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Standardized Mite, Dermatophagoides pteronyssinus

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Overview

What is Standardized Mite, Dermatophagoides pteronyssinus?

DESCRIPTION

D. farinae

D. pteronyssinus

    INGREDIENTS:

standardized quality procedures

no material of human origin.

D. farinae

D. pteronyssinus

Saccharomyces sp.

50

1,2,3,4,5,16



What does Standardized Mite, Dermatophagoides pteronyssinus look like?



What are the available doses of Standardized Mite, Dermatophagoides pteronyssinus?

Sorry No records found.

What should I talk to my health care provider before I take Standardized Mite, Dermatophagoides pteronyssinus?

Sorry No records found

How should I use Standardized Mite, Dermatophagoides pteronyssinus?

INDICATIONS AND USAGE

D. farinae

D. pteronyssinus

PRICK-PUNCTURE TESTING:

     Smaller, less conclusive reactions may be considered positive in conjunction with a definitive history of symptoms on exposure to the mite allergen. The more sensitive the patient the higher the probability that he/she will have symptoms related to the exposure of the offending allergen. Hence, the importance of a good patient history. Less sensitive individuals can be tested intra­dermally with an appropriately diluted extract.     A clinical study using the same patients with positive prick-puncture test (10) using the , has demonstrated the following:     Skin test by prick-puncture test using Standardized Mite, 10,000 AU/ml was per­formed in 10 patients. The mean sum of erythema diameter was 76.6 mm (Range 45-104 mm). Skin test by prick-puncture test using Standardized Mite, 10,000 AU/ml in 10 patients, the mean sum of erythema diameter was 74.7 mm (Range 43-109 mm).

*C = Concentration

SINGLE DILUTION INTRADERMAL TESTING:

INTRADERMAL TESTING–SKIN ENDPOINT TITRATION:

D. farinae Mite

D. pteronyssinus

DOSAGE AND ADMINISTRATION

physician must proceed cautiously in the treatment of the highly sensitive patient who develops large local or systemic reactions

Maintenance dose potency must be established by the physician's clini­cal observation and experience

7

8,12

6,13


What interacts with Standardized Mite, Dermatophagoides pteronyssinus?

Sorry No Records found


What are the warnings of Standardized Mite, Dermatophagoides pteronyssinus?

Sorry No Records found


What are the precautions of Standardized Mite, Dermatophagoides pteronyssinus?

Sorry No Records found


What are the side effects of Standardized Mite, Dermatophagoides pteronyssinus?

Sorry No records found


What should I look out for while using Standardized Mite, Dermatophagoides pteronyssinus?

CONTRAINDICATIONS

WARNINGS

IN THESE CASES BOTH THE POTENCY FOR SKIN TESTS AND THE ESCALATION OF THE TREATMENT DOSE MUST BE ADJUSTED TO THE PATIENT'S SENSITIVITY TOLERANCE.

changing immunotherapy from an unstandard­ized to an AU/ml standardized allergenic extract

dose reduced to 75%.


What might happen if I take too much Standardized Mite, Dermatophagoides pteronyssinus?

OVERDOSAGE

4


How should I store and handle Standardized Mite, Dermatophagoides pteronyssinus?

Store at controlled room temperature 20° to 25°C (68° to 77°F) [see USP] .HOW SUPPLIED Dermatophagoides fari­naeDermatophagoides pteronyssinusHOW SUPPLIED Dermatophagoides fari­naeDermatophagoides pteronyssinusHOW SUPPLIED Dermatophagoides fari­naeDermatophagoides pteronyssinus


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

CLINICAL PHARMACOLOGY

3,5

10,14,15

Non-Clinical Toxicology
CONTRAINDICATIONS

WARNINGS

IN THESE CASES BOTH THE POTENCY FOR SKIN TESTS AND THE ESCALATION OF THE TREATMENT DOSE MUST BE ADJUSTED TO THE PATIENT'S SENSITIVITY TOLERANCE.

changing immunotherapy from an unstandard­ized to an AU/ml standardized allergenic extract

dose reduced to 75%.

PRECAUTIONS

Antihistamines.

Corticosteroids.

Theophylline.

Beta-adrenergic agents.

Cromolyn.

Other drugs.

Specific Immunotherapy.

13,14

11

17,18,19,20,21,22

23

23

23

23

23

23

23

23

23

1

1

1

1

1

2

2

ADVERSE REACTIONS

Patients receiving beta-blockers may not be responsive to epinephrine or inhaled bronchodilators.

beta-blockers

24

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Tips

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Interactions

Interactions

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