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Reasons Keppra is used and important information about this medication
Seizures are symptoms of an abnormality in the nerve centers of the brain. They are brief periods of abnormal electric activity in these nerve centers. Seizures may be convulsive or nonconvulsive in nature. During seizure activity, a change in the person’s consciousness, sensory and motor systems, subjective well-being, and objective behavior is present. Seizure can be triggered by fever, head injury, brain tumor, meningitis, hypoglycemia, drug overdose or withdrawal, or even poisoning. Keppra is an anticonvulsant used for the treatment of seizures. The mechanism of action is unknown, but it promises to reduce frequency of seizures and reduce injury from seizure activity. Keppra is used for the control of grand mal seizures, partial-onset seizures, and seizures of the psychomotor, temporal lobe.
Side effects to expect in Keppra therapy include anorexia, asthenia, ataxia, depression, dizziness, headache, infection, nervousness, pain, pharyngitis, rhinitis, somnolence, and vertigo. Other less common adverse effects include accidental injury, agitation, albuminuria, conjunctivitis, constipation, diarrhea, ecchymosis, emotional lability, flu syndrome, gastroenteritis, hostility, increased cough, nervousness, personality disorder, and vomiting. These may be relieved by gradual increases or decreases in dosage. Encourage the patient not to discontinue therapy without first consulting the health care provider. People who are required to work around machinery, drive a car, or perform other duties in which they must remain alert and awake should be cautious. There are side effects to report immediately to the doctor such as hyperglycemia, blood problems, hepatotoxicity, and dermatologic reactions.
Initiating treatment starts at 1000 mg/day, given as twice-daily dosing or 500 mg twice daily, for the treatment of myoclonic and partial-onset seizures in people 12 years or older. The same initial dose is recommended in adults who have primary generalized tonic-clonic seizures. The dose can be increased 1,000 mg per day every 2 weeks to the recommended dose of 3,000 mg daily.
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