Home

helps physicians and healthcare professionals

Erectile Dysfunction

helps physicians and healthcare professionals

Doctor123.org

helps physicians and healthcare professionals

Cromolyn (Nasal)


General


Pronunciation

(KROE moe lin)


Brand Names: U.S.

  • NasalCrom [OTC]

Indications


Use: Labeled Indications

Prevention and treatment of seasonal and perennial allergic rhinitis


Contraindications


Hypersensitivity to cromolyn or any component of the formulation; acute asthma attacks


Dosing and Administration


Dosing: Adult

Allergic rhinitis (treatment and prophylaxis): Intranasal: Instill 1 spray in each nostril 3-4 times/day; may be increased to 6 times/day (symptomatic relief may require 2-4 weeks)


Dosing: Geriatric

Refer to adult dosing.


Dosing: Pediatric

Allergic rhinitis (treatment and prophylaxis): Intranasal: Children ≥2 years: Refer to adult dosing.


Dosing: Renal Impairment

No dosage adjustment provided in manufacturer 's labeling.


Dosing: Hepatic Impairment

No dosage adjustment provided in manufacturer 's labeling.


Administration

Clear nasal passages by blowing nose prior to use.


Storage

Store at room temperature of 15 ‚ °C to 30 ‚ °C (59 ‚ °F to 86 ‚ °F). Protect from light.


Dosage Forms/Strengths


Dosage Forms

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Aerosol Solution, Nasal, as sodium:

NasalCrom: 5.2 mg/actuation (13 mL, 26 mL) [contains benzalkonium chloride, edetate disodium]

Generic: 5.2 mg/actuation (26 mL)


Drug Interactions

There are no known significant interactions.


Adverse Reactions


Frequency not defined.

>10%:

Dermatologic: Burning sensation of the nose

Respiratory: Nasal mucosa irritation, sneezing, stinging sensation of the nose

1% to 10%:

Central nervous system: Headache

Gastrointestinal: Unpleasant taste

Respiratory: Cough, hoarseness, post-nasal drip

<1% (Limited to important or life-threatening): Epistaxis


Warnings/Precautions


Other warnings/precautions:

- Appropriate use: Prophylactic drug with no benefit for acute situations.

- Withdrawal: Caution should be used when withdrawing the drug or tapering the dose as symptoms may reoccur.


Pregnancy Considerations

Animal reproduction studies have not been conducted; however, studies in pregnant women have not shown signs of adverse effects or increased teratogenicity with use during pregnancy (Gilbert, 2005; Mazzotta, 1999).


Actions


Excretion

Urine and feces (equal amounts as unchanged drug); exhaled gases (small amounts)


Onset of Action

Response to treatment: May occur at 1-2 weeks


Half-Life Elimination

80-90 minutes


Patient and Family Education


Patient Education

- Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?)

- Patient may experience sneezing, burning, or stinging. Have patient report immediately to prescriber severe nasal irritation (HCAHPS).

- Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions.

Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for healthcare professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience and judgment in diagnosing, treating and advising patients.

Copyright © 2016 - 2017
Doctor123.org | Disclaimer