"The US Food and Drug Administration (FDA) is investigating the "rare but serious" risk for slowed or difficult breathing in children 17 and younger treated with the opioid analgesic tramadol.
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Protopam Patient Information including How Should I Take
In this Article
- What is pralidoxime (Protopam)?
- What are the possible side effects of pralidoxime (Protopam)?
- What is the most important information I should know about pralidoxime (Protopam)?
- What should I discuss with my health care provider before receiving pralidoxime (Protopam)?
- How is pralidoxime given (Protopam)?
- What happens if I miss a dose (Protopam)?
- What happens if I overdose (Protopam)?
- What should I avoid after receiving pralidoxime (Protopam)?
- What other drugs will affect pralidoxime (Protopam)?
- Where can I get more information?
What should I discuss with my health care provider before receiving pralidoxime (Protopam)?
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. It is not known whether pralidoxime is harmful to an unborn baby. Tell your doctor if you are pregnant.
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.
How is pralidoxime given (Protopam)?
Pralidoxime is usually given as soon as possible after the onset of poisoning or overdose symptoms. You may need to receive pralidoxime for several days.
Pralidoxime is injected into a muscle, under the skin, or into a vein through an IV. A healthcare provider will give you this injection. Pralidoxime must be given slowly. The IV infusion can take up to 30 minutes to complete.
Your breathing, blood pressure, oxygen levels, kidney function, and other vital signs will be watched closely while you are receiving this medication.
After treatment with pralidoxime, you may be watched for up to 72 hours to make sure the medicine has been effective and you no longer have any effects of the poison or drug overdose.
Additional Protopam Information
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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