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MUCODYNE

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Mucodyne Adverse Events Reported to the FDA Over Time

How are Mucodyne adverse event reports trending over time?

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

Most Common Mucodyne Adverse Events Reported to the FDA

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

Hepatic Function Abnormal
29 (3.54%)
Liver Disorder
25 (3.05%)
Abnormal Behaviour
22 (2.68%)
Pyrexia
20 (2.44%)
Drug Eruption
17 (2.07%)
Rash
16 (1.95%)
Alanine Aminotransferase Increased
14 (1.71%)
Aspartate Aminotransferase Increase...
14 (1.71%)
Leukocytoclastic Vasculitis
14 (1.71%)
Stevens-johnson Syndrome
13 (1.59%)
Gamma-glutamyltransferase Increased
12 (1.46%)
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Pneumonia
12 (1.46%)
Tubulointerstitial Nephritis
12 (1.46%)
Blood Lactate Dehydrogenase Increas...
9 (1.1%)
Decreased Appetite
9 (1.1%)
Erythema Multiforme
9 (1.1%)
Erythema
8 (.98%)
Purpura
8 (.98%)
Rhabdomyolysis
8 (.98%)
Vomiting
8 (.98%)
Agranulocytosis
7 (.85%)
Allergic Granulomatous Angiitis
7 (.85%)
Anaphylactic Shock
7 (.85%)
Asthma
7 (.85%)
Cough
7 (.85%)
Depressed Level Of Consciousness
7 (.85%)
Dyspnoea
7 (.85%)
Face Oedema
7 (.85%)
Hallucination
7 (.85%)
Hepatitis Fulminant
7 (.85%)
Hypothermia
6 (.73%)
Malaise
6 (.73%)
Ocular Hyperaemia
6 (.73%)
Respiratory Failure
6 (.73%)
Somnolence
6 (.73%)
Vasculitis
6 (.73%)
Anorexia
5 (.61%)
Anxiety
5 (.61%)
Arrhythmia
5 (.61%)
Blood Alkaline Phosphatase Increase...
5 (.61%)
Blood Urea Increased
5 (.61%)
Condition Aggravated
5 (.61%)
Lymphocyte Stimulation Test Positiv...
5 (.61%)
Oedema Peripheral
5 (.61%)
Pallor
5 (.61%)
Rash Generalised
5 (.61%)
Toxic Skin Eruption
5 (.61%)
Urticaria
5 (.61%)
Aggression
4 (.49%)
Asthenia
4 (.49%)
Blood Creatine Phosphokinase Increa...
4 (.49%)
Cardiac Failure
4 (.49%)
Cerebral Haemorrhage
4 (.49%)
Convulsion
4 (.49%)
Eosinophilic Pneumonia
4 (.49%)
Hepatitis Acute
4 (.49%)
Lip Swelling
4 (.49%)
Nasopharyngitis
4 (.49%)
Oculomucocutaneous Syndrome
4 (.49%)
Pleural Effusion
4 (.49%)
Atrioventricular Block First Degree
3 (.37%)
Blood Creatinine Increased
3 (.37%)
C-reactive Protein Increased
3 (.37%)
Cerebral Infarction
3 (.37%)
Chromaturia
3 (.37%)
Crying
3 (.37%)
Epistaxis
3 (.37%)
Gait Disturbance
3 (.37%)
Gastroenteritis
3 (.37%)
Gastrointestinal Inflammation
3 (.37%)
Generalised Erythema
3 (.37%)
Haematuria
3 (.37%)
Hepatic Enzyme Increased
3 (.37%)
Hyperglobulinaemia
3 (.37%)
Hyperhidrosis
3 (.37%)
Interstitial Lung Disease
3 (.37%)
Jaundice
3 (.37%)
Mumps
3 (.37%)
Oral Mucosa Erosion
3 (.37%)
Oropharyngeal Pain
3 (.37%)
Platelet Count Decreased
3 (.37%)
Renal Failure Acute
3 (.37%)
Thrombocytopenia
3 (.37%)
Toxic Epidermal Necrolysis
3 (.37%)
White Blood Cell Count Increased
3 (.37%)
Altered State Of Consciousness
2 (.24%)
Amnesia
2 (.24%)
Anaphylactic Reaction
2 (.24%)
Anaphylactoid Reaction
2 (.24%)
Ascites
2 (.24%)
Blood Amylase Increased
2 (.24%)
Blood Pressure Decreased
2 (.24%)
Blood Sodium Decreased
2 (.24%)
Blood Urea Decreased
2 (.24%)
Chills
2 (.24%)
Coma
2 (.24%)
Conjunctival Hyperaemia
2 (.24%)
Conjunctival Oedema
2 (.24%)
Dehydration
2 (.24%)
Delirium
2 (.24%)
Diarrhoea
2 (.24%)

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

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

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

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

Bronchitis
150
Drug Use For Unknown Indication
139
Asthma
131
Productive Cough
110
Bronchitis Chronic
87
Product Used For Unknown Indication
87
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Cough
72
Nasopharyngitis
66
Chronic Obstructive Pulmonary Disea...
58
Sputum Retention
51
Upper Respiratory Tract Inflammatio...
49
Influenza
48
Pneumonia
48
Prophylaxis
37
Sinusitis
35
Emphysema
34
Acute Sinusitis
29
Bronchiectasis
27
Upper Respiratory Tract Infection
18
Bronchitis Acute
18
Chronic Sinusitis
15
Pharyngitis
14
Lung Neoplasm Malignant
12
Otitis Media
11
Metastatic Renal Cell Carcinoma
10
Otitis Media Acute
9
Pyrexia
9
Atypical Mycobacterial Infection
9
Gastritis
8
Interstitial Lung Disease
8
Metastases To Lung
8
Rhinitis Allergic
8
Mycobacterium Avium Complex Infecti...
7
Cryptogenic Organising Pneumonia
5
Bronchopneumonia
5
Pharyngeal Disorder
5
Respiratory Disorder
5
Laryngopharyngitis
5
Diffuse Panbronchiolitis
4
Hepatic Function Abnormal
4
Nasal Congestion
4
Cystic Fibrosis
4
Lung Adenocarcinoma
4
Chronic Respiratory Failure
3
Streptococcal Infection
3
Bronchopulmonary Aspergillosis
3
Laryngotracheo Bronchitis
3
Gastric Ulcer
3
Infection
3
Acute Tonsillitis
3
Gastrointestinal Disorder
3

Mucodyne Case Reports

What Mucodyne 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 Mucodyne. 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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