DETAILED NOTES ON CO-CODAMOL

Detailed Notes on Co-codamol

Detailed Notes on Co-codamol

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Ja Jums rodas jebkādas blakusparādības, konsultējieties ar savu ārstu vai farmaceitu. Tas attiecas arī uz iespējamajām blakusparādībām, kas nav minētas šajā instrukcijā.

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هى مادة مطهرة وفي الوقت ذاته تعتبر مضاد حيوي للبكتيريا اللاهوائية

Opioids can result in addiction and you could get withdrawal signs and symptoms should you quit having it abruptly. Your prescriber ought to have defined how much time you may be getting it for and when it is suitable to prevent, how To accomplish this properly. What's more, it is made up of paracetamol, A different analgesic to relieve suffering.

Iespējamais risks, lietojot vienlaicīgi ar sedatīvām zālēm, piemēram, benzodiazepīniem vai līdzīgām zālēm

Pacienti rūpīgi jānovēro, vai viņiem nerodas elpošanas nomākuma un sedācijas pazīmes un simptomi. Ļoti ieteicams tellēt pacientus un viņu aprūpētājus par šiem simptomiem (skatīt 4.five. apakšpunktu).

Browse all of this leaflet diligently before you start getting this medicine because it consists of critical information for you personally.

Chances are you'll create a tolerance and habit to co-codamol. This could cause withdrawal signs and symptoms When the drug is stopped.

Lietojot iekšķīgi, paracetamols nelielā daudzumā izdalās mātes pienā. Nav ziņots par nelabvēlīgu ietekmi zīdaiņiem.

headaches - make sure you rest and drink loads of fluids. Will not consume an excessive amount of alcohol. Speak with your medical professional Should the headaches very last extended than each week or are extreme.

Tāpat kā visas zāles, šīs zāles var izraisīt blakusparādības, kaut arī ne visiem tās izpaužas.

If you are not guaranteed if any of the above implement to you personally, check with your physician or pharmacist just before using co-codamol.

The performance of co-codamol can minimize by Citalopram because it can inhibit the conversion from co-codamol to morphine. Another person may demand a bigger dose of co-codamol when using citalopram; this is because unique individuals have different quantities of inhibition and it will not be feasible to forecast how much medication will have to be converted.

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