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KENACORT

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Kenacort Adverse Events Reported to the FDA Over Time

How are Kenacort adverse event reports trending over time?

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

Most Common Kenacort Adverse Events Reported to the FDA

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

Anaphylactic Shock
14 (2.58%)
Endophthalmitis
13 (2.4%)
Intraocular Pressure Increased
9 (1.66%)
Retinal Artery Occlusion
9 (1.66%)
Drug Interaction
8 (1.48%)
Scleral Thinning
8 (1.48%)
Anaphylactic Reaction
7 (1.29%)
Cytomegalovirus Chorioretinitis
7 (1.29%)
Injection Site Atrophy
7 (1.29%)
Malaise
7 (1.29%)
Blindness Unilateral
6 (1.11%)
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Cardiac Arrest
6 (1.11%)
Injection Site Pain
6 (1.11%)
Oesophageal Perforation
6 (1.11%)
Retinal Detachment
6 (1.11%)
Synovitis
6 (1.11%)
Tendon Rupture
6 (1.11%)
Adverse Event
5 (.92%)
Arthritis Bacterial
5 (.92%)
Cataract
5 (.92%)
Cellulitis
5 (.92%)
Chorioretinopathy
5 (.92%)
Depressed Mood
5 (.92%)
Drug Ineffective
5 (.92%)
Glaucoma
5 (.92%)
Haemarthrosis
5 (.92%)
Myocardial Infarction
5 (.92%)
Osteoporosis
5 (.92%)
Pregnancy
5 (.92%)
Transmission Of An Infectious Agent...
5 (.92%)
Adrenal Insufficiency
4 (.74%)
Anaphylactoid Reaction
4 (.74%)
Atrophy
4 (.74%)
Conjunctival Haemorrhage
4 (.74%)
Muscle Atrophy
4 (.74%)
Pain
4 (.74%)
Placental Chorioangioma
4 (.74%)
Retinal Pigment Epitheliopathy
4 (.74%)
Retinal Tear
4 (.74%)
Vision Blurred
4 (.74%)
Anxiety Disorder
3 (.55%)
Arthritis
3 (.55%)
Blood Cortisol Decreased
3 (.55%)
Blood Pressure Decreased
3 (.55%)
Cellulitis Orbital
3 (.55%)
Chest Pain
3 (.55%)
Convulsion
3 (.55%)
Crystal Arthropathy
3 (.55%)
Cushingoid
3 (.55%)
Diabetes Mellitus
3 (.55%)
Erythema
3 (.55%)
Extradural Abscess
3 (.55%)
Eye Abscess
3 (.55%)
Fatigue
3 (.55%)
Gastrointestinal Perforation
3 (.55%)
Herpes Zoster
3 (.55%)
Humerus Fracture
3 (.55%)
Hyperglycaemia
3 (.55%)
Hypertension
3 (.55%)
Joint Instability
3 (.55%)
Lichen Planus
3 (.55%)
Lichen Striatus
3 (.55%)
Muscular Weakness
3 (.55%)
Necrotising Scleritis
3 (.55%)
Paraesthesia
3 (.55%)
Psoas Abscess
3 (.55%)
Pyelonephritis Acute
3 (.55%)
Respiratory Arrest
3 (.55%)
Sensation Of Heaviness
3 (.55%)
Skin Atrophy
3 (.55%)
Throat Tightness
3 (.55%)
Tinnitus
3 (.55%)
Urticaria
3 (.55%)
Uterine Disorder
3 (.55%)
Visual Acuity Reduced
3 (.55%)
Accidental Overdose
2 (.37%)
Altered State Of Consciousness
2 (.37%)
Arthralgia
2 (.37%)
Asthma
2 (.37%)
Back Pain
2 (.37%)
Cardio-respiratory Arrest
2 (.37%)
Cerebral Infarction
2 (.37%)
Cerebrovascular Accident
2 (.37%)
Chorioretinal Disorder
2 (.37%)
Cytolytic Hepatitis
2 (.37%)
Death
2 (.37%)
Depression
2 (.37%)
Dermatitis
2 (.37%)
Disseminated Intravascular Coagulat...
2 (.37%)
Eczema
2 (.37%)
Eye Excision
2 (.37%)
Eye Infection Fungal
2 (.37%)
Eye Inflammation
2 (.37%)
Eyelid Ptosis
2 (.37%)
Faecal Incontinence
2 (.37%)
Flushing
2 (.37%)
Haemorrhage
2 (.37%)
Haemorrhagic Anaemia
2 (.37%)
Hypoaesthesia
2 (.37%)
Injection Site Abscess
2 (.37%)
Injection Site Necrosis
2 (.37%)

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

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

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

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

Rheumatoid Arthritis
39
Macular Oedema
20
Product Used For Unknown Indication
17
Back Pain
13
Behcets Syndrome
12
Scleritis
10
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Pain
9
Osteoarthritis
8
Asthma
7
Retinal Vein Occlusion
7
Rhinitis Allergic
7
Keloid Scar
7
Seasonal Allergy
7
Hypersensitivity
6
Uveitis
5
Carpal Tunnel Syndrome
5
Retinopathy Of Prematurity
4
Retinal Detachment
4
Malignant Ascites
4
Diabetic Retinal Oedema
4
Epicondylitis
4
Eye Operation
4
Sinusitis
4
Endophthalmitis
3
Diabetic Retinopathy
3
Bursitis
3
Drug Use For Unknown Indication
3
Nerve Block
3
Alopecia Areata
3
Choroidal Neovascularisation
3
Tendonitis
3
Trigger Finger
3
Sciatica
3
Periarthritis
3
Myalgia
2
Vogt-koyanagi-harada Syndrome
2
Spinal Column Stenosis
2
Chalazion
2
Maculopathy
2
Otitis Media
2
Endocrine Ophthalmopathy
2
Polyarthritis
2
Joint Effusion
2
Swelling
2
Tenosynovitis
2
Parosmia
2
Thyroid Dermatopathy
2
Musculoskeletal Pain
2
Prophylaxis
2
Stomatitis
2
Retinal Vein Thrombosis
1

Kenacort Case Reports

What Kenacort 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 Kenacort. 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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