PARACETAMOL STADA rektaalsuposiit Eesti - eesti - Ravimiamet

paracetamol stada rektaalsuposiit

stadapharm gmbh - paratsetamool - rektaalsuposiit - 1000mg 10tk

LISINOPRIL STADA tablett Eesti - eesti - Ravimiamet

lisinopril stada tablett

stadapharm gmbh - lisinopriil - tablett - 20mg 50tk

PARACETAMOL STADA rektaalsuposiit Eesti - eesti - Ravimiamet

paracetamol stada rektaalsuposiit

stadapharm gmbh - paratsetamool - rektaalsuposiit - 500mg 10tk

ISDN AL 20 toimeainet prolongeeritult vabastav kõvakapsel Eesti - eesti - Ravimiamet

isdn al 20 toimeainet prolongeeritult vabastav kõvakapsel

stadapharm gmbh - isosorbiitdinitraat - toimeainet prolongeeritult vabastav kõvakapsel - 20mg 100tk

ARA-CELL 100MG INJEKTION süstelahus/infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

ara-cell 100mg injektion süstelahus/infusioonilahuse kontsentraat

stadapharm gmbh - tsütarabiin - süstelahus/infusioonilahuse kontsentraat - 20mg 1ml 5ml 10tk

Movymia Euroopa Liit - eesti - EMA (European Medicines Agency)

movymia

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.

GEMCITABINE STADA infusioonilahuse kontsentraat Eesti - eesti - Ravimiamet

gemcitabine stada infusioonilahuse kontsentraat

stada arzneimittel ag - gemtsitabiin - infusioonilahuse kontsentraat - 38mg 1ml 26.3ml 1tk

PICOZETTE õhukese polümeerikattega tablett Eesti - eesti - Ravimiamet

picozette õhukese polümeerikattega tablett

stada arzneimittel ag - letrosool - õhukese polümeerikattega tablett - 2,5mg 30tk; 2,5mg 10tk; 2,5mg 100tk

Cegfila (previously Pegfilgrastim Mundipharma) Euroopa Liit - eesti - EMA (European Medicines Agency)

cegfila (previously pegfilgrastim mundipharma)

mundipharma corporation (ireland) limited - pegfilgrastim - neutropeenia - immunostimulants, - neutropeenia ja febriilse neutropeenia esinemissageduse vähendamine ravitud tsütotoksilise kemoteraapia pahaloomulise kasvaja (välja arvatud krooniline müeloidne leukeemia ja müelodüsplastilised sündroomid).

Oyavas Euroopa Liit - eesti - EMA (European Medicines Agency)

oyavas

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.