TRELSTAR POWDER FOR SUSPENSION, SUSTAINED-RELEASE Канада - Енглески - Health Canada

trelstar powder for suspension, sustained-release

knight therapeutics inc. - triptorelin (triptorelin pamoate) - powder for suspension, sustained-release - 3.75mg - triptorelin (triptorelin pamoate) 3.75mg - antineoplastic agents

TRELSTAR POWDER FOR SUSPENSION, SUSTAINED-RELEASE Канада - Енглески - Health Canada

trelstar powder for suspension, sustained-release

knight therapeutics inc. - triptorelin (triptorelin pamoate) - powder for suspension, sustained-release - 11.25mg - triptorelin (triptorelin pamoate) 11.25mg - antineoplastic agents

TRELSTAR POWDER FOR SUSPENSION, SUSTAINED-RELEASE Канада - Енглески - Health Canada

trelstar powder for suspension, sustained-release

knight therapeutics inc. - triptorelin (triptorelin pamoate) - powder for suspension, sustained-release - 22.5mg - triptorelin (triptorelin pamoate) 22.5mg - antineoplastic agents

TRIPTODUR- triptorelin kit Сједињене Америчке Државе - Енглески - NLM (National Library of Medicine)

triptodur- triptorelin kit

azurity pharmaceuticals, inc. - triptorelin (unii: 9081y98w2v) (triptorelin - unii:9081y98w2v) - triptorelin 22.5 mg in 2 ml - triptodur is indicated for the treatment of pediatric patients 2 years of age and older with central precocious puberty (cpp). - hypersensitivity: triptodur is contraindicated in individuals with a known hypersensitivity to triptorelin, any other component of the product, or other gnrh agonists or gnrh [see adverse reactions (6.2)] . - pregnancy: triptodur may cause fetal harm [see use in specific populations (8.1)] . risk summary triptodur is contraindicated in women who are pregnant [see contraindications (4)] since expected hormonal changes that occur with triptodur treatment increase the risk for pregnancy loss. available data with triptorelin use in pregnant women are insufficient to determine a drug-associated risk of adverse developmental outcomes. based on mechanism of action in humans and findings of increased pregnancy loss in animal studies, triptodur may cause fetal harm when administered to pregnant women. advise pregnant women of the potential risk to a fetus. the estimated background risk of m

DECAPEPTYL 0.1 Израел - Енглески - Ministry of Health

decapeptyl 0.1

ferring pharmaceuticals ltd - triptorelin acetate - solution for injection - triptorelin acetate 0.1 mg/ml - triptorelin - triptorelin - ivf

DECAPEPTYL DEPOT 11.25 MG Израел - Енглески - Ministry of Health

decapeptyl depot 11.25 mg

ferring pharmaceuticals ltd - triptorelin as embonate - powder and solvent for suspension for injection - triptorelin as embonate 11.25 mg - triptorelin - triptorelin - - lowering of sexual hormones and- treatment of advanced hormone-dependent prostate cancer.

TRIPTORELIN ACETATE Аустралија - Енглески - APVMA (Australian Pesticides and Veterinary Medicines Authority)

triptorelin acetate

vetoquinol australia pty ltd - triptorelin acetate - unknown - triptorelin acetate anthelmintic active 0.0 - active constituent

DECAPEPTYL triptorelin acetate 100 micrograms/1 mL solution for injection in 1mL pre-filled syringe with integrated needle Аустралија - Енглески - Department of Health (Therapeutic Goods Administration)

decapeptyl triptorelin acetate 100 micrograms/1 ml solution for injection in 1ml pre-filled syringe with integrated needle

ferring pharmaceuticals pty ltd - triptorelin acetate, quantity: 100 microgram (equivalent: triptorelin, qty 95.6 microgram/ml) - injection, solution - excipient ingredients: glacial acetic acid; water for injections; sodium chloride - decapeptyl 100 micrograms/1 ml is indicated for down-regulation and prevention of premature luteinising hormone (lh) surges in women undergoing controlled ovarian hyperstimulation for assisted reproductive technologies (art).,in clinical trials decapeptyl 100 micrograms/1 ml has been used in cycles where urinary and recombinant human follicle stimulating hormone (fsh) as well as human menopausal gonadotrophin (hmg) were used for stimulation.

DIPHERELINE triptorelin (as embonate) 22.5 mg powder for suspension vial and water for injections ampoule Аустралија - Енглески - Department of Health (Therapeutic Goods Administration)

diphereline triptorelin (as embonate) 22.5 mg powder for suspension vial and water for injections ampoule

ipsen pty ltd - triptorelin embonate, quantity: 31 mg (equivalent: triptorelin, qty 22.5 mg) - suspension, powder for - excipient ingredients: polyglactin; carmellose sodium; polysorbate 80; mannitol - diphereline is indicated for the treatment of hormone-dependent locally advanced or metastatic prostate cancer.,diphereline 22.5mg 6 month formulation only:,diphereline 22.5 mg is indicated for the treatment of children 2 years and older with central precocious puberty (cpp).

DIPHERELINE triptorelin {as embonate} 11.25mg powder for suspension vial and water for injections ampoule Аустралија - Енглески - Department of Health (Therapeutic Goods Administration)

diphereline triptorelin {as embonate} 11.25mg powder for suspension vial and water for injections ampoule

ipsen pty ltd - triptorelin embonate, quantity: 19.32 mg - injection, diluent for - excipient ingredients: water for injections - diphereline is indicated for the treatment of hormone-dependent locally advanced or metastatic prostate cancer.