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IPRATROPIUM BROMIDE

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Ipratropium Bromide Adverse Events Reported to the FDA Over Time

How are Ipratropium Bromide adverse event reports trending over time?

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

Most Common Ipratropium Bromide Adverse Events Reported to the FDA

What are the most common Ipratropium Bromide adverse events reported to the FDA?

Drug Ineffective
965 (6.11%)
Dyspnoea
941 (5.96%)
Dysgeusia
366 (2.32%)
Pneumonia
302 (1.91%)
Cough
272 (1.72%)
Death
240 (1.52%)
Chronic Obstructive Pulmonary Disea...
231 (1.46%)
Dizziness
185 (1.17%)
Asthma
180 (1.14%)
Drug Effect Decreased
164 (1.04%)
Condition Aggravated
129 (.82%)
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Chest Pain
126 (.8%)
Throat Irritation
118 (.75%)
Headache
117 (.74%)
Nausea
111 (.7%)
Tremor
111 (.7%)
Chest Discomfort
109 (.69%)
Wheezing
103 (.65%)
Dysphonia
99 (.63%)
Dry Mouth
98 (.62%)
Bronchitis
95 (.6%)
Respiratory Failure
94 (.6%)
Medication Error
93 (.59%)
Feeling Abnormal
91 (.58%)
Malaise
89 (.56%)
Tachycardia
89 (.56%)
Asthenia
87 (.55%)
Atrial Fibrillation
79 (.5%)
Heart Rate Increased
79 (.5%)
Cardiac Failure Congestive
76 (.48%)
Fatigue
76 (.48%)
Lung Infection
74 (.47%)
Rash
70 (.44%)
Oropharyngeal Pain
69 (.44%)
Overdose
69 (.44%)
Insomnia
68 (.43%)
Burning Sensation
64 (.41%)
Lung Neoplasm Malignant
64 (.41%)
Blood Pressure Increased
62 (.39%)
Confusional State
62 (.39%)
Dyspnoea Exertional
61 (.39%)
Vision Blurred
61 (.39%)
Therapeutic Response Decreased
60 (.38%)
Loss Of Consciousness
57 (.36%)
Myocardial Infarction
57 (.36%)
Palpitations
56 (.35%)
Oedema Peripheral
55 (.35%)
Drug Interaction
53 (.34%)
Hypertension
52 (.33%)
Oxygen Saturation Decreased
50 (.32%)
Pulmonary Congestion
49 (.31%)
Pyrexia
49 (.31%)
Cardiac Arrest
47 (.3%)
Constipation
47 (.3%)
Fall
47 (.3%)
Hypersensitivity
47 (.3%)
Incorrect Dose Administered
47 (.3%)
Increased Upper Airway Secretion
47 (.3%)
Bronchospasm
46 (.29%)
Emphysema
46 (.29%)
Lung Disorder
45 (.28%)
Productive Cough
45 (.28%)
Vomiting
45 (.28%)
Cardiac Failure
44 (.28%)
Glossodynia
44 (.28%)
Hyperhidrosis
44 (.28%)
Oral Discomfort
44 (.28%)
Respiratory Distress
44 (.28%)
Blood Glucose Increased
43 (.27%)
Urticaria
42 (.27%)
Nasopharyngitis
41 (.26%)
Anxiety
40 (.25%)
Convulsion
40 (.25%)
Cyanosis
40 (.25%)
Pruritus
40 (.25%)
Weight Decreased
40 (.25%)
Epistaxis
38 (.24%)
Pulmonary Embolism
38 (.24%)
Urinary Retention
38 (.24%)
Inflammation
37 (.23%)
Muscle Spasms
37 (.23%)
Transient Ischaemic Attack
37 (.23%)
Cardiac Disorder
36 (.23%)
Cerebrovascular Accident
36 (.23%)
Dehydration
36 (.23%)
Pharyngeal Oedema
36 (.23%)
Respiratory Tract Irritation
36 (.23%)
Throat Tightness
36 (.23%)
Diarrhoea
35 (.22%)
Nervousness
35 (.22%)
Product Quality Issue
35 (.22%)
Depressed Level Of Consciousness
34 (.22%)
Drug Exposure During Pregnancy
34 (.22%)
General Physical Health Deteriorati...
34 (.22%)
Hypoaesthesia
34 (.22%)
Pupils Unequal
34 (.22%)
Mesothelioma
33 (.21%)
Mydriasis
33 (.21%)
Nasal Congestion
33 (.21%)
Pain
33 (.21%)
Rhinorrhoea
32 (.2%)

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

What are the most common Ipratropium Bromide adverse events reported to the FDA?

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

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

Chronic Obstructive Pulmonary Disea...
2899
Asthma
1704
Drug Use For Unknown Indication
1035
Product Used For Unknown Indication
795
Dyspnoea
666
Emphysema
539
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Bronchitis
166
Chronic Obstructive Airways Disease
113
Pneumonia
96
Bronchitis Chronic
95
Bronchospasm
93
Wheezing
89
Lung Disorder
63
Cough
53
Respiratory Disorder
52
Rhinorrhoea
48
Ill-defined Disorder
45
Hypersensitivity
39
Status Asthmaticus
30
Prophylaxis
28
Respiratory Distress
27
Respiratory Failure
24
Bronchiectasis
22
Seasonal Allergy
22
Rhinitis
20
Pulmonary Congestion
17
Bronchial Disorder
17
Nasal Congestion
16
Sinus Disorder
15
Multiple Allergies
15
Obstructive Airways Disorder
15
Pulmonary Fibrosis
14
Oxygen Saturation Decreased
13
Unevaluable Event
13
Lower Respiratory Tract Infection
11
Cardiac Failure Congestive
11
Asthmatic Crisis
10
Postnasal Drip
9
Respiratory Therapy
9
Inhalation Therapy
9
Rhinitis Allergic
8
Nasopharyngitis
8
Sarcoidosis
8
Upper-airway Cough Syndrome
8
Antasthmatic Drug Level
8
Sinus Congestion
8
Bronchial Hyperreactivity
8
Bronchial Obstruction
6
Respiratory Tract Infection
6
Sleep Apnoea Syndrome
5
Diffuse Panbronchiolitis
5

Drug Labels

LabelLabelerEffective
Ipratropium BromideMylan Pharmaceuticals Inc.15-APR-09
Ipratropium BromideNephron Pharmaceuticals Corporation09-NOV-09
Ipratropium BromidePhysicians Total Care, Inc.31-DEC-09
Ipratropium BromidePhysicians Total Care, Inc.05-MAY-10
Ipratropium BromidePhysicians Total Care, Inc.05-MAY-10
AtroventhfaPhysicians Total Care, Inc.28-JUL-10
AtroventPhysicians Total Care, Inc.10-SEP-10
AtroventPhysicians Total Care, Inc.10-SEP-10
CombiventPhysicians Total Care, Inc.21-SEP-10
Ipratropium BromideRebel Distributors Corp29-SEP-10
Ipratropium Bromide And Albuterol SulfatePhysicians Total Care, Inc.05-NOV-10
Ipratropium BromideBausch & Lomb Incorporated03-MAY-11
Ipratropium BromideRoxane Laboratories, Inc18-MAY-11
Ipratropium BromideRoxane Laboratories, Inc18-MAY-11
Ipratropium BromideCardinal Health24-MAY-11
AtroventBoehringer Ingelheim Pharmaceuticals, Inc.14-JUL-11
AtroventBoehringer Ingelheim Pharmaceuticals, Inc.14-JUL-11
Ipratropium BromideBausch & Lomb Incorporated01-NOV-11
Ipratropium BromideRitedose Pharmaceuticals, LLC21-NOV-11
Ipratropium BromideRebel Distributors Corp13-DEC-11
Ipratropium Bromide And Albuterol SulfateCardinal Health15-MAY-12
Ipratropium BromideCardinal Health16-MAY-12
Ipratropium BromideMylan Pharmaceuticals Inc.01-JUL-12
Ipratropium Bromide And Albuterol SulfateCobalt Laboratories17-JUL-12
Ipratropium BromidePreferred Pharmaceuticals, Inc.25-JUL-12
Combivent RespimatBoehringer Ingelheim Pharmaceuticals Inc.24-AUG-12
AtroventhfaBoehringer Ingelheim Pharmaceuticals Inc.24-AUG-12
Ipratropium Bromide And Albuterol SulfateEon Labs, Inc.31-AUG-12
Ipratropium Bromide And Albuterol SulfateMylan Pharmaceuticals Inc.31-AUG-12
Ipratropium Bromide And Albuterol SulfateNephron Pharmaceuticals Corporation04-SEP-12
CombiventBoehringer Ingelheim Pharmaceuticals, Inc.20-SEP-12
Ipratropium BromideCantrell Drug Company13-NOV-12
Ipratropium BromideRebel Distributors Corp11-DEC-12
Ipratropium Bromide And Albuterol SulfateRitedose Pharmaceuticals, LLC13-DEC-12
Ipratropium Bromide And Albuterol SulfateTeva Pharmaceuticals USA Inc18-DEC-12
Ipratropium Bromide And Albuterol SulfateWatson Laboratories, Inc.08-FEB-13
Ipratropium BromidePreferred Pharmaceuticals, Inc22-FEB-13
Ipratropium Bromide And Albuterol SulfateMylan Pharmaceuticals, Inc.25-FEB-13
Ipratropium BromideWatson Laboratories, Inc.04-APR-13
Ipratropium BromideSandoz Inc.10-APR-13
Ipratropium BromideCardinal Health25-APR-13

Ipratropium Bromide Case Reports

What Ipratropium Bromide 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 Ipratropium Bromide. 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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