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Do not use any of the following drugs while you are being treated with pralidoxime:
If possible, before you receive pralidoxime, tell your doctor if you have kidney disease, or if you are allergic to any drugs.
FDA pregnancy category C. This medication may be harmful to an unborn baby.
It is not known whether pralidoxime passes into breast milk or if it could harm a nursing baby.
In an emergency situation, it may not be possible before you are treated with pralidoxime to tell your caregivers if you are pregnant or breast-feeding. However, make sure any doctor caring for your pregnancy or your baby knows that you have received this medication.
This medication is usually given as soon as possible after the poisoning or overdose. You may need to receive pralidoxime for several days.
Pralidoxime is given as an injection into a muscle, under the skin, or through a needle placed into a vein. You will receive this injection in a clinic, hospital, or emergency setting.
After treatment with pralidoxime, you will be watched to make sure the medication has been effective and you no longer have any effects of the poison or drug overdose.
To be sure this medication is helping your condition, your blood will need to be tested. You may also need follow-up appointments after you are released from emergency care. Do not miss any scheduled appointments.
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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