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YENTREVE

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Yentreve Adverse Events Reported to the FDA Over Time

How are Yentreve adverse event reports trending over time?

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

Most Common Yentreve Adverse Events Reported to the FDA

What are the most common Yentreve adverse events reported to the FDA?

Nausea
67 (4.11%)
Dizziness
59 (3.62%)
Fall
41 (2.52%)
Headache
34 (2.09%)
Blood Pressure Increased
30 (1.84%)
Vomiting
30 (1.84%)
Fatigue
25 (1.53%)
Syncope
23 (1.41%)
Tremor
23 (1.41%)
Hyponatraemia
21 (1.29%)
Confusional State
19 (1.17%)
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Hyperhidrosis
19 (1.17%)
Dry Mouth
17 (1.04%)
Feeling Abnormal
17 (1.04%)
Hypertension
17 (1.04%)
Anorexia
16 (.98%)
Loss Of Consciousness
16 (.98%)
Drug Withdrawal Syndrome
15 (.92%)
Insomnia
15 (.92%)
Somnolence
15 (.92%)
Anxiety
14 (.86%)
Asthenia
14 (.86%)
Malaise
14 (.86%)
Circulatory Collapse
12 (.74%)
Diarrhoea
11 (.67%)
Disorientation
11 (.67%)
Palpitations
11 (.67%)
Disturbance In Attention
10 (.61%)
Poor Quality Sleep
10 (.61%)
Vision Blurred
10 (.61%)
Abdominal Pain Upper
9 (.55%)
Constipation
9 (.55%)
Mydriasis
9 (.55%)
Restlessness
9 (.55%)
Suicidal Ideation
9 (.55%)
Tachycardia
9 (.55%)
Agitation
8 (.49%)
Drug Interaction
8 (.49%)
Haematoma
8 (.49%)
Body Temperature Increased
7 (.43%)
Cardiovascular Disorder
7 (.43%)
Convulsion
7 (.43%)
Depression
7 (.43%)
Drug Ineffective
7 (.43%)
Dysgeusia
7 (.43%)
Gait Disturbance
7 (.43%)
Hypokalaemia
7 (.43%)
Muscular Weakness
7 (.43%)
Blood Bilirubin Increased
6 (.37%)
Bradycardia
6 (.37%)
Chest Pain
6 (.37%)
Condition Aggravated
6 (.37%)
Elevated Mood
6 (.37%)
General Physical Health Deteriorati...
6 (.37%)
Hallucination
6 (.37%)
Heart Rate Increased
6 (.37%)
Hepatitis
6 (.37%)
Hypertensive Crisis
6 (.37%)
Nightmare
6 (.37%)
Urinary Tract Infection
6 (.37%)
Weight Decreased
6 (.37%)
Abdominal Pain Lower
5 (.31%)
Abdominal Rigidity
5 (.31%)
Anger
5 (.31%)
Aspartate Aminotransferase Increase...
5 (.31%)
Cardiac Failure
5 (.31%)
Chills
5 (.31%)
Decreased Appetite
5 (.31%)
Feeling Drunk
5 (.31%)
Gamma-glutamyltransferase Increased
5 (.31%)
Hepatic Steatosis
5 (.31%)
Hot Flush
5 (.31%)
Hypotension
5 (.31%)
Inappropriate Antidiuretic Hormone ...
5 (.31%)
Liver Function Test Abnormal
5 (.31%)
Loss Of Libido
5 (.31%)
Middle Insomnia
5 (.31%)
Muscle Spasms
5 (.31%)
Nervousness
5 (.31%)
Oedema Peripheral
5 (.31%)
Paraesthesia
5 (.31%)
Psychotic Disorder
5 (.31%)
Serotonin Syndrome
5 (.31%)
Sleep Disorder
5 (.31%)
Stress
5 (.31%)
Stupor
5 (.31%)
Supraventricular Extrasystoles
5 (.31%)
Tinnitus
5 (.31%)
Urinary Retention
5 (.31%)
Ventricular Extrasystoles
5 (.31%)
Vertigo
5 (.31%)
Weight Increased
5 (.31%)
White Blood Cell Count Increased
5 (.31%)
Accidental Drug Intake By Child
4 (.25%)
Amnesia
4 (.25%)
Angina Pectoris
4 (.25%)
Arrhythmia
4 (.25%)
Blood Glucose Increased
4 (.25%)
Blood Lactate Dehydrogenase Increas...
4 (.25%)
C-reactive Protein Increased
4 (.25%)
Cardiomegaly
4 (.25%)

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

What are the most common Yentreve adverse events reported to the FDA?

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

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

Stress Incontinence
124
Urinary Incontinence
78
Stress Urinary Incontinence
46
Incontinence
22
Depression
6
Bladder Disorder
3
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Post Procedural Complication
2
Drug Use For Unknown Indication
2
Transurethral Prostatectomy
1
Urinary Tract Disorder
1
Stress
1
Prostatectomy
1
Neuropathy Peripheral
1
Pain
1
Hypertonic Bladder
1
Urge Incontinence
1
Stress Symptoms
1
Micturition Urgency
1

Yentreve Case Reports

What Yentreve 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 Yentreve. 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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