Darunavir Mylan Europska Unija - danski - EMA (European Medicines Agency)

darunavir mylan

mylan pharmaceuticals limited - darunavir - hiv infektioner - antivirale midler til systemisk anvendelse - darunavir, co-administered with low dose ritonavir is indicated in combination with other antiretroviral medicinal products for the treatment of patients with human immunodeficiency virus (hiv-1) infection (see section 4. darunavir mylan 75 mg, 150 mg, 300 mg and 600 mg tablets may be used to provide suitable dose regimens (see section 4. 2):til behandling af hiv-1 infektion i antiretroviral behandling (art)-erfarne voksne patienter, herunder dem, der har været meget forbehandlet. til behandling af hiv-1 infektion hos pædiatriske patienter fra en alder af 3 år og mindst 15 kg kropsvægt. i beslutter at indlede behandling med darunavir co-administreres med en lav dosis ritonavir, forsigtig, bør det overvejes, om den historie behandling af den enkelte patient og de mønstre af mutationer, der er forbundet med forskellige agenter. genotypic or phenotypic testing (when available) and treatment history should guide the use of darunavir (see sections 4. 2, 4. 4 og 5. darunavir co-administreres med en lav dosis ritonavir er indiceret i kombination med andre antiretrovirale lægemidler til behandling af patienter med human immundefekt virus (hiv-1) infektion.  darunavir co-administered with cobicistat is indicated in combination with other antiretroviral medicinal products for the treatment of human immunodeficiency virus (hiv-1) infection in adults and adolescents (aged 12 years and older, weighing at least 40 kg) (see section 4.  darunavir mylan 400 mg and 800 mg tablets may be used to provide suitable dose regimens for the treatment of hiv-1 infection in adult and paediatric patients from the age of 3 years and at least 40 kg body weight who are: antiretroviral therapy (art)-naïve (see section 4.  art-experienced with no darunavir resistance associated mutations (drv-rams) and who have plasma hiv-1 rna < 100,000 copies/ml and cd4+ cell count ≥ 100 cells x 10⁶/l. i beslutter at indlede behandling med darunavir i en sådan kunst-erfarne patienter, genotypiske test bør vejlede i brugen af darunavir (se afsnit 4. 2, 4. 3, 4. 4 og 5.

Azithromycin "Stada" 500 mg filmovertrukne tabletter Danska - danski - Lægemiddelstyrelsen (Danish Medicines Agency)

azithromycin "stada" 500 mg filmovertrukne tabletter

stada arzneimittel ag - azithromycinmonohydrat - filmovertrukne tabletter - 500 mg

Darunavir "Glenmark" 600 mg filmovertrukne tabletter Danska - danski - Lægemiddelstyrelsen (Danish Medicines Agency)

darunavir "glenmark" 600 mg filmovertrukne tabletter

glenmark arzneimittel gmbh - darunavirpropylenglycolat - filmovertrukne tabletter - 600 mg

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

zinforo

pfizer ireland pharmaceuticals - ceftaroline fosamil - community-acquired infections; skin diseases, infectious; pneumonia - antibakterielle midler til systemisk brug, - zinforo is indicated for the treatment of the following infections in neonates, infants, children, adolescents and adults: , complicated skin and soft tissue infections (cssti), community-acquired pneumonia (cap) , consideration should be given to official guidance on the appropriate use of antibacterial agents.

Piperacillin/Tazobactam "Reig Jofre" 2+0,25 g pulver til infusionsvæske, opløsning Danska - danski - Lægemiddelstyrelsen (Danish Medicines Agency)

piperacillin/tazobactam "reig jofre" 2+0,25 g pulver til infusionsvæske, opløsning

laboratorio reig jofre s.a. - piperacillin, tazobactam - pulver til infusionsvæske, opløsning - 2+0,25 g