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TAZOCIN

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Tazocin Adverse Events Reported to the FDA Over Time

How are Tazocin adverse event reports trending over time?

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

Most Common Tazocin Adverse Events Reported to the FDA

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

Liver Function Test Abnormal
52 (2.6%)
Hepatotoxicity
51 (2.55%)
Dilatation Intrahepatic Duct Acquir...
48 (2.4%)
Alanine Aminotransferase Increased
47 (2.35%)
Venoocclusive Liver Disease
33 (1.65%)
Pyrexia
29 (1.45%)
Blood Alkaline Phosphatase Increase...
28 (1.4%)
Dyspnoea
27 (1.35%)
Aspartate Aminotransferase Increase...
26 (1.3%)
Blood Bilirubin Increased
24 (1.2%)
Rash
24 (1.2%)
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Condition Aggravated
23 (1.15%)
Erythema
23 (1.15%)
Jaundice
23 (1.15%)
Septic Shock
23 (1.15%)
Thrombocytopenia
21 (1.05%)
Dermatitis Exfoliative
19 (.95%)
Malaise
19 (.95%)
White Blood Cell Count Decreased
19 (.95%)
Liver Disorder
18 (.9%)
Diarrhoea
17 (.85%)
Blood Pressure Decreased
16 (.8%)
Drug Ineffective
16 (.8%)
Hypotension
16 (.8%)
Interstitial Lung Disease
16 (.8%)
Multi-organ Failure
16 (.8%)
Blood Lactate Dehydrogenase Increas...
15 (.75%)
Hepatic Function Abnormal
15 (.75%)
Sepsis
15 (.75%)
Death
14 (.7%)
Gastroenteritis Clostridial
14 (.7%)
Renal Failure
14 (.7%)
Cyanosis
13 (.65%)
Pruritus
13 (.65%)
Blood Creatinine Increased
12 (.6%)
Hyperhidrosis
12 (.6%)
Megacolon
12 (.6%)
Nausea
12 (.6%)
Pneumonia
12 (.6%)
Toxic Epidermal Necrolysis
12 (.6%)
Venoocclusive Disease
12 (.6%)
Cardio-respiratory Arrest
11 (.55%)
Chest Pain
11 (.55%)
Chills
11 (.55%)
Clostridial Infection
11 (.55%)
Hepatic Failure
11 (.55%)
Neutropenia
11 (.55%)
Renal Failure Acute
11 (.55%)
Stevens-johnson Syndrome
11 (.55%)
Anaphylactic Reaction
10 (.5%)
Paraesthesia
10 (.5%)
Weight Decreased
10 (.5%)
Acute Respiratory Distress Syndrome
9 (.45%)
Asthenia
9 (.45%)
C-reactive Protein Increased
9 (.45%)
Cough
9 (.45%)
Depressed Level Of Consciousness
9 (.45%)
Disseminated Intravascular Coagulat...
9 (.45%)
Drug Rash With Eosinophilia And Sys...
9 (.45%)
General Physical Health Deteriorati...
9 (.45%)
Infection
9 (.45%)
Pain
9 (.45%)
Swelling Face
9 (.45%)
Toxic Skin Eruption
9 (.45%)
Vomiting
9 (.45%)
Anaemia
8 (.4%)
Blood Urea Increased
8 (.4%)
Concomitant Disease Progression
8 (.4%)
Headache
8 (.4%)
Hepatic Enzyme Increased
8 (.4%)
Loss Of Consciousness
8 (.4%)
Rash Maculo-papular
8 (.4%)
Renal Disorder
8 (.4%)
Abdominal Pain Lower
7 (.35%)
Agranulocytosis
7 (.35%)
Anaphylactic Shock
7 (.35%)
Cardiac Arrest
7 (.35%)
Gamma-glutamyltransferase Increased
7 (.35%)
Hypersensitivity
7 (.35%)
Hypophagia
7 (.35%)
Ileus Paralytic
7 (.35%)
Laryngeal Oedema
7 (.35%)
Leukopenia
7 (.35%)
Myalgia
7 (.35%)
Oxygen Saturation Decreased
7 (.35%)
Tachycardia
7 (.35%)
Drug Interaction
6 (.3%)
Eosinophil Percentage Increased
6 (.3%)
Haemoglobin Decreased
6 (.3%)
Pancytopenia
6 (.3%)
Rash Erythematous
6 (.3%)
Urticaria
6 (.3%)
Body Temperature Increased
5 (.25%)
Drug Hypersensitivity
5 (.25%)
Eosinophilia
5 (.25%)
Face Oedema
5 (.25%)
Fatigue
5 (.25%)
Granulocytopenia
5 (.25%)
Hepatitis
5 (.25%)
Histiocytosis Haematophagic
5 (.25%)
Hot Flush
5 (.25%)

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

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

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

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

Sepsis
80
Drug Use For Unknown Indication
72
Pneumonia
67
Infection
47
Product Used For Unknown Indication
37
Pyrexia
33
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Urinary Tract Infection
16
Febrile Neutropenia
15
Cholecystitis
15
Pyelonephritis
14
Antibiotic Therapy
13
Antibiotic Level
12
Prophylaxis
12
Lower Respiratory Tract Infection
12
Pseudomonas Infection
12
Pneumonia Aspiration
11
Antibiotic Prophylaxis
11
Infection Prophylaxis
10
Pneumonitis
10
Pyelonephritis Acute
10
Lung Infection
9
Cystic Fibrosis
9
Bacterial Infection
8
C-reactive Protein Increased
8
Neutropenic Sepsis
8
Bronchopneumonia
7
Wound Infection
6
Septic Shock
6
Bronchiectasis
6
Liver Abscess
6
Pneumonia Klebsiella
5
Bacteraemia
5
Escherichia Sepsis
5
Anti-infective Therapy
5
Respiratory Tract Infection
5
Abdominal Abscess
4
Osteomyelitis
4
Nosocomial Infection
4
Peritonitis
4
Diabetic Foot Infection
3
Pneumonia Mycoplasmal
3
Oesophageal Operation
3
Abscess
3
Morganella Infection
3
Abdominal Sepsis
3
Pleural Effusion
3
Bacterial Sepsis
3
Staphylococcal Infection
3
Pneumonia Bacterial
3
Condition Aggravated
3
Leukopenia
3

Tazocin Case Reports

What Tazocin 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 Tazocin. 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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