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NATEGLINIDE

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Nateglinide Adverse Events Reported to the FDA Over Time

How are Nateglinide adverse event reports trending over time?

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

Most Common Nateglinide Adverse Events Reported to the FDA

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

Gastritis
45 (2.09%)
Disease Progression
38 (1.76%)
Abdominal Pain
36 (1.67%)
Chest Pain
36 (1.67%)
Gastritis Erosive
32 (1.48%)
Abdominal Pain Upper
29 (1.35%)
Hypertension
29 (1.35%)
Hypoglycaemia
29 (1.35%)
Diarrhoea
28 (1.3%)
Vomiting
27 (1.25%)
Anaemia
26 (1.21%)
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Asthenia
26 (1.21%)
Colonic Polyp
26 (1.21%)
Small Intestinal Haemorrhage
26 (1.21%)
Dizziness
25 (1.16%)
Dyspnoea
25 (1.16%)
Decreased Appetite
24 (1.11%)
Arteriovenous Malformation
22 (1.02%)
Concomitant Disease Progression
22 (1.02%)
Diverticulum Intestinal
22 (1.02%)
Epistaxis
22 (1.02%)
Faeces Discoloured
22 (1.02%)
Gastrointestinal Haemorrhage
22 (1.02%)
Angiodysplasia
21 (.97%)
Angina Pectoris
17 (.79%)
Pancreatitis
17 (.79%)
Convulsion
14 (.65%)
Hepatic Function Abnormal
14 (.65%)
Liver Disorder
14 (.65%)
Pyrexia
14 (.65%)
Blood Glucose Increased
13 (.6%)
Erythema
13 (.6%)
Musculoskeletal Stiffness
13 (.6%)
Pancreatitis Acute
13 (.6%)
Duodenitis
12 (.56%)
Gastric Ulcer
12 (.56%)
Interstitial Lung Disease
12 (.56%)
Renal Impairment
12 (.56%)
Glycosylated Haemoglobin Increased
11 (.51%)
Haemostasis
11 (.51%)
Lethargy
11 (.51%)
Loss Of Consciousness
11 (.51%)
Reflux Oesophagitis
11 (.51%)
Drug Eruption
10 (.46%)
Hypotension
10 (.46%)
Intestinal Operation
10 (.46%)
Jaundice
10 (.46%)
Laparotomy
10 (.46%)
C-reactive Protein Increased
9 (.42%)
Fatigue
9 (.42%)
Gastric Cancer
9 (.42%)
Gastrooesophageal Reflux Disease
9 (.42%)
Malaise
9 (.42%)
Nausea
9 (.42%)
Osteomyelitis
9 (.42%)
Thrombocytopenia
9 (.42%)
White Blood Cell Count Decreased
9 (.42%)
Blood Alkaline Phosphatase Increase...
8 (.37%)
Fall
8 (.37%)
Gamma-glutamyltransferase Increased
8 (.37%)
Hepatic Steatosis
8 (.37%)
Metastases To Lung
8 (.37%)
Nasopharyngitis
8 (.37%)
Palpitations
8 (.37%)
Platelet Count Decreased
8 (.37%)
Pruritus
8 (.37%)
Renal Disorder
8 (.37%)
Small Intestine Carcinoma
8 (.37%)
Blood Lactate Dehydrogenase Increas...
7 (.32%)
Coronary Artery Disease
7 (.32%)
Hepatitis
7 (.32%)
Melaena
7 (.32%)
Urinary Retention
7 (.32%)
Altered State Of Consciousness
6 (.28%)
Atrial Flutter
6 (.28%)
Blood Urea Increased
6 (.28%)
Bronchitis
6 (.28%)
Chest Discomfort
6 (.28%)
Cholangitis
6 (.28%)
Chronic Hepatitis
6 (.28%)
Drug Hypersensitivity
6 (.28%)
Eosinophilia
6 (.28%)
Erosive Oesophagitis
6 (.28%)
Febrile Neutropenia
6 (.28%)
Gastroduodenitis
6 (.28%)
Giardiasis
6 (.28%)
Haematuria
6 (.28%)
Heart Rate Increased
6 (.28%)
Helicobacter Infection
6 (.28%)
Hyperhidrosis
6 (.28%)
Hypoglycaemic Seizure
6 (.28%)
Leukopenia
6 (.28%)
Myocardial Ischaemia
6 (.28%)
Neoplasm Malignant
6 (.28%)
Neutrophil Count Decreased
6 (.28%)
Oedema Peripheral
6 (.28%)
Pityriasis Rosea
6 (.28%)
Prostate Cancer
6 (.28%)
Rash Generalised
6 (.28%)
Shock
6 (.28%)
Splenectomy
6 (.28%)

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

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

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

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

Diabetes Mellitus
188
Glucose Tolerance Impaired
103
Type 2 Diabetes Mellitus
53
Drug Use For Unknown Indication
39
Diabetes Mellitus Non-insulin-depen...
38
Product Used For Unknown Indication
26
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Diabetic Nephropathy
5
Cerebral Infarction
2
Hypertension
2
Ill-defined Disorder
2
Cardiovascular Disorder
1
Blood Glucose
1
Prophylaxis
1
Insulin-requiring Type Ii Diabetes ...
1

Drug Labels

LabelLabelerEffective
NateglinideDr. Reddy's Laboratories Limited10-SEP-09
NateglinideWatson Laboratories, Inc.04-OCT-11
Nateglinide Par Pharmaceutical Inc.28-NOV-11
Nateglinide Physicians Total Care, Inc.12-DEC-11
NateglinideNCS HealthCare of KY, Inc dba Vangard Labs15-AUG-12
NateglinideAmerican Health Packaging22-OCT-12

Nateglinide Case Reports

What Nateglinide 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 Nateglinide. 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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