BODY SYSTEM / ADVERSE
EXPERIENCE |
Bupropion
sustained-release Dosing Group |
||
|
150
mg/d (N=147) |
300
mg/d (N=147) |
Placebo (N=150) |
Cardiovascular |
|||
Palpitations |
3.4% |
3.4% |
1.3% |
Migraine |
0.7% |
0.7% |
0.7% |
Hot Flashes |
1.4% |
0.7% |
0% |
Hypertension |
0% |
0% |
2.0% |
Tachycardia |
1.4% |
0% |
0% |
Infections |
|||
Upper Respiratory Infection |
2.7% |
7.5% |
4.7% |
Flu Syndrome |
8.8% |
1.4% |
4.0% |
Special Senses |
|||
Tinnitus |
4.8% |
6.8% |
0.7% |
Taste Perversion |
0% |
2.7% |
0.7% |
Blurred Vision |
2.7% |
3.4% |
0.7% |
Musculoskeletal |
|||
Arthralgia |
2.7% |
0% |
0% |
Myalgia |
0.7% |
2.7% |
2.0% |
Leg Cramps |
2.0% |
0% |
1.3% |
Twitch |
1.4% |
1.4% |
0% |
Urinary System Disorders |
|||
Urinary Tract Infection |
2.0% |
1.4% |
0% |
Urinary Frequency |
2.0% |
1.4% |
1.3% |
Reproductive Disorders,
Male (percentage based on #
male patients (BUP SR 150=57, BUP SR=49, PLACEBO=51) |
|||
Impotence |
1.8% |
0% |
0% |
Reproductive Disorders, Female (percentage based on #
male patients (BUP SR 150=90, BUP SR=98, PLACEBO=99) |
|||
Dysmenorrhea |
1.1% |
1.0% |
2.0% |
None of the adverse events listed above occurred at
a rate greater than five per cent in at lest one bupropion
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