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CELECOX

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Celecox Adverse Events Reported to the FDA Over Time

How are Celecox adverse event reports trending over time?

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

Most Common Celecox Adverse Events Reported to the FDA

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

Drug Eruption
57 (4.82%)
Pyrexia
40 (3.38%)
Rash
25 (2.12%)
Death
22 (1.86%)
Erythema Multiforme
18 (1.52%)
Cardiac Failure
17 (1.44%)
Loss Of Consciousness
17 (1.44%)
Pneumonia
17 (1.44%)
Toxic Skin Eruption
15 (1.27%)
Fall
14 (1.18%)
Interstitial Lung Disease
14 (1.18%)
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Hepatic Function Abnormal
13 (1.1%)
Rash Generalised
13 (1.1%)
Stevens-johnson Syndrome
13 (1.1%)
Platelet Count Decreased
12 (1.02%)
Gastric Ulcer Haemorrhage
11 (.93%)
Laryngeal Oedema
11 (.93%)
Lip Oedema
11 (.93%)
Altered State Of Consciousness
10 (.85%)
Angina Pectoris
10 (.85%)
Diarrhoea
10 (.85%)
Malaise
9 (.76%)
Vomiting
9 (.76%)
Blister
8 (.68%)
Dizziness
8 (.68%)
Gastric Cancer
8 (.68%)
Renal Impairment
8 (.68%)
Skin Laceration
8 (.68%)
Agranulocytosis
7 (.59%)
Drug Interaction
7 (.59%)
Liver Disorder
7 (.59%)
Lumbar Vertebral Fracture
7 (.59%)
Oropharyngeal Pain
7 (.59%)
Pharyngeal Erythema
7 (.59%)
Rash Maculo-papular
7 (.59%)
Systemic Lupus Erythematosus
7 (.59%)
Tongue Oedema
7 (.59%)
Anaemia
6 (.51%)
Anaphylactic Shock
6 (.51%)
Aortic Aneurysm
6 (.51%)
Arterial Thrombosis
6 (.51%)
Chest Pain
6 (.51%)
Deep Vein Thrombosis
6 (.51%)
Dyspnoea
6 (.51%)
Face Oedema
6 (.51%)
Oral Mucosal Eruption
6 (.51%)
Pain
6 (.51%)
Palpitations
6 (.51%)
Retinal Vein Occlusion
6 (.51%)
Subarachnoid Haemorrhage
6 (.51%)
Thromboangiitis Obliterans
6 (.51%)
Urinary Retention
6 (.51%)
Abdominal Pain Upper
5 (.42%)
Bone Marrow Failure
5 (.42%)
Chills
5 (.42%)
Convulsion
5 (.42%)
Enterocolitis
5 (.42%)
Erythema
5 (.42%)
Feeling Abnormal
5 (.42%)
Muscular Weakness
5 (.42%)
Oedema
5 (.42%)
Oedema Mouth
5 (.42%)
Oedema Peripheral
5 (.42%)
Pulmonary Embolism
5 (.42%)
Purpura
5 (.42%)
Somnolence
5 (.42%)
Acute Generalised Exanthematous Pus...
4 (.34%)
Alcoholism
4 (.34%)
Analgesic Asthma Syndrome
4 (.34%)
Anxiety
4 (.34%)
Aortic Dissection
4 (.34%)
Arrhythmia
4 (.34%)
Asthenia
4 (.34%)
Asthma
4 (.34%)
Atrioventricular Block Complete
4 (.34%)
Cerebral Infarction
4 (.34%)
Cheilitis
4 (.34%)
Circulatory Collapse
4 (.34%)
Confusional State
4 (.34%)
Cross Sensitivity Reaction
4 (.34%)
Delusion
4 (.34%)
Dermatitis Exfoliative
4 (.34%)
Duodenal Ulcer
4 (.34%)
Dyspepsia
4 (.34%)
Emphysema
4 (.34%)
Gait Disturbance
4 (.34%)
Haemorrhage Subcutaneous
4 (.34%)
Hallucination
4 (.34%)
Head Injury
4 (.34%)
Hyperhidrosis
4 (.34%)
Hypoalbuminaemia
4 (.34%)
Intestinal Obstruction
4 (.34%)
Mouth Haemorrhage
4 (.34%)
Organising Pneumonia
4 (.34%)
Pancytopenia
4 (.34%)
Skin Necrosis
4 (.34%)
Sudden Onset Of Sleep
4 (.34%)
Swelling Face
4 (.34%)
Thrombocytopenia
4 (.34%)
Tremor
4 (.34%)
Urticaria
4 (.34%)

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

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

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

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

Rheumatoid Arthritis
184
Osteoarthritis
155
Back Pain
60
Arthralgia
20
Pain
16
Spinal Osteoarthritis
15
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Musculoskeletal Pain
12
Analgesic Therapy
12
Periarthritis
5
Oedema Peripheral
5
Headache
4
Psoriatic Arthropathy
4
Arthritis
4
Product Used For Unknown Indication
4
Cancer Pain
3
Scoliosis
3
Antiinflammatory Therapy
3
Drug Use For Unknown Indication
3
Seronegative Arthritis
3
Multiple Myeloma
3
Lumbar Spinal Stenosis
3
Hypoaesthesia
3
Injury
2
Spinal Column Stenosis
2
Stills Disease Adult Onset
2
Metastatic Renal Cell Carcinoma
1
Spinal Compression Fracture
1
Hip Arthroplasty
1
Muscle Strain
1
Cervicobrachial Syndrome
1
Trigeminal Neuralgia
1
Pain In Extremity
1
Procedural Pain
1
Temporal Arteritis
1
Polymyalgia Rheumatica
1
Knee Deformity
1

Celecox Case Reports

What Celecox 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 Celecox. 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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