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TOLTERODINE TARTRATE

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Tolterodine Tartrate Adverse Events Reported to the FDA Over Time

How are Tolterodine Tartrate adverse event reports trending over time?

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

Most Common Tolterodine Tartrate Adverse Events Reported to the FDA

What are the most common Tolterodine Tartrate adverse events reported to the FDA?

Drug Ineffective
1034 (6.24%)
Dry Mouth
570 (3.44%)
Constipation
325 (1.96%)
Pollakiuria
267 (1.61%)
Dizziness
256 (1.55%)
Urinary Incontinence
245 (1.48%)
Urinary Retention
176 (1.06%)
Drug Effect Decreased
167 (1.01%)
Fall
163 (.98%)
Vision Blurred
150 (.91%)
Condition Aggravated
145 (.88%)
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Headache
144 (.87%)
Death
138 (.83%)
Nocturia
138 (.83%)
Dysuria
136 (.82%)
Hypertension
134 (.81%)
Pain
133 (.8%)
Diarrhoea
126 (.76%)
Fatigue
124 (.75%)
Weight Decreased
122 (.74%)
Nausea
120 (.72%)
Confusional State
118 (.71%)
Insomnia
112 (.68%)
Drug Interaction
111 (.67%)
Oedema Peripheral
109 (.66%)
Abdominal Pain Upper
108 (.65%)
Bladder Disorder
105 (.63%)
Blood Pressure Increased
103 (.62%)
Urinary Tract Infection
102 (.62%)
Malaise
101 (.61%)
Micturition Urgency
94 (.57%)
Vomiting
92 (.56%)
Dry Eye
89 (.54%)
Hypertonic Bladder
86 (.52%)
Cystitis
82 (.49%)
Abdominal Pain
78 (.47%)
Somnolence
78 (.47%)
Weight Increased
78 (.47%)
Feeling Abnormal
77 (.46%)
Blood Cholesterol Increased
74 (.45%)
Rash
72 (.43%)
Loss Of Consciousness
71 (.43%)
Asthenia
67 (.4%)
Glaucoma
67 (.4%)
Cerebrovascular Accident
66 (.4%)
Hypersensitivity
66 (.4%)
Dyspnoea
65 (.39%)
Memory Impairment
65 (.39%)
Arthritis
64 (.39%)
Depression
64 (.39%)
Amnesia
63 (.38%)
Dehydration
61 (.37%)
Dyspepsia
61 (.37%)
Pain In Extremity
61 (.37%)
Pruritus
61 (.37%)
Chest Pain
57 (.34%)
Dysphagia
57 (.34%)
Back Pain
56 (.34%)
Incontinence
56 (.34%)
Muscle Spasms
54 (.33%)
Gastrooesophageal Reflux Disease
53 (.32%)
Heart Rate Increased
53 (.32%)
Tremor
53 (.32%)
Gait Disturbance
52 (.31%)
Blood Glucose Increased
50 (.3%)
Incorrect Dose Administered
50 (.3%)
Pneumonia
50 (.3%)
Cataract
49 (.3%)
Treatment Noncompliance
49 (.3%)
Arthralgia
48 (.29%)
Myocardial Infarction
48 (.29%)
Surgery
48 (.29%)
Abdominal Distension
47 (.28%)
Convulsion
44 (.27%)
Disorientation
43 (.26%)
Dry Throat
42 (.25%)
Body Height Decreased
41 (.25%)
Completed Suicide
41 (.25%)
Abasia
40 (.24%)
Abdominal Discomfort
40 (.24%)
Cardiac Disorder
40 (.24%)
Balance Disorder
39 (.24%)
Post Procedural Complication
39 (.24%)
Bladder Pain
38 (.23%)
Diabetes Mellitus
38 (.23%)
Sleep Disorder
37 (.22%)
Decreased Appetite
36 (.22%)
Fluid Retention
36 (.22%)
Hypotension
36 (.22%)
Hallucination
35 (.21%)
Road Traffic Accident
35 (.21%)
Unevaluable Event
35 (.21%)
Atrial Fibrillation
34 (.21%)
Flatulence
34 (.21%)
Anxiety
33 (.2%)
Visual Acuity Reduced
33 (.2%)
Joint Injury
32 (.19%)
Nervousness
32 (.19%)
Tachycardia
32 (.19%)
Bladder Operation
31 (.19%)
Bladder Spasm
31 (.19%)

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This graph shows the top adverse events submitted to the FDA for Tolterodine Tartrate, 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 Tolterodine Tartrate 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 Tolterodine Tartrate

What are the most common Tolterodine Tartrate adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Tolterodine Tartrate, 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 Tolterodine Tartrate 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 Tolterodine Tartrate According to Those Reporting Adverse Events

Why are people taking Tolterodine Tartrate, according to those reporting adverse events to the FDA?

Hypertonic Bladder
1358
Urinary Incontinence
726
Pollakiuria
523
Bladder Disorder
405
Drug Use For Unknown Indication
385
Incontinence
384
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Ill-defined Disorder
280
Product Used For Unknown Indication
264
Micturition Urgency
231
Bladder Spasm
87
Urge Incontinence
83
Nocturia
71
Neurogenic Bladder
58
Urinary Tract Disorder
50
Urinary Retention
38
Micturition Disorder
38
Dysuria
34
Bladder Irritation
28
Cystitis Interstitial
28
Stress Urinary Incontinence
27
Enuresis
25
Benign Prostatic Hyperplasia
23
Bladder Dysfunction
19
Automatic Bladder
18
Urinary Tract Infection
17
Renal Disorder
14
Prostatomegaly
14
Pain
12
Multiple Sclerosis
11
Bladder Pain
10
Prostatic Disorder
10
Stress Incontinence
9
Cystitis
9
Irritable Bowel Syndrome
8
Bladder Prolapse
8
Prostate Cancer
7
Investigation
6
Salivary Hypersecretion
5
Haematuria
4
Nephrolithiasis
4
Hypertension
4
Convulsion
4
Urine Flow Decreased
4
Polyuria
4
Prophylaxis
3
Bladder Operation
3
Bladder Discomfort
3
Bladder Cancer
3
Cerebral Infarction
3
Prostatism
3
Prostatic Specific Antigen Increase...
3

Drug Labels

LabelLabelerEffective
Tolterodine Tartrate Apotex Corp.15-FEB-11
Detrol LaPD-Rx Pharmaceuticals, Inc.28-SEP-11
Detrol LaLake Erie Medical & Surgical Supply DBA Quality Care Products LLC28-FEB-12
Tolterodine TartrateMylan Pharmaceuticals Inc.23-JUL-12
DetrolPharmacia and Upjohn Company14-AUG-12
Detrol LaPharmacia and Upjohn Company14-AUG-12
Tolterodine TartrateMylan Institutional Inc.07-SEP-12
Tolterodine TartrateTEVA Pharmaceuticals USA Inc18-SEP-12
Detrol LaCardinal Health20-MAR-13

Tolterodine Tartrate Case Reports

What Tolterodine Tartrate 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 Tolterodine Tartrate. 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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