Lipofibrate may be available in the countries listed below.
Ingredient matches for Lipofibrate
Clinofibrate is reported as an ingredient of Lipofibrate in the following countries:
- Japan
International Drug Name Search
Lipofibrate may be available in the countries listed below.
Clinofibrate is reported as an ingredient of Lipofibrate in the following countries:
International Drug Name Search
Doxazosina Ratiopharm may be available in the countries listed below.
Doxazosin mesilate (a derivative of Doxazosin) is reported as an ingredient of Doxazosina Ratiopharm in the following countries:
International Drug Name Search
Rec.INN
0027959-26-8
C34-H32-N4-O9
640
Antilipemic agent
3-Pyridinecarboxylic acid, (2-hydroxy-1,3-cyclohexanediylidene)tetrakis(methylene) ester
International Drug Name Search
Glossary
IS | Inofficial Synonym |
JAN | Japanese Accepted Name |
OS | Official Synonym |
PH | Pharmacopoeia Name |
Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
Octim may be available in the countries listed below.
UK matches:
Desmopressin acetate (a derivative of Desmopressin) is reported as an ingredient of Octim in the following countries:
International Drug Name Search
Glossary
SPC | Summary of Product Characteristics (UK) |
Stela may be available in the countries listed below.
Trifluoperazine hydrochloride (a derivative of Trifluoperazine) is reported as an ingredient of Stela in the following countries:
International Drug Name Search
Purgoxin may be available in the countries listed below.
Digoxin is reported as an ingredient of Purgoxin in the following countries:
International Drug Name Search
In some countries, this medicine may only be approved for veterinary use.
In the US, Betamethasone (betamethasone systemic) is a member of the drug class glucocorticoids and is used to treat Bursitis, Dermatological Disorders, Gouty Arthritis, Inflammatory Conditions and Osteoarthritis.
US matches:
Rec.INN
A07EA04,C05AA05,D07AC01,D07XC01,H02AB01,R01AD06,R03BA04,S01BA06,S01CB04,S02BA07,S03BA03
0000378-44-9
C22-H29-F-O5
392
Adrenal cortex hormone, glucocorticoid
Pregna-1,4-diene-3,20-dione, 9-fluoro-11,17,21-trihydroxy-16-methyl-, (11ß,16ß)-
In the US, Pyrazinamide (pyrazinamide systemic) is a member of the drug class nicotinic acid derivatives and is used to treat Tuberculosis - Active and Tuberculosis - Latent.
US matches:
Rec.INN
J04AK01
0000098-96-4
C5-H5-N3-O
123
Antitubercular agent
Pyrazinecarboxamide
International Drug Name Search
Glossary
BAN | British Approved Name |
DCF | Dénomination Commune Française |
DCIT | Denominazione Comune Italiana |
IS | Inofficial Synonym |
JAN | Japanese Accepted Name |
OS | Official Synonym |
PH | Pharmacopoeia Name |
Rec.INN | Recommended International Nonproprietary Name (World Health Organization) |
WHO | World Health Organization |
In the US, Orapred ODT (prednisolone systemic) is a member of the drug class glucocorticoids and is used to treat Asthma - acute, Bullous Pemphigoid, Dermatitis, Immunosuppression, Inflammatory Conditions, Multiple Sclerosis, Nephrotic Syndrome, Pemphigoid and Pemphigus.
US matches:
Prednisolone 21-(disodium phosphate) (a derivative of Prednisolone) is reported as an ingredient of Orapred ODT in the following countries:
International Drug Name Search
Omeprazol Arafarma may be available in the countries listed below.
Omeprazole is reported as an ingredient of Omeprazol Arafarma in the following countries:
International Drug Name Search
Generic Name: prenatal multivitamins (PRE nay tal VYE ta mins)
Brand Names: Advance Care Plus, Bright Beginnings, Cavan Folate, Cavan One, Cavan-Heme OB, Cenogen Ultra, CitraNatal Rx, Co Natal FA, Complete Natal DHA, Complete-RF, CompleteNate, Concept OB, Docosavit, Dualvit OB, Duet, Edge OB, Elite OB 400, Femecal OB, Folbecal, Folcaps Care One, Folivan-OB, Foltabs, Gesticare, Icar Prenatal, Icare Prenatal Rx, Inatal Advance, Infanate DHA, Kolnatal DHA, Lactocal-F, Marnatal-F, Maternity, Maxinate, Mission Prenatal, Multi-Nate 30, Multinatal Plus, Nata 29 Prenatal, Natachew, Natafort, Natelle, Neevo, Nestabs, Nexa Select with DHA, Novanatal, NovaStart, O-Cal Prenatal, OB Complete, OB Natal One, Ob-20, Obtrex DHA, OptiNate, Paire OB Plus DHA, PNV Select, PNV-Total, PR Natal 400, Pre-H-Cal, Precare, PreferaOB, Premesis Rx, PrenaCare, PrenaFirst, PrenaPlus, Prenatabs OBN, Prenatabs Rx, Prenatal 1 Plus 1, Prenatal Elite, Prenatal Multivitamins, Prenatal Plus, Prenatal S, Prenatal-U, Prenate Advanced Formula, Prenate DHA, Prenate Elite, Prenavite FC, PreNexa, PreQue 10, Previte Rx, PrimaCare, Pruet DHA, RE OB Plus DHA, Renate, RightStep, Rovin-NV, Se-Care, Se-Natal One, Se-Plete DHA, Se-Tan DHA, Select-OB, Seton ET, Strongstart, Stuart Prenatal with Beta Carotene, Tandem OB, Taron-BC, Tri Rx, TriAdvance, TriCare, Trimesis Rx, Trinate, Triveen-PRx RNF, UltimateCare Advance, Ultra-Natal, Vemavite PRX 2, VeNatal FA, Verotin-BY, Verotin-GR, Vinacal OR, Vinatal Forte, Vinate Advanced (New Formula), Vinate AZ, Vinate Care, Vinate Good Start, Vinate II (New Formula), Vinate III, Vinate One, Vitafol-OB, VitaNatal OB plus DHA, Vitaphil, Vitaphil Aide, Vitaphil Plus DHA, Vitaspire, Viva DHA, Vol-Nate, Vol-Plus, Vol-Tab Rx, Vynatal F.A., Zatean-CH, Zatean-PN
There are many brands and forms of prenatal vitamin available and not all brands are listed on this leaflet.
Prenatal vitamins are a combination of many different vitamins that are normally found in foods and other natural sources.
Prenatal vitamins are used to provide the additional vitamins needed during pregnancy. Minerals may also be contained in prenatal multivitamins.
Prenatal vitamins may also be used for purposes not listed in this medication guide.
There are many brands and forms of prenatal vitamin available and not all brands are listed on this leaflet.
Many multivitamin products also contain minerals such as calcium, iron, magnesium, potassium, and zinc. Minerals (especially taken in large doses) can cause side effects such as tooth staining, increased urination, stomach bleeding, uneven heart rate, confusion, and muscle weakness or limp feeling. Read the label of any multivitamin product you take to make sure you are aware of what it contains.
Overdose symptoms may include stomach pain, vomiting, diarrhea, constipation, loss of appetite, hair loss, peeling skin, tingly feeling in or around your mouth, changes in menstrual periods, weight loss, severe headache, muscle or joint pain, severe back pain, blood in your urine, pale skin, and easy bruising or bleeding.
Before taking prenatal vitamins, tell your doctor about all of your medical conditions.
Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.
Many multivitamin products also contain minerals such as calcium, iron, magnesium, potassium, and zinc. Minerals (especially taken in large doses) can cause side effects such as tooth staining, increased urination, stomach bleeding, uneven heart rate, confusion, and muscle weakness or limp feeling. Read the label of any multivitamin product you take to make sure you are aware of what it contains.
Swallow the regular tablet or capsule whole. Do not break, chew, crush, or open it.
The chewable tablet must be chewed or allowed to dissolve in your mouth before swallowing. You may also allow the chewable tablet to dissolve in drinking water, fruit juice, or infant formula (but not milk or other dairy products). Drink this mixture right away.
Use prenatal vitamins regularly to get the most benefit. Get your prescription refilled before you run out of medicine completely.
Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.
Overdose symptoms may include stomach pain, vomiting, diarrhea, constipation, loss of appetite, hair loss, peeling skin, tingly feeling in or around your mouth, changes in menstrual periods, weight loss, severe headache, muscle or joint pain, severe back pain, blood in your urine, pale skin, and easy bruising or bleeding.
Avoid the regular use of salt substitutes in your diet if your multivitamin contains potassium. If you are on a low-salt diet, ask your doctor before taking a vitamin or mineral supplement.
When taken as directed, prenatal vitamins are not expected to cause serious side effects. Less serious side effects may include:
upset stomach;
headache; or
unusual or unpleasant taste in your mouth.
This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Vitamin and mineral supplements can interact with certain medications, or affect how medications work in your body. Before taking a prenatal vitamin, tell your doctor if you also use:
diuretics (water pills);
heart or blood pressure medications;
tretinoin (Vesanoid);
isotretinoin (Accutane, Amnesteen, Clavaris, Sotret);
trimethoprim and sulfamethoxazole (Cotrim, Bactrim, Gantanol, Gantrisin, Septra, TMP/SMX); or
an NSAID (non-steroidal anti-inflammatory drug) such as ibuprofen (Advil, Motrin), naproxen (Aleve, Naprosyn, Naprelan, Treximet), celecoxib (Celebrex), diclofenac (Cataflam, Voltaren), indomethacin (Indocin), meloxicam (Mobic), and others.
This list is not complete and other drugs may interact with prenatal vitamins. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor.
Molsibeta may be available in the countries listed below.
Molsidomine is reported as an ingredient of Molsibeta in the following countries:
International Drug Name Search
Generic Name: Budesonide eent
Class: Corticosteroids
ATC Class: R01AD05
VA Class: NT200
Chemical Name: [11β,16α(R)]-16,17-Butylidene-bis(oxy)-11,21-dihydroxy-pregna-1,4-diene-3,20-dione and 16α,17-[(S)-butylidinebis(oxy)]-11β,21-dihydroxypregna-1,4-diene-3,20-dione
Molecular Formula: C25H34O6
CAS Number: 51333-22-3
REMS:
FDA approved a REMS for budesonide to ensure that the benefits of a drug outweigh the risks. The REMS may apply to one or more preparations of budesonide and consists of the following: communication plan. See the FDA REMS page () or the ASHP REMS Resource Center ().
Synthetic non-halogenated corticosteroid.1 16
Symptomatic treatment of seasonal or perennial allergic rhinitis.1 7 8 9 12 13 14 15 16 17 18 19
For therapeutic effectiveness, use at regular intervals.1
Administer by nasal inhalation using a metered-dose pump spray.1
Shake inhaler gently immediately prior to use.1 17
Prior to initial use, the metered-dose pump spray must be primed with 8 actuations.1 10
If spray pump is not used for 2 consecutive days, partially prime (1 actuation or until a fine spray is observed).1 17 If the spray pump is not used for more than 14 days, rinse the applicator and reprime with 2 sprays or until a fine spray appears.1 Rinse the applicator when not used for more than 14 days.1 17
Clear nasal passages prior to administration.a
Tilt the head slightly forward, insert the spray tip into one nostril, and point the tip toward the back of the nose.a Pump the drug into one nostril while holding the other nostril closed and concurrently inspire through the nose.a Repeat this procedure for the other nostril.a
After priming, nasal spray pump delivers about 32 mcg of budesonide per metered spray and about 120 metered doses per 8.6-g container.1 10
Titrate dosage to the lowest possible effective level.1 (See Pediatric Use under Cautions.)
Children 6–11 years of age: initially, 32 mcg (1 spray) in each nostril once daily (64 mcg total).1 17 May be increased to 64 mcg (2 sprays) in each nostril once daily (128 mcg total).1
Children ≥12 years of age: initially, 32 mcg (1 spray) in each nostril once daily (64 mcg total).1 17 May be increased to 128 mcg (4 sprays) in each nostril once daily (256 mcg total).1
Children 6–11 years of age: initially, 32 mcg (1 spray) in each nostril once daily (64 mcg total).1 17 May be increased to 64 mcg (2 sprays) in each nostril once daily (128 mcg total).1
Children ≥12 years of age: initially, 32 mcg (1 spray) in each nostril once daily (64 mcg total).1 17 May be increased to 128 mcg (4 sprays) in each nostril once daily (256 mcg total).1
Initially, 32 mcg (1 spray) in each nostril once daily (64 mcg total).1 17 May be increased to 128 mcg (4 sprays) in each nostril once daily (256 mcg total).1
Initially, 32 mcg (1 spray) in each nostril once daily (64 mcg total).1 17 May be increased to 128 mcg (4 sprays) in each nostril once daily (256 mcg total).1
Children 6–11 years of age: maximum 128 mcg (2 sprays in each nostril) once daily.1
Children ≥12 years of age: maximum 256 mcg (4 sprays in each nostril) once daily.1
Children 6–11 years of age: maximum 128 mcg (2 sprays in each nostril) once daily.1
Children ≥12 years of age: maximum 256 mcg (4 sprays in each nostril) once daily.1
Maximum 256 mcg (4 sprays in each nostril) once daily.1
Maximum 256 mcg (4 sprays in each nostril) once daily.1
No specific dosage recommendations at this time.1
No specific dosage recommendations at this time.1
No specific dosage recommendations at this time.1
Known hypersensitivity to budesonide or any ingredient of the formulation.1
Possible corticosteroid withdrawal symptoms (e.g., joint pain, muscular pain, lassitude, depression), acute adrenal insufficiency, or severe symptomatic exacerbation of asthma or other clinical conditions if prolonged systemic corticosteroid therapy is replaced with topical corticosteroid therapy; careful monitoring recommended.1
Use particular caution in patients with associated asthma or other conditions that may be exacerbated by too rapid a reduction in systemic corticosteroid dosage.1
Increased susceptibility to infections in patients who are taking immunosuppressant drugs.1 Certain infections (e.g., varicella [chickenpox], measles) can be serious or even fatal in such patients, particularly in children.1
Exposure to varicella and measles should be avoided in previously unexposed patients.1 If exposure to varicella (chickenpox) or measles occurs in susceptible patients, consider administering varicella zoster immune globulin (VZIG) or immune globulin (IG) respectively.1 10 Consider treatment with an antiviral agent if varicella develops.1
Rarely, immediate or delayed hypersensitivity reactions may occur.1 16 Wheezing reported very rarely.1
Possible growth suppression in children and adolescents.1 20 (See Pediatric Use under Cautions.)
Excessive intranasal dosages or use in patients who are particularly sensitive to corticosteroid effects may increase risk of systemic corticosteroid effects (e.g., hypercorticism and adrenal suppression).1
To minimize the systemic effects, titrate dosage to the lowest possible effective level;1 avoid use of higher than recommended dosages.1 If systemic effects occur, slowly reduce dosage and discontinue drug.1
Rarely, localized candidal infections of the nose and/or pharynx have been reported.1 Local treatment of such infections and/or discontinuance of intranasal therapy may be required.1
Rarely, nasal septum perforation and increased intraocular pressure (IOP) have been reported.1
Periodically examine nasal passages for mucosal changes during long-term therapy (several months or longer).1
Use not recommended in patients with recent nasal septal ulcers, nasal surgery, or nasal trauma until healing has occurred.1
Use with caution, if at all, in patients with clinical or asymptomatic Mycobacterium tuberculosis infection of the respiratory tract; in untreated fungal, bacterial, or systemic viral infections; or ocular herpes simplex infections.1
Category B.1 a
Use during pregnancy may result in hypoadrenalism in infants;1 a monitor these infants carefully.1 a
Not known whether budesonide is distributed into milk.1 Caution if used in nursing women.1
Safety and efficacy not established in children <6 years of age.1
Intranasal corticosteroids may reduce growth velocity in pediatric patients.1 Routine monitoring of growth (e.g., via stadiometry) recommended.1 Titrate dosage to the lowest possible effective level.1
No overall substantial differences in safety and efficacy relative to younger patients.1 However, possible increased sensitivity to the drug.1 Frequency of epistaxis may increase with age.1
Possible decreased clearance and increased systemic availability.1
Pharmacokinetics not studied in patients with renal impairment.1
Epistaxis, pharyngitis, bronchospasm, cough, nasal irritation.1
Metabolized by CYP3A4 isoenzyme.1
Potential pharmacokinetic interaction (increased plasma budesonide concentrations) with concomitant use of CYP3A4 isoenzyme inhibitors.1
Inhibitors of the CYP2C19 isoenzyme do not appear to affect the pharmacokinetics of oral budesonide.1
Drug | Interaction |
---|---|
Cimetidine | Decreased budesonide clearance and increased oral bioavailability1 |
Clarithromycin | Increased plasma budesonide concentrations1 |
Erythromycin | Increased plasma budesonide concentrations1 |
Itraconazole | Increased plasma budesonide concentrations1 |
Ketoconazole | Increased plasma budesonide concentrations1 |
Omeprazole | No apparent pharmacokinetic interaction1 |
Relatively well absorbed following intranasal inhalation.1 Following intranasal administration, approximately 34% of a dose reaches systemic circulation.1 Mean peak plasma budesonide concentrations are attained in about 0.7 hours.1
Nasal symptoms improve within 8–12 hours following initiation of therapy.1 7 About 50–66% of the total symptomatic relief is evident within 1–2 days after treatment initiation.1 May require about 2 weeks of therapy for optimum effectiveness.1
Children have plasma drug concentrations approximately twice those observed in adults due to differences in weight.1
Distributes into red blood cells.1 Not known whether the drug crosses the placenta or distributes into breast milk; however, other corticosteroids are distributed into breast milk.1
85-90%.1 Little to no binding to glucocorticosteroid binding globulin.1
Rapidly metabolized to metabolites of low corticosteroid potency by CYP3A4.1
Excreted in urine (66%) and feces (33%) as metabolites.1
2–3 hours.1
Hepatic impairment may affect elimination of corticosteroids by increasing the systemic availability of oral budesonide.1 Intranasally applied budesonide not studied in such patients.1
20–25°C; do not freeze.1 Protect from light.1
Potent glucocorticoid and weak mineralocorticoid activity.1
Decreases the nasal reactivity to allergens and decreases release of inflammatory mediators1 4 and proteolytic enzymes.4
Reduces the number of certain mediator cells (basophils,5 15 eosinophils,1 5 15 T-helper cells,6 mast cells,1 4 and neutrophils)1 5 in the nasal mucosa.
Importance of providing patient a copy of the manufacturer's patient information.1 17
Importance of understanding proper storage, preparation, and administration techniques.1 Importance of shaking container gently prior to each use.1 Importance of avoiding spraying drug into the eyes.1 17
Advise patients that containers of budesonide nasal spray should be discarded after 120 actuations.1
Importance of regular use to obtain therapeutic effectiveness.1 Importance of not exceeding prescribed dosage.1
Advise that the drug usually will provide symptomatic relief within 2 days, but 2 weeks of continuous therapy usually are required for optimum effects.1
Importance of informing clinician if symptoms worsen or fail to improve within 2 weeks.1
Importance of advising clinician if recurrent epistaxis or nasal septum discomfort occurs.1
Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs.1
Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed.1
Importance of informing patients of other important precautionary information. (See Cautions.)
Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.
In 2002, the manufacturer decided to gradually phase out budesonide nasal aerosol (Rhinocort)2 from the US market.3 AstraZeneca will continue to manufacture budesonide nasal spray (Rhinocort Aqua) that unlike budesonide nasal aerosol does not contain fluorocarbons which have been associated with excessive drying of the nasal mucosa in some patients.11
Routes | Dosage Forms | Strengths | Brand Names | Manufacturer |
---|---|---|---|---|
Nasal | Suspension, for intranasal use only | 32 mcg/metered spray | Rhinocort Aqua Nasal Spray | AstraZeneca |
This pricing information is subject to change at the sole discretion of DS Pharmacy. This pricing information was updated 10/2011. Actual costs to patients will vary depending on the use of specific retail or mail-order locations and health insurance copays.
Rhinocort Aqua 32MCG/ACT Suspension (ASTRAZENECA LP): 9/$115.99 or 26/$329.99
This report on medications is for your information only, and is not considered individual patient advice. Because of the changing nature of drug information, please consult your physician or pharmacist about specific clinical use.
The American Society of Health-System Pharmacists, Inc. and Drugs.com represent that the information provided hereunder was formulated with a reasonable standard of care, and in conformity with professional standards in the field. The American Society of Health-System Pharmacists, Inc. and Drugs.com make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information and specifically disclaims all such warranties. Users are advised that decisions regarding drug therapy are complex medical decisions requiring the independent, informed decision of an appropriate health care professional, and the information is provided for informational purposes only. The entire monograph for a drug should be reviewed for a thorough understanding of the drug's actions, uses and side effects. The American Society of Health-System Pharmacists, Inc. and Drugs.com do not endorse or recommend the use of any drug. The information is not a substitute for medical care.
AHFS Drug Information. © Copyright, 1959-2011, Selected Revisions October 27, 2011. American Society of Health-System Pharmacists, Inc., 7272 Wisconsin Avenue, Bethesda, Maryland 20814.
1. AstraZeneca. Rhinocort Aqua (budesonide nasal spray) prescribing information. Wilmington, DE; 2001 Oct.
2. AstraZeneca. Rhinocort (budesonide nasal inhaler) prescribing information (dated 2001 Apr). In: Physicians' desk reference. 56th ed. Montvale, NJ: Medical Economics Company Inc; 2002:640-2.
3. Anon. Dear Pharmacist letter concerning discontinuance of the manufacture of Rhinocort (budesonide nasal inhaler). Wilmington, DE: AstraZeneca; 2002 Nov 15.
4. Meltzer EO, Jalowayski AA, Field EA et al. Intranasal fluticasone propionate reduces histamine and tryptase in the mucosa of allergic rhinitis patients. J Allergy Clin Immunol. 1993; 91:298.
5. Bryson HM, Faulds D. Intranasal fluticasone propionate: a review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in allergic rhinitis. Drugs. 1992; 43:760-75. [IDIS 359172] [PubMed 1379151]
6. Masuyama K, Jacobson MR, Rak S et al. Topical glucocorticosteroid (fluticasone propionate) inhibits cells expressing cytokine mRNA for interleukin-4 in the nasal mucosa in allergen-induced rhinitis. Immunology. 1994; 82:192- 9. [PubMed 7927488]
7. Fokkens WJ, Cserhati E, dos Santos JM et al. Budesonide aqueous nasal spray is an effective treatment in children with perennial allergic rhinitis, with an onset of action within 12 hours. Ann Allergy Asthma Immunol. 2002; 89:279-84. [IDIS 486624] [PubMed 12269648]
8. Ciprandi G, Canonica WG, Grosclaude M et al. Effects of budesonide and fluticasone propionate in a placebo-controlled study on symptoms and quality of life in seasonal allergic rhinitis. Allergy. 2002; 57:586-91. [PubMed 12100298]
9. Bende M, Carrillo T, Vona I et al. A randomized comparison of the effects of budesonide and mometasone furoate aqueous nasal sprays on nasal peak flow rate and symptoms in perennial allergic rhinitis. Ann Allergy Asthma Immunol. 2002; 88:617-23. [IDIS 482210] [PubMed 12086370]
10. AstraZeneca, Wilmington, DE: Personal communication.
11. Mygind N, Clark TJH. Topical steroid treatment for asthma and rhinitis. London: Bailliere Tindall; 1980:89,91,152,159,172.
12. Andersson M, Svensson C, Persson C et al. Dose-dependent effects of budesonide agueous nasal spray on symptoms in a daily nasal allergen challenge model. Ann Allergy Asthma Immunol. 2000; 85:279-83. [IDIS 454624] [PubMed 11061470]
13. Day J, Carrillo T. Comparison of the efficacy of budesonide and fluticasone propionate aqueous nasal spray for once daily treatment of perennial allergic rhinitis. J Allergy Clin Immunol. 1998; 102(6 Part 1):902-8. [IDIS 424214] [PubMed 9847429]
14. Creticos P, Fireman P, Settipane G et al, for the Rhinocort Aqua Study Group. Intranasal budesonide aqueous pump spray (Rhinocort Aqua) for the treatment of seasonal allergic rhinitis. Allergy Asthma Proc. 1998;19:285-94.
15. Meltzer EO. Clinical and antiinflammatory effects of intranasal budesonide aqueous pump spray in the treatment of perennial allergic rhinitis. Ann Allergy Asthma Immunol. 1998; 81:128-34. [IDIS 412928] [PubMed 9723557]
16. Brogden RN, McTavish D. Budesonide: an updated review of its pharmacological properties, and therapeutic efficacy in asthma and rhinitis. Drugs. 1992;44:375-407.
17. AstraZeneca. How to use Rhinocort Aqua. Wilmington, DE; April 2002. From AstraZeneca website (). Accessed 2003 March 4.
18. Yanez A, Rodrigo GJ. Intranasal corticosteroids versus topical H1 receptor antagonists for the treatment of allergic rhinitis: a systematic review with meta-analysis. Ann Allergy Asthma Immunol. 2002; 89:479-84. [IDIS 490491] [PubMed 12452206]
19. Galant SP, Wilkinson R. Clinical prescribing of allergic rhinitis medication in the preschool and young school-age child: what are the options? BioDrugs. 2001; 15:453-63.
20. Pedersen S. Assessing the effect of intranasal steroids on growth. J Allergy Clin Immunol. 2001; 108(1 Suppl):S40-4. [IDIS 467845] [PubMed 11449205]
a. AstraZeneca. Rhinocort Aqua (budesonide nasal spray) prescribing information. Wilmington, DE; 2004 Aug.