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Arcoxia Adverse Events Reported to the FDA Over Time

How are Arcoxia adverse event reports trending over time?

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

Most Common Arcoxia Adverse Events Reported to the FDA

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

Renal Failure Acute
27 (2.75%)
Nausea
25 (2.55%)
Drug Interaction
23 (2.34%)
Melaena
18 (1.83%)
Anaemia
16 (1.63%)
Gastrointestinal Haemorrhage
16 (1.63%)
Drug Ineffective
15 (1.53%)
Duodenal Ulcer
15 (1.53%)
Arthralgia
13 (1.33%)
Diarrhoea
13 (1.33%)
Oedema Peripheral
13 (1.33%)
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Osteonecrosis
13 (1.33%)
Atrial Fibrillation
12 (1.22%)
Pain In Extremity
12 (1.22%)
Vomiting
12 (1.22%)
Weight Increased
12 (1.22%)
Suicide Attempt
11 (1.12%)
Abdominal Pain Upper
10 (1.02%)
Pain
10 (1.02%)
Gastritis Erosive
9 (.92%)
Malaise
9 (.92%)
Stress
9 (.92%)
Blood Cholesterol Increased
8 (.82%)
Haematemesis
8 (.82%)
Blood Triglycerides Increased
7 (.71%)
Cartilage Injury
7 (.71%)
Drug Intolerance
7 (.71%)
Dyspepsia
7 (.71%)
Face Injury
7 (.71%)
Gait Disturbance
7 (.71%)
General Physical Health Deteriorati...
7 (.71%)
Hand Deformity
7 (.71%)
Hepatic Pain
7 (.71%)
Joint Swelling
7 (.71%)
Mouth Injury
7 (.71%)
Pharyngitis
7 (.71%)
Rheumatoid Arthritis
7 (.71%)
Sinusitis
7 (.71%)
Somnolence
7 (.71%)
Abdominal Pain
6 (.61%)
Bradycardia
6 (.61%)
Chest Pain
6 (.61%)
Constipation
6 (.61%)
Dysgeusia
6 (.61%)
Fatigue
6 (.61%)
Hepatitis Acute
6 (.61%)
Hepatitis Toxic
6 (.61%)
Liver Function Test Abnormal
6 (.61%)
C-reactive Protein Increased
5 (.51%)
Cerebrovascular Accident
5 (.51%)
Death
5 (.51%)
Dehydration
5 (.51%)
Depressed Level Of Consciousness
5 (.51%)
Gastric Ulcer Haemorrhage
5 (.51%)
Hypoaesthesia
5 (.51%)
International Normalised Ratio Incr...
5 (.51%)
Intestinal Ulcer
5 (.51%)
Lethargy
5 (.51%)
Blood Creatinine Increased
4 (.41%)
Deep Vein Thrombosis
4 (.41%)
Depression
4 (.41%)
Dialysis
4 (.41%)
Dizziness
4 (.41%)
Drug Abuse
4 (.41%)
Gastric Ulcer
4 (.41%)
Hypotension
4 (.41%)
Insomnia
4 (.41%)
Intentional Overdose
4 (.41%)
Left Atrial Dilatation
4 (.41%)
Loss Of Consciousness
4 (.41%)
Myocardial Infarction
4 (.41%)
Renal Failure
4 (.41%)
Subileus
4 (.41%)
Urinary Tract Infection
4 (.41%)
Weight Decreased
4 (.41%)
Alanine Aminotransferase Increased
3 (.31%)
Asthenia
3 (.31%)
Benign Prostatic Hyperplasia
3 (.31%)
Blood Alkaline Phosphatase Increase...
3 (.31%)
Blood Glucose Increased
3 (.31%)
Blood Pressure Decreased
3 (.31%)
Bundle Branch Block
3 (.31%)
Cardiac Failure
3 (.31%)
Cardioactive Drug Level Increased
3 (.31%)
Cholelithiasis
3 (.31%)
Confusional State
3 (.31%)
Convulsion
3 (.31%)
Crying
3 (.31%)
Diverticulitis
3 (.31%)
Dyspnoea
3 (.31%)
Gout
3 (.31%)
Haemoglobin Decreased
3 (.31%)
Hepatic Necrosis
3 (.31%)
Hypertension
3 (.31%)
Infection
3 (.31%)
Ischaemic Stroke
3 (.31%)
Nephrotic Syndrome
3 (.31%)
Pancytopenia
3 (.31%)
Platelet Count Decreased
3 (.31%)
Pulmonary Arterial Hypertension
3 (.31%)
Pyrexia
3 (.31%)

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

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

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

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

Product Used For Unknown Indication
135
Rheumatoid Arthritis
131
Pain
88
Drug Use For Unknown Indication
80
Osteoarthritis
74
Ankylosing Spondylitis
35
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Arthralgia
23
Arthritis
23
Psoriatic Arthropathy
20
Pain In Extremity
17
Prostate Cancer
9
Back Pain
8
Spondylitis
8
Musculoskeletal Discomfort
6
Osteolysis
5
Tendonitis
5
Rib Fracture
5
Polyarthritis
5
Inflammation
4
Neuralgia
4
Osteoporosis
4
Spinal Cord Disorder
4
Procedural Pain
3
Antiinflammatory Therapy
3
Bone Pain
3
Intervertebral Disc Protrusion
3
Crohns Disease
2
Arthritis Bacterial
2
Depression
2
Analgesia
2
Musculoskeletal Pain
2
Spinal Fracture
2
Behcets Syndrome
2
Neck Pain
2
Lower Limb Fracture
2
Prophylaxis
1
Breast Cancer Metastatic
1
Rotator Cuff Syndrome
1
Renal Cell Carcinoma
1
Spinal Osteoarthritis
1
Rhinitis Allergic
1
Post-traumatic Stress Disorder
1
Spinal Column Injury
1
Ill-defined Disorder
1
Radicular Pain
1
Spinal Pain
1
Hypoaesthesia
1
Analgesic Therapy
1
Osteochondrosis
1
Myalgia
1
Tendon Disorder
1

Arcoxia Case Reports

What Arcoxia 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 Arcoxia. 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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