USA - engelsk - NLM (National Library of Medicine)

allergan, inc. - triptorelin pamoate (unii: 08an7wa2g0) (triptorelin - unii:9081y98w2v) - triptorelin 3.75 mg in 2 ml - trelstar is indicated for the palliative treatment of advanced prostate cancer [see  clinical studies (14) ]. trelstar is contraindicated in individuals with a known hypersensitivity to triptorelin or any other component of the product, or other gnrh agonists or gnrh [see warnings and precautions (5.1) ]. risk summary based on findings in animal studies and mechanism of action, trelstar can cause fetal harm when administered to a pregnant woman [see clinical pharmacology (12.1) ] . expected hormonal changes that occur with trelstar treatment increase the risk for pregnancy loss. in animal developmental and reproductive toxicology studies, daily administration of triptorelin to pregnant rats during the period of organogenesis caused maternal toxicity and embryo-fetal toxicities, including loss of pregnancy, at doses as low as 0.2, 0.8, and 8 times the estimated human daily dose based on body surface area. advise pregnant patients and females of reproductive potential of the potential risk to the fetus. dat

USA - engelsk - NLM (National Library of Medicine)

actavis pharma, inc. - triptorelin pamoate (unii: 08an7wa2g0) (triptorelin - unii:9081y98w2v) - triptorelin 3.75 mg in 2 ml

USA - engelsk - NLM (National Library of Medicine)

verity pharmaceuticals inc. - triptorelin pamoate (unii: 08an7wa2g0) (triptorelin - unii:9081y98w2v) - trelstar is indicated for the treatment of advanced prostate cancer [see  clinical studies (14) ]. trelstar is contraindicated in individuals with a known hypersensitivity to triptorelin or any other component of the product, or other gnrh agonists or gnrh [see warnings and precautions (5.1) ]. risk summary based on findings in animal studies and mechanism of action, trelstar can cause fetal harm when administered to a pregnant woman [see clinical pharmacology (12.1) ] . expected hormonal changes that occur with trelstar treatment increase the risk for pregnancy loss. in animal developmental and reproductive toxicology studies, daily administration of triptorelin to pregnant rats during the period of organogenesis caused maternal toxicity and embryo-fetal toxicities, including loss of pregnancy, at doses as low as 0.2, 0.8, and 8 times the estimated human daily dose based on body surface area. advise pregnant patients and females of reproductive potential of the potential risk to the fetus. data animal data studies in pregnant rats administered triptorelin at doses of 2, 10, and 100 mcg/kg/day (approximately equivalent to 0.2, 0.8, and 8 times the estimated human daily dose based on body surface area) during the period of organogenesis demonstrated maternal toxicity and embryo-fetal toxicities.  embryo-fetal toxicities consisted of pre-implantation loss, increased resorption, and reduced mean number of viable fetuses at the high dose.  teratogenic effects were not observed in viable fetuses in rats or mice.  doses administered to mice were 2, 20, and 200 mcg/kg/day (approximately equivalent to 0.1, 0.7, and 7 times the estimated human daily dose based on body surface area).     the safety and efficacy of trelstar have not been established in females.  there are no data on the presence of triptorelin in human milk, the effects of the drug on milk production, or the effects of the drug on the breastfed child.  because of the potential for serious adverse reactions in a breastfed child from trelstar, a decision should be made to either discontinue breastfeeding, or discontinue the drug taking into account the importance of the drug to the mother. infertility males based on mechanism of action, trelstar may impair fertility in males of reproductive potential [see clinical pharmacology (12.1)] . safety and effectiveness in pediatric patients have not been established. prostate cancer occurs primarily in an older population.  clinical studies with trelstar have been conducted primarily in patients ≥ 65 years [see  clinical pharmacology (12.3) and clinical studies (14) ]. subjects with renal impairment had higher exposure than young healthy males [see  clinical pharmacology (12.3) ]. subjects with hepatic impairment had higher exposure than young healthy males [see  clinical pharmacology (12.3) ].

Hellas - gresk - Εθνικός Οργανισμός Φαρμάκων

ipsen ΕΤΑΙΡΕΙΑ ΠΑΡΑΣΚΕΥΗΣ ΚΑΙ ΕΜΠΟΡΙΑΣ ΦΑΡΜΑΚΕΥΤΙΚΩΝ ΠΡΟΪΟΝΤΩΝ ΜΟΝΟΠΡΟΣΩΠΗ ΕΤΑΙΡΕΙΑ ΠΕΡΙΟΡΙΣΜΕΝΗΣ ΕΥΘΥΝΗΣ Δ.Τ. ipsen ΜΟΝΟΠΡΟΣΩΠΗ ΕΠΕ Αγίου Δημητρίου 63, 17456 Αλιμος Αττικής 210.9843324 - triptoreline pamoate - pd.s.in.pr (ΚΟΝΙΣ ΚΑΙ ΔΙΑΛΥΤΗΣ ΓΙΑ ΠΑΡΑΣΚΕΥΗ ΕΝΕΣΙΜΟΥ ΕΝΑΙΩΡΗΜΑΤΟΣ ΠΑΡΑΤΕΤΑΜΕΝΗΣ ΑΠΟΔΕΣΜΕΥΣΗΣ) - 11.25mg/vial - triptoreline pamoate 17,8mg - triptorelin

Belgia - nederlandsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ipsen sa-nv - triptorelinepamoaat - eq. triptoreline 11,25 mg - poeder en oplosmiddel voor suspensie voor injectie - 11,25 mg - triptorelinepamoaat - triptorelin

Belgia - engelsk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ipsen sa-nv - triptorelin pamoate 31 mg - eq. triptorelin 22,5 mg - powder and solvent for prolonged-release suspension for injection - 22,5 mg - triptorelin pamoate 31 mg - triptorelin

Taiwan - kinesisk - 衛生福利部食品藥物管理署 (Ministry of Health and Welfare, Food And Drug Administration)

友華生技醫藥股份有限公司 臺北市北投區承德路６段128號13樓 (12397982) - triptorelin pamoate - 凍晶注射劑 - triptorelin pamoate (6818000530) [corresponding to hydrous triptorelin pamoate...5.2mg]mg - triptorelin - 1. 用於晚期攝護腺癌之紓解治療(palliative treatment)。2. 用於子宮內膜異位症之治療。3. 女性不孕症在體外受精及胚胎植入(ivf-et)之輔助治療。4. 與tamoxifen或芳香環酶抑制劑併用，做為完成化療後有高復發風險且荷爾蒙受體陽性早期乳癌的停經前婦女之輔助治療。

Belgia - tysk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ipsen - triptorelin pamoate - pulver und lösungsmittel zur herstellung einer injektionssuspension - 11,25 mg - triptorelin pamoate - triptorelin

Belgia - tysk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ipsen - triptorelin pamoate - pulver und lösungsmittel zur herstellung einer depot-injektionssuspension - 22,5 mg - triptorelin pamoate 31 mg - triptorelin

Belgia - fransk - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

ipsen sa-nv - pamoate de triptoréline - eq. triptoréline 11,25 mg - poudre et solvant pour suspension injectable - 11,25 mg - pamoate de triptoréline - triptorelin