DrugCite
Search

ATHYMIL

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Athymil Adverse Events Reported to the FDA Over Time

How are Athymil adverse event reports trending over time?

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

Most Common Athymil Adverse Events Reported to the FDA

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

Fall
38 (3.66%)
Agranulocytosis
26 (2.5%)
Somnolence
22 (2.12%)
Renal Failure Acute
19 (1.83%)
Disorientation
16 (1.54%)
Pyrexia
16 (1.54%)
Confusional State
15 (1.45%)
Malaise
15 (1.45%)
Hypotension
13 (1.25%)
Drug Interaction
11 (1.06%)
Neutropenia
11 (1.06%)
Show More Show More
Renal Failure
11 (1.06%)
Death
10 (.96%)
Hyponatraemia
10 (.96%)
Vomiting
10 (.96%)
Abdominal Pain
9 (.87%)
Asthenia
9 (.87%)
Bradycardia
9 (.87%)
Haematoma
9 (.87%)
Thrombocytopenia
9 (.87%)
Anaemia
8 (.77%)
Cardiomegaly
8 (.77%)
Coma
8 (.77%)
Myoclonus
8 (.77%)
Rhabdomyolysis
8 (.77%)
Bone Marrow Failure
7 (.67%)
Bradyphrenia
7 (.67%)
Cytolytic Hepatitis
7 (.67%)
Electrocardiogram Qt Prolonged
7 (.67%)
Epistaxis
7 (.67%)
Hypernatraemia
7 (.67%)
Pancytopenia
7 (.67%)
Portal Hypertension
7 (.67%)
Respiratory Distress
7 (.67%)
Abdominal Wall Cyst
6 (.58%)
Agitation
6 (.58%)
Alanine Aminotransferase Increased
6 (.58%)
Altered State Of Consciousness
6 (.58%)
Blood Iron Decreased
6 (.58%)
Convulsion
6 (.58%)
Gastric Polyps
6 (.58%)
Inflammation
6 (.58%)
Lactic Acidosis
6 (.58%)
Leukopenia
6 (.58%)
Malnutrition
6 (.58%)
Normochromic Normocytic Anaemia
6 (.58%)
Sepsis
6 (.58%)
Suicide Attempt
6 (.58%)
Tremor
6 (.58%)
Urinary Tract Infection
6 (.58%)
Blood Alkaline Phosphatase Increase...
5 (.48%)
Constipation
5 (.48%)
Cyanosis
5 (.48%)
Dyspnoea
5 (.48%)
Gamma-glutamyltransferase Increased
5 (.48%)
Haemolytic Anaemia
5 (.48%)
Hypothyroidism
5 (.48%)
Loss Of Consciousness
5 (.48%)
Pulmonary Alveolar Microlithiasis
5 (.48%)
Vitamin B12 Decreased
5 (.48%)
Acute Respiratory Distress Syndrome
4 (.39%)
Aspartate Aminotransferase Increase...
4 (.39%)
Blood Folate Increased
4 (.39%)
Blood Lactate Dehydrogenase Increas...
4 (.39%)
C-reactive Protein Increased
4 (.39%)
Cholestasis
4 (.39%)
Electroencephalogram Abnormal
4 (.39%)
Epilepsy
4 (.39%)
Eye Rolling
4 (.39%)
Faecaloma
4 (.39%)
Febrile Bone Marrow Aplasia
4 (.39%)
Gait Disturbance
4 (.39%)
Gastric Ulcer
4 (.39%)
General Physical Condition Abnormal
4 (.39%)
Haemoglobin Decreased
4 (.39%)
Hepatic Enzyme Increased
4 (.39%)
Hypertonia
4 (.39%)
International Normalised Ratio Incr...
4 (.39%)
Interstitial Lung Disease
4 (.39%)
Mechanical Ventilation
4 (.39%)
Melaena
4 (.39%)
Pain In Extremity
4 (.39%)
Pneumonia Aspiration
4 (.39%)
Subileus
4 (.39%)
Thrombosis
4 (.39%)
Urinary Incontinence
4 (.39%)
Aggression
3 (.29%)
Balance Disorder
3 (.29%)
Bundle Branch Block Right
3 (.29%)
Cholelithiasis
3 (.29%)
Condition Aggravated
3 (.29%)
Delirium
3 (.29%)
Diarrhoea
3 (.29%)
Disturbance In Attention
3 (.29%)
Extrapyramidal Disorder
3 (.29%)
Eyelid Oedema
3 (.29%)
Face Oedema
3 (.29%)
General Physical Health Deteriorati...
3 (.29%)
Hepatitis
3 (.29%)
Hepatitis Cholestatic
3 (.29%)
Hyperthermia
3 (.29%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Depression
112
Drug Use For Unknown Indication
78
Product Used For Unknown Indication
21
Insomnia
9
Major Depression
6
Anxiety
5
Show More Show More
Dysthymic Disorder
4
Unevaluable Event
4
Ill-defined Disorder
3
Dementia Alzheimers Type
2
Failure To Thrive
2
Mental Disorder
2
Hallucination, Visual
1
Sleep Disorder
1
Drug Administration Error
1
Cachexia
1
Affective Disorder
1
Multiple Drug Overdose Intentional
1
Bipolar I Disorder
1
Behavioural And Psychiatric Symptom...
1
Dyspnoea
1
Epilepsy
1
Schizophrenia
1
Nonspecific Reaction
1
Death Of Spouse
1

Athymil Case Reports

What Athymil safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Athymil. 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.

Comments

Share your experience with Athymil.