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CELEBRA

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Celebra Adverse Events Reported to the FDA Over Time

How are Celebra adverse event reports trending over time?

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

Most Common Celebra Adverse Events Reported to the FDA

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

Drug Ineffective
31 (2.42%)
Hypersensitivity
28 (2.19%)
Dyspnoea
23 (1.8%)
Abdominal Pain Upper
19 (1.48%)
Arthralgia
19 (1.48%)
Nausea
17 (1.33%)
Vomiting
16 (1.25%)
Fall
14 (1.09%)
Pain
14 (1.09%)
Pain In Extremity
14 (1.09%)
Abdominal Pain
13 (1.02%)
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Dizziness
13 (1.02%)
Erythema
12 (.94%)
Amnesia
11 (.86%)
Asthenia
11 (.86%)
Blood Pressure Increased
11 (.86%)
Malaise
11 (.86%)
Chest Pain
10 (.78%)
Headache
10 (.78%)
Myocardial Infarction
10 (.78%)
Pruritus
10 (.78%)
Swelling Face
10 (.78%)
Tachycardia
10 (.78%)
Tremor
10 (.78%)
Vision Blurred
9 (.7%)
Weight Decreased
9 (.7%)
Feeling Abnormal
8 (.63%)
Renal Pain
8 (.63%)
Somnolence
8 (.63%)
Swelling
8 (.63%)
Anaemia
7 (.55%)
Arrhythmia
7 (.55%)
Blood Pressure Decreased
7 (.55%)
Dehydration
7 (.55%)
Diplopia
7 (.55%)
Fatigue
7 (.55%)
Formication
7 (.55%)
Hypertension
7 (.55%)
Hypoaesthesia
7 (.55%)
Labyrinthitis
7 (.55%)
Oedema Mouth
7 (.55%)
Throat Tightness
7 (.55%)
Blindness
6 (.47%)
Blood Cholesterol Increased
6 (.47%)
Cardiac Disorder
6 (.47%)
Death
6 (.47%)
Drug Hypersensitivity
6 (.47%)
Eye Swelling
6 (.47%)
Feeling Hot
6 (.47%)
Haematemesis
6 (.47%)
Haemorrhage
6 (.47%)
Hypotension
6 (.47%)
Limb Injury
6 (.47%)
Memory Impairment
6 (.47%)
Paraesthesia
6 (.47%)
Purulence
6 (.47%)
Rash Macular
6 (.47%)
Renal Failure
6 (.47%)
Skin Exfoliation
6 (.47%)
Spinal Disorder
6 (.47%)
Stevens-johnson Syndrome
6 (.47%)
Arthropathy
5 (.39%)
Asthma
5 (.39%)
Cardiac Arrest
5 (.39%)
Cerebral Infarction
5 (.39%)
Cerebrovascular Accident
5 (.39%)
Cold Sweat
5 (.39%)
Constipation
5 (.39%)
Crying
5 (.39%)
Face Oedema
5 (.39%)
Hyperhidrosis
5 (.39%)
Insomnia
5 (.39%)
Oedema Peripheral
5 (.39%)
Pruritus Generalised
5 (.39%)
Sensory Disturbance
5 (.39%)
Suffocation Feeling
5 (.39%)
Syncope
5 (.39%)
Abasia
4 (.31%)
Abdominal Distension
4 (.31%)
Acute Myocardial Infarction
4 (.31%)
Anaphylactic Shock
4 (.31%)
Anorexia
4 (.31%)
Blister
4 (.31%)
Blood Glucose Decreased
4 (.31%)
Burning Sensation
4 (.31%)
Bursitis
4 (.31%)
Cardiac Failure
4 (.31%)
Convulsion
4 (.31%)
Cough
4 (.31%)
Diarrhoea
4 (.31%)
Drug Ineffective For Unapproved Ind...
4 (.31%)
Drug Interaction
4 (.31%)
Dysarthria
4 (.31%)
Dysentery
4 (.31%)
Ear Injury
4 (.31%)
Flatulence
4 (.31%)
Gait Disturbance
4 (.31%)
Gastrointestinal Disorder
4 (.31%)
Hyponatraemia
4 (.31%)
Hypophosphataemia
4 (.31%)
Laziness
4 (.31%)

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

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

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

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

Pain
55
Rheumatoid Arthritis
36
Osteoarthritis
31
Arthralgia
22
Back Pain
21
Arthritis
19
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Tendonitis
13
Product Used For Unknown Indication
13
Myalgia
11
Pain In Extremity
8
Ankylosing Spondylitis
8
Postoperative Care
8
Ill-defined Disorder
8
Drug Use For Unknown Indication
7
Inflammation
7
Bursitis
6
Bone Pain
6
Fibromyalgia
5
Prostatitis
4
Headache
4
Spondylitis
4
Limb Injury
4
Arthropathy
3
Musculoskeletal Pain
3
Gastritis
3
Aphthous Stomatitis
3
Bruxism
3
Mouth Injury
3
Spinal Disorder
2
Haemorrhoids
2
Muscle Rupture
2
Bone Disorder
2
Neuritis
2
Temporomandibular Joint Syndrome
2
Head Injury
2
Cough
2
Infection
2
Clavicle Fracture
2
Pelvic Pain
2
Sciatica
2
Back Disorder
2
Swelling
2
Coronary Artery Disease
2
Skin Infection
2
Premedication
2
Torticollis
2
Neck Pain
2
Dysarthria
2
Joint Effusion
2
Tendon Pain
2
Osteopenia
2

Celebra Case Reports

What Celebra 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 Celebra. 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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