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MIXTARD HUMAN

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Mixtard Human Adverse Events Reported to the FDA Over Time

How are Mixtard Human adverse event reports trending over time?

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

Most Common Mixtard Human Adverse Events Reported to the FDA

What are the most common Mixtard Human adverse events reported to the FDA?

Hypoglycaemia
35 (4.32%)
Intentional Drug Misuse
30 (3.7%)
Homicide
25 (3.09%)
Blood Glucose Increased
21 (2.59%)
Victim Of Homicide
16 (1.98%)
Death
14 (1.73%)
Dyspnoea
12 (1.48%)
Fall
11 (1.36%)
Vomiting
10 (1.23%)
Blood Insulin Increased
9 (1.11%)
Hypoglycaemic Coma
9 (1.11%)
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Physical Assault
9 (1.11%)
Suicide Attempt
9 (1.11%)
Eye Swelling
8 (.99%)
Hot Flush
8 (.99%)
Hyperglycaemia
8 (.99%)
Orthostatic Hypotension
8 (.99%)
Pruritus
8 (.99%)
Abdominal Pain Upper
7 (.86%)
Convulsion
7 (.86%)
Erythema
7 (.86%)
Loss Of Consciousness
7 (.86%)
Pneumonia
7 (.86%)
Product Quality Issue
7 (.86%)
Victim Of Crime
7 (.86%)
Aphasia
6 (.74%)
Blood Creatinine Increased
6 (.74%)
Blood Glucose Decreased
6 (.74%)
Chest Pain
6 (.74%)
Device Leakage
6 (.74%)
Diabetic Ketoacidosis
6 (.74%)
Hyperparathyroidism Primary
6 (.74%)
Injection Site Erythema
6 (.74%)
Injection Site Rash
6 (.74%)
Parathyroid Tumour Benign
6 (.74%)
Pulmonary Oedema
6 (.74%)
Renal Disorder
6 (.74%)
Renal Failure
6 (.74%)
Adverse Event
5 (.62%)
Coma
5 (.62%)
Confusional State
5 (.62%)
Device Malfunction
5 (.62%)
Myocardial Infarction
5 (.62%)
Nausea
5 (.62%)
Overdose
5 (.62%)
Renal Failure Acute
5 (.62%)
Syncope
5 (.62%)
Victim Of Child Abuse
5 (.62%)
Asthenia
4 (.49%)
Blood Urea Increased
4 (.49%)
Burning Sensation
4 (.49%)
Cardiac Arrest
4 (.49%)
Cerebrovascular Accident
4 (.49%)
Chills
4 (.49%)
Circulatory Collapse
4 (.49%)
Completed Suicide
4 (.49%)
Dehydration
4 (.49%)
Depressed Level Of Consciousness
4 (.49%)
Dysgeusia
4 (.49%)
Eye Pain
4 (.49%)
Feeling Cold
4 (.49%)
General Physical Health Deteriorati...
4 (.49%)
Hyperhidrosis
4 (.49%)
Hypotension
4 (.49%)
Incorrect Dose Administered
4 (.49%)
Medication Error
4 (.49%)
Pleural Effusion
4 (.49%)
Premature Baby
4 (.49%)
Rash Generalised
4 (.49%)
Arteriovenous Fistula Operation
3 (.37%)
Arteriovenous Fistula Thrombosis
3 (.37%)
Azotaemia
3 (.37%)
Blood Glucose Fluctuation
3 (.37%)
Blood Insulin
3 (.37%)
Cardiac Failure
3 (.37%)
Cerebral Ischaemia
3 (.37%)
Chronic Lymphocytic Leukaemia
3 (.37%)
Drug Ineffective
3 (.37%)
Drug Interaction
3 (.37%)
Enteritis
3 (.37%)
Excoriation
3 (.37%)
Fracture
3 (.37%)
Gastrointestinal Infection
3 (.37%)
Hypersensitivity
3 (.37%)
Intervertebral Disc Disorder
3 (.37%)
Malaise
3 (.37%)
Palpitations
3 (.37%)
Paraesthesia Oral
3 (.37%)
Periorbital Haematoma
3 (.37%)
Pruritus Generalised
3 (.37%)
Pulmonary Fibrosis
3 (.37%)
Pyoderma
3 (.37%)
Respiratory Failure
3 (.37%)
Skin Infection
3 (.37%)
Sudden Death
3 (.37%)
Urticaria
3 (.37%)
Withdrawal Syndrome
3 (.37%)
Abdominal Discomfort
2 (.25%)
Agitation
2 (.25%)
Alcohol Interaction
2 (.25%)
Alcohol Use
2 (.25%)

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

What are the most common Mixtard Human adverse events reported to the FDA?

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

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

Drug Use For Unknown Indication
143
Diabetes Mellitus
138
Product Used For Unknown Indication
62
Off Label Use
47
Type 2 Diabetes Mellitus
45
Type 1 Diabetes Mellitus
28
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Diabetes Mellitus Insulin-dependent
23
Diabetes Mellitus Non-insulin-depen...
12
Ill-defined Disorder
12
Insulin-requiring Type 2 Diabetes M...
9
Insulin-requiring Type Ii Diabetes ...
8
Gestational Diabetes
5

Mixtard Human Case Reports

What Mixtard Human 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 Mixtard Human. 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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