Примери за използване на To carbamazepine на Английски и техните преводи на Български
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No change in exposure to carbamazepine or its metabolite carbamazepine-epoxide was noted.
If you have ever shown unusual sensitivity(rash orany other signs of allergy) to carbamazepine or to any other medicines.
Alternatives to carbamazepine should be used where possible for INI resistant patients.
Examples of moderate or strong CYP3A4 inducers include,but are not limited to carbamazepine, rifampicin, phenytoin and St. John's Wort.
Due to carbamazepine inducing effect, a reduction in atazanavir exposure cannot be ruled out.
Other P-gp inducers(including butnot limited to carbamazepine, phenytoin, and St. John's wort) may decrease talazoparib exposure.
Due to carbamazepine inducing effect, a reduction in REYATAZ/ritonavir exposure cannot be ruled out.
If you have ever shown unusual sensitivity(rash orany other signs of allergy) to carbamazepine or to any other medicines?
The patients were randomized to carbamazepine CR or lacosamide, provided as tablets, in a 1:1 ratio.
If you have ever shown unusual sensitivity(rash orany other signs of allergy) to carbamazepine or to any other medicines.
If you are allergic to carbamazepine there is a one in four(25%) chance that you could also have an allergic reaction to oxcarbazepine.
Efficacy of lacosamide as monotherapy was established in a double-blind, parallel group,noninferiority comparison to carbamazepine CR in 886 patients 16 years of age or older with newly or recently diagnosed epilepsy.
Subjects were randomised to carbamazepine and zonisamide received treatment for a duration of up to 24 months depending on response.
Efficacy of lacosamide as monotherapy was established in a double-blind, parallel group,non- inferiority comparison to carbamazepine CR in 886 patients 16 years of age or older with newly or recently diagnosed epilepsy.
If you are allergic to carbamazepine, the chances are approximately 1 in 4(25%) that you could also have an allergic reaction to oxcarbazepine(Trileptal).
Based on the analysis of data from a non-inferiority monotherapy clinical trial comparing lacosamide to carbamazepine controlled release(CR), the most frequently reported adverse reactions(≥10%) for lacosamide were headache and dizziness.
The patients were randomized to carbamazepine CR 400- 1200 mg/day or levetiracetam 1000- 3000 mg/day, the duration of the treatment was up to 121 weeks depending on the response.
Efficacy of levetiracetam as monotherapy was established in a double-blind, parallel group,noninferiority comparison to carbamazepine controlled release(CR) in 576 patients 16 years of age or older with newly or recently diagnosed epilepsy.
Patients who have had hypersensitivity reactions to carbamazepine should be informed that approximately 25% to 30% of them will experience hypersensitivity reactions with oxcarbazepine.
Efficacy of levetiracetam as monotherapy was established in a double-blind, parallel group,noninferiority comparison to carbamazepine controlled release(CR) in 576 patients 16 years of age or older with newly or recently diagnosed epilepsy.
Patients who are hypersensitive to carbamazepine should be told that approximately 25 to 30 percent of these patients may experience hypersensitivity to oxcarbazepine.
With or without secondary generalisation Efficacy of zonisamide as monotherapy was established in a double-blind,parallel group, non-inferiority comparison to carbamazepine prolonged release(PR) in 583 adult subjects with newly diagnosed partial seizures with or without secondary generalised tonic-clonic seizures.
Patients who have exhibited hypersensitivity reactions to carbamazepine should be informed that approximately 25-30% of the patients experience hypersensitivity reactions to oxcarbazepine.
The concurrent use of strong CYP3A inducers, including butnot limited to carbamazepine, phenobarbital, phenytoin, rifampicin, and St. John's wort, should be avoided(see section 4.4).
Patients who have exhibited hypersensitivity reactions to carbamazepine should be informed that approximately 25-30% of these patients may experience hypersensitivity reactions(e.g. severe skin reactions) with Trileptal(see section 4.8).
In patients who have exhibited hypersensitivity reactions to carbamazepine, approximately 25 to 30% may experience hypersensitivity reactions with oxcarbazepine(Trileptal®).
In the monotherapy clinical trial comparing lacosamide to carbamazepine CR, the extent of increase in PR interval was comparable between lacosamide and carbamazepine.
In the monotherapy clinical trial comparing lacosamide to carbamazepine CR, syncope was reported in 7/444(1.6%) lacosamide patients and in 1/442(0.2%) carbamazepine CR patients.
In patients who have exhibited hypersensitivity reactions to carbamazepine approximately 25 to 30% of these patients may experience hypersensitivity reactions with oxcarbazepine(Trileptal®).
Efficacy of zonisamide as monotherapy was established in a double-blind, parallel group,noninferiority comparison to carbamazepine prolonged release(PR) in 583 adult subjects with newly diagnosed partial seizures with or without secondary generalised tonic-clonic seizures.