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ATROVENT HFA

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Atrovent Hfa Adverse Events Reported to the FDA Over Time

How are Atrovent Hfa adverse event reports trending over time?

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

Most Common Atrovent Hfa Adverse Events Reported to the FDA

What are the most common Atrovent Hfa adverse events reported to the FDA?

Dyspnoea
117 (7.26%)
Drug Ineffective
113 (7.01%)
Dysgeusia
55 (3.41%)
Dizziness
34 (2.11%)
Cough
31 (1.92%)
Dry Mouth
28 (1.74%)
Nausea
27 (1.68%)
Throat Irritation
24 (1.49%)
Feeling Abnormal
21 (1.3%)
Oropharyngeal Pain
21 (1.3%)
Pneumonia
21 (1.3%)
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Insomnia
20 (1.24%)
Drug Effect Decreased
17 (1.06%)
Dysphonia
17 (1.06%)
Fatigue
17 (1.06%)
Rash
17 (1.06%)
Glossodynia
16 (.99%)
Productive Cough
15 (.93%)
Asthenia
14 (.87%)
Chest Discomfort
14 (.87%)
Hyperhidrosis
14 (.87%)
Dyspnoea Exertional
13 (.81%)
Tremor
13 (.81%)
Bronchitis
12 (.74%)
Death
12 (.74%)
Vision Blurred
12 (.74%)
Wheezing
12 (.74%)
Asthma
11 (.68%)
Decreased Appetite
11 (.68%)
Hypersensitivity
11 (.68%)
Malaise
11 (.68%)
Palpitations
11 (.68%)
Weight Decreased
11 (.68%)
Alopecia
10 (.62%)
Back Pain
10 (.62%)
Gait Disturbance
10 (.62%)
Pruritus
10 (.62%)
Therapeutic Response Decreased
10 (.62%)
Urticaria
10 (.62%)
Blood Cholesterol Increased
9 (.56%)
Chest Pain
9 (.56%)
Drug Interaction
9 (.56%)
Muscular Weakness
9 (.56%)
Neuropathy Peripheral
9 (.56%)
Peroneal Nerve Palsy
9 (.56%)
Tongue Coated
9 (.56%)
Burning Sensation
8 (.5%)
Dyspepsia
8 (.5%)
Head Discomfort
8 (.5%)
Retching
8 (.5%)
Skin Discolouration
8 (.5%)
Adverse Drug Reaction
7 (.43%)
Anaphylactic Reaction
7 (.43%)
Blood Glucose Increased
7 (.43%)
Breath Alcohol Test Positive
7 (.43%)
Contusion
7 (.43%)
Convulsion
7 (.43%)
Erythema
7 (.43%)
Heat Rash
7 (.43%)
Oedema Peripheral
7 (.43%)
Pain
7 (.43%)
Rash Pruritic
7 (.43%)
Stress
7 (.43%)
Throat Tightness
7 (.43%)
Aphonia
6 (.37%)
Bipolar Disorder
6 (.37%)
Blood Sodium Decreased
6 (.37%)
Cerebrovascular Accident
6 (.37%)
Chronic Obstructive Pulmonary Disea...
6 (.37%)
Clumsiness
6 (.37%)
Coordination Abnormal
6 (.37%)
Delusion
6 (.37%)
Depressed Mood
6 (.37%)
Headache
6 (.37%)
Heart Rate Increased
6 (.37%)
Hot Flush
6 (.37%)
Hypertension
6 (.37%)
Hypoaesthesia
6 (.37%)
Incorrect Route Of Drug Administrat...
6 (.37%)
Lung Infection
6 (.37%)
Mania
6 (.37%)
Melaena
6 (.37%)
Monoplegia
6 (.37%)
Sudden Onset Of Sleep
6 (.37%)
Swelling Face
6 (.37%)
Atrial Fibrillation
5 (.31%)
Dysuria
5 (.31%)
Heart Rate Irregular
5 (.31%)
Lip Pain
5 (.31%)
Nasal Congestion
5 (.31%)
Oral Discomfort
5 (.31%)
Pharyngeal Oedema
5 (.31%)
Product Quality Issue
5 (.31%)
Speech Disorder
5 (.31%)
Swollen Tongue
5 (.31%)
Abdominal Discomfort
4 (.25%)
Abdominal Pain Upper
4 (.25%)
Chills
4 (.25%)
Choking
4 (.25%)
Constipation
4 (.25%)
Delirium
4 (.25%)

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

What are the most common Atrovent Hfa adverse events reported to the FDA?

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

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

Chronic Obstructive Pulmonary Disea...
196
Asthma
91
Dyspnoea
77
Emphysema
69
Bronchitis Chronic
10
Cough
10
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Bronchitis
9
Rhinorrhoea
5
Drug Use For Unknown Indication
5
Bronchospasm
5
Bronchiectasis
4
Wheezing
4
Respiratory Distress
3
Product Used For Unknown Indication
3
Vocal Cord Disorder
3
Pneumonia
3
Pulmonary Congestion
3
Obstructive Airways Disorder
2
Cardiac Failure Congestive
2
Increased Upper Airway Secretion
2
Exposure To Chemical Pollution
2
Bronchial Obstruction
2
Sinus Disorder
2
Asthma Exercise Induced
1
Bronchial Hyperreactivity
1
Lung Disorder
1
Upper Respiratory Tract Infection
1
Oxygen Saturation Decreased
1
Alpha-1 Anti-trypsin Deficiency
1
Exposure To Toxic Agent
1
Sinus Congestion
1
Cystic Fibrosis
1
Forced Expiratory Volume Decreased
1
Respiratory Tract Infection
1
Panic Attack
1
Upper-airway Cough Syndrome
1
Nasal Discomfort
1
Pleurisy
1
Nasal Congestion
1

Drug Labels

LabelLabelerEffective
AtroventhfaPhysicians Total Care, Inc.28-JUL-10
AtroventhfaBoehringer Ingelheim Pharmaceuticals Inc.24-AUG-12

Atrovent Hfa Case Reports

What Atrovent Hfa 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 Atrovent Hfa. 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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