Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

viatris limited - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 20 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

viatris limited - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 40 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

viatris limited - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 80 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

viatris limited - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 10 mg

Den Europæiske Union - dansk - EMA (European Medicines Agency)

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.

Den Europæiske Union - dansk - EMA (European Medicines Agency)

mylan pharmaceuticals limited - teriflunomide - multipel sklerose, recidiverende-remitterende - immunosuppressiva - teriflunomide mylan is indicated for the treatment of adult patients and paediatric patients aged 10 years and older (body weight > 40 kg) with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 of the smpc for important information on the population for which efficacy has been established).

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

krka sverige ab - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 20 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

krka sverige ab - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 40 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

sandoz a/s - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 80 mg

Danmark - dansk - Lægemiddelstyrelsen (Danish Medicines Agency)

hexal a/s - atorvastatincalcium (trihydrat) - filmovertrukne tabletter - 20 mg