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TRYPTANOL

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Tryptanol Adverse Events Reported to the FDA Over Time

How are Tryptanol adverse event reports trending over time?

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

Most Common Tryptanol Adverse Events Reported to the FDA

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

Pyrexia
11 (2.3%)
Agranulocytosis
10 (2.09%)
Gamma-glutamyltransferase Increased
10 (2.09%)
Vomiting
8 (1.67%)
Dysuria
7 (1.46%)
Platelet Count Decreased
7 (1.46%)
Blood Alkaline Phosphatase Increase...
6 (1.25%)
Blood Creatine Phosphokinase Increa...
6 (1.25%)
Depression
6 (1.25%)
Dizziness
6 (1.25%)
Liver Disorder
6 (1.25%)
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Loss Of Consciousness
6 (1.25%)
Malaise
6 (1.25%)
Nausea
6 (1.25%)
Neuroleptic Malignant Syndrome
6 (1.25%)
White Blood Cell Count Decreased
6 (1.25%)
Alanine Aminotransferase Increased
5 (1.04%)
Aspartate Aminotransferase Increase...
5 (1.04%)
Blood Pressure Decreased
5 (1.04%)
Convulsion
5 (1.04%)
Neutrophil Count Decreased
5 (1.04%)
Somnolence
5 (1.04%)
Abnormal Behaviour
4 (.84%)
Blood Lactate Dehydrogenase Increas...
4 (.84%)
C-reactive Protein Increased
4 (.84%)
Epilepsy
4 (.84%)
Headache
4 (.84%)
Insomnia
4 (.84%)
Interstitial Lung Disease
4 (.84%)
Pain
4 (.84%)
Pruritus
4 (.84%)
Suicide Attempt
4 (.84%)
Weight Increased
4 (.84%)
Anorexia
3 (.63%)
Cardiac Failure Acute
3 (.63%)
Chest X-ray Abnormal
3 (.63%)
Confusional State
3 (.63%)
Constipation
3 (.63%)
Depressed Level Of Consciousness
3 (.63%)
Dyspnoea
3 (.63%)
Fall
3 (.63%)
Hyperhidrosis
3 (.63%)
Intentional Overdose
3 (.63%)
Irritability
3 (.63%)
Lymphocyte Stimulation Test Positiv...
3 (.63%)
Nasopharyngitis
3 (.63%)
Nocturia
3 (.63%)
Optic Nerve Disorder
3 (.63%)
Pain In Extremity
3 (.63%)
Rapid Eye Movements Sleep Abnormal
3 (.63%)
Red Blood Cell Count Decreased
3 (.63%)
Renal Impairment
3 (.63%)
Thrombocytopenia
3 (.63%)
Tremor
3 (.63%)
Urinary Tract Infection
3 (.63%)
Vision Blurred
3 (.63%)
Abdominal Distension
2 (.42%)
Alopecia
2 (.42%)
Altered State Of Consciousness
2 (.42%)
Amnesia
2 (.42%)
Anxiety
2 (.42%)
Basophil Count Decreased
2 (.42%)
Basophil Percentage Decreased
2 (.42%)
Blindness
2 (.42%)
Blood Creatinine Increased
2 (.42%)
Blood Potassium Decreased
2 (.42%)
Blood Urea Increased
2 (.42%)
Chest Discomfort
2 (.42%)
Condition Aggravated
2 (.42%)
Cough
2 (.42%)
Cyanosis
2 (.42%)
Decreased Appetite
2 (.42%)
Dehydration
2 (.42%)
Delirium
2 (.42%)
Diarrhoea
2 (.42%)
Drug Effect Decreased
2 (.42%)
Drug Eruption
2 (.42%)
Drug Hypersensitivity
2 (.42%)
Drug Interaction
2 (.42%)
Drug Toxicity
2 (.42%)
Dysgeusia
2 (.42%)
Enterocolitis
2 (.42%)
Eosinophil Count Decreased
2 (.42%)
Eosinophil Percentage Decreased
2 (.42%)
Epistaxis
2 (.42%)
Eyelids Pruritus
2 (.42%)
Fatigue
2 (.42%)
Feeling Abnormal
2 (.42%)
Fracture
2 (.42%)
Gastroenteritis
2 (.42%)
Haematocrit Decreased
2 (.42%)
Haemoglobin Decreased
2 (.42%)
Herpes Virus Infection
2 (.42%)
Hordeolum
2 (.42%)
Hunger
2 (.42%)
Hyponatraemia
2 (.42%)
Hypothermia
2 (.42%)
Inappropriate Schedule Of Drug Admi...
2 (.42%)
Infected Epidermal Cyst
2 (.42%)
Intervertebral Disc Protrusion
2 (.42%)
Irritable Bowel Syndrome
2 (.42%)

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

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

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

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

Depression
70
Drug Use For Unknown Indication
34
Pain
25
Cancer Pain
14
Product Used For Unknown Indication
14
Insomnia
9
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Pain In Extremity
8
Nocturia
8
Post Herpetic Neuralgia
7
Dysthymic Disorder
7
Headache
5
Abnormal Dreams
4
Hyperventilation
4
Neuropathy Peripheral
4
Migraine
3
Panic Disorder
3
Nervous System Disorder
3
Salivary Hypersecretion
3
Autism
3
Inflammation
3
Hypoaesthesia
3
Herpes Zoster
3
Depressive Symptom
2
Herpes Virus Infection
2
Analgesic Therapy
2
Diabetic Neuropathy
2
Multiple Myeloma
2
Depressed Mood
2
Trigeminal Neuralgia
2
Neuralgia
2
Glossopharyngeal Neuralgia
2
Parkinsons Disease
2
Antidepressant Therapy
1
Eye Pain
1
Analgesic Intervention Supportive T...
1
Hiccups
1
Abnormal Behaviour
1
Sleep Disorder
1
Obsessive-compulsive Disorder
1
Completed Suicide
1
Ill-defined Disorder
1
Neurosis
1
Enuresis
1
Sedative Therapy
1
Anxiety Disorder
1
Anxiety
1

Tryptanol Case Reports

What Tryptanol 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 Tryptanol. 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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