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DALIRESP

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Daliresp Adverse Events Reported to the FDA Over Time

How are Daliresp adverse event reports trending over time?

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

Most Common Daliresp Adverse Events Reported to the FDA

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

Diarrhoea
51 (4.42%)
Insomnia
43 (3.73%)
Nausea
43 (3.73%)
Decreased Appetite
42 (3.64%)
Weight Decreased
37 (3.21%)
Dyspnoea
35 (3.03%)
Dizziness
32 (2.77%)
Headache
30 (2.6%)
Suicidal Ideation
26 (2.25%)
Tremor
26 (2.25%)
Anxiety
24 (2.08%)
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Back Pain
21 (1.82%)
Asthenia
17 (1.47%)
Vomiting
17 (1.47%)
Chest Pain
15 (1.3%)
Abdominal Pain
14 (1.21%)
Chronic Obstructive Pulmonary Disea...
14 (1.21%)
Off Label Use
14 (1.21%)
Condition Aggravated
13 (1.13%)
Influenza Like Illness
12 (1.04%)
Muscular Weakness
12 (1.04%)
Pain
12 (1.04%)
Frequent Bowel Movements
11 (.95%)
Death
10 (.87%)
Fatigue
10 (.87%)
Swelling Face
10 (.87%)
Mood Altered
9 (.78%)
Palpitations
9 (.78%)
Panic Attack
9 (.78%)
Pneumonia
9 (.78%)
Depression
8 (.69%)
Oedema Peripheral
8 (.69%)
Tachycardia
8 (.69%)
Abdominal Pain Upper
7 (.61%)
Atrial Fibrillation
7 (.61%)
Cold Sweat
7 (.61%)
Dehydration
7 (.61%)
Malaise
7 (.61%)
Rash
7 (.61%)
Blood Pressure Increased
6 (.52%)
Convulsion
6 (.52%)
Drug Interaction
6 (.52%)
Dry Mouth
6 (.52%)
Gastrooesophageal Reflux Disease
6 (.52%)
Hallucination
6 (.52%)
Heart Rate Increased
6 (.52%)
Pain In Extremity
6 (.52%)
Paraesthesia
6 (.52%)
Ventricular Tachycardia
6 (.52%)
Bronchitis
5 (.43%)
Delusion
5 (.43%)
Drug Ineffective
5 (.43%)
Dysgeusia
5 (.43%)
Fall
5 (.43%)
Mental Status Changes
5 (.43%)
Mood Swings
5 (.43%)
Pancreatitis Acute
5 (.43%)
Accidental Overdose
4 (.35%)
Ageusia
4 (.35%)
Anger
4 (.35%)
Arthralgia
4 (.35%)
Blood Glucose Increased
4 (.35%)
Eructation
4 (.35%)
Fear
4 (.35%)
Lethargy
4 (.35%)
Liver Function Test Abnormal
4 (.35%)
Muscle Spasms
4 (.35%)
Orthostatic Hypotension
4 (.35%)
Psychotic Disorder
4 (.35%)
Renal Failure Acute
4 (.35%)
Respiratory Tract Congestion
4 (.35%)
Abnormal Dreams
3 (.26%)
Arrhythmia
3 (.26%)
Cardiac Arrest
3 (.26%)
Depressed Mood
3 (.26%)
Dyspepsia
3 (.26%)
Heart Rate Decreased
3 (.26%)
Hypotension
3 (.26%)
International Normalised Ratio Incr...
3 (.26%)
Irritability
3 (.26%)
Melaena
3 (.26%)
Nervousness
3 (.26%)
Overdose
3 (.26%)
Oxygen Saturation Decreased
3 (.26%)
Presyncope
3 (.26%)
Pruritus
3 (.26%)
Suicide Attempt
3 (.26%)
Supraventricular Tachycardia
3 (.26%)
Syncope
3 (.26%)
Therapeutic Response Unexpected
3 (.26%)
Abdominal Discomfort
2 (.17%)
Abdominal Distension
2 (.17%)
Aggression
2 (.17%)
Agitation
2 (.17%)
Angioedema
2 (.17%)
Appendicitis
2 (.17%)
Blister
2 (.17%)
Blood Bilirubin Increased
2 (.17%)
Blood Glucose Decreased
2 (.17%)
Brain Scan Abnormal
2 (.17%)
Bruxism
2 (.17%)

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

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

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

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

Chronic Obstructive Pulmonary Disea...
201
Emphysema
12
Asthma
11
Bronchitis Chronic
6
Lung Disorder
5
Infective Exacerbation Of Chronic O...
2
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Respiratory Disorder
2
Condition Aggravated
1
Lung Infection
1
Dyspnoea
1
Upper Respiratory Tract Infection
1
Pneumonia
1
Pulmonary Oedema
1
Pulmonary Hypertension
1
Chronic Respiratory Failure
1
Respiration Abnormal
1
Obstructive Airways Disorder
1

Drug Labels

LabelLabelerEffective
DalirespForest Laboratories, Inc.21-FEB-13

Daliresp Case Reports

What Daliresp 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 Daliresp. 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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