Estland - estniska - Ravimiamet

stada arzneimittel ag - dabigatraaneteksilaat - kõvakapsel - 75mg 30tk; 75mg 10tk

Estland - estniska - Ravimiamet

stada arzneimittel ag - itrakonasool - kõvakapsel - 100mg 4tk; 100mg 14tk; 100mg 50tk; 100mg 6tk; 100mg 15tk; 100mg 30tk; 100mg 18tk; 100mg 28tk; 100mg 8tk; 100mg 84tk

Estland - estniska - Ravimiamet

stada arzneimittel ag - ibuprofeen+fenüülefriin - õhukese polümeerikattega tablett - 400mg+10mg 24tk; 400mg+10mg 20tk; 400mg+10mg 10tk; 400mg+10mg 16tk; 400mg+10mg 12tk

Estland - estniska - Ravimiamet

stada arzneimittel ag - tramadool - kõvakapsel - 50mg 50tk; 50mg 30tk; 50mg 20tk; 50mg 10tk

Estland - estniska - Ravimiamet

stada arzneimittel ag - tramadool - rektaalsuposiit - 100mg 5tk

Europeiska unionen - estniska - EMA (European Medicines Agency)

stada arzneimittel ag - bevatsizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - antineoplastilised ained - oyavas in combination with fluoropyrimidine based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. oyavas in combination with paclitaxel is indicated for first line treatment of adult patients with metastatic breast cancer. lisateavet inimese epidermaalse kasvufaktori retseptori 2 (her2) seisundi kohta vt palun 5. jaotisest. oyavas in combination with capecitabine is indicated for first line treatment of adult patients with metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. patients who have received taxane and anthracycline containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with oyavas in combination with capecitabine. her2 staatuse kohta lisateabe saamiseks lugege palun 5. jaotist. oyavas, in addition to platinum based chemotherapy, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non small cell lung cancer other than predominantly squamous cell histology. oyavas, in combination with erlotinib, is indicated for first line treatment of adult patients with unresectable advanced, metastatic or recurrent non squamous non small cell lung cancer with epidermal growth factor receptor (egfr) activating mutations (see section 5. oyavas in combination with interferon alfa 2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. oyavas, in combination with carboplatin and paclitaxel is indicated for the front line treatment of adult patients with advanced (international federation of gynecology and obstetrics (figo) stages iii b, iii c and iv) epithelial ovarian, fallopian tube, or primary peritoneal cancer (see section 5. oyavas, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel, is indicated for treatment of adult patients with first recurrence of platinum sensitive epithelial ovarian, fallopian tube or primary peritoneal cancer who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor–targeted agents. oyavas, in combination with topotecan, or pegylated liposomal doxorubicin is indicated for the treatment of adult patients with platinum resistant recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other vegf inhibitors or vegf receptor targeted agents (see section 5. oyavas, in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum therapy, is indicated for the treatment of adult patients with persistent, recurrent, or metastatic carcinoma of the cervix (see section 5.

Europeiska unionen - estniska - EMA (European Medicines Agency)

stada arzneimittel ag - ranibizumab - wet macular degeneration; macular edema; diabetic retinopathy; diabetes complications - oftalmoloogilised vahendid - ximluci is indicated in adults for:the treatment of neovascular (wet) age-related macular degeneration (amd)the treatment of visual impairment due to diabetic macular oedema (dme)the treatment of proliferative diabetic retinopathy (pdr)the treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch rvo or central rvo)the treatment of visual impairment due to choroidal neovascularisation (cnv).

Estland - estniska - Ravimiamet

stada arzneimittel ag - rivaroksabaan - kõvakapsel - 15mg 30tk; 15mg 28tk

Europeiska unionen - estniska - EMA (European Medicines Agency)

stada arzneimittel ag - teriparatiid - osteoporoos - kaltsiumi homöostaas - movymia on näidustatud täiskasvanutel. osteoporoosi ravi postmenopausis naistel ja meestel, kellel on suurem luumurdude risk. postmenopausaalsetel naistel on selgelt ja selgroogsete luumurdude, kuid mitte puusaluumurdude esinemissageduse märkimisväärne vähenemine. ravi osteoporoosi seostatakse pidevat süsteemset glükokortikoidi ravi naiste ja meeste suurenenud risk luumurdude.

Estland - estniska - Ravimiamet

stada arzneimittel ag - alprasolaam - tablett - 0,5mg 90tk; 0,5mg 28tk; 0,5mg 40tk; 0,5mg 20tk; 0,5mg 84tk; 0,5mg 7tk; 0,5mg 1000tk; 0,5mg 14tk; 0,5mg 21tk; 0,5mg 70tk; 0,5mg 200tk; 0,5mg 80tk; 0,5mg 30tk; 0,5mg 500tk; 0,5mg 100tk; 0,5mg 50tk; 0,5mg 10tk; 0,5mg 250tk