Zeltas Nasal Spray
Azelastine + Fluticasone Propionate Nasal prep
125mcg + 50mcg/Metered In
Opsonin Pharma Limited
Pack size | |
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Unite Price | 320.00 BDT |
Indications
Zeltas Nasal Spray is used for:
Seasonal Allergic Rhinitis
Adult Dose
Nasal Spray
Seasonal allergic rhinitis
The recommended dosage is 1 spray each nostril twice daily.
Child Dose
Nasal Spray
Seasonal Allergic Rhinitis
<6 years: Safety and efficacy not established
>6 years: 1 each nostril twice daily.
Renal Dose
Administration
Shake bottle gently prior to each use
Prime the bottle before initial use by releasing 6 sprays or more until a fine mist sprays
Reprime the bottle if unused for >14 days by spraying once or more until fine mist appears
Contra Indications
There is no known contraindication.
Precautions
Avoid spraying directly into eyes; if drug is sprayed into eyes, flush with water for a minimum of 10 minutes
May cause somnolence; avoid operating heavy machinery or engaging in tasks that require mental alertness and coordination
Do not use with history of recent nasal ulcers, nasal surgery, or any nasal trauma
May cause glaucoma or cataracts
As corticosteroids may cause immunosuppression, patients should notify healthcare providers if they experience any symptoms of tuberculosis, viral, bacterial, fungal or parasitic infections or ocular herpes simplex
Due to the potential reduction in growth velocity in children, patients must be monitored routinely
Lactation: Unknown whether distributed in breast milk, exercise caution
Pregnancy-Lactation
Pregnancy
Limited data from postmarketing experience over decades of use in pregnant women have not identified any drug associated risks of miscarriage, birth defects, or other adverse maternal or fetal outcomes
Animal data
Animal reproduction studies with combination product are not available; however, studies are available with its individual components, azelastine hydrochloride and fluticasone propionate
In animal reproduction studies with azelastine, there was no evidence of fetal harm at oral doses approximately 5 times the clinical daily dose; oral administration to pregnant mice, rats, and rabbits, during the period of organogenesis, produced developmental toxicity that included structural abnormalities, decreased embryo-fetal survival, and decreased fetal body weights at doses 270 times and higher than maximum recommended human daily intranasal dose of 1.096 mg; relevance of these findings in animals to pregnant women considered questionable based upon high animal to human dose multiple
In animal reproduction studies, fluticasone propionate administered via nose-only inhalation to rats decreased fetal body weight, but did not induce teratogenicity at a maternal toxic dose less than the MRHDID on a mcg/m2 basis; teratogenicity, characteristic of corticosteroids, decreased fetal body weight and/or skeletal variations, in rats, mice, and rabbits were observed with subcutaneously administered maternal toxic doses of fluticasone propionate less than the MRHDID of 200 mcg on a mcg/m2 basis; experience with corticosteroids suggests that rodents are more prone to teratogenic effects from corticosteroids than humans
Lactation
There are no available data on presence of azelastine hydrochloride or fluticasone propionate in human milk, effects on breastfed infant, or on milk production; breastfed infants should be monitored for signs of milk rejection during combination treatment by lactating women; fluticasone propionate is present in rat milk
Other corticosteroids have been detected in human milk; however, fluticasone propionate concentrations in plasma after intranasal therapeutic doses are low and therefore concentrations in human breast milk are likely to be correspondingly low; developmental and health benefits of breastfeeding should be considered along with mother’s clinical need for combination treatment and any potential adverse effects on breastfed infant from therapy or from underlying maternal condition
Interactions
Additive effects with CNS depressants and ethanol. Increased plasma concentration w/ potent CYP3A4 inhibitors (e.g. ritonavir).
Side Effects
Side effects of Azelastine + Fluticasone Propionate Nasal prep :
1-10%
Dysgeusia (4%), Headache (2%), Epistaxis (2%)
Frequency Not Defined
Somnolence, Nasal effects (eg, nasal ulceration, nasal septal perforation), Impaired wound healing, Candida albicans infection, Glaucoma, Cataracts, Immunosuppression, Hypothalamic-pituitary-adrenal (HPA) axis suppression
Mode of Action
Azelastine: Phthalazinones derivative; elicits histamine H1-receptor antagonist activity; major metabolite (desmethylazelastine) also exhibits histamine H1-receptor antagonist activity
Fluticasone: Corticosteroid possessing anti-inflammatory activity; exact mechanism of action unknown, but shown to exhibit anti-inflammatory effect on multiple cells (eg, neutrophils, eosinophils, macrophages, mast cells, lymphocytes) and mediators (eg, histamine, leukotrienes, cytokines and eicosanoids)
Note
Zeltas 125mcg + 50mcg/Metered In Nasal Spray generic name is Azelastine + Fluticasone Propionate Nasal prep. Zeltas 125mcg + 50mcg/Metered In Nasal Spray is manufactured by Opsonin Pharma LimitedZeltas is availble in all over Bangladesh.
Mes BD drug index information on Zeltas Nasal Spray is not intended for diagnosis, medical advice or treatment; neither intended to be a substitute for the exercise of professional judgment.
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