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STABLON

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Stablon Adverse Events Reported to the FDA Over Time

How are Stablon adverse event reports trending over time?

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

Most Common Stablon Adverse Events Reported to the FDA

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

Hyponatraemia
24 (2.46%)
Fall
21 (2.16%)
Pyrexia
21 (2.16%)
Dehydration
18 (1.85%)
Diarrhoea
18 (1.85%)
Confusional State
17 (1.75%)
Cytolytic Hepatitis
17 (1.75%)
Dysphagia
15 (1.54%)
Vomiting
15 (1.54%)
Agranulocytosis
14 (1.44%)
Cholestasis
14 (1.44%)
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Eosinophilia
13 (1.33%)
Cough
12 (1.23%)
Chills
11 (1.13%)
Nausea
11 (1.13%)
Pancytopenia
11 (1.13%)
Pruritus
11 (1.13%)
Rash Morbilliform
11 (1.13%)
Food Intolerance
10 (1.03%)
Musculoskeletal Chest Pain
8 (.82%)
Oxygen Saturation Decreased
8 (.82%)
Skin Exfoliation
8 (.82%)
Suicide Attempt
8 (.82%)
Hypertension
7 (.72%)
International Normalised Ratio Incr...
7 (.72%)
Malaise
7 (.72%)
Rash Maculo-papular
7 (.72%)
Renal Failure
7 (.72%)
Bacteraemia
6 (.62%)
Cerebellar Haematoma
6 (.62%)
Disorientation
6 (.62%)
Drug Eruption
6 (.62%)
Epilepsy
6 (.62%)
Fatigue
6 (.62%)
General Physical Health Deteriorati...
6 (.62%)
Guillain-barre Syndrome
6 (.62%)
Ischaemic Stroke
6 (.62%)
Lip Disorder
6 (.62%)
Orthostatic Hypotension
6 (.62%)
Pancreatitis Acute
6 (.62%)
Pneumonia
6 (.62%)
Blood Alkaline Phosphatase Increase...
5 (.51%)
Blood Prolactin Increased
5 (.51%)
C-reactive Protein Increased
5 (.51%)
Coma
5 (.51%)
Constipation
5 (.51%)
Convulsion
5 (.51%)
Dizziness
5 (.51%)
Drug Ineffective
5 (.51%)
Galactorrhoea
5 (.51%)
Gamma-glutamyltransferase Increased
5 (.51%)
Hyperkalaemia
5 (.51%)
Leukopenia
5 (.51%)
Myalgia
5 (.51%)
Tongue Necrosis
5 (.51%)
Toxic Skin Eruption
5 (.51%)
Abdominal Pain
4 (.41%)
Anaemia Haemolytic Autoimmune
4 (.41%)
Anorexia
4 (.41%)
Anticoagulation Drug Level Above Th...
4 (.41%)
Cardiac Arrest
4 (.41%)
Cholelithiasis
4 (.41%)
Drug Interaction
4 (.41%)
Dyspepsia
4 (.41%)
Eructation
4 (.41%)
Fungal Infection
4 (.41%)
Gait Disturbance
4 (.41%)
Gastrointestinal Disorder
4 (.41%)
Gastrooesophageal Reflux Disease
4 (.41%)
Haematoma
4 (.41%)
Hypersensitivity
4 (.41%)
Hypokalaemia
4 (.41%)
Infection
4 (.41%)
Leukocytosis
4 (.41%)
Lip Oedema
4 (.41%)
Lung Disorder
4 (.41%)
Oedema
4 (.41%)
Pain
4 (.41%)
Renal Failure Acute
4 (.41%)
Rhabdomyolysis
4 (.41%)
Serotonin Syndrome
4 (.41%)
Thrombocytopenia
4 (.41%)
Tongue Biting
4 (.41%)
Urinary Tract Infection
4 (.41%)
Abdominal Discomfort
3 (.31%)
Abnormal Behaviour
3 (.31%)
Back Pain
3 (.31%)
Bacterial Infection
3 (.31%)
Blood Chloride Decreased
3 (.31%)
Bradycardia
3 (.31%)
Bronchial Obstruction
3 (.31%)
Bronchitis
3 (.31%)
Cerebrovascular Accident
3 (.31%)
Cheilitis
3 (.31%)
Colitis
3 (.31%)
Condition Aggravated
3 (.31%)
Drug Withdrawal Syndrome
3 (.31%)
Face Oedema
3 (.31%)
Fine Motor Delay
3 (.31%)
Gastrointestinal Sounds Abnormal
3 (.31%)
Haematuria
3 (.31%)

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

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

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

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

Depression
135
Drug Use For Unknown Indication
70
Product Used For Unknown Indication
37
Major Depression
6
Ill-defined Disorder
6
Dysthymic Disorder
5
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Generalised Anxiety Disorder
4
Unevaluable Event
2
Insomnia
2
Confusional State
1
Personality Disorder
1
Bipolar I Disorder
1
Childhood Psychosis
1
Psychotic Disorder
1
Dementia Alzheimers Type
1
Gastrointestinal Disorder
1
Depressed Mood
1

Stablon Case Reports

What Stablon 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 Stablon. 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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