Keppra
Overview
- About Keppra
At the start of treatment, Keppra also can cause extreme drowsiness, unusual weakness, and coordination difficulties. Bring such symptoms to your doctor's attention. In a few patients, therapy must be stopped or reduced.
This drug has not been tested in children under age 16.
Possible food and drug interactions when taking Keppra
Return to topNo unwanted interactions have been identified to date.
Special information if you are pregnant or breastfeeding
Return to topIn animal tests, Keppra has produced fetal abnormalities. Accordingly, Keppra is recommended for pregnant women only if its potential benefits outweigh the potential risk to the baby. Notify your physician immediately if you are pregnant or plan to become pregnant.
Keppra makes its way into breast milk and could cause serious reactions in a nursing infant. Do not take this drug while nursing.
Recommended dosage for Keppra
Return to topADULTS
For adults and children over 16, the usual starting dosage of Keppra is 500 milligrams twice a day. The dose may be increased every 2 weeks up to a maximum dose of 1,500 milligrams twice a day. If you have kidney disease, your dosage will be lower.
Overdosage
Return to topAny medication taken in excess can have serious consequences. If you suspect an overdose, seek medical attention immediately.
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Symptoms of Keppra overdose may include:
Aggression, agitation, coma, drowsiness, reduced consciousness, slowed breathing








