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TRYPTIZOL

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Tryptizol Adverse Events Reported to the FDA Over Time

How are Tryptizol adverse event reports trending over time?

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

Most Common Tryptizol Adverse Events Reported to the FDA

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

Coma
6 (5.66%)
Confusional State
4 (3.77%)
Gait Disturbance
4 (3.77%)
Death
3 (2.83%)
Drug Interaction
3 (2.83%)
Hepatocellular Injury
3 (2.83%)
Hypokalaemia
3 (2.83%)
Hyponatraemia
3 (2.83%)
Inappropriate Antidiuretic Hormone ...
3 (2.83%)
Respiratory Failure
3 (2.83%)
Bradyphrenia
2 (1.89%)
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Fatigue
2 (1.89%)
Headache
2 (1.89%)
Hypoaesthesia
2 (1.89%)
Insomnia
2 (1.89%)
Pain In Extremity
2 (1.89%)
Respiratory Acidosis
2 (1.89%)
Suicidal Ideation
2 (1.89%)
Acute Respiratory Failure
1 (.94%)
Aggression
1 (.94%)
Anal Pruritus
1 (.94%)
Anxiety
1 (.94%)
Balance Disorder
1 (.94%)
Cardiac Failure
1 (.94%)
Colon Neoplasm
1 (.94%)
Convulsion
1 (.94%)
Coordination Abnormal
1 (.94%)
Depression
1 (.94%)
Diarrhoea
1 (.94%)
Diplopia
1 (.94%)
Disability
1 (.94%)
Disturbance In Attention
1 (.94%)
Drug Exposure During Pregnancy
1 (.94%)
Drug Ineffective
1 (.94%)
Dysstasia
1 (.94%)
Feeling Abnormal
1 (.94%)
Food Craving
1 (.94%)
Galactorrhoea
1 (.94%)
Gingival Disorder
1 (.94%)
Haematocrit Decreased
1 (.94%)
Homicidal Ideation
1 (.94%)
Hyperhidrosis
1 (.94%)
Hyperventilation
1 (.94%)
Hypomania
1 (.94%)
Ill-defined Disorder
1 (.94%)
Inappropriate Schedule Of Drug Admi...
1 (.94%)
Irritability
1 (.94%)
Libido Decreased
1 (.94%)
Listless
1 (.94%)
Mental Disorder
1 (.94%)
Nasopharyngitis
1 (.94%)
Nausea
1 (.94%)
Neuropathy Peripheral
1 (.94%)
No Therapeutic Response
1 (.94%)
Orthostatic Hypotension
1 (.94%)
Parkinsonism
1 (.94%)
Pneumonia
1 (.94%)
Polyp
1 (.94%)
Postural Orthostatic Tachycardia Sy...
1 (.94%)
Rash Papular
1 (.94%)
Restless Legs Syndrome
1 (.94%)
Restlessness
1 (.94%)
Sensory Loss
1 (.94%)
Serotonin Syndrome
1 (.94%)
Speech Disorder
1 (.94%)
Stress
1 (.94%)
Syncope
1 (.94%)
Tongue Disorder
1 (.94%)
Treatment Noncompliance
1 (.94%)
Tremor
1 (.94%)
Vision Blurred
1 (.94%)
Weight Increased
1 (.94%)
Withdrawal Syndrome
1 (.94%)

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

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

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

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

Drug Use For Unknown Indication
15
Depression
12
Pain
10
Neuralgia
6
Product Used For Unknown Indication
4
Back Pain
3
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Pain In Extremity
2
Sleep Disorder
2
Polyneuropathy
1
Prophylaxis
1
Senile Dementia
1
Headache
1
Ill-defined Disorder
1
Facial Neuralgia
1
Herpes Zoster
1
Trigeminal Neuralgia
1
Neuritis
1
Migraine Prophylaxis
1
Cervical Spinal Stenosis
1

Tryptizol Case Reports

What Tryptizol 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 Tryptizol. 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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