UM Guidelines
Hyperemesis Gravidarum

Home Care (HC) ORG: M-2195

BCBST modification effective August 29, 2008*

Deleted:
   
 

No deletions were made.


Added to RN Treatment Plan: Treatments and Procedures
   

 Commonly Prescribed Anti-emetics for the Treatment of Hyperemesis Gravidarum

AGENT

IV

IM

PO

PR

SQ

DOSAGE

Doxylamine (Unisom)

   

·

   

25 mg PO HS or 12.5 mg PO BID

Dimenhydrinate (Dramamine)

·

·

·

   

50-100 mg PO Q4H; 50 mg IV/IM Q3-4H

Diphenhydramine (Benadryl)

·

·

·

   

50 mg PO TID/QID; 25-50 mg IM/IV Q2-3H

Meclizine (Antivert)

   

·

   

20-50 mg PO QD

Metoclopramide (Reglan)

·

·

·

 

·

5-10 mg PO/IV/IM QID

Chlorpromazine (Thorazine)

·

·

·

·

 

10-25 mg PO Q4-6H

Prochlorperazine (Compazine)

·

·

·

·

 

5-10 mg PO/IM TID-QID; 10-25 mg PR Q4-6H

Promethazine (Phenergan)

·

·

·

·

 

12.5-25 mg IM/PO Q4-6H; 25 mg PR Q4-6H

Scopolamine Patch (Transderm Scop)

         

Transdermal Patch 1.5 mg: 1 patch applied Q1-3 days

Trimethobenzamide (Tigan)

 

·

·

 

250 mg PO Q6-8H; 100-200 mg IM Q6-8H

Ondansetron (Zofran)

·

·

·

Up to 8 mg IV or PO every 6 hours, not to exceed 32 mg/day.

Additional Information

The use of steroids (e.g., Decadron 4 mg IV, along with other antiemetics) is being used post anesthesia to help control nausea.

SOURCES

BlueCross BlueShield of Tennessee network physicians. April - June 2008.

U. S. Food and Drug Administration. (2000, December). Center for Drug Evaluation and Research. Zofran®. Retrieved February 14, 2003 from http://www.fda.gov/cder/foi/nda/99/20781_Zofran.pdf.

U. S. Food and Drug Administration. (2007, April). Center for Drug Evaluation and Research.  FDA announces that companies must stop marketing suppository products containing trimethobenzamide. Retrieved January 16, 2008 from http://www.fda.gov/bbs/topics/NEWS/2007/NEW01601.html.

 
   

* These guideline(s) have been revised from the Milliman USA Milliman Care Guidelines.  The portions of the guideline(s) which have been revised are identified through the use of [insert: italic, boldface, underlined, etc. as appropriate] text, and Milliman USA has neither reviewed nor approved the modified material.  Any statement to the contrary or association of the modified material with Milliman USA is strictly prohibited. This document has been classified as public information.
The above information only contains the modified portion of the Milliman Care Guideline. If you wish to view the complete Milliman Care Guideline, please contact Milliman USA.