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TAZOCILLINE

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Tazocilline Adverse Events Reported to the FDA Over Time

How are Tazocilline adverse event reports trending over time?

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

Most Common Tazocilline Adverse Events Reported to the FDA

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

Pyrexia
102 (2.69%)
Drug Rash With Eosinophilia And Sys...
70 (1.85%)
Cholestasis
62 (1.64%)
Condition Aggravated
62 (1.64%)
Cytolytic Hepatitis
62 (1.64%)
Agranulocytosis
61 (1.61%)
Thrombocytopenia
60 (1.58%)
Eosinophilia
57 (1.5%)
Renal Failure Acute
55 (1.45%)
Neutropenia
54 (1.43%)
Purpura
49 (1.29%)
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Toxic Skin Eruption
49 (1.29%)
Confusional State
48 (1.27%)
Rash Maculo-papular
45 (1.19%)
Convulsion
40 (1.06%)
Pruritus
38 (1%)
Leukopenia
37 (.98%)
Pancytopenia
37 (.98%)
Rash
37 (.98%)
Gamma-glutamyltransferase Increased
35 (.92%)
Anaemia
33 (.87%)
Dermatitis Exfoliative
33 (.87%)
Lymphadenopathy
32 (.84%)
Multi-organ Failure
30 (.79%)
Septic Shock
30 (.79%)
Encephalopathy
27 (.71%)
Skin Exfoliation
27 (.71%)
Face Oedema
26 (.69%)
Alanine Aminotransferase Increased
25 (.66%)
Erythema
25 (.66%)
Rash Erythematous
25 (.66%)
Renal Failure
24 (.63%)
Cardio-respiratory Arrest
23 (.61%)
Chills
22 (.58%)
Haemoglobin Decreased
22 (.58%)
Myoclonus
22 (.58%)
Coma
21 (.55%)
Tumour Lysis Syndrome
21 (.55%)
Dermatitis Bullous
20 (.53%)
Oedema Peripheral
20 (.53%)
Eyelid Oedema
19 (.5%)
Liver Disorder
19 (.5%)
Rash Morbilliform
19 (.5%)
Blood Alkaline Phosphatase Increase...
18 (.48%)
Haematuria
18 (.48%)
Hypersensitivity
18 (.48%)
C-reactive Protein Increased
17 (.45%)
Mydriasis
17 (.45%)
Cerebellar Syndrome
16 (.42%)
Cheilitis
16 (.42%)
Hallucination
16 (.42%)
Overdose
16 (.42%)
Aspartate Aminotransferase Increase...
15 (.4%)
Histiocytosis Haematophagic
15 (.4%)
Hyperthermia
15 (.4%)
Peritonitis
15 (.4%)
Rectal Haemorrhage
15 (.4%)
Bone Marrow Failure
14 (.37%)
International Normalised Ratio Incr...
14 (.37%)
Pancreatitis Acute
14 (.37%)
Rash Generalised
14 (.37%)
Urticaria
14 (.37%)
Blood Creatinine Increased
13 (.34%)
Bronchopulmonary Aspergillosis
13 (.34%)
Eosinophil Count Increased
13 (.34%)
Eye Movement Disorder
13 (.34%)
Hepatitis Cholestatic
13 (.34%)
Rash Pruritic
13 (.34%)
Sinus Bradycardia
13 (.34%)
Ventricular Fibrillation
13 (.34%)
Anuria
12 (.32%)
Decerebration
12 (.32%)
Drug Eruption
12 (.32%)
General Physical Health Deteriorati...
12 (.32%)
Hypotension
12 (.32%)
Inflammation
12 (.32%)
Jaundice
12 (.32%)
Lymphadenitis
12 (.32%)
Respiratory Distress
12 (.32%)
Tachypnoea
12 (.32%)
Acute Respiratory Distress Syndrome
11 (.29%)
Blister
11 (.29%)
Diarrhoea
11 (.29%)
Drug Interaction
11 (.29%)
Staphylococcal Infection
11 (.29%)
Acute Generalised Exanthematous Pus...
10 (.26%)
Delirium
10 (.26%)
Mononucleosis Syndrome
10 (.26%)
Premature Baby
10 (.26%)
Transaminases Increased
10 (.26%)
Abdominal Pain
9 (.24%)
Blast Cell Count Increased
9 (.24%)
Drug Ineffective
9 (.24%)
Gammopathy
9 (.24%)
Generalised Erythema
9 (.24%)
Hyperammonaemia
9 (.24%)
Lung Disorder
9 (.24%)
Platelet Count Decreased
9 (.24%)
Pulmonary Alveolar Haemorrhage
9 (.24%)
Sepsis
9 (.24%)
Status Epilepticus
9 (.24%)

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

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

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

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

Drug Use For Unknown Indication
66
Pyrexia
40
Infection
33
Sepsis
29
Prophylaxis
27
Lung Disorder
27
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Pneumonia
23
Peritonitis
18
Septic Shock
15
Febrile Bone Marrow Aplasia
13
Pseudomonas Infection
13
Antibiotic Prophylaxis
11
Respiratory Tract Infection
11
Cellulitis
8
Staphylococcal Infection
8
Hyperthermia
7
Sepsis Syndrome
7
Lung Abscess
7
Bronchitis
7
Unevaluable Event
7
Osteitis
7
Erysipelas
7
Febrile Neutropenia
7
Escherichia Infection
6
Klebsiella Infection
6
Lung Infection
6
Product Used For Unknown Indication
6
Urinary Tract Infection
6
Enterococcal Infection
6
Bronchopneumonia
5
Pancytopenia
5
Pseudomonal Bacteraemia
5
Endocarditis Bacterial
5
Infection Prophylaxis
5
Drug Exposure During Pregnancy
5
Bacterial Sepsis
5
Staphylococcal Sepsis
5
Oesophageal Varices Haemorrhage
4
Abscess
4
Abdominal Infection
4
Septic Embolus
4
Bronchopulmonary Aspergillosis
4
Escherichia Sepsis
4
Pneumonia Aspiration
3
Superinfection
3
Antibiotic Therapy
3
Bacterial Pyelonephritis
3
Morganella Infection
3
Proteus Infection
3
Escherichia Bacteraemia
3
Urinary Tract Infection Pseudomonal
3

Tazocilline Case Reports

What Tazocilline 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 Tazocilline. 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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