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MODACIN

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Modacin Adverse Events Reported to the FDA Over Time

How are Modacin adverse event reports trending over time?

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

Most Common Modacin Adverse Events Reported to the FDA

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

Hepatic Function Abnormal
44 (4.03%)
Alanine Aminotransferase Increased
31 (2.84%)
Pyrexia
31 (2.84%)
Aspartate Aminotransferase Increase...
29 (2.66%)
Gamma-glutamyltransferase Increased
22 (2.02%)
Blood Alkaline Phosphatase Increase...
19 (1.74%)
Erythema
18 (1.65%)
Liver Disorder
17 (1.56%)
Rash
16 (1.47%)
Toxic Epidermal Necrolysis
16 (1.47%)
Depressed Level Of Consciousness
14 (1.28%)
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Drug Eruption
14 (1.28%)
Renal Failure Acute
14 (1.28%)
Blood Pressure Decreased
13 (1.19%)
Platelet Count Decreased
13 (1.19%)
Wheezing
13 (1.19%)
Acute Generalised Exanthematous Pus...
12 (1.1%)
Convulsion
12 (1.1%)
Eosinophil Count Increased
12 (1.1%)
Generalised Erythema
12 (1.1%)
Shock
12 (1.1%)
Anaphylactic Shock
10 (.92%)
Sepsis
10 (.92%)
Ascites
9 (.82%)
Blood Bilirubin Increased
9 (.82%)
Blood Lactate Dehydrogenase Increas...
9 (.82%)
Dyspnoea
9 (.82%)
Cyanosis
8 (.73%)
Rash Erythematous
8 (.73%)
Stevens-johnson Syndrome
8 (.73%)
Blister
7 (.64%)
C-reactive Protein Increased
7 (.64%)
Diarrhoea
7 (.64%)
Hallucination
7 (.64%)
Hyperhidrosis
7 (.64%)
Nausea
7 (.64%)
Pneumonia
7 (.64%)
Renal Disorder
7 (.64%)
Renal Impairment
7 (.64%)
Urinary Incontinence
7 (.64%)
Delirium
6 (.55%)
Disseminated Intravascular Coagulat...
6 (.55%)
Drug Exposure During Pregnancy
6 (.55%)
Haemorrhage
6 (.55%)
Pallor
6 (.55%)
Parosmia
6 (.55%)
Blood Urea Increased
5 (.46%)
Body Temperature Increased
5 (.46%)
Cachexia
5 (.46%)
Cardiac Failure
5 (.46%)
Conjunctival Hyperaemia
5 (.46%)
Drug Level Increased
5 (.46%)
Dysgeusia
5 (.46%)
Dyskinesia
5 (.46%)
Excoriation
5 (.46%)
Generalised Oedema
5 (.46%)
Hypercapnia
5 (.46%)
Multi-organ Failure
5 (.46%)
Oedema
5 (.46%)
Pancytopenia
5 (.46%)
Respiratory Arrest
5 (.46%)
Staphylococcal Infection
5 (.46%)
Abdominal Pain Upper
4 (.37%)
Abnormal Behaviour
4 (.37%)
Cardiac Arrest
4 (.37%)
Constipation
4 (.37%)
Cough
4 (.37%)
Face Oedema
4 (.37%)
Haematemesis
4 (.37%)
Heart Rate Increased
4 (.37%)
Hypersensitivity
4 (.37%)
Ileus Paralytic
4 (.37%)
Infection
4 (.37%)
Intestinal Dilatation
4 (.37%)
Memory Impairment
4 (.37%)
Mouth Breathing
4 (.37%)
Oliguria
4 (.37%)
Painful Respiration
4 (.37%)
Prolonged Expiration
4 (.37%)
Pseudomembranous Colitis
4 (.37%)
Red Blood Cell Count Decreased
4 (.37%)
Skin Erosion
4 (.37%)
Speech Disorder
4 (.37%)
Stomatitis
4 (.37%)
Thrombocytopenia
4 (.37%)
Urine Output Decreased
4 (.37%)
Vomiting
4 (.37%)
White Blood Cell Count Decreased
4 (.37%)
White Blood Cell Count Increased
4 (.37%)
Abdominal Pain
3 (.27%)
Acute Respiratory Distress Syndrome
3 (.27%)
Altered State Of Consciousness
3 (.27%)
Blood Creatine Phosphokinase Increa...
3 (.27%)
Brain Oedema
3 (.27%)
C-reactive Protein Decreased
3 (.27%)
Clostridium Colitis
3 (.27%)
Cystitis Haemorrhagic
3 (.27%)
Dermatitis Exfoliative
3 (.27%)
Dysphagia
3 (.27%)
Electroencephalogram Abnormal
3 (.27%)
Encephalopathy
3 (.27%)

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

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

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

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

Pneumonia
86
Infection
36
Sepsis
24
Drug Use For Unknown Indication
19
Pyrexia
14
Peritonitis
10
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Infection Prophylaxis
9
Prophylaxis
9
Bacterial Infection
8
Cholangitis
7
Pseudomonas Infection
7
Urinary Tract Infection
6
Appendicitis
5
Febrile Neutropenia
5
Abscess
4
Otitis Externa
4
Bronchitis
4
Staphylococcal Sepsis
3
Prostatitis
3
Type 2 Diabetes Mellitus
3
Uterine Infection
3
Pancreatitis
3
Pneumonia Bacterial
3
Pneumonia Aspiration
3
Wound Infection Staphylococcal
3
Postoperative Infection
2
Bronchitis Acute
2
Interstitial Lung Disease
2
Postoperative Fever
2
Product Used For Unknown Indication
2
Nephritis
2
Systemic Antibacterial Therapy
2
Cytomegalovirus Enterocolitis
2
Pyelonephritis
2
Serratia Infection
2
Antibiotic Therapy
1
Pyothorax
1
Upper Respiratory Tract Inflammatio...
1
Pneumonia Pneumococcal
1
Ill-defined Disorder
1
Enterocolitis
1
Dacryocystitis Infective
1
Cellulitis
1
Abdominal Abscess
1
Duodenal Ulcer Perforation
1
Device Related Infection
1
Meningitis
1
Spondylitis
1
C-reactive Protein Increased
1

Modacin Case Reports

What Modacin 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 Modacin. 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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