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ILETIN

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Iletin Adverse Events Reported to the FDA Over Time

How are Iletin adverse event reports trending over time?

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

Most Common Iletin Adverse Events Reported to the FDA

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

Blood Glucose Increased
116 (8.15%)
Blood Glucose Decreased
87 (6.11%)
Loss Of Consciousness
43 (3.02%)
Blood Glucose Fluctuation
34 (2.39%)
Drug Ineffective
33 (2.32%)
Feeling Abnormal
33 (2.32%)
Myocardial Infarction
24 (1.69%)
Anxiety
20 (1.4%)
Cardiac Failure Congestive
20 (1.4%)
Hypoglycaemia Unawareness
20 (1.4%)
Hypoglycaemia
19 (1.33%)
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Erythema
17 (1.19%)
Connective Tissue Disorder
16 (1.12%)
Fall
16 (1.12%)
Intervertebral Disc Degeneration
16 (1.12%)
Depression
15 (1.05%)
Drug Exposure During Pregnancy
15 (1.05%)
Cataract
14 (.98%)
Drug Hypersensitivity
14 (.98%)
Memory Impairment
14 (.98%)
Skin Exfoliation
14 (.98%)
Vision Blurred
14 (.98%)
Diabetes Mellitus Inadequate Contro...
12 (.84%)
General Physical Health Deteriorati...
12 (.84%)
Glycosylated Haemoglobin Increased
12 (.84%)
Hiatus Hernia
12 (.84%)
Dizziness
11 (.77%)
Sleep Disorder
10 (.7%)
Visual Acuity Reduced
10 (.7%)
Blindness
9 (.63%)
Cardiac Disorder
9 (.63%)
Cerebrovascular Accident
9 (.63%)
Drug Effect Decreased
9 (.63%)
Road Traffic Accident
9 (.63%)
Amnesia
8 (.56%)
Cardiac Arrest
8 (.56%)
Convulsion
8 (.56%)
Diabetic Neuropathy
8 (.56%)
Eye Haemorrhage
8 (.56%)
Hallucination
8 (.56%)
Headache
8 (.56%)
Insomnia
8 (.56%)
Weight Increased
8 (.56%)
Coma
7 (.49%)
Confusional State
7 (.49%)
Fatigue
7 (.49%)
Feeling Cold
7 (.49%)
Hypersensitivity
7 (.49%)
Injection Site Reaction
7 (.49%)
Malaise
7 (.49%)
Morbid Thoughts
7 (.49%)
Pain
7 (.49%)
Anger
6 (.42%)
Asthenia
6 (.42%)
Blindness Unilateral
6 (.42%)
Contusion
6 (.42%)
Diabetic Ketoacidosis
6 (.42%)
Lower Limb Fracture
6 (.42%)
Oedema Peripheral
6 (.42%)
Retinal Detachment
6 (.42%)
Tremor
6 (.42%)
Abortion Spontaneous
5 (.35%)
Disorientation
5 (.35%)
Emotional Distress
5 (.35%)
Impaired Healing
5 (.35%)
Infection
5 (.35%)
Influenza
5 (.35%)
Open Wound
5 (.35%)
Rash Macular
5 (.35%)
Renal Disorder
5 (.35%)
Renal Failure Chronic
5 (.35%)
Skin Disorder
5 (.35%)
Swelling
5 (.35%)
Vomiting
5 (.35%)
Ankle Fracture
4 (.28%)
Cellulitis
4 (.28%)
Drug Exposure Via Breast Milk
4 (.28%)
Dyspnoea
4 (.28%)
Eye Operation
4 (.28%)
Fluid Retention
4 (.28%)
Hypertension
4 (.28%)
Hypoglycaemic Seizure
4 (.28%)
Injection Site Pain
4 (.28%)
Medication Error
4 (.28%)
Neuropathy Peripheral
4 (.28%)
Pain In Extremity
4 (.28%)
Personality Change
4 (.28%)
Premature Baby
4 (.28%)
Respiratory Arrest
4 (.28%)
Retinopathy
4 (.28%)
Scar
4 (.28%)
Surgery
4 (.28%)
Therapy Regimen Changed
4 (.28%)
Treatment Noncompliance
4 (.28%)
Urticaria
4 (.28%)
Weight Decreased
4 (.28%)
Wrong Drug Administered
4 (.28%)
Abnormal Behaviour
3 (.21%)
Anorexia
3 (.21%)
Arterial Disorder
3 (.21%)
Arthritis
3 (.21%)

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

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

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

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

Diabetes Mellitus
538
Diabetes Mellitus Insulin-dependent
56
Type 1 Diabetes Mellitus
13
Drug Use For Unknown Indication
10
Diabetes Mellitus Non-insulin-depen...
6
Type 2 Diabetes Mellitus
4
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Pancreatic Disorder
4
Blood Glucose Increased
3
Hyperglycaemia
2
Gestational Diabetes
2
Product Used For Unknown Indication
1

Iletin Case Reports

What Iletin 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 Iletin. 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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