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OFLOXACIN

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Ofloxacin Adverse Events Reported to the FDA Over Time

How are Ofloxacin adverse event reports trending over time?

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

Most Common Ofloxacin Adverse Events Reported to the FDA

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

Pyrexia
62 (1.62%)
Drug Interaction
56 (1.46%)
Drug Rash With Eosinophilia And Sys...
56 (1.46%)
Corneal Deposits
44 (1.15%)
Thrombocytopenia
44 (1.15%)
Renal Failure Acute
43 (1.12%)
Confusional State
34 (.89%)
Diarrhoea
32 (.84%)
Dyspnoea
32 (.84%)
Eosinophilia
28 (.73%)
Anxiety
26 (.68%)
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Drug Ineffective
26 (.68%)
Neutropenia
26 (.68%)
Headache
24 (.63%)
Alanine Aminotransferase Increased
23 (.6%)
Anaemia
23 (.6%)
Cytolytic Hepatitis
23 (.6%)
Nausea
23 (.6%)
Cholestasis
22 (.58%)
Dizziness
22 (.58%)
Condition Aggravated
21 (.55%)
Rash
21 (.55%)
Toxic Epidermal Necrolysis
21 (.55%)
Encephalopathy
20 (.52%)
Oedema Peripheral
20 (.52%)
Pain
20 (.52%)
Blood Alkaline Phosphatase Increase...
19 (.5%)
Renal Failure
19 (.5%)
Septic Shock
19 (.5%)
White Blood Cell Count Decreased
19 (.5%)
Agranulocytosis
18 (.47%)
Arthralgia
18 (.47%)
Fear
18 (.47%)
General Physical Health Deteriorati...
18 (.47%)
Hepatitis
18 (.47%)
Jaundice
18 (.47%)
Pancytopenia
18 (.47%)
Myalgia
17 (.44%)
Sepsis
17 (.44%)
Asthenia
16 (.42%)
Blood Bilirubin Increased
16 (.42%)
Leukopenia
16 (.42%)
Pruritus
16 (.42%)
Psychotic Disorder
16 (.42%)
Urinary Tract Infection
16 (.42%)
Aphasia
15 (.39%)
Cardiac Arrest
15 (.39%)
Gait Disturbance
15 (.39%)
Gamma-glutamyltransferase Increased
15 (.39%)
Myoclonus
15 (.39%)
Respiratory Distress
15 (.39%)
Staphylococcal Infection
15 (.39%)
Atrial Fibrillation
14 (.37%)
International Normalised Ratio Incr...
14 (.37%)
Medication Error
14 (.37%)
Muscular Weakness
14 (.37%)
Toxic Skin Eruption
14 (.37%)
Wrong Drug Administered
14 (.37%)
Anorexia
13 (.34%)
Aspartate Aminotransferase Increase...
13 (.34%)
Depressed Mood
13 (.34%)
Erythema
13 (.34%)
Immobile
13 (.34%)
Infection
13 (.34%)
Abdominal Pain Upper
12 (.31%)
Back Pain
12 (.31%)
Drug Dispensing Error
12 (.31%)
Drug Hypersensitivity
12 (.31%)
Hyperreflexia
12 (.31%)
Insomnia
12 (.31%)
Negative Thoughts
12 (.31%)
Palpitations
12 (.31%)
Paraesthesia
12 (.31%)
Paranoia
12 (.31%)
Psychotic Disorder Due To A General...
12 (.31%)
Purpura
12 (.31%)
Toxic Anterior Segment Syndrome
12 (.31%)
Urticaria
12 (.31%)
Agitation
11 (.29%)
Blood Urine Present
11 (.29%)
Cardiac Failure
11 (.29%)
Depression
11 (.29%)
Ear Pain
11 (.29%)
Hypertension
11 (.29%)
Pain In Extremity
11 (.29%)
Platelet Count Increased
11 (.29%)
Rhabdomyolysis
11 (.29%)
Tendon Rupture
11 (.29%)
Tendonitis
11 (.29%)
Tumour Lysis Syndrome
11 (.29%)
Urine Analysis Abnormal
11 (.29%)
Vision Blurred
11 (.29%)
Vomiting
11 (.29%)
Anaphylactic Reaction
10 (.26%)
Convulsion
10 (.26%)
Depressed Level Of Consciousness
10 (.26%)
Extensor Plantar Response
10 (.26%)
Gastrointestinal Haemorrhage
10 (.26%)
Haemoglobin Decreased
10 (.26%)
Inflammation
10 (.26%)
Multi-organ Failure
10 (.26%)

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

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

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

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

Drug Use For Unknown Indication
105
Urinary Tract Infection
94
Product Used For Unknown Indication
93
Pelvic Inflammatory Disease
33
Conjunctivitis
27
Ill-defined Disorder
24
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Prostatitis
24
Ulcerative Keratitis
20
Osteitis
18
Infection
17
Ear Infection
17
Tuberculosis
17
Infection Prophylaxis
16
Prophylaxis
14
Lung Disorder
12
Pneumonia
12
Typhoid Fever
11
Postoperative Care
11
Sepsis
10
Bronchitis
9
Keratitis Fungal
8
Corneal Erosion
8
Arthritis Bacterial
8
Pulmonary Tuberculosis
8
Pyelonephritis
8
Cataract Operation
7
Pyrexia
7
Diarrhoea
7
Otitis Externa
7
Pelvic Infection
6
Antibiotic Therapy
6
Device Related Infection
6
Bronchopulmonary Aspergillosis
6
Cystitis
6
Erysipelas
6
Keratitis
6
Conjunctivitis Allergic
6
Lung Infection
5
Bronchopneumonia
5
Eye Infection
5
Uveitis
5
Inflammation
5
Corneal Epithelium Defect
5
Febrile Neutropenia
5
Pyelonephritis Acute
5
Bacterial Infection
4
Escherichia Infection
4
Keratitis Bacterial
4
Endocarditis
4
Staphylococcal Infection
4
External Ear Inflammation
4

Drug Labels

LabelLabelerEffective
OfloxacinPack Pharmaceuticals, LLC04-JAN-10
OfloxacinDr. Reddy's Laboratories Limited08-JAN-10
OfloxacinPharmaForce, Inc.22-JAN-10
OfloxacinPhysicians Total Care, Inc.27-APR-10
OfloxacinKeltman Pharmaceuticals Inc.03-AUG-10
OfloxacinSTAT RX LLC USA15-SEP-10
OfloxacinRebel Distributors Corp22-OCT-10
OfloxacinFalcon Pharmaceuticals, Ltd.11-MAR-11
OfloxacinAscend Laboratories, LLC13-APR-11
OfloxacinFalcon Pharmaceuticals, Ltd.04-AUG-11
OfloxacinSTAT RX USA LLC23-AUG-11
Ofloxacin H.J. Harkins Company, Inc.08-SEP-11
OfloxacinRebel Distributors Corp13-SEP-11
OfloxacinAkorn, Inc.13-DEC-11
OcufloxAllergan, Inc.29-FEB-12
OfloxacinBausch & Lomb Incorporated21-JUN-12
Ofloxacin OticApotex Corp.22-JUN-12
OfloxacinRebel Distributors Corp31-JUL-12
OfloxacinHi-Tech Pharmacal Co., Inc.06-SEP-12
Ofloxacin OphthalmicApotex Corp.07-SEP-12
OfloxacinTeva Pharmaceuticals USA Inc27-SEP-12
OfloxacinHi-Tech Pharmacal Co., Inc.09-OCT-12
OfloxacinPhysicians Total Care, Inc.22-OCT-12
OfloxacinPreferred Pharmaceuticals, Inc14-MAR-13
OfloxacinPreferred Pharmaceuticals, Inc.22-MAR-13
OfloxacinREMEDYREPACK INC. 27-MAR-13
OfloxacinBausch & Lomb Incorporated19-APR-13
OfloxacinBausch & Lomb Incorporated30-APR-13

Ofloxacin Case Reports

What Ofloxacin 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 Ofloxacin. 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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