Trichophyton mentagrophytes and trichophyton rubrum: Difference between revisions

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|indicationType=treatment
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|blackBoxWarningTitle=<span style="color:#FF0000;">ConditionName: </span>
* This product is intended for use by physicians who are experienced in the administration of allergenic extracts or for use under the guidance of an allergy specialist. Skin tests should be performed after the patient's physical well being and allergic history have been evaluated. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician if symptoms occur. As with all allergenic extracts, severe systemic reactions may occur, and in certain individuals these reactions may cause death. Patients should be observed for at least 20 minutes after skin tests have been completed. Emergency measures as well as personnel trained in their use should be immediately available in the event of a life threatening reaction.
|blackBoxWarningBody=* This product is intended for use by physicians who are experienced in the administration of allergenic extracts or for use under the guidance of an allergy specialist. Skin tests should be performed after the patient's physical well being and allergic history have been evaluated. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician if symptoms occur. As with all allergenic extracts, severe systemic reactions may occur, and in certain individuals these reactions may cause death. Patients should be observed for at least 20 minutes after skin tests have been completed. Emergency measures as well as personnel trained in their use should be immediately available in the event of a life threatening reaction.


* This product should never be injected intravenously.
* This product should never be injected intravenously.
|blackBoxWarningTitle=<span style="color:#FF0000;">ConditionName: </span>
|fdaLIADAdult===Indications==
|blackBoxWarningBody=<i><span style="color:#FF0000;">ConditionName: </span></i>
* Intradermal skin tests with Trichophyton extract are indicated for use in persons who are suspected of having Type I hypersensitivity (i.e. allergy) to the fungus.
 
* Content
 
<!--Adult Indications and Dosage-->
 
<!--FDA-Labeled Indications and Dosage (Adult)-->
|fdaLIADAdult======Condition1=====
 
* Dosing Information
 
:* Dosage
 
=====Condition2=====
 
* Dosing Information
 
:* Dosage
 
=====Condition3=====
 
* Dosing Information
 
:* Dosage
 
=====Condition4=====
 
* Dosing Information
 
:* Dosage
 
<!--Off-Label Use and Dosage (Adult)-->
 
<!--Guideline-Supported Use (Adult)-->
|offLabelAdultGuideSupport======Condition1=====
|offLabelAdultGuideSupport======Condition1=====


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<!--Contraindications-->
<!--Contraindications-->
|contraindications=* Condition1
|contraindications=* Conditions under which the administration of allergenic extract may be contraindicated, depending upon individual circumstances, include: EXTREME SENSITIVITY TO AN ALLERGEN - Determined from the allergic history, or from previous anaphylaxis following skin testing or subcutaneous injection; MYOCARDIAL INFARCTION - Patients who have experienced a recent myocardial infarction may be less able to tolerate the life-threatening effects of a serious adverse reaction. ASTHMA - Patients with highly unstable asthma are at greater risk of fatal reactions from skin tests than are patients without asthma, especially during seasonal exacerbations of the disease. Also, the combination of unstable asthma and treatment with B-adrenergic blockers appears to increase this risk5. Allergenic extract should be temporarily withheld from patients if any of the following conditions exist: 1) severe symptoms of hay fever and/or asthma; 2) infection or flu accompanied by fever; and 3) exposure to excessive amounts of clinically relevant allergen(s) prior to skin testing.
 
<!--Warnings-->
|warnings=* Description
|warnings=* Description



Revision as of 19:15, 27 March 2015

Trichophyton mentagrophytes and trichophyton rubrum
Black Box Warning
Adult Indications & Dosage
Pediatric Indications & Dosage
Contraindications
Warnings & Precautions
Adverse Reactions
Drug Interactions
Use in Specific Populations
Administration & Monitoring
Overdosage
Pharmacology
Clinical Studies
How Supplied
Images
Patient Counseling Information
Precautions with Alcohol
Brand Names
Look-Alike Names

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Kiran Singh, M.D. [2]

Disclaimer

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Black Box Warning

ConditionName:
See full prescribing information for complete Boxed Warning.
* This product is intended for use by physicians who are experienced in the administration of allergenic extracts or for use under the guidance of an allergy specialist. Skin tests should be performed after the patient's physical well being and allergic history have been evaluated. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician if symptoms occur. As with all allergenic extracts, severe systemic reactions may occur, and in certain individuals these reactions may cause death. Patients should be observed for at least 20 minutes after skin tests have been completed. Emergency measures as well as personnel trained in their use should be immediately available in the event of a life threatening reaction.
  • This product should never be injected intravenously.

Overview

Trichophyton mentagrophytes and trichophyton rubrum is a {{{drugClass}}} that is FDA approved for the treatment of {{{indication}}}. There is a Black Box Warning for this drug as shown here. Common adverse reactions include {{{adverseReactions}}}.

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

Indications

  • Intradermal skin tests with Trichophyton extract are indicated for use in persons who are suspected of having Type I hypersensitivity (i.e. allergy) to the fungus.

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

Condition1
  • Developed by:
  • Class of Recommendation:
  • Strength of Evidence:
  • Dosing Information
  • Dosage
Condition2

There is limited information regarding Off-Label Guideline-Supported Use of Trichophyton mentagrophytes and trichophyton rubrum in adult patients.

Non–Guideline-Supported Use

Condition1
  • Dosing Information
  • Dosage
Condition2

There is limited information regarding Off-Label Non–Guideline-Supported Use of Trichophyton mentagrophytes and trichophyton rubrum in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

Condition1
  • Dosing Information
  • Dosage
Condition2

There is limited information regarding FDA-Labeled Use of Trichophyton mentagrophytes and trichophyton rubrum in pediatric patients.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

Condition1
  • Developed by:
  • Class of Recommendation:
  • Strength of Evidence:
  • Dosing Information
  • Dosage
Condition2

There is limited information regarding Off-Label Guideline-Supported Use of Trichophyton mentagrophytes and trichophyton rubrum in pediatric patients.

Non–Guideline-Supported Use

Condition1
  • Dosing Information
  • Dosage
Condition2

There is limited information regarding Off-Label Non–Guideline-Supported Use of Trichophyton mentagrophytes and trichophyton rubrum in pediatric patients.

Contraindications

  • Conditions under which the administration of allergenic extract may be contraindicated, depending upon individual circumstances, include: EXTREME SENSITIVITY TO AN ALLERGEN - Determined from the allergic history, or from previous anaphylaxis following skin testing or subcutaneous injection; MYOCARDIAL INFARCTION - Patients who have experienced a recent myocardial infarction may be less able to tolerate the life-threatening effects of a serious adverse reaction. ASTHMA - Patients with highly unstable asthma are at greater risk of fatal reactions from skin tests than are patients without asthma, especially during seasonal exacerbations of the disease. Also, the combination of unstable asthma and treatment with B-adrenergic blockers appears to increase this risk5. Allergenic extract should be temporarily withheld from patients if any of the following conditions exist: 1) severe symptoms of hay fever and/or asthma; 2) infection or flu accompanied by fever; and 3) exposure to excessive amounts of clinically relevant allergen(s) prior to skin testing.

Warnings

ConditionName:
See full prescribing information for complete Boxed Warning.
* This product is intended for use by physicians who are experienced in the administration of allergenic extracts or for use under the guidance of an allergy specialist. Skin tests should be performed after the patient's physical well being and allergic history have been evaluated. Patients should be instructed to recognize adverse reaction symptoms and cautioned to contact the physician if symptoms occur. As with all allergenic extracts, severe systemic reactions may occur, and in certain individuals these reactions may cause death. Patients should be observed for at least 20 minutes after skin tests have been completed. Emergency measures as well as personnel trained in their use should be immediately available in the event of a life threatening reaction.
  • This product should never be injected intravenously.
  • Description

Precautions

  • Description

Adverse Reactions

Clinical Trials Experience

There is limited information regarding Clinical Trial Experience of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous

Postmarketing Experience

There is limited information regarding Postmarketing Experience of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Body as a Whole
Cardiovascular
Digestive
Endocrine
Hematologic and Lymphatic
Metabolic and Nutritional
Musculoskeletal
Neurologic
Respiratory
Skin and Hypersensitivy Reactions
Special Senses
Urogenital
Miscellaneous

Drug Interactions

There is limited information regarding Trichophyton mentagrophytes and trichophyton rubrum Drug Interactions in the drug label.

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA):

  • Pregnancy Category


Pregnancy Category (AUS):

  • Australian Drug Evaluation Committee (ADEC) Pregnancy Category

There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Trichophyton mentagrophytes and trichophyton rubrum in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Trichophyton mentagrophytes and trichophyton rubrum during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum with respect to nursing mothers.

Pediatric Use

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum with respect to pediatric patients.

Geriatic Use

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum with respect to geriatric patients.

Gender

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum with respect to specific gender populations.

Race

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Trichophyton mentagrophytes and trichophyton rubrum in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Trichophyton mentagrophytes and trichophyton rubrum in patients who are immunocompromised.

Administration and Monitoring

Administration

  • Oral
  • Intravenous

Monitoring

There is limited information regarding Monitoring of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

  • Description

IV Compatibility

There is limited information regarding IV Compatibility of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Overdosage

Acute Overdose

Signs and Symptoms

  • Description

Management

  • Description

Chronic Overdose

There is limited information regarding Chronic Overdose of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Pharmacology

There is limited information regarding Trichophyton mentagrophytes and trichophyton rubrum Pharmacology in the drug label.

Mechanism of Action

Structure

File:Trichophyton mentagrophytes and trichophyton rubrum01.png
This image is provided by the National Library of Medicine.

Pharmacodynamics

There is limited information regarding Pharmacodynamics of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Pharmacokinetics

There is limited information regarding Pharmacokinetics of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Nonclinical Toxicology

There is limited information regarding Nonclinical Toxicology of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Clinical Studies

There is limited information regarding Clinical Studies of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

How Supplied

Storage

There is limited information regarding Trichophyton mentagrophytes and trichophyton rubrum Storage in the drug label.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Patient Counseling Information of Trichophyton mentagrophytes and trichophyton rubrum in the drug label.

Precautions with Alcohol

  • Alcohol-Trichophyton mentagrophytes and trichophyton rubrum interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

Look-Alike Drug Names

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

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