home > drugs a-z list > kapidex delayed release capsules (dexlansoprazole delayed release capsules) drug center > kapidex delayed release capsules (dexlansoprazole delayed release capsules) drug - overdosage and contraindications

Recommended Topic Related To:

Kapidex

GERD Facts

  • GERD is a condition in which the acidified liquid content of the stomach up into the esophagus.
  • The causes of GERD include an abnormal lower esophageal sphincter, hiatal hernia, abnormal esophageal contractions, and slow emptying of the stomach.
  • GERD may damage the lining of the esophagus, thereby causing inflammation (esophagitis), although usually it does not.
  • The symptoms of uncomplicated GERD are heartburn, regurgitation, and nausea.
  • Complications of GERD include ulcers and strictures of the esophagus, Barrett's esophagus, cough and asthma, throat and laryngeal inflammation, inflammation and infection of the lungs, and collection of fluid in the sinuses and middle ear.
  • Barrett's esophagus is a pre-cancerous condition that requires periodic endoscopic surveillance for the development of cancer.
  • GERD may be diagnosed or evaluate...

Kapidex Delayed Release Capsules

font size

OVERDOSE

There have been no reports of significant overdose of KAPIDEX (dexlansoprazole delayed release capsules) . Multiple doses of KAPIDEX (dexlansoprazole delayed release capsules) 120 mg and a single dose of KAPIDEX (dexlansoprazole delayed release capsules) 300 mg did not result in death or other severe adverse events. Dexlansoprazole is not expected to be removed from the circulation by hemodialysis. If an overdose occurs, treatment should be symptomatic and supportive.

CONTRAINDICATIONS

KAPIDEX (dexlansoprazole delayed release capsules) is contraindicated in patients with known hypersensitivity to any component of the formulation [see DESCRIPTION]. Hypersensitivity and anaphylaxis have been reported with KAPIDEX use [see ADVERSE REACTIONS].

Last reviewed on RxList: 4/14/2010
This monograph has been modified to include the generic and brand name in many instances.

Report Problems to the Food and Drug Administration

 

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.


Women's Health

Find out what women really need.