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CORTISONE ACETATE

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Cortisone Acetate Adverse Events Reported to the FDA Over Time

How are Cortisone Acetate adverse event reports trending over time?

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

Most Common Cortisone Acetate Adverse Events Reported to the FDA

What are the most common Cortisone Acetate adverse events reported to the FDA?

Drug Ineffective
75 (2.4%)
Arthralgia
51 (1.63%)
Pain
46 (1.47%)
Weight Increased
46 (1.47%)
Nausea
45 (1.44%)
Dyspnoea
39 (1.25%)
Headache
38 (1.22%)
Hypersensitivity
34 (1.09%)
Fatigue
32 (1.02%)
Blood Glucose Increased
30 (.96%)
Drug Hypersensitivity
29 (.93%)
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Pain In Extremity
29 (.93%)
Vision Blurred
29 (.93%)
Vomiting
29 (.93%)
Erythema
25 (.8%)
Malaise
25 (.8%)
Hyperhidrosis
23 (.74%)
Pruritus
23 (.74%)
Asthenia
22 (.7%)
Back Pain
22 (.7%)
Dizziness
21 (.67%)
Glioma
21 (.67%)
Pyrexia
21 (.67%)
Swelling
21 (.67%)
Condition Aggravated
19 (.61%)
Constipation
19 (.61%)
Insomnia
19 (.61%)
Tremor
18 (.58%)
Arthropathy
17 (.54%)
Oedema Peripheral
17 (.54%)
Septic Shock
17 (.54%)
Diabetes Mellitus
16 (.51%)
Fall
16 (.51%)
Asthma
15 (.48%)
Cataract
15 (.48%)
Diarrhoea
15 (.48%)
Dyspepsia
15 (.48%)
Urticaria
15 (.48%)
Muscle Spasms
14 (.45%)
Osteonecrosis
14 (.45%)
Weight Decreased
14 (.45%)
Abdominal Pain
13 (.42%)
Gait Disturbance
13 (.42%)
Rash
13 (.42%)
Dysgeusia
12 (.38%)
Hepatitis
12 (.38%)
Muscular Weakness
12 (.38%)
Rotator Cuff Syndrome
12 (.38%)
Tendonitis
12 (.38%)
Anaemia
11 (.35%)
Fibromyalgia
11 (.35%)
Hypoaesthesia
11 (.35%)
Inflammation
11 (.35%)
Musculoskeletal Pain
11 (.35%)
Oesophageal Pain
11 (.35%)
Somnolence
11 (.35%)
Swelling Face
11 (.35%)
Blood Pressure Increased
10 (.32%)
Depression
10 (.32%)
Feeling Abnormal
10 (.32%)
Intervertebral Disc Protrusion
10 (.32%)
Myalgia
10 (.32%)
Rheumatoid Arthritis
10 (.32%)
Tendon Rupture
10 (.32%)
Burning Sensation
9 (.29%)
Cardiac Arrest
9 (.29%)
Completed Suicide
9 (.29%)
Dysphonia
9 (.29%)
Nerve Injury
9 (.29%)
Pharyngeal Oedema
9 (.29%)
Speech Disorder
9 (.29%)
Atrial Fibrillation
8 (.26%)
Convulsion
8 (.26%)
Feeling Cold
8 (.26%)
Fungaemia
8 (.26%)
Gastrointestinal Disorder
8 (.26%)
Heart Rate Increased
8 (.26%)
Hepatic Enzyme Increased
8 (.26%)
Hepatotoxicity
8 (.26%)
Hypertension
8 (.26%)
Impaired Healing
8 (.26%)
Jaundice
8 (.26%)
Lethargy
8 (.26%)
Osteoporosis
8 (.26%)
Renal Failure
8 (.26%)
Rhinitis
8 (.26%)
Trigger Finger
8 (.26%)
Amnesia
7 (.22%)
Arrhythmia
7 (.22%)
Cerebral Haemorrhage
7 (.22%)
Cholelithiasis
7 (.22%)
Disorientation
7 (.22%)
Drug Interaction
7 (.22%)
Dry Mouth
7 (.22%)
Feeling Jittery
7 (.22%)
Irritability
7 (.22%)
Joint Swelling
7 (.22%)
Loss Of Consciousness
7 (.22%)
Myopia
7 (.22%)
Pneumonia
7 (.22%)
Respiratory Arrest
7 (.22%)

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

What are the most common Cortisone Acetate adverse events reported to the FDA?

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

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

Product Used For Unknown Indication
434
Rheumatoid Arthritis
246
Drug Use For Unknown Indication
205
Crohns Disease
89
Pain
56
Arthritis
46
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Asthma
44
Arthralgia
41
Premedication
33
Blood Corticotrophin Decreased
30
Adrenal Insufficiency
29
Back Pain
28
Acute Lymphocytic Leukaemia
26
Psoriatic Arthropathy
25
Rash
21
Prophylaxis
21
Hypersensitivity
19
Bursitis
19
Pruritus
15
Multiple Sclerosis
15
Addisons Disease
15
Psoriasis
15
Inflammation
14
Ill-defined Disorder
13
Polymyalgia Rheumatica
13
Musculoskeletal Pain
12
Hormone Replacement Therapy
12
Intervertebral Disc Protrusion
11
Renal Transplant
10
Dyspnoea
10
Colitis Ulcerative
10
Hypopituitarism
10
Heart Transplant
10
Juvenile Arthritis
10
Pain In Extremity
10
Multiple Sclerosis Relapse
10
Polyarthritis
10
Urticaria
9
Prophylaxis Against Transplant Reje...
9
Sjogrens Syndrome
9
Ankylosing Spondylitis
9
Autoimmune Hepatitis
8
Back Disorder
7
Joint Swelling
7
Osteoarthritis
7
Systemic Lupus Erythematosus
7
Pulmonary Fibrosis
7
Spondylitis
6
Eczema
6
Swelling
6
Exostosis
6

Drug Labels

LabelLabelerEffective
Cortisone AcetateWest-ward Pharmaceutical Corp08-JUN-10
Cortisone AcetateGolden State Medical Supply, Inc.01-JUL-11

Cortisone Acetate Case Reports

What Cortisone Acetate 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 Cortisone Acetate. 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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