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WELLBUTRIN SR

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Wellbutrin Sr Adverse Events Reported to the FDA Over Time

How are Wellbutrin Sr adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Wellbutrin Sr, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Wellbutrin Sr is flagged as the suspect drug causing the adverse event.

Most Common Wellbutrin Sr Adverse Events Reported to the FDA

What are the most common Wellbutrin Sr adverse events reported to the FDA?

Drug Ineffective
307 (4.9%)
Insomnia
178 (2.84%)
Depression
143 (2.28%)
Nausea
133 (2.12%)
Anxiety
123 (1.96%)
Headache
113 (1.8%)
Dizziness
106 (1.69%)
Rash
98 (1.56%)
Tremor
89 (1.42%)
Convulsion
83 (1.32%)
Agitation
80 (1.28%)
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Fatigue
80 (1.28%)
Feeling Abnormal
78 (1.24%)
Completed Suicide
76 (1.21%)
Tinnitus
67 (1.07%)
Medication Error
58 (.93%)
Overdose
58 (.93%)
Pruritus
57 (.91%)
Urticaria
55 (.88%)
Irritability
54 (.86%)
Suicidal Ideation
53 (.85%)
Malaise
51 (.81%)
Somnolence
49 (.78%)
Crying
48 (.77%)
Dry Mouth
48 (.77%)
Alopecia
45 (.72%)
Vomiting
45 (.72%)
Diarrhoea
43 (.69%)
Disturbance In Attention
43 (.69%)
Drug Interaction
43 (.69%)
Asthenia
41 (.65%)
Drug Administration Error
41 (.65%)
Palpitations
40 (.64%)
Product Quality Issue
39 (.62%)
Dyspnoea
38 (.61%)
Blood Pressure Increased
37 (.59%)
Weight Increased
36 (.57%)
Adverse Event
34 (.54%)
Death
33 (.53%)
Amnesia
32 (.51%)
Confusional State
32 (.51%)
Grand Mal Convulsion
31 (.49%)
Memory Impairment
31 (.49%)
Pain
31 (.49%)
Paraesthesia
31 (.49%)
Loss Of Consciousness
30 (.48%)
Weight Decreased
30 (.48%)
Hyperhidrosis
29 (.46%)
Constipation
28 (.45%)
Condition Aggravated
27 (.43%)
Drug Exposure During Pregnancy
27 (.43%)
Heart Rate Increased
27 (.43%)
Therapeutic Response Unexpected
26 (.41%)
Wrong Technique In Drug Usage Proce...
26 (.41%)
Dysgeusia
25 (.4%)
Nervousness
25 (.4%)
Anger
24 (.38%)
Arthralgia
24 (.38%)
Feeling Jittery
24 (.38%)
Hypersensitivity
24 (.38%)
Panic Attack
24 (.38%)
Suicide Attempt
24 (.38%)
Therapeutic Response Unexpected Wit...
24 (.38%)
Aggression
23 (.37%)
Decreased Appetite
23 (.37%)
Hypertension
23 (.37%)
Mood Altered
22 (.35%)
Tachycardia
21 (.34%)
Abdominal Distension
20 (.32%)
Lethargy
20 (.32%)
Myalgia
20 (.32%)
Restlessness
20 (.32%)
Chest Pain
19 (.3%)
Fall
19 (.3%)
Hot Flush
19 (.3%)
Migraine
19 (.3%)
Abdominal Pain Upper
18 (.29%)
Dyskinesia
18 (.29%)
Ill-defined Disorder
18 (.29%)
Sleep Disorder
18 (.29%)
Emotional Disorder
17 (.27%)
Muscle Twitching
17 (.27%)
Therapeutic Response Decreased
17 (.27%)
Balance Disorder
16 (.26%)
Chest Discomfort
16 (.26%)
Drug Withdrawal Syndrome
16 (.26%)
Hallucination
16 (.26%)
Intentional Overdose
16 (.26%)
Mood Swings
16 (.26%)
Paranoia
16 (.26%)
Vision Blurred
16 (.26%)
Abnormal Behaviour
15 (.24%)
Hypoaesthesia
15 (.24%)
Depressed Mood
14 (.22%)
Flatulence
14 (.22%)
Mental Impairment
14 (.22%)
Product Substitution Issue
14 (.22%)
Psychomotor Hyperactivity
14 (.22%)
Thinking Abnormal
14 (.22%)
Abdominal Discomfort
13 (.21%)
Disorientation
13 (.21%)

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This graph shows the top adverse events submitted to the FDA for Wellbutrin Sr, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Wellbutrin Sr is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Wellbutrin Sr

What are the most common Wellbutrin Sr adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Wellbutrin Sr, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Wellbutrin Sr is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Wellbutrin Sr According to Those Reporting Adverse Events

Why are people taking Wellbutrin Sr, according to those reporting adverse events to the FDA?

Depression
1452
Drug Use For Unknown Indication
468
Product Used For Unknown Indication
117
Anxiety
73
Ill-defined Disorder
51
Bipolar Disorder
43
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Major Depression
41
Attention Deficit/hyperactivity Dis...
30
Smoking Cessation Therapy
20
Ex-smoker
20
Mood Swings
10
Fibromyalgia
9
Seasonal Affective Disorder
9
Bipolar I Disorder
6
Post-traumatic Stress Disorder
6
Depressive Symptom
5
Mental Disorder
5
Obsessive-compulsive Disorder
5
Multiple Sclerosis
5
Schizoaffective Disorder
5
Complicated Migraine
5
Disturbance In Attention
4
Affective Disorder
4
Migraine
4
Sexual Dysfunction
4
Dysthymic Disorder
4
Stress
4
Chronic Fatigue Syndrome
3
Postpartum Depression
3
Accidental Drug Intake By Child
3
Panic Attack
3
Eating Disorder
3
Bipolar Ii Disorder
3
Smoker
3
Insomnia
3
Ex-tobacco User
3
Premenstrual Syndrome
3
Death Of Relative
2
Anger
2
Hypertension
2
Panic Disorder
2
Emotional Disorder
2
Apathy
2
Menopausal Depression
2
Asthenia
2
Social Phobia
2
Antidepressant Therapy
2
Fatigue
2
Stress Symptoms
2
Anxiety Disorder
1
Tremor
1

Drug Labels

LabelLabelerEffective
WellbutrinsrGlaxoSmithKline LLC27-MAR-13

Wellbutrin Sr Case Reports

What Wellbutrin Sr safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Wellbutrin Sr. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

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