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FLIXOTIDE

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Flixotide Adverse Events Reported to the FDA Over Time

How are Flixotide adverse event reports trending over time?

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

Most Common Flixotide Adverse Events Reported to the FDA

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

Asthma
55 (4.9%)
Dyspnoea
24 (2.14%)
Cough
22 (1.96%)
Drug Ineffective
19 (1.69%)
Product Quality Issue
19 (1.69%)
Pyrexia
17 (1.52%)
Asthenia
16 (1.43%)
Pain In Extremity
16 (1.43%)
Malaise
13 (1.16%)
Asthmatic Crisis
12 (1.07%)
Chest Pain
11 (.98%)
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Adrenal Suppression
10 (.89%)
Blood Cortisol Decreased
10 (.89%)
Pneumonia
10 (.89%)
Adrenal Insufficiency
9 (.8%)
Irritability
9 (.8%)
Peritonitis Bacterial
9 (.8%)
Pruritus
9 (.8%)
Tachycardia
9 (.8%)
Back Pain
8 (.71%)
Cardiac Failure
8 (.71%)
Drug Interaction
8 (.71%)
Fatigue
8 (.71%)
Headache
8 (.71%)
Muscular Weakness
8 (.71%)
Vomiting
8 (.71%)
Weight Decreased
8 (.71%)
Escherichia Infection
7 (.62%)
Hepatitis Cholestatic
7 (.62%)
Hypercorticoidism
7 (.62%)
Jaundice
7 (.62%)
Aphonia
6 (.53%)
Chest Discomfort
6 (.53%)
Hyperaesthesia
6 (.53%)
Hypersensitivity
6 (.53%)
Medication Error
6 (.53%)
Myalgia
6 (.53%)
Osteonecrosis
6 (.53%)
Pancreatitis Acute
6 (.53%)
Peritonitis
6 (.53%)
Rhinorrhoea
6 (.53%)
Abasia
5 (.45%)
Abnormal Behaviour
5 (.45%)
Aggression
5 (.45%)
Agitation
5 (.45%)
Anaemia
5 (.45%)
Apathy
5 (.45%)
Blood Bilirubin Increased
5 (.45%)
Bronchospasm
5 (.45%)
Disorientation
5 (.45%)
Encephalitis
5 (.45%)
Oedema Peripheral
5 (.45%)
Overdose
5 (.45%)
Retinopathy
5 (.45%)
Abdominal Pain
4 (.36%)
Accidental Overdose
4 (.36%)
Allergic Granulomatous Angiitis
4 (.36%)
Angina Pectoris
4 (.36%)
Blood Alkaline Phosphatase Increase...
4 (.36%)
Condition Aggravated
4 (.36%)
Cryoglobulinaemia
4 (.36%)
Cutaneous Vasculitis
4 (.36%)
Depressed Level Of Consciousness
4 (.36%)
Drug Administration Error
4 (.36%)
Dysgeusia
4 (.36%)
Dysphagia
4 (.36%)
Dysphonia
4 (.36%)
Ecchymosis
4 (.36%)
Fall
4 (.36%)
Gamma-glutamyltransferase Increased
4 (.36%)
General Physical Health Deteriorati...
4 (.36%)
Ill-defined Disorder
4 (.36%)
Mydriasis
4 (.36%)
Nasopharyngitis
4 (.36%)
Oral Candidiasis
4 (.36%)
Renal Tubular Disorder
4 (.36%)
Toe Amputation
4 (.36%)
Tooth Disorder
4 (.36%)
Wheezing
4 (.36%)
Adrenocortical Insufficiency Acute
3 (.27%)
Aphthous Stomatitis
3 (.27%)
Arthralgia
3 (.27%)
Atrioventricular Block Complete
3 (.27%)
Atrioventricular Block Second Degre...
3 (.27%)
Blood Corticotrophin Abnormal
3 (.27%)
Bronchiectasis
3 (.27%)
Confusional State
3 (.27%)
Conjunctival Disorder
3 (.27%)
Conjunctivitis Infective
3 (.27%)
Convulsion
3 (.27%)
Cyanosis
3 (.27%)
Disturbance In Attention
3 (.27%)
Drug Dependence
3 (.27%)
Drug Exposure During Pregnancy
3 (.27%)
Drug Intolerance
3 (.27%)
Dry Throat
3 (.27%)
Eosinophilia
3 (.27%)
Eye Disorder
3 (.27%)
Gout
3 (.27%)
Hyperhidrosis
3 (.27%)
Hyperthermia
3 (.27%)

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

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

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

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

Asthma
230
Drug Use For Unknown Indication
84
Chronic Obstructive Pulmonary Disea...
43
Product Used For Unknown Indication
23
Bronchitis
6
Unevaluable Event
5
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Rhinitis Allergic
4
Hypersensitivity
3
Bronchiolitis
3
Asthma Prophylaxis
3
Ill-defined Disorder
2
Cough
2
Emphysema
2
Dyspnoea
2
Accidental Drug Intake By Child
2
Respiratory Disorder
2
Laryngitis
2
Obstructive Airways Disorder
2
Rales
2
Prophylaxis
1
Condition Aggravated
1
Bronchopneumopathy
1
Eye Swelling
1
Chronic Obstructive Airways Disease
1
Pseudocroup
1
Bronchiectasis
1
Pharyngitis
1
Pneumonia
1
Pharyngotonsillitis
1
Allergic Bronchitis
1
Influenza
1
Bronchitis Chronic
1
Bronchostenosis
1
Dysphonia
1
Bronchial Obstruction
1
Asthma Exacerbation Prophylaxis
1

Flixotide Case Reports

What Flixotide 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 Flixotide. 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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