SYNACHTEN DEPOT 1 mg/ml România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

synachten depot 1 mg/ml

mallinckrodt specialty pharmaceuticals ireland ltd - irlanda - tetracosactidum - susp. inj. - 1mg/ml - hormoni ai lobului hipofizar anterior si analogi acth

HEXORALETTEN N 5 mg+1,5 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

hexoraletten n 5 mg+1,5 mg

jntl consumer health (france) s.a.s. - franta - combinatii (chlorhexidinum+benzocainum) - pastile - 5mg+1,5mg - medicamente pentru zona oro-faringiana antiseptice

IRINOTECAN KOANAA 20 mg/ml România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

irinotecan koanaa 20 mg/ml

drehm pharma gmbh - austria - irinotecanum - conc. pt. sol. perf. - 20mg/ml - alte antineoplazice alte antineoplazice

Abevmy Uniunea Europeană - română - EMA (European Medicines Agency)

abevmy

biosimilar collaborations ireland limited - bevacizumab - colorectal neoplasms; breast neoplasms; ovarian neoplasms; fallopian tube neoplasms; peritoneal neoplasms; carcinoma, non-small-cell lung; carcinoma, renal cell; uterine cervical neoplasms - agenți antineoplazici - abevmy in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of adult patients with metastatic carcinoma of the colon or rectum. abevmy in combination with paclitaxel is indicated for first-line treatment of adult patients with metastatic breast cancer. pentru informații suplimentare cu privire la starea receptorului factorului de creștere epidermal uman 2 (her2), vă rugăm să consultați secțiunea 5. abevmy 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 abevmy in combination with capecitabine. pentru informații suplimentare cu privire la starea her2, vă rugăm să consultați secțiunea 5. abevmy, 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. abevmy, 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. abevmy in combination with interferon alfa-2a is indicated for first line treatment of adult patients with advanced and/or metastatic renal cell cancer. abevmy, 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. abevmy, 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. abevmy in combination with paclitaxel, 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. abevmy, 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.

Atostin comprimate filmate 10 mg Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

atostin comprimate filmate 10 mg

orchid healthcare (a division of orchid chemicals & pharmaceuticals ltd) - atorvastatinum - comprimate filmate - 10 mg

Atostin comprimate filmate 20 mg Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

atostin comprimate filmate 20 mg

orchid healthcare (a division of orchid chemicals & pharmaceuticals ltd) - atorvastatinum - comprimate filmate - 20 mg

Atostin comprimate filmate 40 mg Republica Moldova - română - AMDM (Agenţia Medicamentului şi Dispozitivelor Medicale)

atostin comprimate filmate 40 mg

orchid healthcare (a division of orchid chemicals & pharmaceuticals ltd) - atorvastatinum - comprimate filmate - 40 mg

Gefitinib Mylan Uniunea Europeană - română - EMA (European Medicines Agency)

gefitinib mylan

mylan pharmaceuticals limited - gefitinib - carcinom, pulmonar non-celulă mică - antineoplastic agents, protein kinase inhibitors - gefitinib mylan este indicat în monoterapie pentru tratamentul pacienților adulți cu avansat local sau metastatic non‑cancer pulmonar cu celule mici (nsclc), cu activarea mutații egfr‑tk.