French System for Monitoring Unexpected or Toxic Drug Reactions (UTDR)

Purpose: To evaluate a drug as a possible explanation for an adverse event in a patient using a method employed in France.

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Evaluation

Are you evaluating a drug as a possible explanation for an adverse event in a patient?

Yes

Are there symptoms or other findings implicating the drug?

Yes

Select the appropriate answer for each finding

Challenge

Dechallenge

Rechallenge with drug

Alternative non-drug explanation

Reliable and specific test finding implicating the drug

Results

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Results Interpretation and Description References Next Steps

Data complete?

Evaluation appropriate?

Chronologic findings

Semeiologic findings

Probability that the drug is the cause of the adverse event

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Interpretation and Description

References

Next Steps in Evaluation

Diagnosis

Risk Factors
Clinical Diagnosis, Including Family History For Genetics
- Findings Suggestive of Possible Adverse Drug Reaction
Other Testing
- Evaluate Causal Relationship in Adverse Drug Reaction (FDA)
Severity, Prognosis, Stage
- Classification for Severity of Adverse Drug Reaction
Complications
- Prediction Rule for Adverse Drug Events in Hospitalized Adult Patient

Therapy

Prevention
- Modified Criteria for Preventability of Adverse Drug Reaction (ADR)

Monitoring

Adverse Effects
Complication Detection
- Prediction Rule for Adverse Drug Events in Hospitalized Adult Patient
Comorbid Conditions
- Adverse Drug Reaction (ADR) in Older Adults | Comorbid Conditions Repeat Hospital Admissions

Specialty

Toxicology
Emergency Medicine
Critical Care

Objective

adverse effects

ICD-10

Z86.4 - Personal history of psychoactive substance abuse

Info

Purpose: To evaluate a drug as a possible explanation for an adverse event in a patient using a method employed in France.

Specialty: Toxicology, Emergency Medicine, Critical Care

Objective: adverse effects

ICD-10: Z86.4,

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