 | |
4 | 4 | 1992-12-15 | 30-060 | PHI | @ | ORL | L (-12) | 0 | 12:00 | .615 | .500 | 7.3 | 32.4 | 17.4 | 0.0 | 3.9 | 5.5 | 17.0 | 19.0 | 110 | 103 | 5.9 | 3.6 |
5 | 5 | 1992-12-16 | 30-061 | PHI | CLE | L (-18) | 0 | 4:00 | 1.000 | 1.000 | 26.1 | 31.6 | 28.6 | 0.0 | 0.0 | 14.6 | 0.0 | 9.8 | 202 | 100 | 3.4 | 20.9 | |
6 | 6 | 1992-12-18 | 30-063 | PHI | UTA | L (-14) | 0 | 3:00 | 1.000 | 1.000 | 32.7 | 0.0 | 18.6 | 0.0 | 0.0 | 0.0 | 0.0 | 26.9 | 200 | 120 | 4.1 | 28.3 | |
7 | 7 | 1992-12-19 | 30-064 | PHI | @ | CHI | W (+2) | 1 | 33:00 | 0.0 | 22.6 | 12.4 | 0.0 | 1.5 | 8.8 | 100.0 | 1.4 | 0 | 96 | 4.8 | 1.5 | ||
8 | 8 | 1992-12-21 | 30-066 | PHI | IND | W (+12) | 1 | 23:00 | .361 | .286 | 21.7 | 13.0 | 17.4 | 10.8 | 2.1 | 8.8 | 19.4 | 18.1 | 92 | 97 | 6.4 | -3.1 | |
9 | 9 | 1992-12-26 | 30-071 | PHI | @ | POR | L (-6) | 1 | 43:00 | .170 | .200 | 11.2 | 24.2 | 17.4 | 2.7 | 1.1 | 6.4 | 25.4 | 7.6 | 64 | 104 | 6.6 | -4.6 |
10 | 10 | 1992-12-27 | 30-072 | PHI | @ | LAC | W (+4) | 1 | 36:00 | .515 | .333 | 11.4 | 5.3 | 7.8 | 0.0 | 0.0 | 4.9 | 0.0 | 4.6 | 150 | 116 | 5.1 | -2.3 |
11 | 11 | 1992-12-30 | 30-075 | PHI | @ | UTA | L (-9) | 1 | 35:00 | .500 | .500 | 3.0 | 20.0 | 11.7 | 3.6 | 0.0 | 7.3 | 20.0 | 5.7 | 94 | 112 | 6.4 | -1.6 |
12 | 12 | 1993-01-02 | 30-078 | PHI | @ | SAC | L (-56) | 1 | 12:00 | 1.000 | 1.000 | 0.0 | 17.8 | 9.6 | 0.0 | 0.0 | 9.0 | 50.0 | 12.5 | 68 | 130 | 1.8 | -7.1 |
13 | 13 | 1993-01-06 | 30-082 | PHI | NJN | W (+26) | 1 | 22:00 | .250 | .250 | 5.2 | 17.5 | 11.9 | 0.0 | 2.2 | 2.3 | 0.0 | 7.4 | 80 | 102 | 1.6 | -8.3 | |
14 | 14 | 1993-01-08 | 30-084 | PHI | @ | WSB | W (+2) | 1 | 26:00 | .667 | .667 | 12.9 | 16.4 | 14.7 | 9.3 | 0.0 | 4.4 | 14.3 | 10.6 | 132 | 114 | 8.9 | 1.3 |
15 | 15 | 1993-01-09 | 30-085 | PHI | CHI | W (+13) | 1 | 28:00 | .333 | .333 | 4.6 | 6.1 | 5.5 | 0.0 | 1.7 | 10.2 | 0.0 | 4.7 | 88 | 91 | 5.7 | 2.9 | |
16 | 16 | 1993-01-12 | 30-088 | PHI | @ | IND | L (-19) | 1 | 34:00 | .333 | .333 | 2.8 | 26.7 | 13.0 | 0.0 | 0.0 | 8.6 | 40.0 | 6.0 | 48 | 108 | 3.8 | -4.6 |
17 | 17 | 1993-01-13 | 30-089 | PHI | GSW | W (+7) | 1 | 17:00 | .563 | .500 | 13.1 | 16.3 | 14.9 | 6.5 | 0.0 | 12.5 | 18.4 | 12.3 | 115 | 107 | 7.0 | 1.4 | |
18 | 18 | 1993-01-15 | 30-091 | PHI | @ | NJN | L (-5) | 1 | 30:00 | .387 | .333 | 0.0 | 11.4 | 6.6 | 4.9 | 0.0 | 1.7 | 34.0 | 8.1 | 59 | 100 | 0.3 | -3.9 |
19 | 19 | 1993-01-16 | 30-092 | PHI | DET | W (+15) | 1 | 24:00 | .250 | .250 | 5.0 | 10.2 | 8.1 | 4.1 | 0.0 | 11.8 | 20.0 | 8.9 | 69 | 114 | 4.3 | -5.6 | |
20 | 20 | 1993-01-18 | 30-094 | PHI | ORL | W (+6) | 1 | 27:00 | .387 | .333 | 9.6 | 19.2 | 14.9 | 8.9 | 1.8 | 10.1 | 34.0 | 9.3 | 82 | 100 | 6.9 | 2.7 | |
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
21 | 21 | 1993-01-20 | 30-096 | PHI | @ | MIA | W (+3) | 1 | 24:00 | .000 | .000 | 0.0 | 30.3 | 16.3 | 6.0 | 0.0 | 13.3 | 50.0 | 7.6 | 14 | 99 | 0.9 | -5.9 |
22 | 22 | 1993-01-22 | 30-098 | PHI | NYK | L (-18) | 1 | 31:00 | .875 | .875 | 3.7 | 27.2 | 17.2 | 6.1 | 0.0 | 6.5 | 42.9 | 9.6 | 84 | 102 | 8.8 | 3.0 | |
23 | 23 | 1993-01-23 | 30-099 | PHI | @ | MIL | W (+9) | 1 | 11:00 | 1.000 | 1.000 | 0.0 | 9.5 | 5.4 | 0.0 | 0.0 | 0.0 | 50.0 | 7.8 | 73 | 114 | 1.0 | -5.8 |
24 | 24 | 1993-01-26 | 30-102 | PHI | @ | NYK | L (-8) | 1 | 11:00 | .532 | .000 | 0.0 | 27.9 | 13.8 | 0.0 | 0.0 | 5.3 | 0.0 | 7.3 | 121 | 95 | 2.5 | -0.9 |
25 | 25 | 1993-01-27 | 30-103 | PHI | IND | L (-2) | 1 | 22:00 | 1.000 | 1.000 | 7.3 | 0.0 | 2.8 | 0.0 | 2.3 | 8.5 | 66.7 | 6.4 | 67 | 123 | 2.3 | -4.4 | |
26 | 26 | 1993-01-29 | 30-105 | PHI | WSB | W (+6) | 1 | 26:00 | .667 | .667 | 6.4 | 20.5 | 13.2 | 0.0 | 5.7 | 11.1 | 25.0 | 6.4 | 105 | 73 | 10.6 | 7.2 | |
27 | 27 | 1993-01-30 | 30-106 | PHI | @ | ATL | L (-26) | 1 | 12:00 | .000 | .000 | 0.0 | 21.6 | 9.8 | 0.0 | 0.0 | 8.6 | 0.0 | 6.7 | 0 | 133 | -0.2 | -12.3 |
28 | 28 | 1993-02-03 | 30-110 | PHI | CHH | L (-11) | 1 | 7:00 | .500 | .500 | 0.0 | 36.1 | 16.1 | 0.0 | 0.0 | 8.1 | 33.3 | 17.5 | 63 | 124 | 0.9 | -11.0 | |
29 | 29 | 1993-02-05 | 30-112 | PHI | @ | BOS | L (-12) | 1 | 12:00 | .000 | .000 | 0.0 | 0.0 | 0.0 | 0.0 | 4.0 | 14.1 | 50.0 | 7.0 | 0 | 95 | 1.4 | -1.1 |
30 | 30 | 1993-02-08 | 30-115 | PHI | NYK | L (-5) | 0 | 6:00 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 9.8 | 100.0 | 7.2 | 0 | 116 | -0.3 | -8.6 | |||
31 | 31 | 1993-02-12 | 30-119 | PHI | @ | DEN | L (-4) | 0 | 13:00 | .000 | .000 | 8.4 | 6.8 | 7.5 | 0.0 | 0.0 | 7.5 | 0.0 | 5.8 | 39 | 117 | -0.6 | -9.5 |
32 | 32 | 1993-02-13 | 30-120 | PHI | @ | DAL | W (+23) | 0 | 7:00 | .000 | .000 | 0.0 | 14.0 | 7.3 | 0.0 | 0.0 | 0.0 | 50.0 | 10.8 | 0 | 98 | -1.4 | -18.2 |
33 | 33 | 1993-02-16 | 30-123 | PHI | @ | HOU | L (-38) | 0 | 4:00 | .000 | .000 | 0.0 | 96.0 | 32.0 | 0.0 | 0.0 | 0.0 | 0.0 | 9.7 | 0 | 136 | -0.5 | -18.1 |
34 | 34 | 1993-02-18 | 30-125 | PHI | @ | SAS | L (-5) | 0 | 10:00 | 0.0 | 20.0 | 10.7 | 0.0 | 0.0 | 0.0 | 100.0 | 4.7 | 0 | 113 | -0.8 | -11.4 | ||
35 | 35 | 1993-02-26 | 30-133 | PHI | MIL | W (+3) | 0 | 15:00 | .333 | .333 | 10.3 | 13.9 | 12.5 | 0.0 | 0.0 | 16.2 | 25.0 | 11.7 | 70 | 107 | 3.4 | -0.3 | |
36 | 36 | 1993-03-01 | 30-136 | PHI | @ | GSW | L (-13) | 0 | 11:00 | .500 | .500 | 11.2 | 25.2 | 19.2 | 10.0 | 0.0 | 4.5 | 33.3 | 11.5 | 93 | 119 | 2.2 | -5.4 |
37 | 37 | 1993-03-03 | 30-138 | PHI | @ | PHO | L (-10) | 0 | 24:00 | .692 | .692 | 4.3 | 8.0 | 6.2 | 0.0 | 0.0 | 7.1 | 13.3 | 25.9 | 113 | 125 | 12.7 | 6.9 |
38 | 38 | 1993-03-05 | 30-140 | PHI | @ | LAL | L (-4) | 0 | 32:00 | .200 | .200 | 3.0 | 7.8 | 5.6 | 4.3 | 1.5 | 15.2 | 28.6 | 8.9 | 42 | 87 | 4.9 | 0.5 |
39 | 39 | 1993-03-06 | 30-141 | PHI | @ | SEA | L (-56) | 0 | 3:00 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0 | 143 | -0.8 | -19.1 | |||
40 | 40 | 1993-03-08 | 30-143 | PHI | @ | MIN | W (+9) | 0 | 10:00 | 0.0 | 21.3 | 11.6 | 0.0 | 0.0 | 6.8 | 0.0 | 0 | 92 | 0.9 | -5.5 | |||
Rk | G | Date | Age | Tm | Opp | GS | MP | TS% | eFG% | ORB% | DRB% | TRB% | AST% | STL% | BLK% | TOV% | USG% | ORtg | DRtg | GmSc | BPM | ||
41 | 41 | 1993-03-10 | 30-145 | PHI | BOS | L (-4) | 0 | 4:00 | 0.0 | 66.7 | 28.2 | 0.0 | 0.0 | 0.0 | 0.0 | 0 | 107 | 0.6 | -1.6 | ||||
42 | 42 | 1993-03-12 | 30-147 | PHI | LAL | L (-6) | 0 | 7:00 | .500 | .500 | 18.0 | 14.9 | 16.3 | 0.0 | 0.0 | 0.0 | 0.0 | 13.2 | 125 | 114 | 1.6 | -4.3 | |
43 | 43 | 1993-03-16 | 30-151 | PHI | @ | CLE | L (-12) | 0 | 2:00 | .000 | .000 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 23.0 | 0 | 125 | -0.7 | -28.2 |
44 | 44 | 1993-03-19 | 30-154 | PHI | DAL | L (-2) | 0 | 10:00 | .500 | .500 | 14.5 | 41.7 | 30.4 | 0.0 | 0.0 | 6.5 | 0.0 | 9.5 | 121 | 86 | 2.8 | -1.0 | |
45 | 45 | 1993-03-20 | 30-155 | PHI | @ | MIL | L (-26) | 0 | 12:00 | 10.8 | 9.3 | 10.0 | 0.0 | 0.0 | 16.4 | 0.0 | 217 | 121 | 2.7 | 2.4 | |||
46 | 46 | 1993-03-23 | 30-158 | PHI | DEN | W (+8) | 0 | 8:00 | .500 | .500 | 0.0 | 12.0 | 5.9 | 0.0 | 0.0 | 32.9 | 50.0 | 21.5 | 42 | 64 | 1.3 | -3.6 | |
47 | 47 | 1993-03-24 | 30-159 | PHI | CHI | L (-13) | 0 | 9:00 | 0.0 | 14.8 | 7.3 | 0.0 | 0.0 | 0.0 | 100.0 | 5.4 | 0 | 130 | -0.7 | -9.7 | |||
48 | 48 | 1993-03-26 | 30-161 | PHI | CLE | L (-19) | 0 | 8:00 | .000 | .000 | 0.0 | 34.0 | 15.9 | 0.0 | 0.0 | 27.6 | 0.0 | 10.4 | 0 | 82 | 1.9 | 3.1 | |
49 | 49 | 1993-03-28 | 30-163 | PHI | PHO | L (-10) | 0 | 6:00 | 0.0 | 19.5 | 8.8 | 20.5 | 8.6 | 11.9 | 100.0 | 7.2 | 38 | 95 | 1.7 | 9.8 | |||
50 | 50 | 1993-03-30 | 30-165 | PHI | @ | NJN | L (-14) | 0 | 3:00 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 100.0 | 15.6 | 0 | 110 | -1.0 | -24.0 | ||
51 | 51 | 1993-04-04 | 30-170 | PHI | SAC | W (+10) | 0 | 9:00 | .000 | .000 | 12.7 | 43.5 | 29.3 | 0.0 | 0.0 | 0.0 | 50.0 | 9.7 | 34 | 100 | 0.2 | -12.3 | |
52 | 52 | 1993-04-06 | 30-172 | PHI | @ | ORL | L (-26) | 0 | 10:00 | 0.0 | 28.2 | 11.7 | 0.0 | 0.0 | 0.0 | 0.0 | 0 | 125 | 0.6 | -6.9 | |||
53 | 53 | 1993-04-07 | 30-173 | PHI | @ | WSB | W (+8) | 0 | 3:00 | 1.000 | 1.000 | 34.8 | 0.0 | 18.6 | 0.0 | 0.0 | 0.0 | 0.0 | 14.0 | 204 | 103 | 2.0 | 5.8 |
54 | 54 | 1993-04-18 | 30-184 | PHI | MIN | W (+27) | 0 | 9:00 | 1.500 | 1.500 | 0.0 | 20.5 | 11.9 | 0.0 | 0.0 | 12.5 | 0.0 | 5.1 | 300 | 79 | 4.7 | 16.6 | |
55 | 55 | 1993-04-20 | 30-186 | PHI | @ | CHI | L (-29) | 0 | 16:00 | .643 | .700 | 0.0 | 40.5 | 18.8 | 11.5 | 0.0 | 0.0 | 15.5 | 18.1 | 102 | 124 | 5.5 | 2.8 |
56 | 56 | 1993-04-21 | 30-187 | PHI | MIA | W (+10) | 0 | 9:00 | .375 | .375 | 0.0 | 10.7 | 5.5 | 0.0 | 0.0 | 21.6 | 33.3 | 28.1 | 49 | 90 | 0.6 | -8.8 | |
57 | 57 | 1993-04-23 | 30-189 | PHI | NYK | L (-15) | 0 | 11:00 | 0.0 | 26.2 | 12.8 | 14.5 | 0.0 | 5.1 | 100.0 | 4.0 | 31 | 96 | 0.9 | -2.1 | |||
58 | 58 | 1993-04-25 | 30-191 | PHI | @ | CLE | L (-4) | 0 | 2:00 | .000 | .000 | 0.0 | 52.2 | 28.2 | 0.0 | 0.0 | 0.0 | 0.0 | 21.7 | 0 | 101 | -0.4 | -24.2 |
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