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NPH INSULIN

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Nph Insulin Adverse Events Reported to the FDA Over Time

How are Nph Insulin adverse event reports trending over time?

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

Most Common Nph Insulin Adverse Events Reported to the FDA

What are the most common Nph Insulin adverse events reported to the FDA?

Hypoglycaemia
76 (9.18%)
Blood Glucose Increased
34 (4.11%)
Blood Glucose Decreased
32 (3.86%)
Loss Of Consciousness
20 (2.42%)
Renal Failure Acute
16 (1.93%)
Confusional State
13 (1.57%)
Glycosylated Haemoglobin Increased
13 (1.57%)
Mental Status Changes
13 (1.57%)
Pneumonia
13 (1.57%)
Hyperhidrosis
12 (1.45%)
Acute Respiratory Failure
10 (1.21%)
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Coma
10 (1.21%)
Pancreatitis Acute
10 (1.21%)
Blood Urea Increased
9 (1.09%)
Nausea
9 (1.09%)
Blood Cholesterol Increased
8 (.97%)
Dehydration
8 (.97%)
Dyspnoea
8 (.97%)
Fall
8 (.97%)
Syncope
8 (.97%)
Asthenia
7 (.85%)
Blood Triglycerides Increased
7 (.85%)
Dizziness
7 (.85%)
Feeling Abnormal
7 (.85%)
Medication Error
7 (.85%)
Tremor
7 (.85%)
Depressed Level Of Consciousness
6 (.72%)
Diabetes Mellitus
6 (.72%)
Diabetes Mellitus Inadequate Contro...
6 (.72%)
Hypertension
6 (.72%)
Pancreatitis
6 (.72%)
Renal Failure
6 (.72%)
Treatment Noncompliance
6 (.72%)
Cardiac Arrest
5 (.6%)
Cardiac Failure Congestive
5 (.6%)
Diabetic Ketoacidosis
5 (.6%)
Drug Dose Omission
5 (.6%)
Microalbuminuria
5 (.6%)
Acute Prerenal Failure
4 (.48%)
Aortic Disorder
4 (.48%)
Aortic Valve Stenosis
4 (.48%)
Blood Creatinine Increased
4 (.48%)
Creatinine Renal Clearance Decrease...
4 (.48%)
Drug Ineffective
4 (.48%)
Hyperglycaemia
4 (.48%)
Incorrect Dose Administered
4 (.48%)
Left Ventricular Hypertrophy
4 (.48%)
Mitral Valve Incompetence
4 (.48%)
Myocardial Ischaemia
4 (.48%)
Unresponsive To Stimuli
4 (.48%)
Vomiting
4 (.48%)
Anorexia
3 (.36%)
Back Pain
3 (.36%)
Blood Pressure Diastolic Increased
3 (.36%)
Blood Pressure Increased
3 (.36%)
Cardio-respiratory Arrest
3 (.36%)
Cardiogenic Shock
3 (.36%)
Completed Suicide
3 (.36%)
Diarrhoea
3 (.36%)
Drug Administration Error
3 (.36%)
Dyslipidaemia
3 (.36%)
General Physical Health Deteriorati...
3 (.36%)
Haemothorax
3 (.36%)
Hepatic Function Abnormal
3 (.36%)
Hyperkalaemia
3 (.36%)
Hypoglycaemic Encephalopathy
3 (.36%)
Hypophagia
3 (.36%)
Impaired Gastric Emptying
3 (.36%)
Lethargy
3 (.36%)
Malaise
3 (.36%)
Multiple Fractures
3 (.36%)
Multiple Injuries
3 (.36%)
Obesity
3 (.36%)
Oedema Peripheral
3 (.36%)
Orthostatic Hypotension
3 (.36%)
Polydipsia
3 (.36%)
Polyuria
3 (.36%)
Proteinuria
3 (.36%)
Respiratory Arrest
3 (.36%)
Retroperitoneal Neoplasm
3 (.36%)
Somnolence
3 (.36%)
Agitation
2 (.24%)
Agonal Death Struggle
2 (.24%)
Anaemia
2 (.24%)
Anaphylactic Reaction
2 (.24%)
Angina Pectoris
2 (.24%)
Anxiety
2 (.24%)
Blindness
2 (.24%)
Blood Creatine Phosphokinase Increa...
2 (.24%)
Blood Glucose Abnormal
2 (.24%)
Blood Glucose Fluctuation
2 (.24%)
Blood Potassium Increased
2 (.24%)
Blood Pressure Systolic Increased
2 (.24%)
Blood Uric Acid Increased
2 (.24%)
Body Mass Index Increased
2 (.24%)
Bradycardia
2 (.24%)
Brain Natriuretic Peptide Increased
2 (.24%)
C-reactive Protein Increased
2 (.24%)
Cardiac Disorder
2 (.24%)
Chest Pain
2 (.24%)
Cold Sweat
2 (.24%)

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

What are the most common Nph Insulin adverse events reported to the FDA?

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

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

Diabetes Mellitus
269
Type 2 Diabetes Mellitus
48
Product Used For Unknown Indication
47
Diabetes Mellitus Insulin-dependent
46
Drug Use For Unknown Indication
32
Diabetes Mellitus Non-insulin-depen...
16
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Type 1 Diabetes Mellitus
12
Hyperglycaemia
6
Gestational Diabetes
5
Insulin-requiring Type 2 Diabetes M...
5
Blood Glucose Increased
3
Ill-defined Disorder
2
Hypoglycaemia
1
Unevaluable Event
1
Diabetes Complicating Pregnancy
1
Insulin-requiring Type Ii Diabetes ...
1
Blood Glucose Abnormal
1
Diabetic Ketoacidosis
1

Nph Insulin Case Reports

What Nph Insulin 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 Nph Insulin. 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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