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Zosyn Adverse Events Reported to the FDA Over Time

How are Zosyn adverse event reports trending over time?

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

Most Common Zosyn Adverse Events Reported to the FDA

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

Pyrexia
282 (2.15%)
Renal Failure Acute
261 (1.99%)
Thrombocytopenia
200 (1.52%)
Rash
188 (1.43%)
Drug Rash With Eosinophilia And Sys...
144 (1.1%)
Neutropenia
142 (1.08%)
Alanine Aminotransferase Increased
141 (1.07%)
Toxic Epidermal Necrolysis
133 (1.01%)
Aspartate Aminotransferase Increase...
123 (.94%)
Sepsis
120 (.91%)
Pruritus
110 (.84%)
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Stevens-johnson Syndrome
110 (.84%)
Condition Aggravated
109 (.83%)
Diarrhoea
109 (.83%)
Pancytopenia
109 (.83%)
Hepatic Function Abnormal
98 (.75%)
Renal Failure
97 (.74%)
Death
96 (.73%)
Pneumonia
96 (.73%)
Drug Interaction
92 (.7%)
Multi-organ Failure
90 (.68%)
Acute Respiratory Distress Syndrome
87 (.66%)
Hypotension
87 (.66%)
Rash Maculo-papular
84 (.64%)
Septic Shock
83 (.63%)
Agranulocytosis
80 (.61%)
Interstitial Lung Disease
79 (.6%)
Rash Erythematous
79 (.6%)
Dyspnoea
77 (.59%)
Eosinophilia
74 (.56%)
Platelet Count Decreased
74 (.56%)
Leukopenia
73 (.56%)
Blood Creatinine Increased
72 (.55%)
Respiratory Failure
72 (.55%)
Liver Disorder
69 (.53%)
White Blood Cell Count Decreased
68 (.52%)
Gamma-glutamyltransferase Increased
67 (.51%)
Blood Alkaline Phosphatase Increase...
65 (.49%)
Cholestasis
65 (.49%)
Renal Impairment
65 (.49%)
Tubulointerstitial Nephritis
64 (.49%)
Drug Hypersensitivity
63 (.48%)
Erythema
63 (.48%)
Disseminated Intravascular Coagulat...
60 (.46%)
Clostridial Infection
59 (.45%)
Paraesthesia
58 (.44%)
Drug Ineffective
57 (.43%)
Blood Bilirubin Increased
56 (.43%)
Hepatic Failure
56 (.43%)
Anaemia
55 (.42%)
Chills
55 (.42%)
Encephalopathy
54 (.41%)
Jaundice
52 (.4%)
Tachycardia
52 (.4%)
Hypoglycaemia
51 (.39%)
Haemorrhage Intracranial
50 (.38%)
Clostridium Difficile Colitis
49 (.37%)
Anaphylactic Reaction
48 (.37%)
Cytolytic Hepatitis
48 (.37%)
Nausea
46 (.35%)
Vomiting
46 (.35%)
Blood Pressure Decreased
45 (.34%)
Oedema Peripheral
45 (.34%)
Urticaria
44 (.33%)
Bone Marrow Failure
42 (.32%)
Convulsion
41 (.31%)
Hypersensitivity
41 (.31%)
Liver Function Test Abnormal
41 (.31%)
Haemoglobin Decreased
40 (.3%)
Rash Generalised
40 (.3%)
Febrile Neutropenia
39 (.3%)
Rash Pruritic
39 (.3%)
Renal Tubular Necrosis
39 (.3%)
Blister
38 (.29%)
Cardio-respiratory Arrest
38 (.29%)
Pain
38 (.29%)
Cardiac Arrest
37 (.28%)
Cardiac Failure
37 (.28%)
Skin Exfoliation
37 (.28%)
Weight Decreased
37 (.28%)
Anaphylactic Shock
36 (.27%)
Drug Eruption
36 (.27%)
Haemolytic Anaemia
36 (.27%)
Lung Disorder
36 (.27%)
Blood Lactate Dehydrogenase Increas...
35 (.27%)
Confusional State
35 (.27%)
Hepatic Enzyme Increased
35 (.27%)
Nephropathy Toxic
35 (.27%)
Dialysis
34 (.26%)
Haemodialysis
34 (.26%)
Decreased Appetite
33 (.25%)
Pleural Effusion
33 (.25%)
Pneumonia Aspiration
33 (.25%)
Renal Disorder
33 (.25%)
Dehydration
32 (.24%)
Dermatitis Exfoliative
32 (.24%)
Hypokalaemia
32 (.24%)
Toxic Skin Eruption
32 (.24%)
Blood Urea Increased
31 (.24%)
International Normalised Ratio Incr...
31 (.24%)
Rhabdomyolysis
31 (.24%)

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

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

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

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

Pneumonia
592
Product Used For Unknown Indication
469
Infection
280
Drug Use For Unknown Indication
239
Sepsis
236
Pyrexia
158
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Pneumonia Aspiration
115
Urinary Tract Infection
108
Febrile Neutropenia
105
Infection Prophylaxis
101
Osteomyelitis
90
Cellulitis
75
Pseudomonas Infection
69
Prophylaxis
69
Antibiotic Therapy
60
Antibiotic Prophylaxis
53
Pyelonephritis
50
Bacteraemia
47
Abdominal Infection
45
Pneumonia Bacterial
41
Lung Disorder
35
Cystic Fibrosis
34
Bacterial Infection
32
Septic Shock
32
Lung Infection
28
Peritonitis
27
Bronchopneumonia
26
Staphylococcal Infection
25
Liver Abscess
24
Urosepsis
24
Ill-defined Disorder
21
Lower Respiratory Tract Infection
21
Antifungal Prophylaxis
20
Wound Infection
20
Cholecystitis
19
Evidence Based Treatment
19
Abscess
19
Pyelonephritis Acute
18
Pneumonia Mycoplasmal
17
Upper Respiratory Tract Infection
17
Lung Infection Pseudomonal
15
Bronchitis
15
Skin Infection
14
Abdominal Abscess
14
Respiratory Tract Infection
14
Anti-infective Therapy
14
Drug Therapy
14
Interstitial Lung Disease
14
Neutropenic Sepsis
14
Empyema
12
Condition Aggravated
11

Drug Labels

LabelLabelerEffective
ZosynCardinal Health07-JUN-11
Zosyn In Galaxy ContainersPfizer Pharmaceuticals LLC, Pfizer Pharmaceutical LLC - Piperacillin08-JUN-12
Zosyn Pharmacy Bulk PackagePfizer Pharmaceuticals LLC, Pfizer Pharmaceutical LLC - Piperacillin08-JUN-12
ZosynPfizer Pharmaceuticals LLC, Pfizer Pharmaceutical LLC - Piperacillin02-JUL-12
Zosyn Pharmacy Bulk PackageWyeth Piperacillin Division of Wyeth Holdings Corporation, a subsidiary of Pfizer20-SEP-12
ZosynWyeth 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

Zosyn Case Reports

What Zosyn 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 Zosyn. 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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