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REVELLEX

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Revellex Adverse Events Reported to the FDA Over Time

How are Revellex adverse event reports trending over time?

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

Most Common Revellex Adverse Events Reported to the FDA

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

Death
27 (4.49%)
Infusion Related Reaction
24 (3.99%)
Tuberculosis
19 (3.16%)
Myocardial Infarction
11 (1.83%)
Dyspnoea
10 (1.66%)
Pneumonia
10 (1.66%)
Nausea
9 (1.5%)
Drug Ineffective
7 (1.16%)
Headache
7 (1.16%)
Dehydration
6 (1%)
Lupus-like Syndrome
6 (1%)
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Pyrexia
6 (1%)
Road Traffic Accident
6 (1%)
Sinusitis
6 (1%)
Arthralgia
5 (.83%)
Chest Pain
5 (.83%)
Diarrhoea
5 (.83%)
Disseminated Tuberculosis
5 (.83%)
Fatigue
5 (.83%)
Flushing
5 (.83%)
Lung Infection
5 (.83%)
Pruritus
5 (.83%)
Pulmonary Oedema
5 (.83%)
Sepsis
5 (.83%)
Urticaria
5 (.83%)
Abdominal Pain
4 (.67%)
Arthrodesis
4 (.67%)
Blood Glucose Increased
4 (.67%)
Blood Pressure Increased
4 (.67%)
Bone Graft
4 (.67%)
Bronchospasm
4 (.67%)
Cardiac Disorder
4 (.67%)
Colitis Ulcerative
4 (.67%)
Decreased Appetite
4 (.67%)
Diaphragmalgia
4 (.67%)
Diplopia
4 (.67%)
Discomfort
4 (.67%)
Drug Specific Antibody Present
4 (.67%)
Heart Rate Increased
4 (.67%)
Hip Arthroplasty
4 (.67%)
Hypersensitivity
4 (.67%)
Intestinal Stenosis
4 (.67%)
Large Intestinal Haemorrhage
4 (.67%)
Liver Function Test Abnormal
4 (.67%)
Malaise
4 (.67%)
Menorrhagia
4 (.67%)
Menstruation Irregular
4 (.67%)
Oxygen Saturation Decreased
4 (.67%)
Pulmonary Tuberculosis
4 (.67%)
Rectal Abscess
4 (.67%)
Restless Legs Syndrome
4 (.67%)
Subarachnoid Haemorrhage
4 (.67%)
Surgery
4 (.67%)
Vomiting
4 (.67%)
Accidental Overdose
3 (.5%)
Back Pain
3 (.5%)
Body Temperature Increased
3 (.5%)
Herpes Virus Infection
3 (.5%)
Hospitalisation
3 (.5%)
Hyperhidrosis
3 (.5%)
Intestinal Obstruction
3 (.5%)
Malignant Melanoma
3 (.5%)
Muscle Spasms
3 (.5%)
Oesophageal Candidiasis
3 (.5%)
Pain
3 (.5%)
Palpitations
3 (.5%)
Pneumonia Aspiration
3 (.5%)
Psoriasis
3 (.5%)
Rash
3 (.5%)
Renal Failure
3 (.5%)
Respiratory Failure
3 (.5%)
Rheumatoid Arthritis
3 (.5%)
Systemic Lupus Erythematosus
3 (.5%)
Tremor
3 (.5%)
Abasia
2 (.33%)
Adverse Event
2 (.33%)
Antibody Test Positive
2 (.33%)
Appendicitis Perforated
2 (.33%)
Atrial Flutter
2 (.33%)
Blood Creatinine Increased
2 (.33%)
Blood Sodium Increased
2 (.33%)
Bronchitis
2 (.33%)
Cardiac Arrest
2 (.33%)
Colectomy
2 (.33%)
Convulsion
2 (.33%)
Coronary Artery Disease
2 (.33%)
Cyanosis
2 (.33%)
Cytomegalovirus Infection
2 (.33%)
Deafness
2 (.33%)
Demyelination
2 (.33%)
Dystonia
2 (.33%)
Encephalitis
2 (.33%)
Erythema
2 (.33%)
Eye Swelling
2 (.33%)
Feeling Hot
2 (.33%)
Haemoglobin Decreased
2 (.33%)
Herpes Zoster
2 (.33%)
Hyperaesthesia
2 (.33%)
Hypoglycaemia
2 (.33%)
Hypotension
2 (.33%)
Hypovolaemic Shock
2 (.33%)

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

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

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

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

Rheumatoid Arthritis
71
Crohns Disease
47
Product Used For Unknown Indication
19
Colitis Ulcerative
18
Ankylosing Spondylitis
12
Drug Use For Unknown Indication
9
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Psoriatic Arthropathy
8
Juvenile Arthritis
6
Arthritis
1
Colitis
1
Pyoderma Gangrenosum
1
Inflammatory Bowel Disease
1

Revellex Case Reports

What Revellex 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 Revellex. 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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