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For your pediatric patients aged 12 to 17 with GERD


Percentage of patients with treatement-related adverse events

               (n=148)

Data from a multicenter, randomized, double-blind, parallel-group study of patients aged 12 to 17 years with clinically diagnosed GERD treated with NEXIUM 20 mg or NEXIUM 40 mg once daily for up to 8 weeks.

NEXIUM:

Safety data
  • NEXIUM is approved for the short-term treatment (up to 8 weeks) of GERD in patients aged 12 to 17 years.
  • Safety and effectiveness for the treatment of symptomatic GERD in patients less than 12 years of age have not been established. Safety and effectiveness for other pediatric uses have not been established.
 
Pecentage of patients with symptomatic improvement by week 8

               (n=94)

Secondary endpoint based on symptomatic improvement in a subgroup of 94 patients with moderate-to-severe symptoms of GERD at baseline from a multicenter, randomized, double-blind, parallel-group study evaluating safety and tolerability of NEXIUM in 149 patients aged 12 to 17 years with GERD treated once daily with NEXIUM 20 mg or NEXIUM 40 mg for up to 8 weeks. Symptomatic improvement defined as improvement by at least 1 grade in the Physicians Global Assessment score for those with moderate-to-severe GERD.

Data on file, DA-NEX-81.

Symptom relief in patients aged 12 to 17 years

The use of NEXIUM in adolescents is supported by extrapolation of results, already included in the approved labeling, from adequate and well-controlled studies that supported the approval of NEXIUM for adults and safety and pharmacokinetic studies in patients aged 12 to 17 years.

  • NEXIUM 20 mg and NEXIUM 40 mg are the FDA-approved doses for the short-term treatment (up to 8 weeks) of GERD in patients aged 12 to 17 years.

How would you treat this patient?
View pediatric patient profile.




Important Information

Approved Uses

Healing of EE
NEXIUM (esomeprazole magnesium) is indicated for the short-term treatment (4 to 8 weeks) in the healing and symptomatic resolution of diagnostically-confirmed erosive esophagitis.

For those patients who have not healed after 4-8 weeks of treatment, an additional 4-8 week course of NEXIUM may be considered.

Maintenance of EE Healing
NEXIUM is indicated for the maintenance of healing of erosive esophagitis. Controlled studies do not extend beyond 6 months.

Symptomatic GERD
NEXIUM is indicated for treatment of heartburn and other symptoms associated with GERD.

Pathological Hypersecretory Conditions
NEXIUM is indicated for the long-term treatment of pathological hypersecretory conditions. Dosage regimens should be adjusted to individual patient needs.

Pediatric Use
NEXIUM is approved for the short-term treatment (up to 8 weeks) of GERD in patients aged 12 to 17 years. Safety and effectiveness for the treatment of symptomatic GERD in patients less than 12 years of age have not been established. Safety and effectiveness for other pediatric uses have not been established.

I.V. Indication
NEXIUM I.V. for Injection is indicated for the short-term treatment (up to 10 days) of GERD adult patients with a history of erosive esophagitis as an alternative to oral therapy in patients when therapy with NEXIUM Delayed-Release Capsules is not possible or appropriate.

When oral therapy is possible or appropriate, intravenous therapy with NEXIUM I.V. for Injection should be discontinued and the therapy should be continued orally.

 

Important Safety Information
NEXIUM and NEXIUM I.V. are contraindicated in patients with known hypersensitivity to any component of the formulation or to substituted benzimidazoles.

The most frequently reported adverse events with NEXIUM include headache, diarrhea, and abdominal pain. Injection site reactions have also been reported with NEXIUM I.V.

In patients aged 12 to 17 years, the most frequently reported adverse events with NEXIUM include headache, diarrhea, abdominal pain, and nausea.

Atrophic gastritis has been noted occasionally in gastric corpus biopsies from patients treated long-term with omeprazole, of which NEXIUM is an enantiomer.

As with all PPIs, patients treated concomitantly with warfarin may need to be monitored for increases in INR and prothrombin time. Like other proton pump inhibitors, esomeprazole may interfere with the absorption of drugs where gastric pH is an important determinant of bioavailability (eg, ketoconazole, iron salts, and digoxin).

Concomitant administration of esomeprazole may reduce the plasma levels of atazanavir.

NEXIUM should be used only for the conditions, dosages, and durations specified in the Prescribing Information. Please see full Prescribing Information for NEXIUM.

 
 

NEXIUM and the color purple as applied to the capsule are registered trademarks and Purple Plus is a trademark of the AstraZeneca group of companies.
238402 5/07
Copyright © 2007 AstraZeneca LP. All rights reserved.

This product information is intended for US healthcare professionals only.
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