Atrovent 40 mikrogram Inhalationspulver, hård kapsel Szwecja - szwedzki - Läkemedelsverket (Medical Products Agency)

atrovent 40 mikrogram inhalationspulver, hård kapsel

orifarm ab - ipratropiumbromid (monohydrat) - inhalationspulver, hård kapsel - 40 mikrogram - ipratropiumbromid (monohydrat) 42 mikrog aktiv substans; glukos (vattenfri) hjälpämne - ipratropiumbromid

Atrovent 40 mikrogram Inhalationspulver, hård kapsel Szwecja - szwedzki - Läkemedelsverket (Medical Products Agency)

atrovent 40 mikrogram inhalationspulver, hård kapsel

medartuum ab - ipratropiumbromid (monohydrat) - inhalationspulver, hård kapsel - 40 mikrogram - ipratropiumbromid (monohydrat) 42 mikrog aktiv substans; glukos (vattenfri) hjälpämne - ipratropiumbromid

Zoely Unia Europejska - szwedzki - EMA (European Medicines Agency)

zoely

theramex ireland limited - nomegestrol acetat, estradiol - preventivmedel - könshormoner och modulatorer av könsorganen, - oral contraception,.

Atrovent 20 mikrogram/dos Inhalationsspray, lösning Szwecja - szwedzki - Läkemedelsverket (Medical Products Agency)

atrovent 20 mikrogram/dos inhalationsspray, lösning

ebb medical ab - ipratropiumbromid (monohydrat) - inhalationsspray, lösning - 20 mikrogram/dos - ipratropiumbromid (monohydrat) 21 mikrog aktiv substans; etanol, vattenfri hjälpämne

ellaOne Unia Europejska - szwedzki - EMA (European Medicines Agency)

ellaone

laboratoire hra pharma - ulipristal - antikonception, postcoital - könshormoner och modulatorer av könsorganen, , akut p-piller - nödkontrumception inom 120 timmar (fem dagar) av oskyddad samlag eller preventiv misslyckande.

Thalidomide BMS (previously Thalidomide Celgene) Unia Europejska - szwedzki - EMA (European Medicines Agency)

thalidomide bms (previously thalidomide celgene)

bristol-myers squibb pharma eeig - talidomid - multipelt myelom - immunsuppressiva - thalidomide bms in combination with melphalan and prednisone as first line treatment of patients with untreated multiple myeloma, aged >/= 65 years or ineligible for high dose chemotherapy. thalidomide bms is prescribed and dispensed according to the thalidomide celgene pregnancy prevention programme (see section 4.

Comirnaty Unia Europejska - szwedzki - 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. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.

Jcovden (previously COVID-19 Vaccine Janssen) Unia Europejska - szwedzki - EMA (European Medicines Agency)

jcovden (previously covid-19 vaccine janssen)

janssen-cilag international nv - adenovirus type 26 encoding the sars-cov-2 spike glycoprotein (ad26.cov2-s) - covid-19 virus infection - vacciner - jcovden is indicated for active immunisation to prevent covid-19 caused by sars-cov-2 in individuals 18 years of age and older. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.

Vaxzevria (previously COVID-19 Vaccine AstraZeneca) Unia Europejska - szwedzki - EMA (European Medicines Agency)

vaxzevria (previously covid-19 vaccine astrazeneca)

astrazeneca ab - chadox1-sars-cov-2 - covid-19 virus infection - vacciner - vaxzevria is indicated for active immunisation to prevent covid 19 caused by sars cov 2, in individuals 18 years of age and older. användning av detta vaccin bör ske i enlighet med officiella rekommendationer.

Lydisilka Unia Europejska - szwedzki - EMA (European Medicines Agency)

lydisilka

estetra sprl - estetrol monohydrate, drospirenone - contraceptives, oral - könshormoner och modulatorer av könsorganen, - oral preventivmedel. the decision to prescribe lydisilka should take into consideration the individual woman’s current risk factors, particularly those for venous thromboembolism (vte), and how the risk of vte with lydisilka compares with other combined hormonal contraceptives (chcs) (see sections 4. 3 and 4.