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PIPERACILLIN AND TAZOBACTAM

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Piperacillin And Tazobactam Adverse Events Reported to the FDA Over Time

How are Piperacillin And Tazobactam adverse event reports trending over time?

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

Most Common Piperacillin And Tazobactam Adverse Events Reported to the FDA

What are the most common Piperacillin And Tazobactam adverse events reported to the FDA?

Renal Failure Acute
142 (2.31%)
Pyrexia
123 (2%)
Thrombocytopenia
105 (1.71%)
Rash
86 (1.4%)
Pruritus
66 (1.07%)
Condition Aggravated
64 (1.04%)
Drug Rash With Eosinophilia And Sys...
63 (1.02%)
Neutropenia
61 (.99%)
Rash Maculo-papular
61 (.99%)
Drug Interaction
58 (.94%)
Rash Erythematous
57 (.93%)
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Pancytopenia
55 (.89%)
Stevens-johnson Syndrome
55 (.89%)
Death
54 (.88%)
Sepsis
54 (.88%)
Septic Shock
53 (.86%)
Paraesthesia
50 (.81%)
Alanine Aminotransferase Increased
49 (.8%)
Hypotension
48 (.78%)
Agranulocytosis
47 (.76%)
Drug Ineffective
46 (.75%)
Renal Failure
46 (.75%)
Eosinophilia
45 (.73%)
Multi-organ Failure
43 (.7%)
Leukopenia
42 (.68%)
Cholestasis
41 (.67%)
Tachycardia
39 (.63%)
Aspartate Aminotransferase Increase...
38 (.62%)
Dyspnoea
38 (.62%)
Erythema
38 (.62%)
Cytolytic Hepatitis
36 (.58%)
Encephalopathy
35 (.57%)
Toxic Epidermal Necrolysis
35 (.57%)
Diarrhoea
34 (.55%)
Acute Respiratory Distress Syndrome
32 (.52%)
Clostridium Difficile Colitis
32 (.52%)
Blood Creatinine Increased
30 (.49%)
Pneumonia
30 (.49%)
Anaphylactic Reaction
28 (.45%)
Dermatitis Exfoliative
28 (.45%)
Hepatotoxicity
28 (.45%)
Tubulointerstitial Nephritis
28 (.45%)
Clostridial Infection
27 (.44%)
Liver Function Test Abnormal
27 (.44%)
Renal Impairment
27 (.44%)
Skin Warm
27 (.44%)
Blood Alkaline Phosphatase Increase...
26 (.42%)
Drug Hypersensitivity
26 (.42%)
Hepatic Failure
26 (.42%)
Toxic Skin Eruption
25 (.41%)
Cardio-respiratory Arrest
24 (.39%)
Platelet Count Decreased
24 (.39%)
White Blood Cell Count Decreased
24 (.39%)
Anaemia
23 (.37%)
Chills
23 (.37%)
Coma
23 (.37%)
Confusional State
23 (.37%)
Renal Tubular Necrosis
23 (.37%)
Haemoglobin Decreased
22 (.36%)
Respiratory Failure
22 (.36%)
Hepatic Function Abnormal
21 (.34%)
Petechiae
21 (.34%)
Staphylococcal Infection
21 (.34%)
Dermatitis Bullous
20 (.32%)
Dialysis
20 (.32%)
Haemodialysis
20 (.32%)
Product Contamination Microbial
20 (.32%)
Blood Urea Increased
19 (.31%)
Bone Marrow Failure
19 (.31%)
Gamma-glutamyltransferase Increased
19 (.31%)
Haemolytic Anaemia
19 (.31%)
Rash Pruritic
19 (.31%)
Urticaria
19 (.31%)
Vomiting
19 (.31%)
Drug Toxicity
18 (.29%)
General Physical Health Deteriorati...
18 (.29%)
Lung Disorder
18 (.29%)
Pain
18 (.29%)
Pleural Effusion
18 (.29%)
Respiratory Distress
18 (.29%)
Abdominal Pain
17 (.28%)
Acute Generalised Exanthematous Pus...
17 (.28%)
Anuria
17 (.28%)
Blister
17 (.28%)
Bronchopulmonary Aspergillosis
17 (.28%)
Cardiac Arrest
17 (.28%)
Chest Pain
17 (.28%)
Blood Bilirubin Increased
16 (.26%)
Blood Lactate Dehydrogenase Increas...
16 (.26%)
Convulsion
16 (.26%)
Infection
16 (.26%)
Klebsiella Infection
16 (.26%)
Liver Disorder
16 (.26%)
Blood Pressure Decreased
15 (.24%)
Febrile Neutropenia
15 (.24%)
Hypokalaemia
15 (.24%)
Myoclonus
15 (.24%)
Nausea
15 (.24%)
Purpura
15 (.24%)
White Blood Cell Count Increased
15 (.24%)
Dehydration
14 (.23%)

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This graph shows the top adverse events submitted to the FDA for Piperacillin And Tazobactam, 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 Piperacillin And Tazobactam 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 Piperacillin And Tazobactam

What are the most common Piperacillin And Tazobactam adverse events reported to the FDA?

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

Why are people taking Piperacillin And Tazobactam, according to those reporting adverse events to the FDA?

Pneumonia
202
Product Used For Unknown Indication
177
Infection
128
Sepsis
122
Pyrexia
105
Drug Use For Unknown Indication
75
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Febrile Neutropenia
61
Urinary Tract Infection
45
Lung Disorder
35
Cellulitis
33
Antibiotic Therapy
33
Pseudomonas Infection
28
Osteomyelitis
28
Prophylaxis
26
Pneumonia Aspiration
25
Antibiotic Prophylaxis
23
Abdominal Infection
22
Septic Shock
21
Bacteraemia
21
Bronchopneumonia
21
Lung Infection
20
Bacterial Infection
20
Antifungal Prophylaxis
20
Infection Prophylaxis
18
Lower Respiratory Tract Infection
17
Ill-defined Disorder
16
Cystic Fibrosis
16
Pyelonephritis
15
Upper Respiratory Tract Infection
15
Peritonitis
14
Evidence Based Treatment
14
Urosepsis
14
Staphylococcal Infection
14
Neutropenic Sepsis
13
Abdominal Abscess
12
Wound Infection
11
Lung Infection Pseudomonal
11
Respiratory Tract Infection
10
Cholecystitis
9
Pyelonephritis Acute
9
Pneumonia Bacterial
8
Liver Abscess
8
Abscess
8
Empyema
8
C-reactive Protein Increased
7
Febrile Bone Marrow Aplasia
7
Acinetobacter Infection
6
Abdominal Sepsis
6
Drug Therapy
6
Bronchitis
6
Pneumonia Staphylococcal
6

Drug Labels

LabelLabelerEffective
Piperacillin And TazobactamAPP Pharmaceuticals, LLC02-JUN-11
ZosynCardinal Health07-JUN-11
Piperacillin And TazobactamHospira, Inc21-OCT-11
Piperacillin And TazobactamHospira, Inc21-OCT-11
Piperacillin And TazobactamHospira, Inc21-OCT-11
Piperacillin And TazobactamSandoz Inc21-OCT-11
Piperacillin And TazobactamHospira, Inc21-OCT-11
Piperacillin And TazobactamAPP Pharmaceuticals, LLC31-MAR-12
Piperacillin, TazobactamSagent Pharmaceuticals25-MAY-12
Zosyn In Galaxy ContainersPfizer Pharmaceuticals LLC, Pfizer Pharmaceutical LLC - Piperacillin08-JUN-12
Zosyn Pharmacy Bulk PackagePfizer Pharmaceuticals LLC, Pfizer Pharmaceutical LLC - Piperacillin08-JUN-12
Piperacillin And TazobactamAuroMedics Pharma LLC25-JUN-12
ZosynPfizer Pharmaceuticals LLC, Pfizer Pharmaceutical LLC - Piperacillin02-JUL-12
ZosynWyeth Piperacillin Division of Wyeth Holdings Corporation, a subsidiary of Pfizer20-SEP-12
Zosyn Pharmacy Bulk PackageWyeth Piperacillin Division of Wyeth Holdings Corporation, a subsidiary of Pfizer20-SEP-12
Zosyn In Galaxy ContainersWyeth Piperacillin Division of Wyeth Holdings Corporation, a subsidiary of Pfizer21-SEP-12
Piperacillin And TazobactamWG Critical Care, LLC31-JAN-13
Piperacillin And TazobactamWG Critical Care, LLC31-JAN-13
Piperacillin And TazobactamApotex Corporation04-FEB-13
Piperacillin And TazobactamApotex Corporation04-FEB-13
Piperacillin And TazobactamCardinal Health29-APR-13

Piperacillin And Tazobactam Case Reports

What Piperacillin And Tazobactam 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 Piperacillin And Tazobactam. 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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