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NOVORAPID CHU FLEXPEN

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Novorapid Chu Flexpen Adverse Events Reported to the FDA Over Time

How are Novorapid Chu Flexpen adverse event reports trending over time?

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

Most Common Novorapid Chu Flexpen Adverse Events Reported to the FDA

What are the most common Novorapid Chu Flexpen adverse events reported to the FDA?

Hypoglycaemia
114 (9.91%)
Anti-insulin Antibody Positive
79 (6.87%)
Diabetes Mellitus Inadequate Contro...
49 (4.26%)
Suicide Attempt
42 (3.65%)
Hyperglycaemia
41 (3.57%)
Intentional Overdose
40 (3.48%)
Blood Glucose Fluctuation
36 (3.13%)
Blood Glucose Increased
36 (3.13%)
Hypoglycaemic Coma
29 (2.52%)
Anti-insulin Antibody
26 (2.26%)
Anti-insulin Antibody Increased
26 (2.26%)
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Hepatic Function Abnormal
26 (2.26%)
Hypoglycaemic Encephalopathy
17 (1.48%)
Hypoglycaemic Unconsciousness
16 (1.39%)
Drug Hypersensitivity
15 (1.3%)
Diabetic Ketoacidosis
14 (1.22%)
Glycosylated Haemoglobin Increased
13 (1.13%)
Alanine Aminotransferase Increased
11 (.96%)
Aspartate Aminotransferase Increase...
11 (.96%)
Erythema Multiforme
11 (.96%)
Injection Site Erythema
11 (.96%)
Liver Disorder
11 (.96%)
Rash
11 (.96%)
Blood Glucose Decreased
9 (.78%)
Loss Of Consciousness
8 (.7%)
Oedema Peripheral
8 (.7%)
Weight Increased
8 (.7%)
Autoantibody Positive
7 (.61%)
Blood Insulin Increased
7 (.61%)
Fracture
7 (.61%)
Injection Site Induration
7 (.61%)
Interstitial Lung Disease
7 (.61%)
Erythema
6 (.52%)
Vomiting
6 (.52%)
Abdominal Pain
5 (.43%)
Anti-gad Antibody Positive
5 (.43%)
Ascites
5 (.43%)
Cardio-respiratory Arrest
5 (.43%)
Device Failure
5 (.43%)
Diabetic Neuropathy
5 (.43%)
Face Oedema
5 (.43%)
Hepatitis
5 (.43%)
Injection Site Pain
5 (.43%)
Nasopharyngitis
5 (.43%)
Neuralgia
5 (.43%)
Oedema
5 (.43%)
Pericardial Effusion
5 (.43%)
Pleural Effusion
5 (.43%)
Allodynia
4 (.35%)
Cerebral Infarction
4 (.35%)
Disseminated Intravascular Coagulat...
4 (.35%)
Drug Eruption
4 (.35%)
Dysphonia
4 (.35%)
Dyspnoea
4 (.35%)
Hepatitis Acute
4 (.35%)
Hyperinsulinaemia
4 (.35%)
Injection Site Swelling
4 (.35%)
Insomnia
4 (.35%)
Insulin Autoimmune Syndrome
4 (.35%)
Nausea
4 (.35%)
Premature Rupture Of Membranes
4 (.35%)
Pyrexia
4 (.35%)
Threatened Labour
4 (.35%)
Wrong Drug Administered
4 (.35%)
Burning Sensation
3 (.26%)
Cardiac Arrest
3 (.26%)
Cerebral Haemorrhage
3 (.26%)
Death
3 (.26%)
Decreased Appetite
3 (.26%)
Dehydration
3 (.26%)
Diplopia
3 (.26%)
Eczema
3 (.26%)
Feeling Abnormal
3 (.26%)
Gamma-glutamyltransferase Increased
3 (.26%)
Gastroenteritis
3 (.26%)
Generalised Oedema
3 (.26%)
Hepatic Enzyme Increased
3 (.26%)
Hepatitis Fulminant
3 (.26%)
Hypoglycaemia Unawareness
3 (.26%)
Hypothermia
3 (.26%)
Ill-defined Disorder
3 (.26%)
Injection Site Pruritus
3 (.26%)
Injection Site Reaction
3 (.26%)
Liver Function Test Abnormal
3 (.26%)
Localised Oedema
3 (.26%)
Malaise
3 (.26%)
Maternal Condition Affecting Foetus
3 (.26%)
Osteomyelitis
3 (.26%)
Pemphigoid
3 (.26%)
Pregnancy
3 (.26%)
Pruritus Generalised
3 (.26%)
Retinal Haemorrhage
3 (.26%)
Sepsis
3 (.26%)
Toxic Skin Eruption
3 (.26%)
Weight Decreased
3 (.26%)
Abdominal Pain Upper
2 (.17%)
Abortion
2 (.17%)
Anti-insulin Receptor Antibody Posi...
2 (.17%)
Back Pain
2 (.17%)
Body Temperature Decreased
2 (.17%)
Brain Oedema
2 (.17%)

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This graph shows the top adverse events submitted to the FDA for Novorapid Chu Flexpen, 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 Novorapid Chu Flexpen 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 Novorapid Chu Flexpen

What are the most common Novorapid Chu Flexpen adverse events reported to the FDA?

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

Why are people taking Novorapid Chu Flexpen, according to those reporting adverse events to the FDA?

Type 2 Diabetes Mellitus
126
Type 1 Diabetes Mellitus
84
Insulin-requiring Type Ii Diabetes ...
55
Diabetes Mellitus
39
Diabetes Mellitus Insulin-dependent
24
Insulin-requiring Type 2 Diabetes M...
17
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Drug Use For Unknown Indication
9
Off Label Use
5
Product Used For Unknown Indication
3
Latent Autoimmune Diabetes In Adult...
2
Diabetes Mellitus Non-insulin-depen...
1
Homicide
1
Pancreatogenous Diabetes
1
Suicide Attempt
1
Intentional Overdose
1

Novorapid Chu Flexpen Case Reports

What Novorapid Chu Flexpen 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 Novorapid Chu Flexpen. 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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