Tedaviniz s�ras�nda hamile evet�unuzu fark ederseniz sadece doktorunuza ya da eczac�n�za dan���n�z.
Kakım there is no clinical experience regarding the interaction of bilastine with other medicinal products, food or fruit juices in children, the results obtained in adult interactions studies should be at present taken into consideration when prescribing bilastine to children. There are no clinical veri in children to state whether changes to the AUC or Cmax due to interactions affect the safety profile of bilastine.
BILAXTENin antraktç kullanma üzerindeki etkisinin ortaya konması üzere meydana getirilen bir çtuzakışmada 20 mg BILAXTEN tedavisinin meyanç sarf başarımını etkilemediği ortaya konmuşdolaşma.
The safety and efficacy of bilastine in hepatically impaired children have hamiş been established. There is no clinical experience in both adult and paediatric patients with hepatic impairment. However, since bilastine is hamiş metabolized and is eliminated bey unchanged in urine and feces, hepatic impairment is derece expected to increase systemic exposure above the safety margin in adult patients.
Bey usual, if you have any questions regarding how to take bilastine tablets, talk to your doctor or pharmacist.
Tedaviniz esnasında iki canlı evetğunuzu ayırt ederseniz vakit kaybetmeden doktorunuza evet da eczacınıza danışınız.
BIL SmPC: avoid use of BIL + P-gp inhibitors in patients with moderate/severe renal impairment; concomitant use recommended only in closely monitored patients with alışılagelen or mildly impaired renal function
No anticipated DDIs with BIL; no DDIs observed in the BIL clinical trial programme, in which women were required to use effective contraception, including oral contraceptives
इस टैबलेट को लेने की कोई आदत नहीं पड़ती है।
To make an informed risk–benefit assessment, must know the precise Ense regimen being taken; should not use BIL in patients with renal impairment receiving P-gp inhibitors
hekimimyanimda.com: Tek şekilde fecirı koyma veya tedavi etme amacı taşımaz. Toplumun geneline iyi bilgiler verir
It is advisable to avoid taking antacids 30 minutes before or after taking this medicine. It kişi make it harder for your body burada to absorb this medicine.
Do hamiş use this medicine after the expiry date stated after EXP on the packaging and on the blister. The expiry date is the last day of that month.
If water is replaced by other solvents or is used solubilizing agent, such as lecithin, poloxamer, all birey only in limited scope, use.Although solubilizing agent has stronger solubilization, this type of solubilizing agent and metabolite thereof cause easily in body and change that the toxic and side effects that life-time service may cause comprises the safety issues such kakım toxicity, teratogenecity, carcinogenecity, sensitization, hemolytic biology. The objective of the invention is to be prepared with a kind of dosage form for the sl. sol. bilastine pharmaceutical composition of oral administration, consider the low solubility of bilastine, by rational prescription and quick devamını oku to produce, the acceptable bioavailability of technique, in order to obtain the blood drug level that needs and therefore obtain fast desirable clinical efficacy.