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ASMANEX TWISTHALER

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Asmanex Twisthaler Adverse Events Reported to the FDA Over Time

How are Asmanex Twisthaler adverse event reports trending over time?

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

Most Common Asmanex Twisthaler Adverse Events Reported to the FDA

What are the most common Asmanex Twisthaler adverse events reported to the FDA?

Product Quality Issue
65 (5.01%)
Drug Dose Omission
64 (4.93%)
Dyspnoea
37 (2.85%)
No Adverse Event
34 (2.62%)
Asthma
30 (2.31%)
Condition Aggravated
20 (1.54%)
Drug Ineffective
20 (1.54%)
Cough
19 (1.46%)
Device Malfunction
18 (1.39%)
Wheezing
17 (1.31%)
Chest Pain
13 (1%)
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Off Label Use
12 (.93%)
Swollen Tongue
12 (.93%)
Death
11 (.85%)
Loss Of Consciousness
11 (.85%)
Oropharyngeal Pain
11 (.85%)
Chest Discomfort
10 (.77%)
Device Failure
10 (.77%)
Nausea
10 (.77%)
Palpitations
10 (.77%)
Rash
10 (.77%)
Abdominal Pain
9 (.69%)
Headache
9 (.69%)
Tremor
9 (.69%)
Aphonia
8 (.62%)
Asthenia
8 (.62%)
Candidiasis
8 (.62%)
Drug Hypersensitivity
8 (.62%)
Epistaxis
8 (.62%)
Fatigue
8 (.62%)
Incorrect Dose Administered
8 (.62%)
Insomnia
8 (.62%)
Pain
8 (.62%)
Convulsion
7 (.54%)
Depression
7 (.54%)
Dizziness
7 (.54%)
Pain In Extremity
7 (.54%)
Pneumonia
7 (.54%)
Throat Tightness
7 (.54%)
Urticaria
7 (.54%)
Weight Decreased
7 (.54%)
Anaphylactic Reaction
6 (.46%)
Blindness Unilateral
6 (.46%)
Dysphonia
6 (.46%)
Malaise
6 (.46%)
Medical Device Complication
6 (.46%)
Myocardial Infarction
6 (.46%)
Throat Irritation
6 (.46%)
Blood Pressure Increased
5 (.39%)
Burning Sensation
5 (.39%)
Fall
5 (.39%)
Haemoptysis
5 (.39%)
Hypersensitivity
5 (.39%)
Lip Swelling
5 (.39%)
Nervousness
5 (.39%)
Oedema Peripheral
5 (.39%)
Overdose
5 (.39%)
Paraesthesia
5 (.39%)
Staphylococcal Infection
5 (.39%)
Subcutaneous Abscess
5 (.39%)
Syncope
5 (.39%)
Vision Blurred
5 (.39%)
Vomiting
5 (.39%)
Weight Increased
5 (.39%)
Accidental Exposure
4 (.31%)
Aggression
4 (.31%)
Anxiety
4 (.31%)
Arthralgia
4 (.31%)
Bronchopulmonary Aspergillosis
4 (.31%)
Cardiac Disorder
4 (.31%)
Cardiac Failure Congestive
4 (.31%)
Diarrhoea
4 (.31%)
Dysgeusia
4 (.31%)
Feeling Abnormal
4 (.31%)
Gait Disturbance
4 (.31%)
Gastrooesophageal Reflux Disease
4 (.31%)
Glossodynia
4 (.31%)
Hot Flush
4 (.31%)
Hypertension
4 (.31%)
Hypoaesthesia
4 (.31%)
Lung Infection
4 (.31%)
Mouth Ulceration
4 (.31%)
Myalgia
4 (.31%)
Myopathy
4 (.31%)
Oral Pain
4 (.31%)
Paranoia
4 (.31%)
Product Contamination
4 (.31%)
Pruritus
4 (.31%)
Rash Erythematous
4 (.31%)
Sleep Disorder
4 (.31%)
Suicidal Ideation
4 (.31%)
Swelling Face
4 (.31%)
Transient Ischaemic Attack
4 (.31%)
Unevaluable Event
4 (.31%)
Wrong Technique In Drug Usage Proce...
4 (.31%)
Anorexia
3 (.23%)
Anosmia
3 (.23%)
Bronchospasm
3 (.23%)
Cataract
3 (.23%)
Cerebrovascular Accident
3 (.23%)
Chronic Obstructive Pulmonary Disea...
3 (.23%)

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

What are the most common Asmanex Twisthaler adverse events reported to the FDA?

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

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

Asthma
364
Drug Use For Unknown Indication
173
Chronic Obstructive Pulmonary Disea...
122
Product Used For Unknown Indication
95
Emphysema
15
Bronchitis
10
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Dyspnoea
9
Hypersensitivity
7
Lung Disorder
4
Respiratory Disorder
4
Chest Discomfort
4
Idiopathic Pulmonary Fibrosis
2
Bronchiectasis
2
Pneumoconiosis
2
Cough
2
Asthma Exercise Induced
1
Seasonal Allergy
1
Prophylaxis
1
Tremor
1
Sinusitis
1
Bronchial Hyperreactivity
1
Acute Lung Injury
1
Oesophagitis
1
Pulmonary Congestion
1
Pneumonia
1
Antiinflammatory Therapy
1
Pulmonary Fibrosis
1
Spirometry Abnormal
1
Multiple Allergies
1
Inflammation
1

Drug Labels

LabelLabelerEffective
AsmanexPhysicians Total Care, Inc.13-OCT-10
AsmanexMerck Sharp & Dohme Corp.12-DEC-12

Asmanex Twisthaler Case Reports

What Asmanex Twisthaler 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 Asmanex Twisthaler. 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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