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Lexatin Adverse Events Reported to the FDA Over Time

How are Lexatin adverse event reports trending over time?

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

Most Common Lexatin Adverse Events Reported to the FDA

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

Foetal Distress Syndrome
8 (5.52%)
Hepatitis Cholestatic
8 (5.52%)
Caesarean Section
7 (4.83%)
Atrial Septal Defect
6 (4.14%)
Hypocalcaemia
6 (4.14%)
Premature Baby
6 (4.14%)
Anaemia Neonatal
5 (3.45%)
Macrocephaly
5 (3.45%)
Stevens-johnson Syndrome
5 (3.45%)
Maternal Drugs Affecting Foetus
4 (2.76%)
Patent Ductus Arteriosus
4 (2.76%)
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Periventricular Leukomalacia
4 (2.76%)
Apathy
3 (2.07%)
Depressed Level Of Consciousness
3 (2.07%)
Drug Interaction
3 (2.07%)
Hyperinsulinism
3 (2.07%)
Hypoglycaemia Neonatal
3 (2.07%)
Hypoparathyroidism
3 (2.07%)
Respiratory Failure
3 (2.07%)
Somnolence
3 (2.07%)
Asthenia
2 (1.38%)
Congenital Hypoparathyroidism
2 (1.38%)
Fall
2 (1.38%)
General Physical Health Deteriorati...
2 (1.38%)
Interstitial Lung Disease
2 (1.38%)
Lung Infiltration
2 (1.38%)
Neonatal Hypoparathyroidism
2 (1.38%)
Pulmonary Fibrosis
2 (1.38%)
Respiratory Depression
2 (1.38%)
Toxic Encephalopathy
2 (1.38%)
Twin Pregnancy
2 (1.38%)
Aggression
1 (.69%)
Agranulocytosis
1 (.69%)
Anaemia
1 (.69%)
Antisocial Behaviour
1 (.69%)
Anxiety
1 (.69%)
Balance Disorder
1 (.69%)
Bradykinesia
1 (.69%)
Bradyphrenia
1 (.69%)
Cardiac Pacemaker Replacement
1 (.69%)
Confusional State
1 (.69%)
Cytolytic Hepatitis
1 (.69%)
Fatigue
1 (.69%)
Flushing
1 (.69%)
Hepatomegaly
1 (.69%)
Joint Injury
1 (.69%)
Loss Of Consciousness
1 (.69%)
Medication Error
1 (.69%)
Meningitis
1 (.69%)
Pancytopenia
1 (.69%)
Partner Stress
1 (.69%)
Portal Hypertension
1 (.69%)
Pyrexia
1 (.69%)
Rib Fracture
1 (.69%)
Sepsis
1 (.69%)
Shock
1 (.69%)
Sudden Onset Of Sleep
1 (.69%)
Treatment Noncompliance
1 (.69%)
Upper Gastrointestinal Haemorrhage
1 (.69%)
Urinary Sediment Abnormal
1 (.69%)
Urine Analysis
1 (.69%)
White Blood Cell Count Decreased
1 (.69%)

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

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

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

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

Anxiety
60
Depression
13
Insomnia
8
Drug Use For Unknown Indication
8
Product Used For Unknown Indication
7
Sleep Disorder
6
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Mental Disorder
3
Anxiety Disorder
2
Nervousness
2
Neurosis
1
Nervous System Disorder
1
Relaxation Therapy
1

Lexatin Case Reports

What Lexatin 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 Lexatin. 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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