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BECLOMETHASONE DIPROPIONATE

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Beclomethasone Dipropionate Adverse Events Reported to the FDA Over Time

How are Beclomethasone Dipropionate adverse event reports trending over time?

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

Most Common Beclomethasone Dipropionate Adverse Events Reported to the FDA

What are the most common Beclomethasone Dipropionate adverse events reported to the FDA?

Drug Ineffective
97 (3.68%)
Dyspnoea
64 (2.43%)
Asthma
57 (2.16%)
Drug Exposure During Pregnancy
45 (1.71%)
Mesothelioma
28 (1.06%)
Aortic Dissection
27 (1.02%)
Chronic Obstructive Pulmonary Disea...
24 (.91%)
Cough
22 (.83%)
Hypospadias
22 (.83%)
Headache
21 (.8%)
Malaise
21 (.8%)
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Product Quality Issue
21 (.8%)
Pruritus
21 (.8%)
Joint Contracture
20 (.76%)
Lung Neoplasm Malignant
20 (.76%)
Anosmia
19 (.72%)
Urticaria
19 (.72%)
Skull Malformation
18 (.68%)
Dizziness
17 (.65%)
Epistaxis
17 (.65%)
Nasal Discomfort
17 (.65%)
Pulmonary Congestion
17 (.65%)
Foetal Growth Retardation
16 (.61%)
Hypertension
15 (.57%)
Insomnia
15 (.57%)
Chest Pain
14 (.53%)
Condition Aggravated
14 (.53%)
Congenital Foot Malformation
14 (.53%)
Pneumonia
14 (.53%)
Anuria
13 (.49%)
Arthralgia
13 (.49%)
Hypersensitivity
13 (.49%)
Neonatal Hypotension
13 (.49%)
Oligohydramnios
13 (.49%)
Bladder Agenesis
12 (.46%)
Erythema
12 (.46%)
Kidney Malformation
12 (.46%)
Multiple Congenital Abnormalities
12 (.46%)
Oedema Peripheral
12 (.46%)
Premature Baby
12 (.46%)
Rash
12 (.46%)
Chest Discomfort
11 (.42%)
Nausea
11 (.42%)
Osteonecrosis
11 (.42%)
Vomiting
11 (.42%)
Antepartum Haemorrhage
10 (.38%)
Cranial Sutures Widening
10 (.38%)
Dysgeusia
10 (.38%)
Face Oedema
10 (.38%)
Migraine
10 (.38%)
Pyrexia
10 (.38%)
Single Functional Kidney
10 (.38%)
Anxiety
9 (.34%)
Drug Interaction
9 (.34%)
Hypotension
9 (.34%)
Maternal Drugs Affecting Foetus
9 (.34%)
Nasal Congestion
9 (.34%)
Throat Irritation
9 (.34%)
Vision Blurred
9 (.34%)
Bronchospasm
8 (.3%)
Diarrhoea
8 (.3%)
Fatigue
8 (.3%)
Foetal Heart Rate Abnormal
8 (.3%)
Lung Infection
8 (.3%)
Muscle Spasms
8 (.3%)
Oral Candidiasis
8 (.3%)
Palpitations
8 (.3%)
Talipes
8 (.3%)
Weight Increased
8 (.3%)
Abortion Induced
7 (.27%)
Ageusia
7 (.27%)
Agitation
7 (.27%)
Aphasia
7 (.27%)
Arrhythmia
7 (.27%)
Atrial Fibrillation
7 (.27%)
Blood Glucose Increased
7 (.27%)
Blood Pressure Increased
7 (.27%)
Cushingoid
7 (.27%)
Dry Mouth
7 (.27%)
Dysphonia
7 (.27%)
Dyspnoea Exertional
7 (.27%)
Gait Disturbance
7 (.27%)
Growth Retardation
7 (.27%)
Hypoaesthesia
7 (.27%)
Kidney Enlargement
7 (.27%)
Muscular Weakness
7 (.27%)
Myalgia
7 (.27%)
Pain
7 (.27%)
Rhinorrhoea
7 (.27%)
Sinusitis
7 (.27%)
Stevens-johnson Syndrome
7 (.27%)
Swelling
7 (.27%)
Swelling Face
7 (.27%)
Tongue Oedema
7 (.27%)
Adrenal Insufficiency
6 (.23%)
Adrenal Suppression
6 (.23%)
Burnout Syndrome
6 (.23%)
Completed Suicide
6 (.23%)
Congenital Anomaly In Offspring
6 (.23%)
Congenital Bladder Anomaly
6 (.23%)
Convulsion
6 (.23%)

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

What are the most common Beclomethasone Dipropionate adverse events reported to the FDA?

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

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

Asthma
955
Drug Use For Unknown Indication
408
Product Used For Unknown Indication
346
Chronic Obstructive Pulmonary Disea...
172
Hypersensitivity
37
Dyspnoea
37
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Seasonal Allergy
36
Rhinitis Allergic
36
Ill-defined Disorder
26
Rhinitis
25
Emphysema
25
Cough
19
Respiratory Disorder
14
Sinusitis
13
Bronchitis Chronic
13
Sinus Disorder
12
Crohns Disease
10
Stomatitis
9
Bronchitis
9
Multiple Allergies
7
Chronic Sinusitis
7
Bronchospasm
6
Colitis Ulcerative
6
Wheezing
6
Chronic Obstructive Airways Disease
6
Viral Infection
5
Lung Disorder
5
Nasopharyngitis
4
Graft Versus Host Disease
4
Sinus Congestion
4
Oropharyngeal Pain
4
Nasal Congestion
4
Psoriasis
4
Nasal Polyps
4
Respiratory Failure
3
Immunosuppression
3
Allergic Respiratory Symptom
3
Nasal Decongestion Therapy
3
Prophylaxis
3
Ear Infection
3
Obstructive Airways Disorder
2
Oedema
2
Vasculitis
2
Spirometry Abnormal
2
Sleep Apnoea Syndrome
2
Acute Graft Versus Host Disease
2
Rheumatoid Arthritis
2
Postnasal Drip
2
Mucosal Inflammation
2
Rhinitis Seasonal
2
Pulmonary Fibrosis
2

Drug Labels

LabelLabelerEffective
Beconase AqStat Rx USA LLC08-SEP-10
QnaslTeva Respiratory, LLC01-SEP-12
QvarTeva Respiratory, LLC11-DEC-12

Beclomethasone Dipropionate Case Reports

What Beclomethasone Dipropionate 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 Beclomethasone Dipropionate. 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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