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HUMULIN N

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Humulin N Adverse Events Reported to the FDA Over Time

How are Humulin N adverse event reports trending over time?

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

Most Common Humulin N Adverse Events Reported to the FDA

What are the most common Humulin N adverse events reported to the FDA?

Blood Glucose Increased
870 (6.29%)
Blood Glucose Decreased
454 (3.28%)
Drug Exposure During Pregnancy
344 (2.49%)
Drug Ineffective
278 (2.01%)
Hypoglycaemia
196 (1.42%)
Loss Of Consciousness
182 (1.32%)
Visual Acuity Reduced
170 (1.23%)
Fall
150 (1.08%)
Cerebrovascular Accident
149 (1.08%)
Blindness
142 (1.03%)
Blood Glucose Fluctuation
133 (.96%)
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Myocardial Infarction
132 (.95%)
Malaise
118 (.85%)
Dyspnoea
117 (.85%)
Feeling Abnormal
114 (.82%)
Cardiac Disorder
106 (.77%)
Dizziness
99 (.72%)
Hospitalisation
97 (.7%)
Hyperglycaemia
95 (.69%)
Renal Failure
94 (.68%)
Cataract
93 (.67%)
Incorrect Dose Administered
93 (.67%)
Cardiac Failure Congestive
86 (.62%)
Diabetes Mellitus Inadequate Contro...
86 (.62%)
Vomiting
85 (.61%)
Weight Decreased
83 (.6%)
Premature Baby
81 (.59%)
Eye Haemorrhage
78 (.56%)
Hypertension
76 (.55%)
Memory Impairment
75 (.54%)
Pain In Extremity
71 (.51%)
Blindness Unilateral
67 (.48%)
Headache
65 (.47%)
Asthenia
64 (.46%)
Convulsion
63 (.46%)
Death
62 (.45%)
Weight Increased
61 (.44%)
Abortion Spontaneous
60 (.43%)
Tremor
60 (.43%)
Fatigue
59 (.43%)
Medication Error
59 (.43%)
Hyperhidrosis
58 (.42%)
Arthralgia
57 (.41%)
Nausea
57 (.41%)
Oedema Peripheral
57 (.41%)
Pain
57 (.41%)
Arthritis
56 (.4%)
Glycosylated Haemoglobin Increased
54 (.39%)
Visual Impairment
54 (.39%)
Diabetic Retinopathy
52 (.38%)
Drug Dose Omission
52 (.38%)
Road Traffic Accident
52 (.38%)
Syncope
52 (.38%)
Pneumonia
51 (.37%)
Gait Disturbance
50 (.36%)
Renal Disorder
50 (.36%)
Diarrhoea
48 (.35%)
Chest Pain
47 (.34%)
Injection Site Pain
47 (.34%)
Vision Blurred
46 (.33%)
Blood Glucose Abnormal
43 (.31%)
Glaucoma
43 (.31%)
Confusional State
42 (.3%)
Hypoglycaemic Unconsciousness
42 (.3%)
Coma
41 (.3%)
Pruritus
41 (.3%)
Drug Hypersensitivity
39 (.28%)
Hypersensitivity
38 (.27%)
Infection
38 (.27%)
Depression
37 (.27%)
Hypoacusis
37 (.27%)
Urticaria
36 (.26%)
Depressed Level Of Consciousness
35 (.25%)
Pyrexia
35 (.25%)
Dehydration
34 (.25%)
Macular Degeneration
34 (.25%)
Asthma
33 (.24%)
Blood Pressure Decreased
33 (.24%)
Diabetic Ketoacidosis
33 (.24%)
Expired Drug Administered
33 (.24%)
Insomnia
33 (.24%)
Poor Quality Drug Administered
33 (.24%)
Fluid Retention
32 (.23%)
Hypoaesthesia
32 (.23%)
Urinary Tract Infection
32 (.23%)
Wrong Drug Administered
32 (.23%)
Blood Pressure Increased
31 (.22%)
Limb Injury
31 (.22%)
Stress
31 (.22%)
Amnesia
30 (.22%)
Hip Fracture
30 (.22%)
Anaemia
29 (.21%)
Eye Disorder
29 (.21%)
Hypoglycaemia Unawareness
29 (.21%)
Neuropathy Peripheral
29 (.21%)
Cardiac Failure
28 (.2%)
Mobility Decreased
28 (.2%)
Cataract Operation
27 (.2%)
Injection Site Haemorrhage
27 (.2%)
Retinal Haemorrhage
27 (.2%)
Skin Ulcer
27 (.2%)

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

What are the most common Humulin N adverse events reported to the FDA?

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

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

Diabetes Mellitus
2364
Type 2 Diabetes Mellitus
319
Type 1 Diabetes Mellitus
156
Gestational Diabetes
156
Diabetes Mellitus Insulin-dependent
144
Diabetes Mellitus Non-insulin-depen...
97
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Drug Use For Unknown Indication
50
Product Used For Unknown Indication
43
Blood Glucose Increased
25
Hyperglycaemia
5
Blood Glucose Abnormal
4
Diabetes Mellitus Inadequate Contro...
3
Diabetic Ketoacidosis
2
Blood Glucose
2
Hypoglycaemia
2
Pancreatic Disorder
2
Insulin-requiring Type Ii Diabetes ...
2
Blood Insulin
1
Hyperlipidaemia
1
Pancreatic Carcinoma Stage Iv
1
Diabetic Coma
1
Prophylaxis
1
Blood Glucose Fluctuation
1
Insulin-requiring Type 2 Diabetes M...
1

Drug Labels

LabelLabelerEffective
Humulin NPhysicians Total Care, Inc.08-NOV-10
Humulin NEli Lilly and Company09-NOV-11
Humulin NEli Lilly and Company09-MAR-13

Humulin N Case Reports

What Humulin N 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 Humulin N. 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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