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REPAGLINIDE

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Repaglinide Adverse Events Reported to the FDA Over Time

How are Repaglinide adverse event reports trending over time?

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

Most Common Repaglinide Adverse Events Reported to the FDA

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

Hypoglycaemia
81 (5.77%)
Renal Failure
26 (1.85%)
Renal Failure Acute
25 (1.78%)
Diarrhoea
24 (1.71%)
Drug Interaction
22 (1.57%)
Dizziness
21 (1.5%)
Lactic Acidosis
19 (1.35%)
Thrombocytopenia
19 (1.35%)
Dehydration
18 (1.28%)
Hypoglycaemic Coma
18 (1.28%)
Hypotension
18 (1.28%)
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Anaemia
17 (1.21%)
Eosinophilia
14 (1%)
Nephropathy
13 (.93%)
Confusional State
12 (.85%)
Somnolence
12 (.85%)
Hepatic Cirrhosis
11 (.78%)
Leukopenia
11 (.78%)
Rhabdomyolysis
11 (.78%)
Vomiting
11 (.78%)
Alanine Aminotransferase Increased
10 (.71%)
Dyspnoea
10 (.71%)
Pruritus
10 (.71%)
Rash Maculo-papular
10 (.71%)
Renal Impairment
10 (.71%)
Tubulointerstitial Nephritis
10 (.71%)
Aspartate Aminotransferase Increase...
9 (.64%)
Fatigue
9 (.64%)
Hepatitis
9 (.64%)
Leukocytoclastic Vasculitis
9 (.64%)
Psychomotor Hyperactivity
9 (.64%)
Blood Creatinine Increased
8 (.57%)
Condition Aggravated
8 (.57%)
Dysarthria
8 (.57%)
Jaundice
8 (.57%)
Rash Erythematous
8 (.57%)
Asthenia
7 (.5%)
Colitis
7 (.5%)
Cytolytic Hepatitis
7 (.5%)
Depressed Level Of Consciousness
7 (.5%)
Epistaxis
7 (.5%)
Gait Disturbance
7 (.5%)
Gamma-glutamyltransferase Increased
7 (.5%)
Haematoma
7 (.5%)
Hypothermia
7 (.5%)
Injection Site Haemorrhage
7 (.5%)
Intentional Overdose
7 (.5%)
Intestinal Obstruction
7 (.5%)
Myoclonus
7 (.5%)
Oedema
7 (.5%)
Pancreatic Enzymes Increased
7 (.5%)
Proctocolitis
7 (.5%)
Rales
7 (.5%)
Sopor
7 (.5%)
Anion Gap Increased
6 (.43%)
Atrial Fibrillation
6 (.43%)
Death
6 (.43%)
Disturbance In Attention
6 (.43%)
Encephalopathy
6 (.43%)
Hyperglycaemia
6 (.43%)
Hyperkalaemia
6 (.43%)
Hyperuricaemia
6 (.43%)
Inflammation
6 (.43%)
Malaise
6 (.43%)
Neurotoxicity
6 (.43%)
Pancreatitis Acute
6 (.43%)
Rash
6 (.43%)
Suicide Attempt
6 (.43%)
Vascular Purpura
6 (.43%)
Acute Coronary Syndrome
5 (.36%)
Aphasia
5 (.36%)
Blood Glucose Increased
5 (.36%)
Cardiac Failure
5 (.36%)
Cardiogenic Shock
5 (.36%)
Drug Rash With Eosinophilia And Sys...
5 (.36%)
Haematuria
5 (.36%)
Hepatic Function Abnormal
5 (.36%)
Idiopathic Urticaria
5 (.36%)
Interstitial Lung Disease
5 (.36%)
Myocardial Ischaemia
5 (.36%)
Purpura
5 (.36%)
Unresponsive To Stimuli
5 (.36%)
Acute Generalised Exanthematous Pus...
4 (.28%)
Agranulocytosis
4 (.28%)
Anaemia Haemolytic Autoimmune
4 (.28%)
Angina Pectoris
4 (.28%)
Bladder Cancer
4 (.28%)
Cardiac Arrest
4 (.28%)
Completed Suicide
4 (.28%)
Drug Intolerance
4 (.28%)
Fall
4 (.28%)
Haemodialysis
4 (.28%)
Haemoglobin Decreased
4 (.28%)
Haemolytic Anaemia
4 (.28%)
Heart Rate Decreased
4 (.28%)
Hemiparesis
4 (.28%)
Hepatic Steatosis
4 (.28%)
Hepatitis Acute
4 (.28%)
Hydrocephalus
4 (.28%)
Hyperthermia
4 (.28%)
Inappropriate Schedule Of Drug Admi...
4 (.28%)

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

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

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

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

Type 2 Diabetes Mellitus
256
Diabetes Mellitus
256
Product Used For Unknown Indication
73
Drug Use For Unknown Indication
68
Diabetes Mellitus Non-insulin-depen...
25
Ill-defined Disorder
12
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Hyperglycaemia
10
Insulin-requiring Type 2 Diabetes M...
5
Insulin-requiring Type Ii Diabetes ...
4
Diabetes Mellitus Malnutrition-rela...
3
Blood Glucose Increased
3
Prophylaxis
3
Type 1 Diabetes Mellitus
2
Diabetes Prophylaxis
2
Ascites
1
Drug Dispensing Error
1
Renal Failure
1
Glucose Tolerance Impaired
1

Drug Labels

LabelLabelerEffective
PrandinPhysicians Total Care, Inc.14-MAY-10
PrandimetNovo Nordisk24-APR-12
PrandinCardinal Health30-MAY-12
PrandinNovo Nordisk11-APR-13
PrandinCardinal Health30-APR-13

Repaglinide Case Reports

What Repaglinide 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 Repaglinide. 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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