July 23, 2016
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Morrhuate Sodium

"The US Food and Drug Administration (FDA) today approved a drug for children and adults with hemophilia B called albutrepenonacog alfa (Idelvion, CSL Behring), which combines albumin with factor IX to reduce injection frequency.


Morrhuate Sodium

Morrhuate Sodium Side Effects Center

Medical Editor: John P. Cunha, DO, FACOEP

Last reviewed on RxList 4/21/2016

Morrhuate Sodium Injection is a sclerosing agent used for the obliteration of primary varicosed veins that consist of simple dilation with competent valves. Morrhuate sodium injection is available in generic form. Side effects of morrhuate sodium injection include:

  • drowsiness
  • headache
  • burning or cramping sensations
  • blood clot in the lung (pulmonary embolism)
  • severe allergic (anaphylactic) reactions, and
  • injection site reactions

Dosage of morrhuate sodium injection depends on the size and degree of varicosity. The usual adult dose for obliteration of small or medium veins is 50- 100 mg (1-2 mL of the 5% injection). For large veins, 150- 250 (3-5 mL of the injection) is used. Morrhuate sodium injection may interact with other drugs. Tell your doctor all medications and supplements you use. During pregnancy, morrhuate sodium injection should be used only if prescribed. Consult your doctor before breastfeeding.

Our Morrhuate Sodium Injection Side Effects Drug Center provides a comprehensive view of available drug information on the potential side effects when taking this medication.

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.

What is Prescribing information?

The FDA package insert formatted in easy-to-find categories for health professionals and clinicians.

Morrhuate Sodium FDA Prescribing Information: Side Effects
(Adverse Reactions)


No information provided.

Read the entire FDA prescribing information for Morrhuate Sodium (Morrhuate Sodium Injection)

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.

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