People who use the drug Qualaquin to treat or prevent nighttime leg cramps may be at risk for serious and life-threatening reactions, according to the Food and Drug Administration (FDA).
Qualaquin (quinine sulfate) is FDA-approved only to treat a certain type of malaria (uncomplicated malaria) caused by the parasite Plasmodium falciparum.This infection, which is rare in the United States, is found mainly in travelers who have been to countries where malaria occurs.
However, most of Qualaquin’s use in the U.S. is for the treatment or prevention of nighttime leg cramps—a use not approved by FDA.
FDA has received reports of side effects after people used Qualaquin to prevent or treat leg cramps or restless leg syndrome. Side effects included serious and life-threatening reactions in 38 reports.
Of these 38 reports, there were 24 blood-related reactions, including a severe lowering of platelets in the blood. Some of the blood-related side effects resulted in permanent kidney damage, hospitalization, and two deaths.
If you take Qualaquin for nighttime leg cramps, you should discuss other treatment options with your health care professional.
Contact your health care professional immediately if you experience easy bruising, severe nose bleeding, blood in your urine or stool, bleeding gums, or the appearance of unusual purple, brown, or red spots on your skin.
Read the medication guide given to you at the pharmacy when you pick up a prescription for Qualaquin.
As part of a risk management plan, FDA requires that patients receive a medication guide at the pharmacy when they pick up a prescription for Qualaquin. The medication guide explains what the drug is and is not approved for, as well as its potential side effects.