Dexavit 4 mg/ml injektions-/infusionsvæske, opløsning Danska - danski - Lægemiddelstyrelsen (Danish Medicines Agency)

dexavit 4 mg/ml injektions-/infusionsvæske, opløsning

vital pharma nordic aps - dexamethasonnatriumphosphat - injektions-/infusionsvæske, opløsning - 4 mg/ml

Spikevax (previously COVID-19 Vaccine Moderna) Europska Unija - danski - EMA (European Medicines Agency)

spikevax (previously covid-19 vaccine moderna)

moderna biotech spain, s.l. - single-stranded, 5’-capped messenger rna (mrna) produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacciner - spikevax is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older. spikevax bivalent original/omicron ba. 1 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 years of age and older who have previously received at least a primary vaccination course against covid-19. spikevax bivalent original/omicron ba. 4-5 is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 6 months of age and older.  spikevax xbb. 5 is indicated for active immunisation to prevent covid 19 caused by sars-cov-2 in individuals 6 months of age and older. the use of this vaccine should be in accordance with official recommendations.

RevitaCAM Europska Unija - danski - EMA (European Medicines Agency)

revitacam

zoetis belgium sa - meloxicam - oxicams - hunde - forbedring af inflammation og smerte i både akutte og kroniske muskuloskeletale lidelser hos hunde.

Bemfola Europska Unija - danski - EMA (European Medicines Agency)

bemfola

gedeon richter plc. - follitropin alfa - anovulation - køn hormoner og modulatorer af den genitale system, - in adult women:anovulation (including polycystic ovarian disease, pcod) in women who have been unresponsive to treatment with clomiphene citrate;stimulation of multifollicular development in patients undergoing superovulation for assisted reproductive technologies (art) such as in vitro fertilisation (ivf), gamete intra-fallopian transfer (gift) and zygote intra-fallopian transfer (zift);follitropin alfa in association with a luteinising hormone (lh) preparation is recommended for the stimulation of follicular development in women with severe lh and fsh deficiency. i kliniske forsøg skal disse patienter blev defineret ved en endogen serum lh niveau < 1. 2 ie / l. in adult men:follitropin alfa is indicated for the stimulation of spermatogenesis in men who have congenital or acquired hypogonadotrophic hypogonadism with concomitant human chorionic gonadotrophin (hcg) therapy.

Rekovelle Europska Unija - danski - EMA (European Medicines Agency)

rekovelle

ferring pharmaceuticals a/s - follitropin delta - anovulation - køn hormoner og modulatorer af den genitale system, - kontrolleret ovariestimulation for udviklingen af flere follikler hos kvinder undergår assisterede reproduktive teknologier (art) som en in vitro-befrugtning (ivf) eller intracytoplasmatisk sperm injektion (icsi) cyklus.

Orgalutran Europska Unija - danski - EMA (European Medicines Agency)

orgalutran

n.v. organon - ganirelix - reproductive techniques, assisted; ovulation induction; infertility, female - hypofysiske og hypotalamiske hormoner og analoger - forebyggelse af for tidlig luteiniserende hormonforstyrrelser hos kvinder, der gennemgår kontrolleret ovariehyperstimulering for assisterede reproduktionsteknikker. i kliniske undersøgelser, orgalutran blev brugt med rekombinant human follikel-stimulerende hormon eller corifollitropin alfa, vedvarende follikel stimulerende.

Ovaleap Europska Unija - danski - EMA (European Medicines Agency)

ovaleap

theramex ireland limited - follitropin alfa - anovulation - køn hormoner og modulatorer af den genitale system, - i voksen womenanovulation (herunder polycystisk ovarie syndrom) hos kvinder, der ikke har responderet på behandling med clomifene citrat, stimulering af multifollicular udvikling hos kvinder, der gennemgår superovulation for art (assisted reproductive technologies), såsom in vitro-fertilisering (ivf), gamete intra-fallopian transfer og zygote intra-fallopian transfer;ovaleap i forening med en luteiniserende hormon (lh) forberedelse anbefales til stimulering af follikulært udvikling hos kvinder med alvorlige lh og fsh-mangel. i kliniske forsøg skal disse patienter blev defineret ved en endogen serum lh niveau < 1. 2 iu/l. i voksen menovaleap er indiceret til stimulation af spermatogenese hos mænd, der har medfødt eller erhvervet hypogonadotrop hypogonadisme med samtidig human chorionic gonadotropin (hcg) terapi.

Comirnaty Europska Unija - danski - EMA (European Medicines Agency)

comirnaty

biontech manufacturing gmbh - single-stranded, 5’-capped messenger rna produced using a cell-free in vitro transcription from the corresponding dna templates, encoding the viral spike (s) protein of sars-cov-2 - covid-19 virus infection - vacciner - comirnaty 30 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older.  comirnaty 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty original/omicron ba. 1 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older who have previously received at least a primary vaccination course against covid-19. comirnaty original/omicron ba. 4-5 (15/15 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty original/omicron ba. 4-5 (5/5 micrograms)/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years.  comirnaty original/omicron ba. 4-5 (1. 5/1. 5 micrograms)/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years.  comirnaty omicron xbb. 5 30 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in individuals 12 years of age and older. comirnaty omicron xbb. 5 10 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 10 micrograms/dose dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in children aged 5 to 11 years. comirnaty omicron xbb. 5 3 micrograms/dose concentrate for dispersion for injection is indicated for active immunisation to prevent covid-19 caused by sars-cov-2, in infants and children aged 6 months to 4 years. brug af denne vaccine bør være i overensstemmelse med de officielle anbefalinger.

Ganirelix Gedeon Richter Europska Unija - danski - EMA (European Medicines Agency)

ganirelix gedeon richter

chemical works of gedeon richter plc. (gedeon richter plc.) - ganirelix acetate - reproductive techniques, assisted; ovulation induction; infertility, female - hypofysiske og hypotalamiske hormoner og analoger - prevention of premature luteinising hormone (lh) surges in women undergoing controlled ovarian hyperstimulation (coh) for assisted reproduction techniques (art).