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FORADIL

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Foradil Adverse Events Reported to the FDA Over Time

How are Foradil adverse event reports trending over time?

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

Most Common Foradil Adverse Events Reported to the FDA

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

Dyspnoea
398 (5.04%)
Asthma
205 (2.6%)
Death
165 (2.09%)
Cough
152 (1.93%)
Fatigue
144 (1.83%)
Pneumonia
143 (1.81%)
Malaise
128 (1.62%)
Hallucination
90 (1.14%)
Tremor
88 (1.12%)
Chronic Obstructive Pulmonary Disea...
79 (1%)
Drug Ineffective
76 (.96%)
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Influenza
74 (.94%)
Device Malfunction
73 (.93%)
Emphysema
73 (.93%)
Hypertension
72 (.91%)
Chest Pain
70 (.89%)
Blood Pressure Increased
67 (.85%)
Wheezing
63 (.8%)
Oedema Peripheral
62 (.79%)
Dizziness
61 (.77%)
Tachycardia
61 (.77%)
Bronchitis
59 (.75%)
Lung Disorder
59 (.75%)
Insomnia
56 (.71%)
Cardiac Disorder
55 (.7%)
Throat Irritation
51 (.65%)
Asthenia
48 (.61%)
Incorrect Route Of Drug Administrat...
46 (.58%)
Pain
46 (.58%)
Headache
45 (.57%)
Fall
44 (.56%)
Nausea
44 (.56%)
Condition Aggravated
43 (.55%)
Chest Discomfort
42 (.53%)
Dysphonia
41 (.52%)
Diabetes Mellitus
40 (.51%)
Pyrexia
40 (.51%)
Heart Rate Increased
39 (.49%)
Nasopharyngitis
39 (.49%)
Wrong Technique In Drug Usage Proce...
39 (.49%)
Depression
38 (.48%)
Respiratory Failure
36 (.46%)
Feeling Abnormal
35 (.44%)
Syncope
35 (.44%)
Vomiting
35 (.44%)
Hypersensitivity
34 (.43%)
Back Pain
33 (.42%)
Weight Increased
33 (.42%)
Bronchospasm
32 (.41%)
Cerebrovascular Accident
31 (.39%)
Gait Disturbance
31 (.39%)
Abdominal Pain Upper
30 (.38%)
Pruritus
30 (.38%)
Drug Exposure During Pregnancy
29 (.37%)
Medication Error
29 (.37%)
Memory Impairment
29 (.37%)
Somnolence
29 (.37%)
Weight Decreased
29 (.37%)
Arrhythmia
28 (.35%)
Lung Neoplasm Malignant
28 (.35%)
Anxiety
27 (.34%)
Palpitations
27 (.34%)
Cardiac Arrest
26 (.33%)
Confusional State
26 (.33%)
Infarction
26 (.33%)
Myocardial Infarction
26 (.33%)
Productive Cough
26 (.33%)
Incorrect Dose Administered
25 (.32%)
Muscle Spasms
25 (.32%)
Respiratory Disorder
25 (.32%)
Dry Mouth
24 (.3%)
Lung Infection
24 (.3%)
Pain In Extremity
24 (.3%)
Erythema
23 (.29%)
Sepsis
23 (.29%)
Dyspnoea Exertional
22 (.28%)
Hypoaesthesia
22 (.28%)
Hypotension
22 (.28%)
Blood Glucose Increased
21 (.27%)
Diarrhoea
20 (.25%)
Oxygen Saturation Decreased
20 (.25%)
Arthralgia
19 (.24%)
Speech Disorder
19 (.24%)
Abdominal Distension
18 (.23%)
Cardiomegaly
18 (.23%)
Gastrooesophageal Reflux Disease
18 (.23%)
Pulmonary Arterial Hypertension
18 (.23%)
Apparent Death
17 (.22%)
Atrial Fibrillation
17 (.22%)
Coma
17 (.22%)
Diverticulitis
17 (.22%)
Glaucoma
17 (.22%)
Increased Bronchial Secretion
17 (.22%)
Infection
17 (.22%)
Musculoskeletal Pain
17 (.22%)
Normal Newborn
17 (.22%)
Pleural Effusion
17 (.22%)
Thrombosis
17 (.22%)
Cardio-respiratory Arrest
16 (.2%)
Cataract
16 (.2%)
Epistaxis
16 (.2%)

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

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

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

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

Asthma
903
Chronic Obstructive Pulmonary Disea...
545
Drug Use For Unknown Indication
242
Product Used For Unknown Indication
224
Emphysema
159
Dyspnoea
106
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Bronchitis
93
Lung Disorder
45
Chronic Obstructive Airways Disease
27
Bronchospasm
22
Respiratory Disorder
19
Bronchitis Chronic
18
Cough
16
Hypersensitivity
13
Respiratory Failure
12
Pulmonary Fibrosis
10
Pneumonia
10
Fatigue
8
Ill-defined Disorder
8
Bronchial Disorder
6
Allergic Bronchitis
5
Hypertension
5
Bronchiectasis
4
Interstitial Lung Disease
4
Lung Neoplasm Malignant
4
Obstructive Airways Disorder
4
Depression
4
Silicosis
3
Wheezing
3
Pulmonary Eosinophilia
2
Respiration Abnormal
2
Inhalation Therapy
2
Embolism
2
Rhinitis
2
Pulmonary Embolism
2
Suicide Attempt
2
Pulmonary Congestion
2
Infection
2
Cardiopulmonary Failure
2
Sympathomimetic Effect
2
Musculoskeletal Pain
2
Fibrosis
2
Malignant Melanoma
2
Tobacco User
2
Seasonal Allergy
2
Asthma Exercise Induced
2
Multiple Allergies
2
Cellulitis
1
Haemorrhage
1
Cardiac Failure
1
Chronic Sinusitis
1

Drug Labels

LabelLabelerEffective
ForadilPhysicians Total Care, Inc.01-MAR-12
ForadilMerck Sharp & Dohme Corp.30-NOV-12

Foradil Case Reports

What Foradil 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 Foradil. 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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