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TEICOPLANIN

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Teicoplanin Adverse Events Reported to the FDA Over Time

How are Teicoplanin adverse event reports trending over time?

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

Most Common Teicoplanin Adverse Events Reported to the FDA

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

Pyrexia
36 (2.73%)
Thrombocytopenia
36 (2.73%)
Drug Interaction
21 (1.59%)
Hyphaema
20 (1.51%)
Septic Shock
20 (1.51%)
Neutropenia
19 (1.44%)
Blood Bilirubin Increased
18 (1.36%)
International Normalised Ratio Incr...
18 (1.36%)
Neutropenic Sepsis
18 (1.36%)
Intraocular Pressure Increased
16 (1.21%)
Toxic Epidermal Necrolysis
16 (1.21%)
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Clostridium Difficile Colitis
14 (1.06%)
Drug Ineffective
14 (1.06%)
Erythema
14 (1.06%)
Nausea
14 (1.06%)
Respiratory Failure
14 (1.06%)
Anaphylactic Reaction
13 (.98%)
Death
13 (.98%)
Headache
13 (.98%)
Renal Failure
13 (.98%)
Staphylococcal Infection
13 (.98%)
Alanine Aminotransferase Increased
12 (.91%)
Anaemia
12 (.91%)
Aspartate Aminotransferase Increase...
12 (.91%)
Renal Failure Acute
12 (.91%)
Sepsis
12 (.91%)
Eosinophilia
11 (.83%)
Hepatic Failure
11 (.83%)
Leukopenia
11 (.83%)
Multi-organ Failure
11 (.83%)
Platelet Count Decreased
11 (.83%)
Rash
11 (.83%)
Agranulocytosis
10 (.76%)
Condition Aggravated
10 (.76%)
Decreased Appetite
10 (.76%)
Febrile Neutropenia
10 (.76%)
Hallucination, Visual
10 (.76%)
Skin Exfoliation
10 (.76%)
Cardiac Failure
9 (.68%)
Hepatic Function Abnormal
9 (.68%)
White Blood Cell Count Decreased
9 (.68%)
Confusional State
8 (.61%)
Diarrhoea
8 (.61%)
Eye Pain
8 (.61%)
General Physical Health Deteriorati...
8 (.61%)
Pancytopenia
8 (.61%)
Renal Impairment
8 (.61%)
Stevens-johnson Syndrome
8 (.61%)
Cardiac Arrest
7 (.53%)
Cardio-respiratory Arrest
7 (.53%)
Dyspnoea
7 (.53%)
Hepatotoxicity
7 (.53%)
Pleural Effusion
7 (.53%)
Pneumonia
7 (.53%)
Staphylococcal Sepsis
7 (.53%)
Cellulitis
6 (.45%)
Disseminated Intravascular Coagulat...
6 (.45%)
Gamma-glutamyltransferase Increased
6 (.45%)
Haemodialysis
6 (.45%)
Hepatic Enzyme Increased
6 (.45%)
Intestinal Perforation
6 (.45%)
Liver Injury
6 (.45%)
Purpura
6 (.45%)
Bronchopulmonary Aspergillosis
5 (.38%)
Candidiasis
5 (.38%)
Convulsion
5 (.38%)
Drug Resistance
5 (.38%)
Haemoglobin Decreased
5 (.38%)
Hypotension
5 (.38%)
Liver Disorder
5 (.38%)
Mycobacterium Fortuitum Infection
5 (.38%)
Rash Maculo-papular
5 (.38%)
Vomiting
5 (.38%)
Cardiac Failure Congestive
4 (.3%)
Chalazion
4 (.3%)
Coagulation Time Prolonged
4 (.3%)
Dermatitis Exfoliative
4 (.3%)
Drug Rash With Eosinophilia And Sys...
4 (.3%)
Haemoptysis
4 (.3%)
Hyperglycaemia
4 (.3%)
Influenza
4 (.3%)
Leukocytosis
4 (.3%)
Lymphangitis
4 (.3%)
Metabolic Acidosis
4 (.3%)
Oral Mucosa Erosion
4 (.3%)
Pseudomonas Infection
4 (.3%)
Rash Generalised
4 (.3%)
Rash Scarlatiniform
4 (.3%)
Renal Failure Chronic
4 (.3%)
Respiratory Distress
4 (.3%)
Acute Myeloid Leukaemia
3 (.23%)
Ascites
3 (.23%)
Aspergillosis
3 (.23%)
Blood Alkaline Phosphatase Increase...
3 (.23%)
C-reactive Protein Increased
3 (.23%)
Cheilitis
3 (.23%)
Chills
3 (.23%)
Device Related Infection
3 (.23%)
Diabetic Retinopathy
3 (.23%)
Drug Hypersensitivity
3 (.23%)
Drug Ineffective For Unapproved Ind...
3 (.23%)

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

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

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

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

Pneumonia
72
Infection
55
Product Used For Unknown Indication
51
Infection Prophylaxis
46
Sepsis
41
Antibiotic Prophylaxis
36
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Pyrexia
23
Drug Use For Unknown Indication
23
Prophylaxis
21
Staphylococcal Infection
17
Cellulitis
14
Antibiotic Therapy
13
Febrile Neutropenia
12
Staphylococcal Sepsis
10
Endocarditis
9
Neutropenic Sepsis
9
Ill-defined Disorder
9
Periorbital Cellulitis
8
Pneumonia Staphylococcal
8
Evidence Based Treatment
7
Septic Shock
6
Osteomyelitis
6
Bronchopulmonary Aspergillosis
6
Chalazion
6
Bacterial Infection
6
Abdominal Infection
6
Anti-infective Therapy
5
Skin Ulcer
5
Antibacterial Prophylaxis
5
Device Related Infection
5
Lung Disorder
5
Enterococcal Infection
5
Antibiotic Level
4
Spinal Cord Infection
4
Lung Infection
4
Bacteraemia
4
Postoperative Wound Infection
4
Respiratory Tract Infection
3
Peritonitis
3
Bronchitis
3
Lobar Pneumonia
3
Neonatal Infection
3
Intervertebral Discitis
3
Dermatitis
3
Diffuse Large B-cell Lymphoma
2
Pneumonia Mycoplasmal
2
Urinary Tract Infection
2
Multiple-drug Resistance
2
Agranulocytosis
2
Liver Abscess
2
Sickle Cell Anaemia
2

Teicoplanin Case Reports

What Teicoplanin 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 Teicoplanin. 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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