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DOPAMINE

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Dopamine Adverse Events Reported to the FDA Over Time

How are Dopamine adverse event reports trending over time?

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

Most Common Dopamine Adverse Events Reported to the FDA

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

Hypotension
37 (3.02%)
Blood Pressure Decreased
36 (2.93%)
Cardiac Arrest
36 (2.93%)
Medication Error
34 (2.77%)
Drug Ineffective
21 (1.71%)
Metabolic Acidosis
19 (1.55%)
Acute Respiratory Distress Syndrome
16 (1.3%)
Device Failure
16 (1.3%)
Ventricular Tachycardia
15 (1.22%)
Convulsion
14 (1.14%)
Device Malfunction
14 (1.14%)
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Drug Interaction
14 (1.14%)
Bradycardia
12 (.98%)
Incorrect Dose Administered
12 (.98%)
Renal Failure Acute
11 (.9%)
Multi-organ Failure
10 (.81%)
Death
9 (.73%)
Electrocardiogram St Segment Elevat...
9 (.73%)
Tachycardia
9 (.73%)
Arteriospasm Coronary
8 (.65%)
Condition Aggravated
8 (.65%)
Hypertension
8 (.65%)
Hypoxia
8 (.65%)
Propofol Infusion Syndrome
8 (.65%)
Wrong Drug Administered
8 (.65%)
Atrial Fibrillation
7 (.57%)
Cardio-respiratory Arrest
7 (.57%)
Circumstance Or Information Capable...
7 (.57%)
Drug Administration Error
7 (.57%)
Haemodynamic Instability
7 (.57%)
Loss Of Consciousness
7 (.57%)
Pneumonia
7 (.57%)
Pulse Absent
7 (.57%)
Pyrexia
7 (.57%)
Ventricular Fibrillation
7 (.57%)
Anuria
6 (.49%)
Blood Pressure Systolic Decreased
6 (.49%)
General Physical Health Deteriorati...
6 (.49%)
Myocardial Ischaemia
6 (.49%)
Renal Failure
6 (.49%)
Torsade De Pointes
6 (.49%)
Atrial Tachycardia
5 (.41%)
Blood Pressure Increased
5 (.41%)
Coma
5 (.41%)
Confusional State
5 (.41%)
Drug Dispensing Error
5 (.41%)
Drug Exposure During Pregnancy
5 (.41%)
Heart Rate Increased
5 (.41%)
Hyperkalaemia
5 (.41%)
Hypernatraemia
5 (.41%)
Hypoglycaemia
5 (.41%)
Oxygen Saturation Decreased
5 (.41%)
Oxygen Saturation Increased
5 (.41%)
Pericardial Effusion
5 (.41%)
Pneumothorax
5 (.41%)
Respiratory Failure
5 (.41%)
Sepsis
5 (.41%)
Supraventricular Tachycardia
5 (.41%)
Tachyarrhythmia
5 (.41%)
Vasoconstriction
5 (.41%)
Abdominal Distension
4 (.33%)
Alanine Aminotransferase Increased
4 (.33%)
Anaemia
4 (.33%)
Aspartate Aminotransferase Increase...
4 (.33%)
Cardiac Failure
4 (.33%)
Cardiogenic Shock
4 (.33%)
Depressed Level Of Consciousness
4 (.33%)
Device Leakage
4 (.33%)
Drug Toxicity
4 (.33%)
Extrasystoles
4 (.33%)
Extravasation
4 (.33%)
Haemoglobin Decreased
4 (.33%)
Nausea
4 (.33%)
Renal Impairment
4 (.33%)
Sinus Tachycardia
4 (.33%)
Thirst
4 (.33%)
Air Embolism
3 (.24%)
Anaphylactic Shock
3 (.24%)
Apnoea
3 (.24%)
Arrhythmia Supraventricular
3 (.24%)
Atrioventricular Block First Degree
3 (.24%)
Atrioventricular Block Second Degre...
3 (.24%)
Bacteraemia
3 (.24%)
Blood Chloride Decreased
3 (.24%)
Blood Pressure Abnormal
3 (.24%)
Blood Pressure Immeasurable
3 (.24%)
Brachial Plexus Injury
3 (.24%)
Choreoathetosis
3 (.24%)
Circulatory Collapse
3 (.24%)
Congenital Hypothyroidism
3 (.24%)
Depression
3 (.24%)
Device Occlusion
3 (.24%)
Diarrhoea
3 (.24%)
Drug Effect Decreased
3 (.24%)
Dyspnoea
3 (.24%)
Electrocardiogram Qt Prolonged
3 (.24%)
Encephalitis
3 (.24%)
Erythema
3 (.24%)
Flushing
3 (.24%)
Gangrene
3 (.24%)
Heart Sounds Abnormal
3 (.24%)

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

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

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

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

Product Used For Unknown Indication
241
Drug Use For Unknown Indication
183
Hypotension
106
Cardiac Failure
45
Septic Shock
34
Blood Pressure Decreased
32
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Blood Pressure Management
28
Shock
27
Blood Pressure
15
Circulatory Collapse
12
Cardiogenic Shock
11
Ill-defined Disorder
10
Haemodynamic Instability
10
Parkinsons Disease
9
Polyuria
9
Prophylaxis
8
Blood Pressure Increased
8
Blood Antidiuretic Hormone
8
Anaesthesia
7
Cardiac Disorder
7
Cardiovascular Disorder
6
Cardiac Operation
6
General Anaesthesia
5
Bradycardia
5
Oliguria
5
Pulmonary Oedema
5
Pneumonia
5
Renal Failure
5
Supportive Care
4
Blood Pressure Abnormal
4
Sepsis
4
Staphylococcal Sepsis
4
Urinary Retention
3
Pulmonary Hypertension
3
Myelodysplastic Syndrome
3
Blood Pressure Fluctuation
3
Hypertension
3
Positive Cardiac Inotropic Effect
3
Cardiac Index
3
Vasopressive Therapy
3
Ventricular Fibrillation
3
Cerebral Disorder
3
Cardiac Failure Congestive
3
Catheterisation Cardiac
3
Vasodilatation
3
Adrenocortical Insufficiency Acute
3
Neutropenia
3
Cardiac Arrest
2
Weaning Failure
2
Cardio-respiratory Arrest
2
Blood Pressure Systolic
2

Drug Labels

LabelLabelerEffective
Dopamine Hydrochloride And DextroseHospira, Inc.28-JUN-10
DopamineApotheca Company29-JUN-10
Dopamine HydrochlorideGeneral Injectables & Vaccines, Inc03-AUG-10
Dopamine HydrochlorideHospira, Inc.26-JUL-11
DopamineApotheca Company08-AUG-11
Dopamine HclAmerican Regent, Inc.08-OCT-11
Dopamine Hydrochloride And DextroseBaxter Healthcare Corporation23-JAN-12
DopamineGeneral Injectables & Vaccines, Inc24-JAN-12
Dopamine HydrochlorideGeneral Injectables & Vaccines, Inc24-JAN-12
Dopamine HydrochlorideCardinal Health09-APR-12
DopamineBioActive Nutritional, Inc.01-MAY-12
Dopamine Hydrochloride And DextroseHospira, Inc.10-JUL-12
DopamineDeseret Biologicals, Inc.14-NOV-12

Dopamine Case Reports

What Dopamine 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 Dopamine. 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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