AJ-VINORELBINE SOLUTION Kanada - inglise - Health Canada

aj-vinorelbine solution

agila jamp canada inc - vinorelbine (vinorelbine tartrate) - solution - 10mg - vinorelbine (vinorelbine tartrate) 10mg - antineoplastic agents

Vinorelbine Accord 20 mg soft capsules Iirimaa - inglise - HPRA (Health Products Regulatory Authority)

vinorelbine accord 20 mg soft capsules

accord healthcare ireland ltd. - vinorelbine tartrate - capsule, soft - vinorelbine

Vinorelbine Accord 30 mg soft capsules Iirimaa - inglise - HPRA (Health Products Regulatory Authority)

vinorelbine accord 30 mg soft capsules

accord healthcare ireland ltd. - vinorelbine tartrate - capsule, soft - vinorelbine

Vinorelbine Ebewe Uus-Meremaa - inglise - Medsafe (Medicines Safety Authority)

vinorelbine ebewe

sandoz new zealand limited - vinorelbine tartrate 13.85 mg/ml equivalent to 10 mg/ml of vinorelbine - concentrate for injection - 10 mg/ml - active: vinorelbine tartrate 13.85 mg/ml equivalent to 10 mg/ml of vinorelbine excipient: water for injection - treatment of advanced breast cancer after failure of standard therapy, as a single agent or in combination; and as first-line treatment for advanced non-small cell lung cancer, as a single agent or in combination.

VINORELBINE injection solution concentrate Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

vinorelbine injection solution concentrate

teva parenteral medicines, inc. - vinorelbine tartrate (unii: 253gqw851q) (vinorelbine - unii:q6c979r91y) - vinorelbine 10 mg in 1 ml

VINORELBINE injection Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

vinorelbine injection

ingenus pharmaceuticals, llc - vinorelbine tartrate (unii: 253gqw851q) (vinorelbine - unii:q6c979r91y) - vinorelbine injection is indicated: -   in combination with cisplatin for first-line treatment of patients with locally advanced or metastatic non-small cell lung cancer (nsclc) -   as a single agent for the treatment of patients with metastatic nsclc none risk summary based on findings from animal studies and its mechanism of action [see clinical pharmacology (12.1)], vinorelbine injection can cause fetal harm when administered to a pregnant woman. available human data are insufficient to inform the drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. in animal reproduction studies in mice and rabbits, embryo and fetal toxicity were observed with administration of vinorelbine at doses approximately 0.33 and 0.18 times the human therapeutic dose, respectively (see data). advise pregnant women of the potential risk to a fetus. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies are

Vinorelbine Strides 10mg per ml (1ml vial) Malta - inglise - Medicines Authority

vinorelbine strides 10mg per ml (1ml vial)

strides arcolab international limited unit 4, metro centre, tolpits lane, watford, hertfordshire, wd 189 ss, united kingdom - vinorelbine tartrate - concentrate for solution for infusion - vinorelbine tartrate 10 mg/ml - antineoplastic agents

Vinorelbine Strides 10mg per ml (5ml vial) Malta - inglise - Medicines Authority

vinorelbine strides 10mg per ml (5ml vial)

strides arcolab international limited unit 4, metro centre, tolpits lane, watford, hertfordshire, wd 189 ss, united kingdom - vinorelbine tartrate - concentrate for solution for infusion - vinorelbine tartrate 10 mg/ml - antineoplastic agents