DrugCite
Search

ADVICOR

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Advicor Adverse Events Reported to the FDA Over Time

How are Advicor adverse event reports trending over time?

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

Most Common Advicor Adverse Events Reported to the FDA

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

Flushing
230 (12.95%)
Pruritus
62 (3.49%)
Myalgia
40 (2.25%)
Dizziness
37 (2.08%)
Paraesthesia
35 (1.97%)
Feeling Hot
30 (1.69%)
Nausea
25 (1.41%)
Diarrhoea
24 (1.35%)
Oedema Peripheral
22 (1.24%)
Arthralgia
20 (1.13%)
Rash
19 (1.07%)
Show More Show More
Vomiting
19 (1.07%)
Erythema
18 (1.01%)
Fall
17 (.96%)
Loss Of Consciousness
16 (.9%)
Asthenia
15 (.84%)
Drug Ineffective
14 (.79%)
Headache
14 (.79%)
Pain
14 (.79%)
Pain In Extremity
14 (.79%)
Blood Glucose Increased
13 (.73%)
Insomnia
13 (.73%)
Muscle Spasms
13 (.73%)
Abdominal Pain Upper
12 (.68%)
Chills
12 (.68%)
Dyspnoea
12 (.68%)
Fatigue
12 (.68%)
Medication Error
12 (.68%)
Urticaria
12 (.68%)
Blood Pressure Decreased
11 (.62%)
Burning Sensation
11 (.62%)
Hot Flush
11 (.62%)
Malaise
11 (.62%)
Amnesia
10 (.56%)
Back Pain
10 (.56%)
Heart Rate Increased
10 (.56%)
Hyperhidrosis
10 (.56%)
Muscular Weakness
10 (.56%)
Skin Burning Sensation
10 (.56%)
Blood Pressure Increased
9 (.51%)
Chromaturia
9 (.51%)
Syncope
9 (.51%)
Chest Pain
8 (.45%)
Intervertebral Disc Protrusion
8 (.45%)
Rhabdomyolysis
8 (.45%)
Abdominal Pain
7 (.39%)
Alanine Aminotransferase Increased
7 (.39%)
Blister
7 (.39%)
Blood Triglycerides Increased
7 (.39%)
Confusional State
7 (.39%)
Constipation
7 (.39%)
Dehydration
7 (.39%)
Hypersensitivity
7 (.39%)
Joint Swelling
7 (.39%)
Medication Residue
7 (.39%)
Activities Of Daily Living Impaired
6 (.34%)
Drug Dispensing Error
6 (.34%)
Haemorrhage
6 (.34%)
Hepatic Steatosis
6 (.34%)
Hepatitis
6 (.34%)
Hepatitis Acute
6 (.34%)
Jaundice
6 (.34%)
Swelling
6 (.34%)
Abdominal Distension
5 (.28%)
Anxiety
5 (.28%)
Blood Creatine Phosphokinase Increa...
5 (.28%)
Cerebrovascular Accident
5 (.28%)
Depression
5 (.28%)
Disturbance In Attention
5 (.28%)
Faeces Pale
5 (.28%)
Head Injury
5 (.28%)
Hepatic Infiltration Eosinophilic
5 (.28%)
Hepatic Necrosis
5 (.28%)
Hepatitis C Antibody Positive
5 (.28%)
Hypertension
5 (.28%)
Muscle Twitching
5 (.28%)
Nerve Compression
5 (.28%)
Peptic Ulcer Haemorrhage
5 (.28%)
Pollakiuria
5 (.28%)
Pyrexia
5 (.28%)
Scar
5 (.28%)
Tremor
5 (.28%)
Weight Decreased
5 (.28%)
Weight Increased
5 (.28%)
Abasia
4 (.23%)
Abdominal Discomfort
4 (.23%)
Ankle Fracture
4 (.23%)
Anorexia
4 (.23%)
Aspartate Aminotransferase Increase...
4 (.23%)
Blood Cholesterol Increased
4 (.23%)
Drug Interaction
4 (.23%)
Epistaxis
4 (.23%)
Erectile Dysfunction
4 (.23%)
Fear
4 (.23%)
Gastrooesophageal Reflux Disease
4 (.23%)
Generalised Erythema
4 (.23%)
Gynaecomastia
4 (.23%)
Hepatic Enzyme Increased
4 (.23%)
High Density Lipoprotein Decreased
4 (.23%)
Intervertebral Disc Compression
4 (.23%)
Musculoskeletal Pain
4 (.23%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Blood Cholesterol Increased
226
Drug Use For Unknown Indication
114
High Density Lipoprotein Decreased
55
Product Used For Unknown Indication
48
Blood Triglycerides Increased
46
Blood Cholesterol
36
Show More Show More
Low Density Lipoprotein Increased
29
Dyslipidaemia
14
Hyperlipidaemia
13
Blood Cholesterol Abnormal
11
Hypercholesterolaemia
8
Prophylaxis
4
Lipids Increased
3
Low Density Lipoprotein Decreased
3
Lipoprotein (a) Increased
3
High Density Lipoprotein Abnormal
2
Cardiac Disorder
2
Blood Cholesterol Decreased
2
Coronary Artery Disease
2
Blood Pressure
2
Attention Deficit/hyperactivity Dis...
1
High Density Lipoprotein Increased
1
Intermittent Claudication
1
Low Density Lipoprotein Abnormal
1
Coronary Arterial Stent Insertion
1
Ldl/hdl Ratio
1
Arteriosclerosis
1
Diabetes Mellitus
1
Hypolipidaemia
1
Very Low Density Lipoprotein
1
Hypertriglyceridaemia
1
High Density Lipoprotein
1

Drug Labels

LabelLabelerEffective
AdvicorPhysicians Total Care, Inc.04-OCT-12
AdvicorAbbott Laboratories05-NOV-12

Advicor Case Reports

What Advicor safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Advicor. 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.

Comments

Share your experience with Advicor.