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Cefuroxime Adverse Events Reported to the FDA Over Time

How are Cefuroxime adverse event reports trending over time?

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

Most Common Cefuroxime Adverse Events Reported to the FDA

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

Vomiting
196 (1.94%)
Diarrhoea
169 (1.67%)
Anaphylactic Shock
156 (1.54%)
Dyspnoea
151 (1.49%)
Pruritus
142 (1.4%)
Rash
137 (1.35%)
Nausea
133 (1.31%)
Pyrexia
133 (1.31%)
Drug Ineffective
116 (1.15%)
Hypotension
107 (1.06%)
Erythema
104 (1.03%)
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Hypersensitivity
101 (1%)
Urticaria
95 (.94%)
Drug Interaction
82 (.81%)
Drug Hypersensitivity
74 (.73%)
Anaphylactic Reaction
71 (.7%)
Renal Failure Acute
69 (.68%)
Blood Pressure Decreased
68 (.67%)
Product Quality Issue
67 (.66%)
Abdominal Pain
63 (.62%)
Drug Exposure During Pregnancy
60 (.59%)
Loss Of Consciousness
60 (.59%)
Bronchospasm
59 (.58%)
Asthenia
57 (.56%)
Clostridium Difficile Colitis
57 (.56%)
Toxic Epidermal Necrolysis
53 (.52%)
Alanine Aminotransferase Increased
52 (.51%)
Dizziness
51 (.5%)
Malaise
51 (.5%)
Visual Acuity Reduced
51 (.5%)
Headache
50 (.49%)
Tachycardia
50 (.49%)
Pneumonia
47 (.46%)
Urinary Tract Infection
46 (.45%)
Chills
45 (.44%)
Cough
44 (.43%)
Fatigue
43 (.43%)
Abdominal Pain Upper
41 (.41%)
Blood Bilirubin Increased
41 (.41%)
Swelling Face
41 (.41%)
Jaundice
40 (.4%)
Oedema Peripheral
38 (.38%)
Rash Erythematous
38 (.38%)
Aspartate Aminotransferase Increase...
37 (.37%)
Dehydration
37 (.37%)
Face Oedema
37 (.37%)
General Physical Health Deteriorati...
37 (.37%)
Angioedema
36 (.36%)
Endophthalmitis
36 (.36%)
Rash Generalised
36 (.36%)
Convulsion
35 (.35%)
Dysgeusia
35 (.35%)
Hypertension
35 (.35%)
Circulatory Collapse
34 (.34%)
Syncope
34 (.34%)
Hyperhidrosis
33 (.33%)
Thrombocytopenia
33 (.33%)
Abortion Spontaneous
32 (.32%)
Flushing
32 (.32%)
Gamma-glutamyltransferase Increased
32 (.32%)
Blister
31 (.31%)
Dysphagia
31 (.31%)
Sepsis
31 (.31%)
Arthralgia
30 (.3%)
Multi-organ Failure
29 (.29%)
Pain
29 (.29%)
Pallor
29 (.29%)
Clostridial Infection
28 (.28%)
Blindness
27 (.27%)
Confusional State
26 (.26%)
Incorrect Route Of Drug Administrat...
26 (.26%)
Intraocular Pressure Increased
26 (.26%)
Oxygen Saturation Decreased
26 (.26%)
Parophthalmia
26 (.26%)
Wheezing
26 (.26%)
Back Pain
25 (.25%)
Choking
25 (.25%)
Conjunctival Oedema
25 (.25%)
Corneal Deposits
25 (.25%)
Cyanosis
25 (.25%)
Generalised Erythema
25 (.25%)
Lip Swelling
25 (.25%)
Sinusitis
25 (.25%)
Acute Respiratory Distress Syndrome
24 (.24%)
Condition Aggravated
24 (.24%)
Hepatic Failure
24 (.24%)
Oedema
24 (.24%)
Pharyngeal Oedema
24 (.24%)
Shock
24 (.24%)
Swollen Tongue
24 (.24%)
Blood Alkaline Phosphatase Increase...
23 (.23%)
Corneal Opacity
23 (.23%)
Hepatitis
23 (.23%)
Hypokalaemia
23 (.23%)
Leukocytoclastic Vasculitis
23 (.23%)
Swelling
23 (.23%)
Tremor
23 (.23%)
Anxiety
22 (.22%)
Chest Discomfort
22 (.22%)
Eosinophilia
22 (.22%)
Fall
22 (.22%)

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

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

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

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

Drug Use For Unknown Indication
307
Product Used For Unknown Indication
302
Sinusitis
163
Urinary Tract Infection
156
Pneumonia
148
Prophylaxis
130
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Bronchitis
110
Infection
110
Antibiotic Prophylaxis
94
Infection Prophylaxis
81
Upper Respiratory Tract Infection
77
Pyrexia
53
Cataract Operation
47
Ear Infection
41
Respiratory Tract Infection
38
Otitis Media Acute
37
Pharyngitis
36
Lyme Disease
34
Tonsillitis
34
Bacterial Infection
30
Sepsis
29
Postoperative Care
26
Antibiotic Therapy
24
Lobar Pneumonia
20
Lower Respiratory Tract Infection
20
Ill-defined Disorder
19
Bronchopneumonia
15
Nasopharyngitis
14
Lung Infection
14
Cellulitis
13
Eye Infection
13
Otitis Media
13
Endocarditis
13
Surgery
12
Acute Sinusitis
12
Cough
12
Diverticulitis
12
Skin Infection
11
Pyelonephritis
11
Cystitis
11
Peritonitis
11
Pneumonia Aspiration
10
Staphylococcal Infection
9
Erysipelas
9
Periodontitis
9
Inflammation
9
Influenza
9
Cholecystitis
9
Preoperative Care
8
Asthma
8
Keratitis Fungal
8

Drug Labels

LabelLabelerEffective
CefuroximeWest-ward Pharmaceutical Corp13-JAN-10
CefuroximeWest-ward Pharmaceutical Corp14-JAN-10
Cefuroxime SodiumSamson Medical Technologies, L.L.C.08-FEB-10
CefuroximeHospira, Inc.07-JUN-10
CefuroximeHospira, Inc.07-JUN-10
Cefuroxime AxetilMedVantx, Inc.22-JUN-10
CefuroximeAPP Pharmaceuticals, LLC30-AUG-10
Cefuroxime AxetilRebel Distributors Corp22-SEP-10
Cefuroxime AxetilAscend Laboratories, LLC03-DEC-10
Cefuroxime AxetilPhysicians Total Care, Inc.09-DEC-10
CefuroximeSagent Pharmaceuticals28-DEC-10
Cefuroxime Axetil LUPIN PHARMACEUTICALS INC29-MAR-11
CefuroximeAPP Pharmaceuticals, LLC24-MAY-11
ZinacefGlaxoSmithKline LLC07-JUN-11
Cefuroxime SodiumSagent Pharmaceuticals21-OCT-11
Cefuroxime Axetil H.J. Harkins Company, Inc.22-DEC-11
Cefuroxime Axetil H.J. Harkins Company, Inc.29-DEC-11
Cefuroxime AxetilGreenstone LLC18-JAN-12
Cefuroxime AxetilPD-Rx Pharmaceuticals, Inc.02-FEB-12
Cefuroxime AxetilPD-Rx Pharmaceuticals, Inc.02-FEB-12
Cefuroxime AxetilPD-Rx Pharmaceuticals, Inc.02-FEB-12
Cefuroxime AxetilWockhardt USA LLC.02-FEB-12
Cefuroxime AxetilWockhardt Limited08-FEB-12
Cefuroxime And DextroseB. Braun Medical Inc.17-APR-12
Cefuroxime AxetilNorthstar Rx LLC28-AUG-12
Cefuroxime AxetilSTAT Rx USA LLC30-AUG-12
CefuroximeWG Critical Care, LLC04-OCT-12
CefuroximeWG Critical Care, LLC04-OCT-12
Cefuroxime AxetilApotex Corp.21-NOV-12
Cefuroxime AxetilAurobindo Pharma Limited21-JAN-13
Cefuroxime AxetilPreferred Pharmaceuticals, Inc.15-MAR-13

Cefuroxime Case Reports

What Cefuroxime 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 Cefuroxime. 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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