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CEFZON

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Cefzon Adverse Events Reported to the FDA Over Time

How are Cefzon adverse event reports trending over time?

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

Most Common Cefzon Adverse Events Reported to the FDA

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

Pyrexia
84 (4.66%)
Toxic Epidermal Necrolysis
63 (3.5%)
Liver Disorder
56 (3.11%)
Aspartate Aminotransferase Increase...
42 (2.33%)
Stevens-johnson Syndrome
37 (2.05%)
Hepatic Function Abnormal
31 (1.72%)
Alanine Aminotransferase Increased
29 (1.61%)
Gamma-glutamyltransferase Increased
26 (1.44%)
Rash
26 (1.44%)
Erythema
25 (1.39%)
Blood Alkaline Phosphatase Increase...
21 (1.17%)
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Depressed Level Of Consciousness
21 (1.17%)
Pneumonia
21 (1.17%)
Pallor
19 (1.05%)
Drug Eruption
18 (1%)
Haemolytic Anaemia
17 (.94%)
Multi-organ Failure
17 (.94%)
Platelet Count Decreased
17 (.94%)
Renal Failure Acute
17 (.94%)
Blood Bilirubin Increased
16 (.89%)
C-reactive Protein Increased
16 (.89%)
Conjunctival Hyperaemia
16 (.89%)
Disseminated Intravascular Coagulat...
16 (.89%)
Erythema Multiforme
16 (.89%)
Blood Lactate Dehydrogenase Increas...
15 (.83%)
Convulsion
15 (.83%)
White Blood Cell Count Increased
14 (.78%)
Asthenia
13 (.72%)
Ocular Icterus
13 (.72%)
Chromaturia
12 (.67%)
Drug Exposure During Pregnancy
12 (.67%)
Haematochezia
12 (.67%)
Pruritus
12 (.67%)
Dyspnoea
11 (.61%)
Anorexia
10 (.56%)
Diarrhoea
10 (.56%)
Histiocytosis Haematophagic
10 (.56%)
Sepsis
10 (.56%)
Body Temperature Increased
9 (.5%)
Feeling Abnormal
9 (.5%)
Hypertension
9 (.5%)
Nephrotic Syndrome
9 (.5%)
Restlessness
9 (.5%)
Urinary Retention
9 (.5%)
Wheezing
9 (.5%)
Acute Generalised Exanthematous Pus...
8 (.44%)
Agranulocytosis
8 (.44%)
Alanine Aminotransferase
8 (.44%)
Condition Aggravated
8 (.44%)
Cough
8 (.44%)
Cytomegalovirus Infection
8 (.44%)
Eye Discharge
8 (.44%)
Hepatitis Cholestatic
8 (.44%)
Ocular Hyperaemia
8 (.44%)
Thirst
8 (.44%)
Ulcerative Keratitis
8 (.44%)
Abnormal Behaviour
7 (.39%)
Acute Hepatic Failure
7 (.39%)
Blood Pressure Decreased
7 (.39%)
Constipation
7 (.39%)
Dehydration
7 (.39%)
Dyspepsia
7 (.39%)
Eosinophil Count Increased
7 (.39%)
Generalised Erythema
7 (.39%)
Hepatitis Fulminant
7 (.39%)
Infection
7 (.39%)
Lip Swelling
7 (.39%)
Nasopharyngitis
7 (.39%)
Arthralgia
6 (.33%)
Cardiac Arrest
6 (.33%)
Cheilitis
6 (.33%)
Confusional State
6 (.33%)
Decreased Appetite
6 (.33%)
Dizziness
6 (.33%)
Eosinophilic Pneumonia
6 (.33%)
Fall
6 (.33%)
Heart Rate Decreased
6 (.33%)
Infectious Mononucleosis
6 (.33%)
Iron Deficiency Anaemia
6 (.33%)
Lymphocyte Stimulation Test Positiv...
6 (.33%)
Movement Disorder
6 (.33%)
Muscle Disorder
6 (.33%)
Nausea
6 (.33%)
Neutropenia
6 (.33%)
Oral Herpes
6 (.33%)
Shock
6 (.33%)
Spinal Compression Fracture
6 (.33%)
Swelling
6 (.33%)
Threatened Labour
6 (.33%)
Urticaria
6 (.33%)
White Blood Cell Count Decreased
6 (.33%)
Aplastic Anaemia
5 (.28%)
Blood Creatinine Increased
5 (.28%)
Blood Immunoglobulin E Increased
5 (.28%)
Chills
5 (.28%)
Death
5 (.28%)
Drug Hypersensitivity
5 (.28%)
Excoriation
5 (.28%)
Faeces Discoloured
5 (.28%)
Gait Disturbance
5 (.28%)
Haematuria
5 (.28%)

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

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

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

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

Drug Use For Unknown Indication
91
Upper Respiratory Tract Inflammatio...
44
Pyrexia
40
Nasopharyngitis
30
Pharyngitis
28
Infection Prophylaxis
24
Show More Show More
Infection
21
Product Used For Unknown Indication
16
Urinary Tract Infection
14
Cellulitis
11
Influenza
11
Bronchitis
10
Acute Tonsillitis
9
Inflammation
9
Bronchitis Acute
9
Pneumonia
8
Bacterial Infection
8
Contusion
8
Laryngopharyngitis
8
Prophylaxis
8
Herpes Zoster
7
Post Procedural Infection
7
Drug Exposure During Pregnancy
6
Cystitis
6
Skin Ulcer
5
Impetigo
5
Upper Respiratory Tract Infection
5
Antibacterial Prophylaxis
4
Wound Abscess
4
Hordeolum
4
Wound Infection
4
Postoperative Infection
4
Tonsillitis
3
Arthritis Bacterial
3
Purulence
3
Gastroenteritis
3
Otitis Media Acute
3
Pneumonia Streptococcal
3
Subcutaneous Abscess
3
Antibiotic Prophylaxis
3
Injury
3
Antipyresis
3
Rash Pustular
2
Pharyngitis Streptococcal
2
Balanoposthitis
2
Thermal Burn
2
Periodontitis
2
Pyoderma
2
Hyperthermia
2
Toothache
2
Penile Discharge
2

Cefzon Case Reports

What Cefzon 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 Cefzon. 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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