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LIPIDIL

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Lipidil Adverse Events Reported to the FDA Over Time

How are Lipidil adverse event reports trending over time?

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

Most Common Lipidil Adverse Events Reported to the FDA

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

Liver Disorder
40 (3.01%)
Malaise
30 (2.26%)
Pyrexia
28 (2.11%)
Hepatic Function Abnormal
23 (1.73%)
Gamma-glutamyltransferase Increased
22 (1.65%)
Renal Failure Acute
22 (1.65%)
Drug Interaction
21 (1.58%)
Aspartate Aminotransferase Increase...
20 (1.5%)
Blood Creatinine Increased
20 (1.5%)
Myalgia
20 (1.5%)
Pneumonia
20 (1.5%)
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High Density Lipoprotein Decreased
19 (1.43%)
Liver Function Test Abnormal
18 (1.35%)
Blood Creatine Phosphokinase Increa...
17 (1.28%)
Fatigue
17 (1.28%)
Jaundice
16 (1.2%)
Pruritus
16 (1.2%)
Abdominal Pain
15 (1.13%)
Headache
15 (1.13%)
Interstitial Lung Disease
15 (1.13%)
Nausea
15 (1.13%)
Renal Impairment
15 (1.13%)
Alanine Aminotransferase Increased
14 (1.05%)
Dizziness
13 (.98%)
Rhabdomyolysis
13 (.98%)
Asthenia
12 (.9%)
Haematuria
12 (.9%)
Renal Failure
12 (.9%)
Blood Urea Increased
11 (.83%)
Chromaturia
11 (.83%)
Hepatic Failure
11 (.83%)
Anaemia
10 (.75%)
Arthralgia
10 (.75%)
Body Temperature
10 (.75%)
Rash
10 (.75%)
Confusional State
9 (.68%)
Gait Disturbance
9 (.68%)
Pancreatitis Acute
9 (.68%)
Abdominal Pain Upper
8 (.6%)
Blood Lactate Dehydrogenase Increas...
8 (.6%)
Blood Potassium Increased
8 (.6%)
Diabetes Mellitus
8 (.6%)
Dyspnoea
8 (.6%)
Hepatitis
8 (.6%)
Hypertriglyceridaemia
8 (.6%)
Pain In Extremity
8 (.6%)
Abdominal Compartment Syndrome
7 (.53%)
Abdominal Distension
7 (.53%)
Insomnia
7 (.53%)
Intestinal Perforation
7 (.53%)
Multi-organ Failure
7 (.53%)
Muscular Weakness
7 (.53%)
Myocardial Infarction
7 (.53%)
Oedema Peripheral
7 (.53%)
Pain
7 (.53%)
Sepsis
7 (.53%)
Tachypnoea
7 (.53%)
Toxic Epidermal Necrolysis
7 (.53%)
Unresponsive To Stimuli
7 (.53%)
Urticaria
7 (.53%)
White Blood Cell Count Increased
7 (.53%)
Abdominal Discomfort
6 (.45%)
Anorexia
6 (.45%)
Face Oedema
6 (.45%)
Insulin Resistance
6 (.45%)
Muscle Spasms
6 (.45%)
Thrombocytopenia
6 (.45%)
Abdominal Rigidity
5 (.38%)
Amnesia
5 (.38%)
Apnoea
5 (.38%)
Blister
5 (.38%)
Blood Bilirubin Increased
5 (.38%)
Choking
5 (.38%)
Diarrhoea
5 (.38%)
Eczema
5 (.38%)
Erythema
5 (.38%)
Eye Pain
5 (.38%)
Gastrooesophageal Reflux Disease
5 (.38%)
Intentional Overdose
5 (.38%)
Toxic Skin Eruption
5 (.38%)
Visual Field Defect
5 (.38%)
Angina Pectoris
4 (.3%)
Blood Triglycerides Increased
4 (.3%)
Cardiac Failure Congestive
4 (.3%)
Decreased Appetite
4 (.3%)
Discomfort
4 (.3%)
Dyspepsia
4 (.3%)
Generalised Erythema
4 (.3%)
Gout
4 (.3%)
Hypertension
4 (.3%)
Hypocholesterolaemia
4 (.3%)
Impaired Driving Ability
4 (.3%)
Lip Swelling
4 (.3%)
Lipase Increased
4 (.3%)
Memory Impairment
4 (.3%)
Muscle Disorder
4 (.3%)
Musculoskeletal Pain
4 (.3%)
Ocular Icterus
4 (.3%)
Overdose
4 (.3%)
Paresis
4 (.3%)
Shock
4 (.3%)

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

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

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

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

Hyperlipidaemia
175
Drug Use For Unknown Indication
93
Product Used For Unknown Indication
53
Dyslipidaemia
39
Hypercholesterolaemia
32
Blood Cholesterol Increased
29
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Metabolic Disorder
15
Blood Cholesterol
14
Hypertriglyceridaemia
8
Blood Triglycerides Increased
7
Lipids Abnormal
6
Lipid Metabolism Disorder
5
Neuropathy Peripheral
5
Cardiac Disorder
4
Blood Triglycerides Abnormal
3
Blood Cholesterol Abnormal
3
Hypertension
3
Mixed Hyperlipidaemia
2
Blood Triglycerides
2
Prophylaxis
2
Hyperuricaemia
2
Lipids Increased
2
Arteriosclerosis Obliterans
2
Ill-defined Disorder
2
Low Density Lipoprotein Decreased
1
Unevaluable Event
1
Arrhythmia
1
Rheumatoid Arthritis
1
Hepatic Steatosis
1
High Density Lipoprotein Decreased
1
Xanthomatosis
1
Myocardial Ischaemia
1
Blood Triglycerides Decreased
1
Fat Tissue Increased
1

Lipidil Case Reports

What Lipidil 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 Lipidil. 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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