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DITROPAN XL

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Ditropan Xl Adverse Events Reported to the FDA Over Time

How are Ditropan Xl adverse event reports trending over time?

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

Most Common Ditropan Xl Adverse Events Reported to the FDA

What are the most common Ditropan Xl adverse events reported to the FDA?

Drug Ineffective
21 (3.54%)
Dry Mouth
20 (3.37%)
Death
13 (2.19%)
Drug Interaction
13 (2.19%)
Hypertension
13 (2.19%)
Urinary Incontinence
11 (1.85%)
Fall
9 (1.52%)
Dry Throat
8 (1.35%)
Dyspnoea
8 (1.35%)
Lung Disorder
8 (1.35%)
Constipation
7 (1.18%)
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Loss Of Consciousness
7 (1.18%)
Macular Degeneration
7 (1.18%)
Confusional State
6 (1.01%)
Dehydration
6 (1.01%)
Intestinal Obstruction
6 (1.01%)
Medication Error
6 (1.01%)
Mental Status Changes
6 (1.01%)
Pollakiuria
6 (1.01%)
Tachycardia
6 (1.01%)
Urinary Tract Infection
6 (1.01%)
Amnesia
5 (.84%)
Asthenia
5 (.84%)
Chest Pain
5 (.84%)
Circulatory Collapse
5 (.84%)
Decreased Appetite
5 (.84%)
Product Quality Issue
5 (.84%)
Pyrexia
5 (.84%)
Transient Ischaemic Attack
5 (.84%)
Alanine Aminotransferase Increased
4 (.67%)
Aspartate Aminotransferase Increase...
4 (.67%)
Balance Disorder
4 (.67%)
Blood Pressure Decreased
4 (.67%)
Cholelithiasis
4 (.67%)
Dementia
4 (.67%)
Dysuria
4 (.67%)
Gait Disturbance
4 (.67%)
Nausea
4 (.67%)
Nocturia
4 (.67%)
Oedema Peripheral
4 (.67%)
Oesophageal Carcinoma
4 (.67%)
Pruritus
4 (.67%)
Vision Blurred
4 (.67%)
Weight Increased
4 (.67%)
Abdominal Mass
3 (.51%)
Abdominal Pain
3 (.51%)
Acne
3 (.51%)
Bacterial Infection
3 (.51%)
Blood Alkaline Phosphatase Increase...
3 (.51%)
Blood Cholesterol Increased
3 (.51%)
Cerebral Atrophy
3 (.51%)
Condition Aggravated
3 (.51%)
Dental Caries
3 (.51%)
Diarrhoea
3 (.51%)
Disease Progression
3 (.51%)
Dry Skin
3 (.51%)
Fatigue
3 (.51%)
Fluid Retention
3 (.51%)
Glaucoma
3 (.51%)
Headache
3 (.51%)
Intervertebral Disc Protrusion
3 (.51%)
Large Intestine Perforation
3 (.51%)
Liver Disorder
3 (.51%)
Myocardial Infarction
3 (.51%)
Obstructive Uropathy
3 (.51%)
Pain
3 (.51%)
Rectal Haemorrhage
3 (.51%)
Renal Haemorrhage
3 (.51%)
Therapeutic Response Decreased
3 (.51%)
Vomiting
3 (.51%)
Weight Decreased
3 (.51%)
Wheezing
3 (.51%)
Abnormal Faeces
2 (.34%)
Abortion Spontaneous
2 (.34%)
Ammonia Increased
2 (.34%)
Anorexia
2 (.34%)
Aphasia
2 (.34%)
Appendicitis Perforated
2 (.34%)
Arthropathy
2 (.34%)
Atrial Fibrillation
2 (.34%)
Bile Duct Stone
2 (.34%)
Biliary Tract Disorder
2 (.34%)
Bladder Pain
2 (.34%)
Bladder Prolapse
2 (.34%)
Bladder Spasm
2 (.34%)
Blood Glucose Decreased
2 (.34%)
Blood Glucose Increased
2 (.34%)
Blood Potassium Decreased
2 (.34%)
Blood Urine Present
2 (.34%)
Breast Cancer Metastatic
2 (.34%)
Cardiac Failure
2 (.34%)
Cerebrovascular Accident
2 (.34%)
Chromaturia
2 (.34%)
Cognitive Disorder
2 (.34%)
Cystitis
2 (.34%)
Disorientation
2 (.34%)
Drug Administered At Inappropriate ...
2 (.34%)
Drug Exposure During Pregnancy
2 (.34%)
Dyskinesia
2 (.34%)
Encephalopathy
2 (.34%)
Eye Pain
2 (.34%)

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This graph shows the top adverse events submitted to the FDA for Ditropan Xl, 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 Ditropan Xl 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 Ditropan Xl

What are the most common Ditropan Xl adverse events reported to the FDA?

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

Why are people taking Ditropan Xl, according to those reporting adverse events to the FDA?

Drug Use For Unknown Indication
54
Urinary Incontinence
47
Hypertonic Bladder
41
Incontinence
26
Bladder Disorder
26
Pollakiuria
25
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Product Used For Unknown Indication
24
Micturition Urgency
5
Urinary Tract Disorder
5
Urinary Tract Infection
5
Cystitis Interstitial
5
Benign Prostatic Hyperplasia
4
Neurogenic Bladder
4
Stress Incontinence
3
Ill-defined Disorder
3
Urge Incontinence
2
Urine Abnormality
2
Enuresis
2
Bladder Spasm
2
Cystitis
1
Bladder Cancer
1
Nocturia
1
Urinary Retention
1
Bladder Dysfunction
1
Stress Urinary Incontinence
1

Drug Labels

LabelLabelerEffective
DitropanxlPhysicians Total Care, Inc.16-FEB-12
DitropanxlJanssen Pharmaceuticals, Inc.26-NOV-12

Ditropan Xl Case Reports

What Ditropan Xl 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 Ditropan Xl. 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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