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PROPULSID

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Propulsid Adverse Events Reported to the FDA Over Time

How are Propulsid adverse event reports trending over time?

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

Most Common Propulsid Adverse Events Reported to the FDA

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

Electrocardiogram Qt Prolonged
114 (13.27%)
Death
26 (3.03%)
Dehydration
14 (1.63%)
Vomiting
14 (1.63%)
Renal Failure
12 (1.4%)
Cerebrovascular Accident
11 (1.28%)
Mental Disorder
10 (1.16%)
Nausea
10 (1.16%)
Pollakiuria
10 (1.16%)
Atrioventricular Block First Degree
9 (1.05%)
Decreased Appetite
9 (1.05%)
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Drug Ineffective
9 (1.05%)
Malaise
9 (1.05%)
Aggression
8 (.93%)
Diarrhoea
8 (.93%)
Dyspnoea
8 (.93%)
Palpitations
8 (.93%)
Pneumonia
8 (.93%)
Respiratory Failure
8 (.93%)
Cardiac Disorder
7 (.81%)
Electrolyte Imbalance
7 (.81%)
Gastrointestinal Obstruction
7 (.81%)
Tachycardia
7 (.81%)
Anorexia
6 (.7%)
Cachexia
6 (.7%)
Electrocardiogram T Wave Amplitude ...
6 (.7%)
Gastrointestinal Disorder
6 (.7%)
Pleural Effusion
6 (.7%)
Post Procedural Complication
6 (.7%)
Pyrexia
6 (.7%)
Adhesion
5 (.58%)
Arrhythmia
5 (.58%)
Bundle Branch Block Right
5 (.58%)
Condition Aggravated
5 (.58%)
Gastric Cancer
5 (.58%)
Hypertension
5 (.58%)
Impaired Gastric Emptying
5 (.58%)
Intestinal Obstruction
5 (.58%)
Respiratory Disorder
5 (.58%)
Sinus Tachycardia
5 (.58%)
Spinal Fracture
5 (.58%)
Sudden Infant Death Syndrome
5 (.58%)
Surgery
5 (.58%)
Urticaria
5 (.58%)
Ventricular Tachycardia
5 (.58%)
Bradypnoea
4 (.47%)
C-reactive Protein Increased
4 (.47%)
Cholecystitis Acute
4 (.47%)
Constipation
4 (.47%)
Depression
4 (.47%)
Escherichia Infection
4 (.47%)
Hirsutism
4 (.47%)
Malignant Neoplasm Progression
4 (.47%)
Myocardial Infarction
4 (.47%)
Pneumonia Legionella
4 (.47%)
Pulmonary Oedema
4 (.47%)
Renal Failure Acute
4 (.47%)
Ruptured Cerebral Aneurysm
4 (.47%)
Ventricular Extrasystoles
4 (.47%)
Abdominal Pain Upper
3 (.35%)
Anxiety
3 (.35%)
Apnoea
3 (.35%)
Atrial Fibrillation
3 (.35%)
Blood Calcium Increased
3 (.35%)
Blood Magnesium Increased
3 (.35%)
Blood Pressure Decreased
3 (.35%)
Bronchopneumopathy
3 (.35%)
Cardiac Failure Congestive
3 (.35%)
Chest Pain
3 (.35%)
Confusional State
3 (.35%)
Cyanosis
3 (.35%)
Electrocardiogram T Wave Abnormal
3 (.35%)
Fall
3 (.35%)
Fatigue
3 (.35%)
Food Intolerance
3 (.35%)
Gastrooesophageal Reflux Disease
3 (.35%)
Headache
3 (.35%)
Heart Rate Increased
3 (.35%)
Heart Rate Irregular
3 (.35%)
Hypertrophic Cardiomyopathy
3 (.35%)
Infarction
3 (.35%)
Loss Of Consciousness
3 (.35%)
Ovarian Cyst
3 (.35%)
Pneumonia Aspiration
3 (.35%)
Porphyria
3 (.35%)
Screaming
3 (.35%)
Sepsis
3 (.35%)
Shock
3 (.35%)
Syncope
3 (.35%)
Varicose Ulceration
3 (.35%)
Abdominal Adhesions
2 (.23%)
Abdominal Pain
2 (.23%)
Acute Myocardial Infarction
2 (.23%)
Alopecia
2 (.23%)
Androgens Abnormal
2 (.23%)
Aneurysm Ruptured
2 (.23%)
Blood Follicle Stimulating Hormone ...
2 (.23%)
Blood Potassium Decreased
2 (.23%)
Blood Potassium Increased
2 (.23%)
Bradycardia
2 (.23%)
Bronchitis
2 (.23%)

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

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

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

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

Gastrooesophageal Reflux Disease
194
Impaired Gastric Emptying
54
Diabetic Gastroparesis
50
Drug Use For Unknown Indication
44
Gastrointestinal Motility Disorder
36
Gastrointestinal Disorder
22
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Dyspepsia
15
Product Used For Unknown Indication
10
Gastric Disorder
9
Gastritis
6
Obstruction
5
Oesophageal Disorder
5
Oesophagitis
5
Presbyoesophagus
4
Hiatus Hernia
4
Mobility Decreased
4
Abdominal Discomfort
4
Encephalopathy
4
Constipation
3
Vomiting
3
Scleroderma
3
Reflux Oesophagitis
3
Aspiration
2
Infantile Spasms
2
Ill-defined Disorder
2
Bronchial Hyperactivity
2
Metastases To Stomach
2
Abdominal Pain
2
Abdominal Pain Upper
2
Oesophageal Anastomosis
2
Ulcer
2
Diabetes Mellitus
1
Dyskinesia Oesophageal
1
Eating Disorder
1
Unevaluable Event
1
Pneumonia Aspiration
1
Barretts Oesophagus
1
Flatulence
1
Burn Of Internal Organs
1

Propulsid Case Reports

What Propulsid 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 Propulsid. 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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